U.S. patent application number 14/831199 was filed with the patent office on 2016-02-11 for dosage and administration for preventing cardiotoxicity in treatment with erbb2-targeted immunoliposomes comprising anthracycline chemotherapeutic agents.
The applicant listed for this patent is MERRIMACK PHARMACEUTICALS, INC.. Invention is credited to ELENA GERETTI, BART S. HENDRIKS, STEPHAN KLINZ, KENNETH J. OLIVIER, JR., JOSEPH G. REYNOLDS, THOMAS WICKHAM.
Application Number | 20160038416 14/831199 |
Document ID | / |
Family ID | 46207695 |
Filed Date | 2016-02-11 |
United States Patent
Application |
20160038416 |
Kind Code |
A1 |
REYNOLDS; JOSEPH G. ; et
al. |
February 11, 2016 |
DOSAGE AND ADMINISTRATION FOR PREVENTING CARDIOTOXICITY IN
TREATMENT WITH ERBB2-TARGETED IMMUNOLIPOSOMES COMPRISING
ANTHRACYCLINE CHEMOTHERAPEUTIC AGENTS
Abstract
Methods for determining dosage of HER2-targeted
anthracycline-containing immunoliposomes are disclosed, as are
methods of treating cancer patients with HER2-positive tumors using
dosages so determined. Upon administration, the dosages share the
low cardiotoxicity profile of standard dosages of
non-immunoliposomal (untargeted), anthracycline-containing
liposomes.
Inventors: |
REYNOLDS; JOSEPH G.; (NORTH
ANDOVER, MA) ; OLIVIER, JR.; KENNETH J.; (ATTLEBORO,
MA) ; HENDRIKS; BART S.; (BELMONT, MA) ;
WICKHAM; THOMAS; (GROTON, MA) ; KLINZ; STEPHAN;
(NORWOOD, MA) ; GERETTI; ELENA; (CAMBRIDGE,
MA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
MERRIMACK PHARMACEUTICALS, INC. |
CAMBRIDGE |
MA |
US |
|
|
Family ID: |
46207695 |
Appl. No.: |
14/831199 |
Filed: |
August 20, 2015 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
13912167 |
Jun 6, 2013 |
|
|
|
14831199 |
|
|
|
|
PCT/US2011/063623 |
Dec 6, 2011 |
|
|
|
13912167 |
|
|
|
|
61449602 |
Mar 4, 2011 |
|
|
|
61420688 |
Dec 7, 2010 |
|
|
|
61420225 |
Dec 6, 2010 |
|
|
|
Current U.S.
Class: |
424/450 ;
514/34 |
Current CPC
Class: |
G01N 33/566 20130101;
A61P 7/00 20180101; A61K 9/0019 20130101; A61K 47/6851 20170801;
A61K 31/7042 20130101; A61K 9/127 20130101; A61K 47/42 20130101;
A61K 31/704 20130101; A61P 17/00 20180101; A61P 15/00 20180101;
C07K 16/32 20130101; A61K 9/1272 20130101; A61P 35/00 20180101;
A61K 47/6913 20170801 |
International
Class: |
A61K 9/127 20060101
A61K009/127; A61K 9/00 20060101 A61K009/00; A61K 31/704 20060101
A61K031/704 |
Claims
1-20. (canceled)
21. An injectable pharmaceutical composition comprising an
immunoliposome encapsulating about 1.8 to about 2.2 mg/mL of
doxorubicin, the immunoliposome having a diameter of approximately
75-110 nm, wherein the immunoliposome comprises an antibody
fragment that binds to HER2 and the immunoliposome is internalized
into a cell having at least 200,000 HER2 receptors per cell to a
greater degree than into a cell having less than 200,000 HER2
receptors per cell, wherein the degree of internalization is
determined after treatment of the cell with 15 .mu.g/ml of the
immunoliposome for 180 minutes.
22. The composition of claim 21, wherein the pharmaceutical
composition is formulated for intravenous administration.
23. The composition of claim 21, wherein the immunoliposome
comprises hydrogenated soy phosphatidylcholine (HSPC), cholesterol
and polyethylene glycol-disteroylphosphoethanolamine (PEG-DSPE) at
a molar ratio of 3:2:0.3, the liposome having a. a total of about
10 mmol/L of lipid and a total of polyethyleneglycol-derivatized
phosphatidylethanolamine in the amount of approximately one
polyethyleneglycol (PEG) molecule for 200 phospholipid molecules,
of which approximately one PEG molecule for each 1780 phospholipid
molecules bears at its end an F5 single-chain Fv antibody fragment
that binds to HER2 (DSPE-PEG-F5), wherein F5 is an anti-ErbB2
(anti-HER2) scFv antibody fragment (encoded by ATCC plasmid deposit
designation PTA-7843); b. a HSPC lipid concentration of about 40
mmol/L; c. a total of about 0.16 to about 0.30 mg/mL DSPE-PEG-F5 d.
a total of about 130 to about 170 g doxorubicin/mol phospholipid;
and e. about 12 to about 22 g DSPE-PEG-F5/mol phospholipid.
24. The composition of claim 23, comprising 10 mM/L histidine-HCl
as a buffer (pH 6.5), and 10% sucrose.
25. A doxorubicin liposome formulation comprising doxorubicin
encapsulated in a unilamellar lipid bilayer vesicle of
approximately 75-110 nm in diameter composed of
phosphatidylcholine, cholesterol, and a
polyethyleneglycol-derivatized phosphatidylethanolamine in the
amount of approximately one PEG molecule for 200 phospholipid
molecules, of which approximately one PEG chain for each 1780
phospholipid molecules bears at its end an F5 single-chain Fv
antibody fragment that binds to HER2, wherein F5 is an anti-ErbB2
(anti-HER2) scFv antibody fragment (encoded by ATCC plasmid deposit
designation PTA-7843).
26. The formulation of claim 25, wherein the unilamellar lipid
bilayer comprises HSPC:cholesterol:PEG-DSPE at a molar ratio of
3:2:0.3.
27. The formulation of claim 26, wherein the total HSPC lipid
concentration of the liposome is about 40 mmol/L.
28. The formulation of claim 25, comprising a total of about 10
mmol/L of lipid, and about 2 mg/mL of doxorubicin.
29. The formulation of claim 25, comprising a total of about 1.8 to
about 2.2 mg/mL of doxorubicin in liposomes that contain about 0.16
to about 0.30 mg/mL DSPE-PEG-F5.
30. The formulation of claim 25, comprising about 130 to about 170
g doxorubicin/mol phospholipid and about 12 to about 22 g
DSPE-PEG-F5/mol phospholipid.
31. The formulation of claim 25, comprising 10 mM/L histidine-HCl
as a buffer (pH 6.5), and 10% sucrose to maintain isotonicity.
32. The formulation of claim 27, formulated for intravenous
injection.
33. A pharmaceutical composition comprising an immunoliposome
encapsulating about 1.8 to about 2.2 mg/mL of doxorubicin, the
immunoliposome having a diameter of approximately 75-110 nm, and is
composed of phosphatidylcholine, cholesterol, and a
polyethyleneglycol-derivatized phosphatidylethanolamine in the
amount of approximately one PEG molecule for 200
phosphatidylethanolamine phospholipid molecules, and wherein a
plurality of the immunoliposomes bear on average about 45 F5
anti-ErbB2 (anti-HER2) scFv antibody fragments per immunoliposome,
the scFv antibody fragments being encoded by ATCC plasmid deposit
designation PTA-7843.
34. The composition of claim 33, comprising 10 mM/L histidine-HCl
as a buffer (pH 6.5), and 10% sucrose.
35. The composition of claim 33, wherein the composition is
formulated for intravenous administration.
Description
CROSS-REFERENCES TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 13/912,167, filed Jun. 6, 2013, which is a
continuation of PCT Application No.: PCT/US2011/063623, filed Dec.
6, 2011, which claims the benefit under 35 U.S.C. .sctn.119 to U.S.
Provisional Patent Application No(s). 61/420,225, filed Dec. 6,
2010; 61/420,688, filed Dec. 7, 2010; and 61/449,602, filed Mar. 4,
2011. The contents of each of the foregoing applications are
incorporated herein by reference in their entirety.
STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSORED
RESEARCH AND DEVELOPMENT
[0002] NOT APPLICABLE
REFERENCE TO A "SEQUENCE LISTING," A TABLE, OR A COMPUTER PROGRAM
LISTING APPENDIX SUBMITTED ON A COMPACT DISK
[0003] NOT APPLICABLE
BACKGROUND OF THE INVENTION
[0004] Anthracyclines have been an effective backbone of cancer
therapies for decades. Despite consistent clinical benefit observed
with anthracycline-based regimens in breast cancer, significant
toxicities such as acute and/or chronic cardiac dysfunction
associated with such treatment have limited more expansive
therapeutic use. While liposomal doxorubicin formulations have
succeeded in reducing cardiotoxicity to some extent, they have
failed to demonstrate clear-cut efficacy advantages and can involve
other toxicities such as palmar-plantar erythrodysesthesia (hand
foot syndrome). In an effort to improve upon efficacy of currently
available anthracyclines, a new immunoliposomal formulation,
MM-302, has been prepared that targets doxorubicin to HER2
(ErbB2)-overexpressing tumor cells. Antibody fragments that bind to
HER2 without blocking HER2-mediated signaling are coupled to the
outer surface of pegylated liposomal doxorubicin.
[0005] Doxorubicin (dox) is an anthracyline chemotherapeutic agent
used to treat a variety of cancers. The use of doxorubicin is
dose-limited by the cardiotoxicity of the drug. In order to address
this problem, doxorubicin has been formulated as a pegylated
liposomal preparation. Liposomal encapsulation of drugs enables
delivery of potent cytotoxic drugs with an improved therapeutic
index or therapeutic window. doxorubicin HCl liposome injection
(DOXIL.RTM.) is a pegylated liposome-encapsulated (liposomal) form
of doxorubicin. DOXIL is a commercial form of pegylated liposomal
doxorubicin (PLD). DOXIL alters the tissue distribution and
pharmacokinetic profile of doxorubicin. Use of DOXIL results in a
significantly lower rate of left ventricular cardiac dysfunction
and symptomatic congestive heart failure as compared to therapy
with free doxorubicin, both alone and in combination with
trastuzumab in anthracycline-naive and previously treated patients.
DOXIL.RTM. is approved for use to treat Kaposi's sarcoma, ovarian
cancer, and multiple myeloma. Doxorubicin HCl liposome injection is
also sold as CAELYX.RTM..
[0006] Immunoliposomes are antibody (typically antibody fragment)
targeted liposomes that provide advantages over non-immunoliposomal
preparations because they are selectively internalized by cells
bearing cell surface antigens targeted by the antibody. Such
antibodies and immunoliposomes are described, for example, in the
following US patents and patent applications: US 2010-0068255, U.S.
Pat. Nos. 6,214,388, 7,135,177, and 7,507,407 ("Immunoliposomes
that optimize internalization into target cells"); U.S. Pat. No.
6,210,707 ("Methods of forming protein-linked lipidic
microparticles and compositions thereof"); U.S. Pat. No. 7,022,336
("Methods for attaching protein to lipidic microparticles with high
efficiency") and US 2008-0108135 and U.S. Pat. No. 7,244,826
("Internalizing ErbB2 antibodies."). The following US and
international patents and patent applications describe assays, cell
lines, and related technologies that are relevant to this
disclosure: U.S. Pat. No. 7,846,440 ("Antibodies against ErbB3 and
uses thereof") and U.S. Ser. No. 12/757,801, PCT/US2009/040259, and
PCT/US2009/60721 ("Human Serum Albumin Linkers and Conjugates
Thereof").
[0007] Immunoliposomes targeting ErbB2 (HER2) can be prepared in
accordance with the foregoing patent disclosures. Such HER2
targeted immunoliposomes include MM-302, which comprises the F5
anti-HER2 antibody fragment and contains doxorubicin. MM-302
contains 45 copies of mammalian-derived F5-scFv (anti-HER2) per
liposome. The F5-scFv was selected for its ability to internalize
while not affecting HER2 signaling. Characterization of the F5-scFv
indicates that it does not cross react with mouse, rat or rabbit
HER2 and does not interfere with HER2 signaling in the free scFv
form. Because cardiomyocytes are known to express HER2, concerns
have been expressed regarding the potential cardiotoxicity of
MM-302 and related HER2-targeted immunoliposomes.
[0008] Dosage and administration of commercially available
liposomal doxorubicin:
[0009] DOXIL.RTM. (doxorubicin HCl liposome injection) is an
exemplary liposomal anthracycline chemotherapeutic drug. DOXIL is
typically administered intravenously at a dose indicated in
mg/m.sup.2 and characterized as doxorubicin HCl equivalent (dox
equiv., meaning the total mass of doxorubicin in each dose). Each
dose is typically administered at an interval measured in weeks, to
yield a dosage of x mg/m.sup.2 (dox equiv.) every y weeks. The
first liposomal doxorubicin dose is typically administered at an
initial rate of 1 mg/min to minimize the risk of infusion-related
reactions. If no infusion-related adverse reactions are observed,
the infusion rate is typically increased to complete the
administration of the drug over one hour.
[0010] Patients with Ovarian Cancer:
[0011] DOXIL is typically administered to ovarian cancer patients
intravenously at a dose of 50 mg/m.sup.2 dox equiv. The patient is
typically dosed once every 4 weeks, for as long as the patient does
not progress, shows no evidence of cardiotoxicity and continues to
tolerate treatment. A minimum of 4 courses is recommended because
median time to response in clinical trials was 4 months. To manage
adverse reactions such as hand-foot syndrome (HFS), stomatitis, or
hematologic toxicity the doses may be delayed or reduced.
Pretreatment with or concomitant use of antiemetics should be
considered.
[0012] Patients with AIDS-Related Kaposi's Sarcoma (KS):
[0013] DOXIL is typically administered to KS patients intravenously
at a dose of 20 mg/m.sup.2 (dox equiv.). In KS patients the dose is
typically repeated once every three weeks, for as long as patients
respond satisfactorily and tolerate treatment.
[0014] Patients with Multiple Myeloma:
[0015] To treat patients with multiple myeloma, DOXIL is
administered with VELCADE.RTM. (bortezomib). Bortezomib is
administered at a dose of 1.3 mg/m.sup.2 as intravenous bolus on
days 1, 4, 8 and 11, every three weeks. DOXIL is typically
administered to these patients at a dose of 30 mg/m.sup.2 as a 1-hr
intravenous infusion following each day 4 bortezomib
administration. Patients are typically treated for up to 8 cycles
until disease progression or the occurrence of unacceptable
toxicity.
[0016] HERCEPTIN.RTM. (trastuzumab) is a therapeutic anti-HER2
antibody that is very widely used to treat HER2 overexpressing
tumors. A key dosage-limiting effect of trastuzumab is
cardiotoxicity. Cardiomyocytes are known to express HER2, and
trastuzumab-mediated cardiotoxicity is generally accepted as being
caused by damage to HER2-expressing cardiomyocytes resulting from
trastuzumab binding to the cardiomyocyte-expressed HER2--see, e.g.,
Hysing J and Wist E, "Cardiotoxic Effects of Trastuzumab,". Tidsskr
Nor Laegeforen, 2011 Nov. 15; 131(22):2239-2241. Anthracycline
drugs such as doxorubicin are known to exert dose-limiting
cardiotoxic effects, which are considered a major limitation in
their use--see, e.g., Sawyer et al., "Mechanisms of Anthracycline
Cardiac Injury: Can we identify strategies for cardio-protection?"
Prog Cardiovasc Dis., 2010 September-October; 53(2):105-13.
[0017] Doxorubicin-induced cardiac damage is irreversible,
resulting in acute injury and also damage that can manifest itself
years after treatment. Exposure to cumulative concentrations of
doxorubicin above 550 mg/m.sup.2 increases the potential for
cardiomyopathy and heart failure. The development of HER2-directed
therapy for the treatment of HER2-positive breast cancer has led to
the investigation of the clinical benefit of the combination of
doxorubicin and trastuzumab. The clinical efficacy of doxorubicin
plus trastuzumab was superior to that of paclitaxel plus
trastuzumab; however, there was an increased incidence of cardiac
toxicity observed on the doxorubicin plus trastuzumab arm of the
study, and the combination was not approved for marketing. The
clinical benefit of anthracycline-based therapy, specifically in
HER2-positive breast cancer, remains controversial.
[0018] Liposomal encapsulation of drugs has enabled delivery of
potent cytotoxic drugs with an improved therapeutic index.
Pegylated liposomal doxorubicin (PLD) alters the tissue
distribution and pharmacokinetic profile of doxorubicin. PLD has
demonstrated a significantly lower rate of left ventricular cardiac
dysfunction and symptomatic congestive heart failure as compared to
therapy with conventional doxorubicin, alone and in combination
with trastuzumab in anthracycline-naive and previously treated
patients. A proposed mechanism for the reduced cardiotoxicity of
PLD is that its greater size relative to conventional doxorubicin
prevents it from crossing the endothelial barrier in the heart,
thereby minimizing doxorubicin exposure to heart tissue.
[0019] MM-302 is a HER2-targeted, pegylated liposome designed to
deliver doxorubicin directly to HER2-overexpressing cancers.
HER2-targeted PLD deposits in tumors through the enhanced
permeability and retention effect similar to PLD. In the tumor
microenvironment, targeting HER2-overexpressing cells with
HER2-targeted PLD results in superior efficacy relative to PLD in
preclinical models. During the development of MM-302, concern was
expressed by regulatory authorities that due to its HER2-targeting,
MM-302 would deliver cardiotoxic doxorubicin directly to
cardiomyocytes, resulting in increased cardiotoxicity compared to
doxorubicin HCl liposome injection, and reduced dosages of MM-302
were suggested to avoid such life-threatening toxicities.
BRIEF SUMMARY OF THE INVENTION
[0020] The present invention provides methods to determine safe
doses and to safely use anti-HER2 immunoliposomal anthracycline to
treat HER2-expressing cancers, e.g., without increased risk of
cardiotoxicity as compared to doxorubicin HCl liposome injection
(DOXIL), and provides other advantages.
[0021] It has now been discovered that anti-ErbB2 targeted,
anthracycline-containing immunoliposomes, e.g., MM-302, are not any
more cardiotoxic than doxorubicin HCl liposome injection
(DOXIL.RTM.), and can be dosed using exactly the same dosages
(i.e., dose and administration amounts and schedules) as used for
doxorubicin HCl liposome injection without any increase in
cardiotoxicity risk or decrease in efficacy. Furthermore, it has
now been demonstrated that MM-302 can be effectively targeted to
cells expressing 200,000 or more ErbB2 (HER2) receptors per cell in
vitro and in vivo, indicating that it can be used to treat patients
with HER2-overexpressing tumors that are either HER2 "3+" (e.g., by
HERCEPTEST.RTM.), HER2 FISH+ (fluorescence in situ hybridization
for HER2 gene amplification) or HER2 "2+" (e.g., by
HERCEPTEST).
[0022] Therefore, disclosed herein are methods for determining a
safe and effective dosage for use in treating a human cancer
patient by administration of anthracycline-comprising anti-HER2
immunoliposomes, the patient being diagnosed with a cancer
characterized by expression of HER2 receptor,
the methods comprising determining a first dosage, such a dosage
indicating a dose magnitude and frequency of dosing, for a patient
diagnosed with a cancer characterized by expression of HER2
receptor, the first dosage being for a liposomal anthracycline
chemotherapeutic agent that does not comprise an immunoliposome,
which dosage is determined to provide to the patient a safe and
effective amount of the liposomal anthracycline chemotherapeutic
agent; and determining a dosage for the administration of the
anthracycline-comprising anti-HER2 immunoliposomes, a plurality of
which immunoliposomes is each bearing a plurality of anti-HER2
antibody molecules on its surface and each containing the
anthracycline chemotherapeutic agent, where the safe and effective
dosage for the administration of the anthracycline-comprising
anti-HER2 immunoliposomes is the first dosage.
[0023] Also disclosed are methods of treating a human cancer
patient by administration of anthracycline-comprising anti-HER2
immunoliposomes, the methods comprising determining a first dosage,
such a dosage indicating a dose magnitude and frequency of dosing,
for a patient diagnosed with a cancer characterized by expression
of HER2 receptor, the first dosage being for a liposomal
anthracycline chemotherapeutic agent that does not comprise an
immunoliposome, which dosage is determined to provide to the
patient a safe and effective amount of the liposomal formulation,
and administering anthracycline-comprising anti-HER2
immunoliposomes, a plurality of which immunoliposomes is each
bearing a plurality of anti-HER2 antibody molecules on its surface
and each containing the anthracycline chemotherapeutic agent, where
the anthracycline-comprising anti-HER2 immunoliposomes are
administered to the patient at the first dosage.
[0024] In certain aspects the anthracycline is doxorubicin. In
other aspects the liposomal anthracycline chemotherapeutic agent
that does not comprise an immunoliposome is doxorubicin HCl
liposome injection and the HER2-targeted immunoliposomes are
MM-302. In others, the cancer is breast cancer, Kaposi's sarcoma,
ovarian cancer, or multiple myeloma. In yet other aspects, the
first dosage is 50 mg/m.sup.2, 40 mg/m.sup.2, 30 mg/m.sup.2, 20
mg/m.sup.2, or 10 mg/m.sup.2 every two weeks or every three weeks
or every four weeks. In other aspects the cancer characterized by
expression of HER2 receptor is further characterized as being
HER2.sup.2+, HER2.sup.3+, or HER2 FISH positive. In others the
cancer characterized by expression of ErbB2 receptor is further
characterized as expressing an average of at least 200,000 cell
surface ErbB2 receptors per cell. In yet others, the administration
of the immunoliposomes at the first dosage is effective to treat
the cancer and in others the administration of the immunoliposomes
at the first dosage does not result in increased cardiotoxicity as
compared to administration at the first dosage of the liposomal
anthracycline chemotherapeutic agent that does not comprise an
immunoliposome. In other aspects, the administration of the
immunoliposomes to the patient at the first dosage results in a
peak concentration of the immunoliposomes in the patient's
bloodstream, and treating human cardiomyocytes in vitro by
culturing in medium comprising the immunoliposomes at about the
peak concentration does not reduce, or reduces by no more than 5%,
heregulin-stimulated increase of pERK or pAKT in the cultured
cardiomyocytes as compared to in control human cardiomyocytes
cultured in medium free of the immunoliposomes. In other aspects
the immunoliposome concentration in the patient's bloodstream is
measured as a serum immunoliposome concentration. In yet other
aspects each of the HER2 immunoliposomes bears on its surface, on
average, 45 anti-HER2 antibody molecules.
BRIEF DESCRIPTION OF THE DRAWINGS
[0025] FIG. 1A depicts a graph of the expression of HER2 in
multiple cell lines after being treated with 15 .mu.g/ml of MM-302
immunoliposomes containing doxorubicin (dox) for 2 hr and levels of
total cellular doxorubicin internalized as determined using HPLC.
The y-axes represent femtograms dox per cell (left) and liposomes
per cell (right) and the x-axes represent the number of HER2
receptors per cell (log scale).
[0026] FIG. 1B depicts a graph of the expression of HER2 in
multiple cell lines after being treated with 15 .mu.g/ml of
untargeted pegylated liposomal dox (UT-PLD) containing doxorubicin
(dox) for 2 hr and levels of total cellular doxorubicin
internalized as determined using HPLC. The y-axes represent
femtograms dox per cell (left) and liposomes per cell (right) and
the x-axes represent the number of HER2 receptors per cell (log
scale).
[0027] FIG. 1C is a graph depicting the expression of HER2
receptors in Mouse tumor 4T1 cells transfected with human HER2 to
generate stable clones with varying levels of expression.
Individual clones (represented by triangles, circles, or squares)
were treated with F5-targeted liposomes containing a fluorescent
marker (DiI5-F5-PL), and total binding/uptake was determined by
FACS.
[0028] FIG. 1D is a graph depicting the expression of HER2
receptors in endogenously low HER2 expressing HeLa cells
transfected with human HER2 to generate stable clones with varying
levels of expression. Individual clones (represented by triangles,
circles, or squares) were treated with F5-targeted liposomes
containing a fluorescent marker (DiI5-F5-PL), and total
binding/uptake was determined by FACS.
[0029] FIG. 2A is a line graph depicting the total cellular
doxorubicin quantified by HPLC (y-axis, femtograms/cell) in
HER2-overexpressing BT474-M3 cells when treated with 15 .mu.g/ml of
MM-302 (circle), PLD (square), and free doxorubicin (triangle) for
the indicated times (x-axis, in min.).
[0030] FIG. 2B is a line graph depicting nuclear doxorubicin
delivery quantified by high content microscopy (y-axis, signal per
cell above background) when treated with 15 .mu.g/ml of MM-302
(square), PLD (triangle), and free doxorubicin (circle) 24 h
following the indicated incubation times (x-axis, in min.).
[0031] FIG. 2C is a line graph depicting the anti-tumor activity of
MM-302 and PLD in a BT474-M3 orthotopic breast cancer model. Both
MM-302 (square) and PLD (triangle) significantly inhibited tumor
growth compared to control (circle). The y-axis indicates tumor
volume in mm.sup.3 and the x-axis indicates days after
inoculation.
[0032] FIG. 2D is a line graph depicting the pharmacokinetics of
MM-302 and UT-PLD in BT474-M3 xenografts administered with 3 mg/kg
or 6 mg/kg (dox equiv) at q7d. The y-axis is .mu.g/mL dox in plasma
and the x-axis is time in hours.
[0033] FIG. 3A represents a line graph showing HER2 level
(receptors per cell, x-axis) as a function of liposome Di15-labeled
MM-302 (Di15-F5-PLD) or UT-PLD (Di15-UT-PLD) binding to BT474-M3
xenograft tumor cells (percent cells positive, y-axis).
[0034] FIG. 3B represents a line graph demonstrating the
heterogeneity of HER2 expression on a single cell basis as measured
in tumor tissue sections.
[0035] FIG. 4A depicts a line graph illustrating the uptake of
MM-302 (circle), PLD (square) and doxorubicin (triangle) in human
embryonic stem cell-derived (ESCd) cardiomyocytes. Total cellular
doxorubicin was quantified by HPLC. The y-axes represents uptake in
femtograms/cell and the x-axes represent incubation time in
min.
[0036] FIG. 4B depicts a line graph illustrating the uptake of
MM-302 (circle), PLD (square) and doxorubicin (triangle) in human
induced pluripotent stem cell-derived (iPSd) cardiomyocytes. Total
cellular doxorubicin was quantified by HPLC. The y-axes represents
uptake in femtograms/cell and the x-axes represent incubation time
in min.
[0037] FIG. 4C depicts a line graph illustrating the cell viability
of ESCd cardiomyocytes after treatment for 3 h with drug (free
doxorubicin (circle), PLD (square) or MM-302 (triangle)) at the
indicated concentrations and incubated for an additional 24 h with
fresh media. The y-axis represents cell viability as % compared to
control and the x-axis represents concentration in .mu.g/ml.
[0038] FIG. 4D depicts a line graph illustrating the cell viability
of human induced pluripotent stem cell-derived (iPSd)
cardiomyocytes after treatment for 24 hours with drug (free
doxorubicin (circle), PLD (square) or MM-302 (triangle)) at the
indicated concentrations and incubated for an additional 24 h with
fresh media. The y-axis represents cell viability as % compared to
control and the x-axis represents concentration in .mu.g/ml. The
supernatant was collected and a PrestoBlue.RTM. cell viability
assay was performed on the remaining cells.
[0039] FIG. 4E depicts expression of human Troponin I using an
ELISA assay performed on the supernatant collected in (FIG. 4D).
The untreated line (dotted line) represents the value of soluble
Troponin I detectable in untreated wells. All values are normalized
against dilutions of a supplied standard.
[0040] FIG. 5A depicts a line graph representing expression the DNA
damage marker gamma-H2AX in ESCd cardiomyocytes after treatment for
3 h with MM-302 (circle), PLD (square), and free doxorubicin
(triangle) at the indicated concentrations and then incubated for
an additional 24 h with fresh media. Single cell intensity for each
stain was quantified and represented as the mean relative intensity
of individual cells.
[0041] FIG. 5B depicts a line graph representing expression of the
cell stress protein phospho-p53 in ESCd cardiomyocytes after
treatment for 3 h with MM-302 (circle), PLD (square), and free
doxorubicin (triangle) at the indicated concentrations and then
incubated for an additional 24 h with fresh media. Single cell
intensity for each stain was quantified and represented as the mean
relative intensity of individual cells.
[0042] FIG. 5C depicts a line graph representing expression of the
cell stress protein phospho-HSP27 in ESCd cardiomyocytes after
treatment for 3 h with MM-302 (circle), PLD (square), and free
doxorubicin (triangle) at the indicated concentrations and then
incubated for an additional 24 h with fresh media. Single cell
intensity for each stain was quantified and represented as the mean
relative intensity of individual cells.
[0043] FIG. 5D depicts a line graph representing expression of the
cleaved form of the apoptosis protein PARP (cPARP) in ESCd
cardiomyocytes after treatment for 3 h with MM-302 (circle), PLD
(square), and free doxorubicin (triangle) at the indicated
concentrations and then incubated for an additional 24 h with fresh
media. Single cell intensity for each stain was quantified and
represented as the mean relative intensity of individual cells.
[0044] FIG. 6A depicts a bar graph illustrating the effects of F5
scFv alone, F5 scFv bound to empty (i.e. without encapsulated dox)
liposomes ("F5 lipo"-liposomes equivalent to MM-302 but not
containing doxorubicin), Herceptin.RTM. (trastuzumab) and lapatinib
on basal and heregulin stimulated pAKT levels in iPS-derived human
cardiomyocytes.
[0045] FIG. 6B depicts a bar graph illustrating the effects of F5
scFv alone, F5 scFv bound to empty (i.e. without encapsulated dox)
liposomes ("F5 lipo"-liposomes equivalent to MM-302 but not
containing doxorubicin), Herceptin.RTM. (trastuzumab) and lapatinib
on basal and heregulin stimulated pERK levels in iPS-derived human
cardiomyocytes.
[0046] FIG. 7A is a line graph illustrating the biodistribution and
accumulation of doxorubicin in heart tissue after administration of
MM-302 (square), PLD (triangle) and free doxorubicin (circle) in
NCI-N87 tumor bearing mice (n=4/time point/group).
[0047] FIG. 7B is a line graph illustrating the biodistribution and
accumulation of doxorubicin in tumor tissue after administration of
MM-302 (square), PLD (triangle) and free doxorubicin (circle) in
NCI-N87 tumor bearing mice (n=4/time point/group).
[0048] FIG. 7C is a line graph illustrating the biodistribution and
accumulation of doxorubicin in paw tissue after administration of
MM-302 (square), PLD (triangle) and free doxorubicin (circle) in
NCI-N87 tumor bearing mice (n=4/time point/group).
[0049] FIG. 7D represents confocal fluorescence microscopy
photomicrographs illustrating the biodistribution and accumulation
of doxorubicin in heart tissue over time in Nu/nu mice injected
intravenously with MM-302-Di15, PLD-Di15, and free doxorubicin at 3
mg/kg (dox equiv.).
[0050] FIG. 7E depicts a higher magnification (2 x) of the confocal
fluorescence microscopy photomicrograph illustrating the overlay of
the nuclei and doxorubicin signal images as shown in FIG. 7D for
the 0.5 h time points for doxorubicin and MM-302.
[0051] FIG. 7F depicts a line graph illustrating the percentage of
doxorubicin positive nuclei in heart tissue of Nu/nu mice injected
intravenously with MM-302-Di15, PLD-Di15, and free doxorubicin at 3
mg/kg (dox equiv.) quantified using Definiens.RTM. Developer
XD.TM..
[0052] FIG. 8A depicts a graphical illustration of a computational
model developed and calibrated on literature and in-house data for
free and liposomal doxorubicin. The model can be applied to
understand the competing kinetic processes that determine drug
concentration and exposure for liposomal versus free doxorubicin in
various tissues.
[0053] FIG. 8B depicts a graphical illustration of a computational
model developed and calibrated on literature and in-house data for
tissue deposition of free and liposomal doxorubicin in mouse.
[0054] FIG. 8C depicts a graphical illustration of a theoretical
kinetic model to provide a framework for understanding the role of
HER2 expression in MM-302 uptake and doxorubicin cellular
trafficking.
DETAILED DESCRIPTION OF THE INVENTION
[0055] An MM-302 liposome is a unilamellar lipid bilayer vesicle of
approximately 75-110 nm in diameter that encapsulates an aqueous
space which contains doxorubicin in a gelated or precipitated
state. The lipid membrane is composed of phosphatidylcholine,
cholesterol, and a polyethyleneglycol-derivatized
phosphatidylethanolamine in the amount of approximately one PEG
molecule for 200 phospholipid molecules, of which approximately one
PEG chain for each 1780 phospholipid molecules bears at its end an
F5 single-chain Fv antibody fragment that binds to HER2. MM-302
liposomes are prepared from HSPC (Hydrogenated soy
phosphatidylcholine):Cholesterol (plant-derived):PEG-DSPE
(polyethylene glycol-disteroylphosphoethanolamine) at a molar ratio
of 3:2:0.3. The total HSPC lipid concentration of MM-302 is about
40 mmol/L. MM-302 contains about 10 mmol/L of lipid, and about 2
mg/mL of doxorubicin. MM-302 comprises 1.8-2.2 mg/mL of doxorubicin
in liposomes that contain 0.16-0.30 mg/mL DSPE-PEG-F5 (prepared as
described in U.S. Pat. No. 6,210,707). F5 is an anti-ErbB2 (HER2)
scFv antibody fragment (encoded by ATCC plasmid deposit designation
PTA-7843). MM-302 liposomes comprise 130-170 g doxorubicin/mol
phospholipid and 12-22 g F5-PEG-DSPE/mol phospholipid. MM-302 is
formulated in sterile 10 mM/L histidine-HCl as a buffer (pH 6.5),
and 10% sucrose to maintain isotonicity. MM-302 liposomes are
loaded using pre-loaded ammonium sulfate
MM-302 Dosing
TABLE-US-00001 [0056] Dose 1 Dose 2 Dose 3 Dose 4 Dose 5 Every week
10 mg/m.sup.2 20 mg/m.sup.2 30 mg/m.sup.2 40 mg/m.sup.2 50
mg/m.sup.2 Every 10 mg/m.sup.2 20 mg/m.sup.2 30 mg/m.sup.2 40
mg/m.sup.2 50 mg/m.sup.2 two weeks Every 10 mg/m.sup.2 20
mg/m.sup.2 30 mg/m.sup.2 40 mg/m.sup.2 50 mg/m.sup.2 three weeks
Every 10 mg/m.sup.2 20 mg/m.sup.2 30 mg/m.sup.2 40 mg/m.sup.2 50
mg/m.sup.2 four weeks Every 10 mg/m.sup.2 20 mg/m.sup.2 30
mg/m.sup.2 40 mg/m.sup.2 50 mg/m.sup.2 five weeks
"mg/m.sup.2" indicates mg of doxorubicin (formulated as MM-302) per
square meter of body surface area of the patient. For breast
cancer, dose 3, 4, or 5 is preferred. For Kaposi's sarcoma dose 1,
2, or 3 is preferred, for ovarian cancer, dose 3, 4, or 5 is
preferred and for multiple myeloma dose 2, 3, 4, or 5 is preferred.
Dosing regimens may vary in patients with solid tumors that are
"early" (pre-metastatic, e.g., adjuvant breast cancer) as compared
to "advanced" (metastatic tumors).
[0057] Preferred tumors are those in which the tumor cells
overexpress HER2. A tumor that overexpresses HER2 is one that is
identified as being HER2 "3+" or HER2 "2+" by HercepTest.TM., or
HER2 FISH+ by fluorescence in situ hybridization. Alternatively, a
preferred tumor that overexpresses HER2 is one that expresses an
average of 200,000 or more receptors per cell, as quantified by the
methods described in the Examples.
MM-302 Therapy of Advanced Breast Cancer
[0058] MM-302 is administered once every 4 weeks by intravenous
(IV) infusion over 60 minutes at 8, 16, 30, 40, or 50 mg/m.sup.2 to
patients with locally advanced/unresectable or metastatic advanced
breast cancer that overexpresses HER2 as determined by FISH or by
IHC or by determination of the average number of HER2 receptors per
cell. Patients should have adequate bone marrow reserves as
evidenced by: 1) absolute neutrophil count (ANC)
.gtoreq.1,500/.mu.L; 2) platelet count .gtoreq.100,000/.mu.L and 3)
hemoglobin .gtoreq.9 g/dL (Transfusions allowed). Patients should
have adequate hepatic function as evidenced by: 1) serum total
bilirubin .ltoreq.1.5.times.ULN and 2) Aspartate aminotransferase
(AST), Alanine aminotransferase (ALT) and Alkaline Phosphatase
(ALP) normal or up to 2.5.times. upper limit of normal (ULN;
5.times.ULN is acceptable for ALP if liver metastases and/or bone
metastases are present). Patients should have adequate renal
function as evidenced by a serum creatinine .ltoreq.1.5.times.ULN.
Patients should be recovered from any clinically relevant toxic
effects of any prior surgery, radiotherapy or other therapy
intended for the treatment of breast cancer. Women of childbearing
potential as well as fertile men and their partners must be warned
to abstain from sexual intercourse or to use an effective form of
contraception during treatment and for 90 days following the last
dose of MM-302. Patients should have adequate cardiac function as
evidenced by a measured left ventricular ejection fraction of
.gtoreq.50% by ECHO or MUGA within approximately 30 days of
treatment. Patients who are pregnant or lactating and those with
NYHA Class III or IV congestive heart failure or left ventricular
ejection fraction (LVEF)<50%, or a prolonged QTc interval
(.gtoreq.460 ms), are preferably not be treated with MM-302.
[0059] The following Examples are merely illustrative and should
not be construed as limiting the scope of this disclosure in any
way as many variations and equivalents will become apparent to
those skilled in the art upon reading the present disclosure.
EXAMPLES
Materials and Methods Used in these Examples
[0060] Materials:
[0061] Doxorubicin is from SIGMA-ALDRICH, Inc. (St. Louis, Mo.).
FITC-conjugated lectin (lycopersicon esculentum (tomato) lectin,
Cat # FL-1171) is purchased from Vector Laboratories, Inc.
(Burlingame, Calif.). Acetic acid, Methanol, and Acetonitrile are
from EMD Chemicals Inc. (Gibbstown, N.J.). Water and
Trifluoroacetic Acid (TFA) are from J. T. Baker (Phillipsburg,
N.J.). HOECHST 33342 trihydrochloride trihydrate, ProLong
Gold.RTM., and DiIC18(5)-DS (Di15) are from Invitrogen (Carlsbad,
Calif.). Cholesterol and
1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[amino(polyethylene
glycol)-2000] (ammonium salt) (PEG-DSPE) are from Avanti Polar
Lipids Inc. Hydrogenated soy phosphatidylcholine (HSPC) is from
Lipoid (Newark, N.J.). RPMI is from Lonza (Walkersville, Md.),
Fetal Bovine Serum (FBS) is from Tissue Culture Biologicals and
penicillin G/streptomycin sulphate mixture is from GIBCO
(Invitrogen).
[0062] Preparation of Immunoliposomes:
[0063] Liposomes are prepared and loaded with doxorubicin using an
ammonium sulfate gradient as previously described (Kirpotin et.
al., Cancer Res. 2006; 66:6732-40; Park et al., Clin Cancer Res.
2002; 8:1172-81). The lipid components are HSPC, cholesterol, and
PEG-DSPE (3:2:0.3, mol:mol:mol). The anti-ErbB2 (F5)-PEG-DSPE
conjugate is prepared and inserted into the liposome to form
immunoliposomes as reported by Nellis et al., (Biotechnol Prog.
2005; 21:205-20; Biotechnol Prog. 2005; 21:221-32). The
DiI-5-labelled liposomes, MM-302-Di15 and PLD-Di15, are prepared as
above with the difference that the DiIC18(5)-DS (Di15) dye is
solubilized with the lipid components at a concentration of 0.3 mol
% of total phospholipid. In all cases unloaded free doxorubicin is
removed using a Sephadex.RTM. G-75 size exclusion column eluted
with Hepes buffered saline (pH 6.5). F5-lipo-Di15 is prepared in a
similar fashion as above but without doxorubicin, and incorporating
an aqueous solution of HEPES buffered saline (pH 6.5).
[0064] Tumor Cell Culture:
[0065] BT474-M3 cells (see Noble, Cancer Chemother. Pharmacol. 2009
64:741-51), are HER2-overexpressing human breast cancer cells.
BT474-M3 cells are grown in RPMI medium containing 10% FBS and 1%
penicillin G/streptomycin sulphate. Embryonic stem cell-derived
(ESCd) cardiomyocytes are obtained from P. W. Zandstra, Institute
of Biomaterials and Biomedical Engineering, University of Toronto,
Toronto, Ontario, Canada; (Bauwens et al., Tissue Eng Part A. 2011
Apr. 25, PMID 21417693;). These cells have been shown to express
appropriate cellular markers of cardiomyocytes such as LIM domain
homeobox gene Isl-1, Troponin T, and Myosin Light Chain 2c. The
percentage of Troponin T positive cells is determined following
differentiation. Batches containing less than 70% positive for
Troponin T are discarded. Induced pluripotent stem cell-derived
(iPSd) cells are obtained from Cell Dynamics International and are
handled per the manufacturer's protocol.
[0066] Xenograft Studies:
[0067] 5-7-week-old female nude mice are purchased from Charles
River Laboratories or Taconic Farms, Inc (NCr nude mice). Unless
otherwise indicated, mice are inoculated with BT474-M3 breast
cancer cells or NCI-N87 gastric cancer cells (NCI-DTP,
10.times.10.sup.6 cells in 100 .mu.l RPMI) into the right dorsal
flank of the mice (subcutaneous injection, s.c.). When the tumors
reach an average volume of -200 mm.sup.3, studies are performed as
described below.
[0068] Testing of Tumor HER2 Levels:
[0069] Homozygous NCr nude mice are inoculated with
15.times.10.sup.6 BT474-M3 cells in the mammary fat pad 2nd from
the top right hand side. BT474-M3 tumors are injected with a single
dose of 4 mg/ml fluorescently-labeled (with Di15 as described
below) HER2-targeted or untargeted liposomes without doxorubicin.
Twenty-four hours later, the tumors are excised and dissociated by
mechanical and enzymatic means. After surface staining with
anti-HER2 cells are analyzed by flow cytometry on a FACSCalibur.TM.
instrument (BD Biosciences). The flow cytometry dataset is analyzed
for the relationship between HER2 surface expression levels and
uptake of liposomes above a given threshold by plotting the overall
percentage of cells with elevated liposome content in narrowly
gated cell subsets defined by increasing HER2 signals.
[0070] Single Cell Distribution of Cell Surface HER2:
[0071] BT474-M3 tumor xenograft tissue is stained with an anti-HER2
antibody and counterstained with DAPI. The slide is imaged with an
Aperio.RTM. Scanscope.RTM. at 20.times. magnification and the image
is analyzed. The intensity of the HER2 membrane staining is
quantified on a single-cell basis as the (mean of the inner border
of the HER2 layer)+(mean of the outer border of the HER2
layer).
[0072] Efficacy Study:
[0073] Mice are randomized into three treatment groups (n=7/group)
based on an average tumor volume from mice that receive PBS
(control), MM-302 or PLD, dosed at 3 mg/kg (q7d, n=3 total doses).
Tumors are measured twice/week with a caliper. Tumor volumes are
calculated using the formula: width.sup.2.times.length.times.0.52.
Mice are weighed twice/week to monitor weight loss.
[0074] Uptake of Liposomes in HER2-Expressing Cell Lines:
[0075] Multiple cell lines expressing various levels of HER2 are
treated with 15 .mu.g/ml of MM-302 or PLD for 2 h and total
cellular doxorubicin is quantified by HPLC. Murine 4T1 breast
cancer cells and human HeLa cervical cancer cells are obtained from
the ATCC and propagated according to ATCC recommendations. Cells
are characterized for human HER2 expression by flow cytometry using
a commercial anti-HER2 antibody (BD Biosciences #340552). This
antibody does not cross-react with murine HER2 but detects human
HER2. A neomycin-selectable expression vector encoding human HER2
is obtained from GeneCopeia (Z2866). 4T1 and HeLa cells are
transfected with this construct using the non-lipid polymer
transfection reagent MegaTran.RTM. 1.0 (Origene) according to the
manufacturer's instructions. Transfected cells are selected with
400-500 .mu.g/ml Geneticin/Neomycin (Invitrogen). Surviving cells
are allowed to expand under reduced Geneticin/Neomycin
concentrations (100 .mu.g/ml) and are sorted on a BD Biosciences
FACSAria.TM. instrument to obtain enriched cell populations with
human HER2 expression exceeding those observed in parental HeLa
cells. The sort-enriched cells are then sub-cloned by limited
dilutions, and colonies are ranked by HER2 surface levels to obtain
representative populations of 4T1 and HeLa cells that express
different ranges of HER2. Fluorescent intensity of HER2 surface
staining measured by flow cytometry is compared to staining with
the same antibody bound to Quantum.TM. Simply Cellular.RTM.
anti-mouse IgG microspheres (Bangs Laboratories #815) according to
the manufacturer's instructions to calculate the number of HER2
surface receptors of the cells.
[0076] Uptake of Liposomes in Cardiomyocytes:
[0077] iPSd cardiomyocytes are plated per the manufacturer's
instructions (Cell Dynamics International Cat# CMC-100-110-001) in
a 24-well tissue culture plate at 250,000 cells/well. Two days
later, the 0.5 ml of media in the wells is removed and replaced
with 0.5 ml of 15.0 .mu.g/ml (dox equiv.) of MM-302, PLD or free
doxorubicin. The plates are swirled in a "figure 8 fashion" 20
times to maximize exposure of the cells to the liposomes. Cells are
incubated with MM-302, PLD or free doxorubicin for the indicated
time period after which the media are removed and the cells are
washed once with 0.5 ml of PBS. The PBS is removed and 0.5 ml of
0.05% trypsin is added to each well. The cells are monitored, and
once detachment begins, 0.5 ml of medium containing FBS is added to
each well to inactivate the trypsin. The cells are collected and
placed in microcentrifuge tubes. The cells are spun at 1,500 rpm
for 5 minutes at 4.degree. C. The cell pellet is resuspended by
vortexing and pipetting in 0.5 ml of 1.0% acetic acid in methanol
and placed at -80.degree. C. for 1 hour to extract the doxorubicin.
The microcentrifuge tube containing the resuspended cell pellet is
spun at 10,000 rpm for 10 minutes in the cold room, and 450 .mu.l
of the supernatant is transferred to a HPLC Tube.
[0078] Samples are run on the HPLC machine and concentration per
sample is determined by relating values to a doxorubicin standard
curve.
[0079] Biodistribution of Liposomes:
[0080] Mice are randomized into 4 groups that received a single
intravenous (i.v.) dose of either PBS, doxorubicin, MM-302-Di15 or
PLD-Di15 (all at 3 mg/kg), respectively. Mice (n=4/time
point/group) are sacrificed at 0.5, 4, 24 and 96 h (doxorubicin) or
168 h (MM-302-Di15 and PLD-Di15) after the single dose. Five
minutes before sacrificing, mice are injected i.v. with 100 .mu.l
of FITC-lectin, to label the vasculature.
[0081] HPLC Quantification of Doxorubicin:
[0082] Heart tissues are weighed and disaggregated with 1 mL
H.sub.2O using a TissueLyser.TM. (Qiagen) for 3 min. 100 .mu.l of
the homogenate is then transferred into a new tube and 900 .mu.l of
1% acetic acid/methanol is added. For the cultured cells, cells are
treated with drug, as described above, trypsinized and lysed using
1.0% acetic acid in methanol. Lysates are vortexed for 10 sec. and
placed at -80.degree. C. for 1 h. Samples are spun at room
temperature (RT) for 10 min at 10,000 RPM. Supernatants and
doxorubicin standards are analyzed by HPLC (Dionex) using a C18
reverse phase column (Synergi.TM. POLAR-RP.RTM. 80 .ANG.,
250.times.4.60 mm 4 .mu.m column). Doxorubicin is eluted running a
gradient from 30% acetonitrile; 70% 0.1% trifluoroacetic acid
(TFA)/H.sub.2O to 55% acetonitrile; 45% 0.1% TFA/H2O during a 7 min
span at a flow rate of 1.0 ml/min. The doxorubicin peak is detected
at 6.5 min using an in-line fluorescence detector excited at 485
nm, and emitting at 590 nm. The extraction efficiency of
doxorubicin from the heart tissue was 83% as determined by a
control heart spiked with a known amount of doxorubicin.
[0083] Confocal Microscopy and Image Analysis of Heart Snap-Frozen
Sections:
[0084] 10 .mu.m-thick heart sections are air-dried for 30 min at
RT, counterstained with Hoechst.RTM. 33342 diluted 1:10,000 in
mounting media (ProLong.RTM. Gold, Invitrogen) and mounted. Slides
are imaged on a LSM 510 Zeiss.RTM. confocal microscope equipped
with Enterprise (351, 364 nm), Argon (458, 477, 488, 514 nm), HeNe1
(543 nm) and HeNe2 (594 nm) lasers with a Plan-Neofluar.RTM.
40.times./1.3 oil DIC objective. Image analysis and quantification
of nuclear doxorubicin is carried out using Definiens.RTM.
Developer XD.TM. (Definiens, Parsippany, N.J.). Nuclei are
segmented in the Hoechst channel. Doxorubicin positive nuclei are
segmented in the doxorubicin channel. The percentage of doxorubicin
positive nuclei is quantified as a ratio of the number of objects
in the doxorubicin channel divided by the total nuclei objects in
the Hoechst channel.
[0085] Receptor Quantification:
[0086] Stem cell-derived cardiomyocytes are trypsinized, washed,
and HER2 levels are determined as described above under "Uptake of
liposomes in HER2-expressing cell lines."
[0087] Viability:
[0088] ESCd cardiomyocytes are treated for 3 h at the indicated
concentrations of MM-302, PLD and doxorubicin. Cells are washed
twice with PBS, fresh medium is added and the cells are incubated
for an additional 24 h. Cell viability is assessed using
CellTiter-Glo.RTM. from Promega (Madison, Wis.) and the percent of
viable cells is determined relative to the untreated
population.
[0089] Troponin I ELISA:
[0090] 15,000 iPSd (iCELL.RTM.) cardiomyocytes (Cellular Dynamics
International, Madison Wis.) cells are plated per the
manufacturer's protocol. Cells are treated for 24 h with the
indicated concentrations of free doxorubicin, PLD or MM-302. The
supernatant is collected and analyzed using a human Troponin I
ELISA (Catalog #: GWB-83A61F, Genway Biotech, San Diego Calif.) per
the manufacturer's protocol. A PrestoBlue.RTM. Cell Viability Assay
(Catalog #: A-13261, Invitrogen, Grand Island, N.Y.) is performed
on the remaining cells in 100 .mu.l per the manufacturer's
protocol.
[0091] High-Content Analysis:
[0092] Cardiomyocytes are treated as described above. Cells are
fixed using 3.7% formaldehyde, washed twice with PBS containing
0.1% Tween-20 (PBS-T), and permeabilized with methanol. Cells are
blocked using a 1:1 mixture of LI-COR.RTM. Odyssey.RTM. Blocking
Buffer (Lincoln, Nebr.) and PBS-T for 1 h at room temperature (RT).
Cells are stained with a 1:400 dilution of the indicated primary
antibody from Cell Signaling Technology (Beverly, Mass.) and
incubated shaking at 4.degree. C. overnight. Cells are washed and
incubated with a 1:2,000 dilution of the fluorescently labeled
secondary antibody for 1 h at RT. Cells are stained with a 1:10,000
dilution of Hoechst 33342 and 1:1,000 dilution of Whole Cell Stain
from Pierce Protein Research Products (Rockford, Ill.) for 30 min
at RT to allow visualization of DNA and the whole cell,
respectively. Plates are scanned using the Applied Precision
Instruments ArrayWorx.RTM. High Content Scanner (Issaquah, Wash.)
with a 10.times. objective for Hoechst 33342/Whole Cell Stain (460
nm), doxorubicin (595 nm), and APC/DiI5 (657 nm). Images are
analyzed using the software ImageRail (as described in Millard et
al., Nat Methods. 2011; 8:487-92). An intensity threshold is
established for nuclear and whole cell signals. This threshold is
then applied to all images and used to segment individual cells.
Data is presented as the mean pixel intensity for all cells in a
given well for the indicated channel.
[0093] Signaling in Cardiomyocytes:
[0094] iPS-derived cardiomyocytes (iCell.TM. iPS-derived human
cardiomyocytes--Cellular Dynamics International (CDI), Madison,
Wis.--CDI # CMC-100-010-001, Lot 1258680) are cultured using
iCell.TM. Plating Medium (CDI # CMM-100-110-005, Lot 1013740 and
iCell.TM. Maintenance Medium (CDI # CMM-100-120-005, Lot 1000305)
and are exposed to components of MM-302. Levels of phospho-AKT
(pAKT) and phospho-ERK (pERK) in the cardiomyocytes are then
measured using immunostaining and high content microscopy. Cells
are pretreated for 24 hours with either trastuzumab, lapatinib, or
the MM-302 antibody (F5-scFv) and an MM-302 molecule (liposome) not
containing doxorubicin (F5-lipo) at an equivalent concentration to
5.0 ug/ml of MM-302. Cells are stained and imaged using high
content microscopy as described above for (A) pAKT and (B) pERK
following a 10 minute stimulation with 10 nM and 5 nM of heregulin,
respectively. The following primary antibodies are used at a 1:400
dilution in blocking buffer: pERK antibody--Cell Signaling
Technology (CST--Danvers Mass.)--Catalog 9106L (Phospho-p44/42 MAPK
(Erk1/2) (Thr202/Tyr204) (E10) Mouse mAb #9106); pAKT
antibody--CST--Catalog 4060L (Phospho-Akt (Ser473) (D9E) XP.TM.
Rabbit mAb #4060). Secondary antibodies are Anti-mouse IgG (H+L),
F(ab')2 Fragment (Alexa Fluor.RTM. 647 Conjugate)--CST--Catalog
4410; Anti-rabbit IgG (H+L), F(ab')2 Fragment (Alexa Fluor.RTM. 647
Conjugate)--CST--Catalog 4414. Whole cell stain and DNA stain
(Hoechst 33342) are used as described above. Images are analyzed
and individual cells are segmented on the basis of Hoechst 33342
nuclear staining Single cell signal intensity for each stain is
quantified and represented as the mean relative intensity of
individual cells.
[0095] The results in the following Examples were obtained using
the above methods or minor variations thereof. Cellular uptake
studies in tumor cell lines expressing various levels of HER2
demonstrate that MM-302 delivers significantly higher doxorubicin
levels to HER2 over-expressing tumor cells compared to PLD as well
as similar or higher levels than highly permeable free doxorubicin.
However, in human cardiomyocytes, while free doxorubicin was again
taken up at high levels, doxorubicin uptake was dramatically lower
with both MM-302 and PLD. Pharmacokinetic studies in mice
demonstrate that MM-302 has a similar half-life, clearance, and
organ distribution compared to PLD. In HER2-overexpressing BT474
breast and NCI-N87 gastric tumor xenografts, MM-302 exhibits
superior anti-tumor activity to both free anthracyclines and PLD.
Tumor microdistribution studies further suggest that differences in
the localization of doxorubicin in the tumor may be responsible for
the enhanced activity of MM-302 compared to free doxorubicin and
PLD.
Example 1
Correlation Between HER2 Expression and MM-302 Uptake In Vitro
[0096] The level of cell surface HER2 expression on multiple cell
lines was determined as described above. These same cell lines were
then treated with 15 .mu.g/ml of MM-302 (FIG. 1A, Table 1) or PLD
(FIG. 1B, Table 2) for 180 minutes, after which the cells were
collected and the amount of cell associated doxorubicin was
quantified by HPLC. By plotting the number of HER2 receptors per
cell for each cell line vs. the quantity of doxorubicin present per
cell in that same cell line following treatment, a relationship
between increasing HER2 levels and increasing doxorubicin becomes
evident. Through this representation, there appears to be an
inflection point at approximately 200,000 HER2 receptors per cell
where cells expressing greater than this number appear to have
consistently higher levels of cell associated doxorubicin. Taken
together, these results support the specificity of MM-302, with
high uptake by cells expressing levels of HER2 above the inflection
point (such as HER2 overexpressing cancers) and no-to-minimal
uptake in cells expressing levels of HER2 below the inflection
point (such as cells in normal tissues, e.g., cardiomyocytes).
TABLE-US-00002 TABLE 1 HER2 levels vs MM-302 uptake FIG. HER2 fg 1A
Cell line Source (#/cell) dox/cell A 4T1-clone- ATCC # CRL-2539
.TM. 650,000 1,758.63 12W7 B ADRr ATCC # HTB-22 .TM. (MCF7
derivative) 40,792 26.47 C AdRr-Her2 ATCC # HTB-22 .TM., stably
transfected with HER2 722,000 519.04 D BT474-M3 Noble, Cancer
Chemother. Pharmacol. 2009 64: 741-51 1,706,601 1,123.51 E Calu-3
ATCC # HTB-55 .TM. 1,196,976 84.06 F HCC1954 ATCC # CRL-2338 .TM.
700,000 1,174.60 G HeLa ATCC # CCL-2 .TM. 123,713 31.61 H IGROV1
NCI 60-cell panel from NCI-DTP, DCTD TUMOR 158,418 51.54
REPOSITORY, Operated by Charles River Laboratories, Inc. (NCI-DTP)
I JIMT-1 DSMZ # ACC-589 850,000 126.85 J MCF7 ATCC # HTB-22 74,745
17.52 K MCF7-c18 Gift from Dr. Christopher Bentz, Director, Cancer
and 1,031,247 531.31 Developmental Therapeutics Program, Buck
Institute for Age Research, UCSF L MDA-MB-361 ATCC # HBT-27 .TM.
371,731 112.79 M MDA-MB-453 ATCC # HBT-131 .TM. 393,441 185.51 N
MKN-7 Health Science Research Resource Bank of the Japanese
1,217,989 181.73 Health Sciences Foundation #JCRB1025 O NCI-N87
ATCC # CRL-5822 .TM. 1,233,479 366.10 P OVCAR8 NCI 60-cell panel
from NCI-DTP 53,272 99.79 Q OVCAR8- NCI 60-cell panel from NCI-DTP,
stably transfected 673,300 711.87 Her2 with HER2 R SkBr3 ATCC #
HBT-30 .TM. 1,315,512 228.68 S SKOV3 ATCC # HTB-77 .TM. 1,377,661
600.81 T ZR75-1 ATCC # CRL-1500 .TM. 199,132 30.32 (Results for
MKN-45 cells were below detection level)
TABLE-US-00003 TABLE 2 HER2 levels vs PLD uptake FIG. HER2 fg 1B
Cell Line Source (#/cell) dox/cell A 4T1-clone- ATCC # CRL-2539
.TM. 650,000 13.54 12W7 B ADRr ADR-RES (NCI-DTP) 40,792 23.24 D
BT474-M3 Noble, Cancer Chemother. Pharmacol. 2009 64: 741-51
1,706,601 106.60 E Calu-3 ATCC # HTB-55 .TM. 1,196,976 41.64 G HeLa
ATCC # CCL-2 .TM. 123,713 291.11 H IGROV1 NCI 60-cell panel from
NCI-DTP 158,418 34.94 I JIMT-1 DSMZ # ACC-589 850,000 155.46 J MCF7
ATCC # HTB-22 74,745 13.57 K MCF7-c18 Gift from Dr. Christopher
Bentz, Director, Cancer and 1,031,247 115.88 Developmental
Therapeutics Program, Buck Institute for Age Research, UCSF M
MDA-MB-453 ATCC # HBT-131 .TM. 393,441 59.97 N MKN-7 Health Science
Research Resource Bank of the Japanese 1,217,989 48.24 Health
Sciences Foundation #JCRB1025 O NCI-N87 ATCC # CRL-5822 .TM.
1,233,479 47.44 P OVCAR8 NCI 60-cell panel from NCI-DTP 53,272
90.53 Q OVCAR8- NCI 60-cell panel from NCI-DTP, 673,300 37.00 Her2
stably transfected with HER2 S SKOV3 ATCC # HTB-77 .TM. 1,377,661
43.83 T ZR75-1 ATCC # CRL-1500 .TM. 199,132 26.10 U MKN-45 DSMZ #
ACC-409 152,197 57.02 (Results for AdRr-Her2, HCC1954, and
MDA-MB-361 cells were below detection level)
[0097] In order to quantify uptake into the different cell
populations, MM-302 was prepared to contain a red-fluorescent
carbocyanine tracer DiIC18(5)-DS (Invitrogen D12730--abbreviated
DiI5). Di15 is a lipophilic fluorescent dye that intercalates into
the lipid bilayer of the liposome during the extrusion process.
4T1-Her2 cell populations expressing different ranges of human HER2
were incubated with 10 .mu.g/ml fluorescently labeled MM-302 for 3
hrs, washed and incubated for an additional 21 hrs. Cells were
harvested, stained for cell surface human HER2 and analyzed for
both HER2 levels and liposome binding via flow cytometry. While the
4T1 cell line expresses murine HER2, MM-302 does not bind to the
murine receptor. The figure shows that uptake of these liposomes
into 4T1 cells was strongly dependent on human HER2 expression
(FIG. 1C). Similar results were obtained for populations of the
HeLa cell lines expressing different ranges of HER2 (FIG. 1D).
These results further demonstrate that MM-302 is highly effective
in binding cells with high HER2 levels but has little or no binding
to cells with relatively lower HER2 protein expression.
Example 2
MM-302 is Effectively Internalized into HER2-Overexpressing Tumor
Cells and Significantly Inhibits Tumor Growth in a Xenograft
Model
[0098] To determine levels of binding and internalization of MM-302
into HER2 over-expressing tumor cells, BT474-M3 cells
(1.7.times.10.sup.6 HER2/cell) were incubated with MM-302, PLD or
free doxorubicin at 15 .mu.g/ml for up to 3 h (FIG. 2A). MM-302 was
efficiently taken into tumor cells, as evidenced by total cell
binding (FIG. 2A) and nuclear doxorubicin accumulation (FIG. 2B).
By contrast, the untargeted analogue, PLD, did not show any
appreciable accumulation demonstrating the requirement of targeting
to effectively deliver liposomal doxorubicin in vitro. As a
control, free doxorubicin was shown to freely enter cells and
accumulate in the nucleus. Results showed effective binding and
internalization of MM-302 (but not PLD) into HER2-overexpressing
tumor cells.
[0099] The anti-tumor activity of MM-302 was evaluated in a breast
cancer xenograft model. Mice were inoculated with BT474-M3 cells
and when the tumor volumes reached an average of 250 mm.sup.3,
treatment with PBS (control), MM-302 or PLD (both at 6 mg/kg dox
equiv.) was started (q7d, n=3 doses). Both MM-302 and PLD
significantly inhibited tumor growth relative to control (t-test at
day 55; p<0.0001). MM-302 resulted in a stronger inhibition of
tumor growth relative to PLD (t-test at day 55; p=0.0310) (FIG.
2C). At study termination, 3 complete regressions were observed
with MM-302 and only 1 with PLD. MM-302 and PLD had similar
pharmacokinetic profiles (FIG. 2D) indicating that the improved
efficacy was as a result of HER2-targeting, rather than prolonged
exposure.
Example 3
Impact of HER2 Levels on MM-302 Uptake In Vivo
[0100] Experiments were conducted to demonstrate HER2-mediated
uptake of MM-302 into target tumor cells from xenograft models
compared with untargeted liposomal doxorubicin. Mice bearing
BT474-M3 xenograft tumors in the mammary fat pad were injected with
Di15-labeled MM-302 (Di15-F5-PLD) or UT-PLD (Di15-UT-PL). A tumor
single cell suspension was prepared and stained with FITC-HER2
antibodies. Di15-positive-HER2-positive cells were determined by
FACS. A distinct population of cells with elevated doxorubicin
levels was identified, indicating that liposomes had not just been
deposited in the tumor interstitial space, but had been taken up
into the cells themselves (FIG. 3A). This was particularly evident
in cell samples derived from tumors treated with HER2-targeted
liposomes. The percentage of cells with elevated liposome content
began to rise in cell subsets expressing on average 100,000 and
200,000 HER2 receptors per cell. Untargeted liposomes did not show
any preferential uptake into HER2 positive cells. These results
demonstrate that MM-302 uptake in tumor cells in vivo is
HER2-dependent and further support a level of at least
100,000-200,000 HER2 receptors per cell necessary to allow
significant binding and internalization of MM-302.
[0101] The distribution of HER2 membrane intensity was determined
on a single-cell basis in full tissue sections and is shown in FIG.
3B, representing the variability of expression in the tissue.
Example 4
Human Cardiomyocytes do not Express Sufficient HER2 Levels to
Actively Take Up MM-302
[0102] Human cardiomyocytes have been reported to express low
levels of HER2, and therefore were thought to have potential for
MM-302 uptake. ESCd and iPSd human cardiomyocytes were obtained to
study the effect of MM-302 on human cardiac cells in vitro. HER2
receptor levels on cardiomyocytes were determined by qFACS to be
approximately 70,000 and 200,000 receptors per cell in human ESCd
and iPSd cardiomyocytes, respectively. These results are consistent
with the reported low HER2 expression in human cardiac tissue
(Fuchs et al., Breast Cancer Res Treat. 2003; 82:23-8).
[0103] HER2 expression levels on normal and diseased human heart
tissue were measured via quantitative immunohistochemistry. A human
heart Tissue Microarray (TMA) was stained for HER2 and DAPI and the
(Mean HER2 intensity)/core was quantified with Definiens.RTM.
software. A cell pellet array with cell lines at different HER2
expression levels was stained as above and the (Mean HER2
intensity)/core was quantified and plotted against the
correspondent LOG (HER2 receptor #) to generate a standard. Based
on the generated standard, the average HER2 receptor #/core for the
different human heart TMA cores was interpolated (Table 3).
TABLE-US-00004 TABLE 3 Interpolated HER2 Receptor Number HER2 ID
Pathology Diagnosis # 1 Chronic rheumatic valvular disease 40,000
with calcification 2-pt1 Chronic rheumatic valvular disease 38,000
2-pt2 Chronic rheumatic valvular disease 38,000 2-pt3 Chronic
rheumatic valvular disease 47,000 2-pt4 Chronic rheumatic valvular
disease 47,000 2-pt5 Chronic rheumatic valvular disease 39,000
2-pt6 Chronic rheumatic valvular disease 38,000 2-pt7 Chronic
rheumatic valvular disease 42,000 2-pt8 Chronic rheumatic valvular
disease 42,000 2-pt9 Chronic rheumatic valvular disease 41,000 3
Hepatocellular carcinoma embolus of 44,000 cardiac atrium 4
Hypertrophic cardiomyopathy 38,000 5 Normal great arteries tissue
37,000 6 Normal cardiac atrium tissue 37,000 7 Normal myocardial
tissue (focal 38,000 mild hypertrophy) 8 Normal auricle of heart
tissue 48,000 9 Normal myocardial tissue (mild 38,000 hypertrophy)
10 Normal myocardial tissue 38,000
[0104] To determine if the level of HER2 expression on
cardiomyocytes is sufficient to induce uptake of MM-302, total
cellular doxorubicin was quantified by HPLC following treatment of
ESCd (FIG. 4A) and iPSd (FIG. 4B) cardiomyocytes. Cardiomyocytes
(and cancer cells) treated with free doxorubicin result in
doxorubicin accumulation in all cells. Treatment with PLD did not
result in an increase in doxorubicin delivery in either
cardiomyocyte cell type. In contrast to HER2-overexpressing cancer
cells, the HER2 expression level on cardiomyocytes was not
sufficient to promote active uptake of MM-302. Taken together,
these results demonstrate delivery of doxorubicin via MM-302 does
not enhance doxorubicin exposure to low level HER2 expressing
non-target cells such as cardiomyocytes as compared to PLD.
Example 5
MM-302 does not Reduce Human Cardiomyocyte Viability or Stimulate
Apoptotic Responses
[0105] Exposure to low levels of doxorubicin can be cytotoxic. To
determine if treatment with MM-302 or PLD affected cardiomyocyte
viability, ESCd cardiomyocytes were incubated with free dox, PLD or
MM-302 for 3 h at the indicated concentration followed by washing
and incubation in fresh media for 24 h. Treatment with free
doxorubicin resulted in a loss of viability at concentrations as
low as 0.2 .mu.g/ml (FIG. 4C). Conversely, treatment with MM-302
and PLD did not lead to reductions in viability at any
concentration tested, including super-therapeutic concentrations up
to 45 .mu.g/ml. To further test whether treatment with MM-302 or
PLD affected cardiomyocyte viability, iPSd cardiomyocytes were
treated with the indicated concentration of free doxorubicin, PLD
or MM-302 for 24 hours. Treatment with doxorubicin resulted in a
marked decrease in viability as compared to treatment with PLD and
MM-302 (FIG. 4D). The presence of elevated levels of cardiac
troponins is a clinical indicator of cardiac damage. The
supernatant from the iPSd cardiomyocytes in (D) was analyzed for
levels of troponin I. As shown in FIG. 4E, doxorubicin treatment
resulted in a marked increase of Troponin I compared to treatment
with PLD or MM-302. These results demonstrate that ESCd and iPSd
cardiomyocytes are sensitive to doxorubicin, and that treatment
with MM-302 and PLD does not provide sufficient doxorubicin
exposure to affect cardiomyocyte viability.
[0106] Exposure of cells to low levels of doxorubicin may induce
subtle cellular changes not revealed by cell viability
measurements, including DNA damage, cell stress and incipient
apoptosis. Following treatment with MM-302, PLD and free
doxorubicin, cardiomyocytes were stained for proteins in each of
these response pathways and imaged using high-content microscopy.
Single-cell data were generated by analyzing the resulting images
using ImageRail.
[0107] In response to double-stranded DNA damage, histone H2AX
becomes phosphorylated, forming gamma-H2AX. Treatment of
cardiomyocytes with free doxorubicin resulted in a dose-dependent
increase in nuclear gamma-H2AX (FIG. 5A). However, treatment with
MM-302 and PLD did not increase nuclear gamma-H2AX signal at any
concentration tested, indicating that liposomal encapsulation
prevented DNA damage to cardiomyocytes in vitro.
[0108] In response to cellular stress, HSP27 and p53 can be
phosphorylated, leading to cell cycle arrest, followed by DNA
repair or apoptosis depending on the extent of injury. Cardiac
cells exposed to free doxorubicin demonstrate a dose-dependent
increase in phospho-HSP27 and phospho-p53 indicating an induction
of cellular stress following treatment (FIGS. 5B and 5C). However,
an increase in phospho-HSP27 was not observed in cells treated with
either MM-302 or PLD regardless of concentration. In most cases,
there did not appear to be an effect on phospho-p53 in cells
treated with MM-302 or PLD, with the exception of a slight increase
in phospho-p53 following treatment with 5.0 .mu.g/ml of MM-302.
However, treatment at this and higher concentrations did not result
in increased cell death.
[0109] In cases of severe DNA damage and cell stress, the cell may
initiate the apoptotic pathway including activation of a caspase
cascade, ultimately resulting in the cleavage of the DNA repair
protein PARP. Treatment with 5.0 .mu.g/ml of free doxorubicin led
to an increase in nuclear cleaved PARP (cPARP) (FIG. 5D),
correlating with the observed increase in cell death. However,
treatment with MM-302 or PLD did not result in increased nuclear
cPARP suggesting that treatment under these conditions is not
sufficient to induce apoptosis.
Example 6
Impacts of HER2-Targeted Agents on Intracellular Signaling in
Cardiomyocytes
[0110] The concurrent use of doxorubicin and trastuzumab is
contraindicated due to an unacceptably high incidence of cardiac
events observed in patients treated with the combination. The
mechanism of action for the cardiotoxicity associated with this
combination is believed to be the simultaneous induction of
cellular stress by doxorubicin and by trastuzumab-mediated
inhibition of HER2 signaling pathways that is necessary to respond
to the cellular stress induced by doxorubicin.
[0111] To determine if pretreatment with MM-302 alters
HER2-mediated signaling (an essential pathway in cardiomyocytes),
iPDd cardiomyocytes were pretreated for 24 hours with trastuzumab,
lapatinib (a small molecule HER2 tyrosine kinase inhibitor), or the
MM-302 antibody (F5-scFv) and an empty liposome identical to MM-302
except that it does not contain doxorubicin) (F5-lipo). After
stimulation with 10 nM (FIG. 6A) and 5 nM (FIG. 6B) of heregulin
(HRG) for 10 min, the levels of phospho-AKT (pAKT, FIG. 6A) and
phospho-ERK (pERK, FIG. 6B) were measured by high content
microscopy as described above. Pretreatment with trastuzumab for 24
h resulted in a reduction in HRG-mediated phosphorylation of both
proteins. Pretreatment with lapatinib led to a reduction in basal
phosphorylation of AKT and ERK as well as a complete inhibition of
HRG-induced phosphorylation of these proteins. Pretreatment F5-lipo
did not inhibit HRG-induced phosphorylation of AKT or ERK. These
results suggest that, despite targeting HER2, MM-302 does not
inhibit ligand-induced phospho-AKT and phospho-ERK signaling in
cardiomyocytes, leaving these critical signaling pathways
functional.
[0112] These results also show that trastuzumab and lapatinib have
a significantly greater negative impact on this signaling pathway
in cardiomyocytes than do F5 scFv or F5 lipo. This in turn is an
indication that the anti-HER2 antibody component of MM-302 is less
cardiotoxic than the anti-HER2 antibody trastuzumab. The results
show that F5, either alone or linked to the exterior of an MM-302
liposome, does not interfere with heregulin (ligand)-stimulated
HER2/HER3 heterodimer-mediated signaling in cardiomyocytes which is
an essential intracellular signaling modality, inhibition of which
is believed to be a key mechanism mediating trastuzumab-induced
cardiotoxicity.
Example 7
MM-302 has a Lower Accumulation in Mouse Heart Tissue Compared to
Free Doxorubicin
[0113] Liposome targeting with a highly specific antibody fragment
such as F5 generally does not alter the total tissue deposition of
liposomes, but rather alters their microdistribution following
extravasation. The macro-level biodistributions of MM-302 (square),
PLD (UT-PLD, triangle) and doxorubicin (free dox, circle) were
compared in mouse heart tissue (FIG. 7A), human xenograft tumor
tissue (FIG. 7B) and paw tissue (FIG. 7C) in NCI-N87 tumor bearing
mice inoculated as described above. Mice (n=4/time point/group)
were injected i.v. with MM-302, PLD, or free doxorubicin (all at 3
mg/kg dox equiv.) and hearts were collected at 0.5, 4, 24, and 96 h
(for dox) or 168 h (for MM-302 and PLD) post injection and
doxorubicin quantified by HPLC (FIG. 7A). Injection of free
doxorubicin resulted in a high peak exposure in the heart at 0.5 h
(10% of injected dose (i.d.)/g tissue) compared to the two
liposomal formulations. The clearance of doxorubicin from the heart
tissue after free doxorubicin injection was faster compared to
MM-302 and PLD and at 24 h the amount of detected doxorubicin
(0.77% of i.d./g tissue) was close to background. Both MM-302 and
PLD had a sustained accumulation profile that peaked at 24 h (2.8%
and 2.6% for MM-302 and PLD, respectively) while values returned to
background at 168 h. These results are in a range similar to that
of previously reported data on the heart biodistribution of other
PLD formulations. No significant differences were observed between
the heart biodistribution of MM-302 and PLD.
Example 8
MM-302 Results in Lower Nuclear Doxorubicin Accumulation in Mouse
Tissue Compared to Free Doxorubicin
[0114] The microdistribution of doxorubicin (naturally fluorescent)
and liposomes (DiI5-labelled) was analyzed in cryosections
generated from heart tissues of mice injected with either free
doxorubicin, MM-302-DiI5 or PLD-DiI5 (all at 3 mg/kg dox equiv) at
0.5, 4 and 24 h post injection. In order to visualize the heart
vasculature, mice were injected i.v. with FITC-lectin 5 min before
sacrificing. Heart slices were imaged by fluorescence confocal
microscopy. Representative fields for the different treatment
groups at the three time points analyzed (0.5, 4 and 24 h) are
shown in FIG. 7D. Untreated hearts were also imaged and a
representative image is shown in FIG. 7D (left panels).
Co-localization of doxorubicin with the nuclear signal is shown in
the bottom panels of FIG. 7D. Higher magnification images of the
nuclear doxorubicin signal are shown in FIG. 7E, for both
doxorubicin and MM-302 at the 0.5 h time point. While with MM-302
no doxorubicin signal is visible in the nuclei, with free
doxorubicin the majority of the nuclei are doxorubicin-positive.
The images were analyzed as described above and the percent of
doxorubicin-positive nuclei determined. Injection of free
doxorubicin resulted in a prominent nuclear accumulation of
doxorubicin at 0.5 h, with about 50% of the nuclei positive for
doxorubicin. By 4 h, however, only 23% of the nuclei were positive
for doxorubicin and the signal returned to basal levels at 24
h.
[0115] With the liposomal formulations, little to no signal was
detected for the majority of fields of view. Occasional signal in
the DiI5 channel (liposome) was detected. In these cases, the
liposome signal predominantly co-localized with the FITC-lectin
signal, indicating liposomes that had not extravasated into the
heart tissue but still remained in the vascular compartment. Upon
MM-302-DiI5 or PLD-DiI5 treatment, doxorubicin was not detected in
the nucleus in the majority of the heart fields analyzed,
independent of time point. In one of the four MM-302-DiI5 hearts
collected at 0.5 h and in one of the four MM-302-DiI5 hearts
collected at 4 h, a liposomal signal was detected in the
extravascular space and doxorubicin was found in a small percentage
of the nuclei. Similarly, in one of four PLD hearts collected at
0.5 h and in two of four PLD heart collected at 24 h, images
revealed the extravascular liposomal signal and presence of nuclear
doxorubicin. These fields are not presented as representative
images, however their values were considered for the quantification
shown in FIG. 7F. The area under the curves of both MM-302 and PLD
were statistically significantly lower than the free doxorubicin
AUC (p<0.001). No significant differences were observed between
the AUCs of MM-302 and PLD.
[0116] In order to get a broader visualization of the distribution
of doxorubicin and of the liposomes in the heart tissue, full heart
section scans were taken. The full section heart scans visually
confirmed the results of the confocal microscopy, showing a broad
doxorubicin distribution with nuclear localization upon free
doxorubicin injection, and only rare liposome and doxorubicin
signals in the hearts of mice injected with either Di15 MM-302 or
DiI5 PLD.
[0117] In summary, treatment with either MM-302 or PLD showed
significantly lower nuclear doxorubicin accumulation than was seen
following treatment with free doxorubicin, while this did not
differ significantly between MM-302 and PLD.
EQUIVALENTS
[0118] Those skilled in the art will recognize, or be able to
ascertain and implement using no more than routine experimentation,
many equivalents of the specific embodiments described herein. Such
equivalents are intended to be encompassed by the following claims.
Any combinations of the embodiments disclosed in the dependent
claims are contemplated to be within the scope of the
disclosure.
INCORPORATION BY REFERENCE
[0119] The disclosure of each and every U.S. and foreign patent and
pending patent application and publication referred to herein is
specifically incorporated by reference herein in its entirety.
* * * * *