U.S. patent application number 11/229250 was filed with the patent office on 2006-01-12 for dual lumen device for biopsy and treatment of breast tumors and method for use.
This patent application is currently assigned to Sanarus, Inc.. Invention is credited to Glenn Foy, Paul Mikus, Seth Stabinsky, Kevin H. Van Bladel, Lisa Zindel.
Application Number | 20060009712 11/229250 |
Document ID | / |
Family ID | 24394333 |
Filed Date | 2006-01-12 |
United States Patent
Application |
20060009712 |
Kind Code |
A1 |
Van Bladel; Kevin H. ; et
al. |
January 12, 2006 |
Dual lumen device for biopsy and treatment of breast tumors and
method for use
Abstract
A device for diagnosis and treatment of tumors and lesions
within the body. A cannula adapted to apply suction through the
lumen of the catheter to the tumor or lesion is described. The
lumen has a self sealing valve through which a cryoprobe is
inserted while the suction is being applied. The cryoprobe is then
inserted into the lesion, and operated to ablate the lesion.
Inventors: |
Van Bladel; Kevin H.;
(Pleasanton, CA) ; Stabinsky; Seth; (Pleasanton,
CA) ; Zindel; Lisa; (Pleasanton, CA) ; Foy;
Glenn; (Pleasanton, CA) ; Mikus; Paul;
(Irvine, CA) |
Correspondence
Address: |
CROCKETT & CROCKETT
24012 CALLE DE LA PLATA
SUITE 400
LAGUNA HILLS
CA
92653
US
|
Assignee: |
Sanarus, Inc.
|
Family ID: |
24394333 |
Appl. No.: |
11/229250 |
Filed: |
September 16, 2005 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
10321136 |
Dec 16, 2002 |
6945942 |
|
|
11229250 |
Sep 16, 2005 |
|
|
|
09598124 |
Jun 21, 2000 |
6494844 |
|
|
10321136 |
Dec 16, 2002 |
|
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Current U.S.
Class: |
600/566 ;
600/567; 606/20; 606/27 |
Current CPC
Class: |
A61B 10/0041 20130101;
A61B 2018/00291 20130101; A61B 18/02 20130101; A61B 10/0283
20130101 |
Class at
Publication: |
600/566 ;
600/567; 606/020; 606/027 |
International
Class: |
A61B 10/00 20060101
A61B010/00; A61B 18/18 20060101 A61B018/18; A61B 18/04 20060101
A61B018/04 |
Claims
1. A system for treating or sampling a mass of tissue within a
human patient, said device comprising: a cannula having a distal
end adapted for insertion into the body of the patient, a proximal
end, and a first lumen extending through the cannula and defining a
first lumen distal opening in the cannula, and a second lumen
extending through the cannula and defining a second lumen proximal
opening and a second lumen distal opening in the cannula, said
second lumen distal opening being proximate the first lumen distal
opening; a fitting disposed on the proximal end of the cannula,
said fitting adapted for connection to a vacuum source to the first
lumen; at least one elongate medical device sized and dimensioned
to pass into the second lumen through second lumen distal opening
and extend beyond the distal end of the cannula, said elongate
medical device having a distal tip adapted for penetration into
body tissue proximate the distal end of the cannula.
2. The system of claim 1 wherein the elongate medical device is a
biopsy needle.
3. The system of claim 1 wherein the elongate medical device is a
cryoprobe.
4. The system of claim 1 wherein the elongate medical device is an
ablation device suitable for ablation of the mass.
5. The system of claim 1 further comprising an additional elongate
medical device sized and dimensioned to pass into the first lumen
through first lumen distal opening and extend beyond the distal end
of the cannula.
6. A method for treating or sampling a mass of tissue within a
human patient, said method comprising: providing a cannula having a
distal end adapted for insertion into the body of the patient, a
proximal end, and a first lumen extending through the cannula and
defining a first lumen distal opening in the cannula, and a second
lumen extending through the cannula and defining a second lumen
proximal opening and a second lumen distal opening in the cannula,
said second lumen distal opening being proximate the first lumen
distal opening; a fitting disposed on the proximal end of the
cannula, said fitting adapted for connection to a vacuum source to
the first lumen; an elongate medical device sized and dimensioned
to pass into the second lumen through second lumen distal opening
and extend beyond the distal end of the cannula, said elongate
medical device having a distal tip adapted for penetration into
body tissue proximate the distal end of the cannula; inserting the
cannula into the body of the patient so that the distal end of the
cannula is proximate the mass; selectively drawing the mass toward
the cannula by applying suction to the first lumen of the cannula;
inserting the elongate medical device through the second lumen of
the cannula and into the vicinity of the mass; operating the
elongate medical device treat or sample the mass.
7. The method of claim 6 further comprising the steps of: providing
the elongate medical device in the form of a cryoprobe; extending
the distal tip of the cryoprobe beyond the distal tip of the
cannula; and operating the cryoprobe to treat the mass.
8. The method of claim 7 further comprising the step of: locating
the distal tip of the cryoprobe such that the mass is superficial
to the distal tip upon extension from the distal end of the
cannula.
Description
[0001] This application is a continuation of U.S. application Ser.
No. 10/321,136, filed Dec. 16, 2002, now U.S. Pat. No. 6,945,942,
which is a continuation of U.S. application Ser. No. 09/598,124,
filed Jun. 21, 2000, now U.S. Pat. No. 6,494,844.
FIELD OF THE INVENTIONS
[0002] The devices and method described below relate to the
diagnosis and treatment of breast lesions, and more generally, to
the diagnosis and treatment of tumors and lesions throughout the
body.
BACKGROUND OF THE INVENTIONS
[0003] Biopsy is an important procedure used for the diagnosis of
patients with cancerous tumors, pre-malignant conditions, and other
diseases and disorders. Typically, in the case of cancer, when the
physician establishes by means of procedures such as palpation,
mammography or x-ray, or ultrasound imaging that suspicious
circumstances exist, a biopsy is performed. The biopsy will help
determine whether the cells are cancerous, the type of cancer, and
what treatment should be used to treat the cancer. Biopsy may be
done by an open or percutaneous technique. Open biopsy, which is an
invasive surgical procedure using a scalpel and involving direct
vision of the target area, removes the entire mass (excisional
biopsy) or a part of the mass (incisional biopsy). Percutaneous
biopsy, on the other hand, is usually done with a needle-like
instrument through a relatively small incision, blindly or with the
aid of an imaging device, and may be either a fine needle
aspiration (FNA) or a core biopsy. In FNA biopsy, individual cells
or clusters of cells are obtained for cytologic examination and may
be prepared such as in a Papanicolaou smear. In core biopsy, as the
term suggests, a core or fragment of tissue is obtained for
histologic examination which may be done via a frozen section or
paraffin section. One important area where biopsies are performed
is the diagnosis of breast tumors.
[0004] Traditionally, the biopsy technique for breast tumors
involves placing a biopsy device multiple times into the breast and
taking several samples of tissue from a mass or tumor which is
suspected of being cancerous. Several samples are required to be
sure that some tissue from the suspect mass has been captured, and
enough tissue has been sampled to ensure that, if disperse cancer
cells exist in the suspect mass some of those cancer cells will be
captured in the samples. Each time the device is placed the
physician must locate and direct the device with ultrasound imaging
into the correct position near the suspect mass. Some breast tumors
and lesions are very well defined, hard spherical masses which grow
within the soft, compliant breast tissue. It is difficult to force
a needle into these lesions because they are resistant to puncture
and fairly mobile. Forcing the biopsy needle into the lesion is
like trying to spear an apple floating in water.
[0005] Vacuum assisted biopsy system proposed by Biopsys involves
sucking a breast lesion into a cannula and shearing off the
captured edge of the lesion to obtain a biopsy sample. The device
uses a vacuum to collect tissue into the side of an open tubular
device, and then uses a rotating corer to cut the tissue collected.
The rotating corer is slidable within the tubular section and can
be pulled back to remove the tissue collected in the rotating
corer. An additional stylet inside the rotating corer can be used
to push the tissue out of the core. The device can be rotated on
its axis to remove a sample, 360 degrees around the central
placement of the device. Typically, physicians sample six to eight
cores. One advantage of this device is that the physician does not
have to remove the device for additional biopsy samples. However,
the tumor itself must be re-engaged after every coring operation,
which entails substantial effort in relocation and confirmation
that the target suspect mass has been engaged by the side aperture.
Tumors may be too tough to yield to the suction and deform as
necessary to enter the side opening of the cannula. Doctors also
currently use the device to take a circular sequence of cores by
rotating the device about its long axis or by sideways movement of
the suction head to take a line of cores.
[0006] After biopsy and analysis, the tumor must be treated with a
separate device, as Biopsys teaches that their coring device should
not be used for resection. Indeed, the device is not designed to
perform resection with assurance that complete resection of a
suspect mass has been accomplished. Mechanical cutting and
disruption of the tissue structure and cancer cell dispersion (that
is, tearing of the tissue around the cancer and movement of the
cancer cells amongst normal tissue) will result in unintentional
delivery of cancer cells into healthy tissue adjacent the
lesion.
SUMMARY
[0007] The devices and methods described below provide for
diagnosis and treatment of tumors within the breast. The devices
include structures which permit the surgeon to secure a suspect
mass or tumor within the breast for an extended period of time and
for several biopsies, coring procedures, or resections. The suspect
mass or tumor is secured to a cannula for the entire diagnostic and
treatment procedure, or subsets of the procedure such as biopsy or
ablation. This allows the placement of the cannula with a single
step utilizing methods such as ultrasound to guide the cannula
toward the tumor.
[0008] The cannula includes a lumen adapted to be connected to a
source of vacuum, which can be used to secure a breast lesion to
the cannula. A ring seal on the proximal end of the catheter
permits biopsy needles, cryoprobes or other ablation devices to be
inserted through the cannula and into the lesion while the vacuum
on the cannula is maintained. In this manner, the needles and
ablation devices may be inserted into the lesion while the lesion
in held securely in place by the suction applied to the
cannula.
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] FIG. 1 illustrates the cannula adapted for use in securing a
breast tumor during a biopsy or ablation procedure.
[0010] FIG. 2 illustrates the biopsy needle in use with the cannula
of FIG. 1.
[0011] FIG. 3 illustrates a multiple coring needle which may be
used with the cannula of FIG. 1.
[0012] FIG. 4 illustrates the placement of a cryoprobe or other
ablative device within the cannula of FIG. 1.
[0013] FIG. 5 illustrates a method of breast tumor ablation for
tumors located near the skin.
[0014] FIG. 6 illustrates a method of breast tumor ablation for
tumors located near the skin.
[0015] FIG. 7 illustrates an adaptation of the cannula to provide
additional protection to the skin.
DETAILED DESCRIPTION OF THE INVENTIONS
[0016] FIG. 1 illustrates the biopsy and treatment device adapted
for use in securing a breast tumor during the biopsy and treatment
procedure. The patient 1 and the patient's breast 2 and skin 3 of
the breast are shown schematically. The tumor, lesion or other
suspect mass 4 is located within the breast, surrounded by soft
tissue and fatty tissue. The tumor in this illustration is a well
defined, hard mass ranging in size from 3 to 40 mm in diameter,
typical of a benign palpable tumor or fibro-adenoma, although the
device and method may be used to treat fibrocystic disease and
other conditions. The device comprises a cannula 5 with a straight
cut distal edge 6 adapted for insertion through a small incision in
the skin overlying the tumor and a proximal end 7 which remains
outside the breast. The proximal end of the cannula is fitted with
hub 8 which serves as a handle and a manifold for the several
connections to the cannula. This hub may be integral with the
cannula or provided as a separate piece secured to the proximal end
of the cannula. The cannula has a lumen 9 extending through the
cannula from the distal edge to the proximal end of the cannula. On
the hub, a vacuum connection 10 in the form of Luer fitting
provides a fluid connection between the lumen of the cannula and a
vacuum hose 11. The vacuum hose may be connected to any source of
vacuum or suction. On the proximal end of the hub, a valve 12 seals
the cannula proximal end against air pressure but allows passage of
the needles and probes used in the procedure. The valve may be a
self-sealing silicone plug 13 provided with a slit 14 capable of
accommodating the needles and probes by resiliently expanding and
conforming around a needle or probe when a needle or probe is
forced through the slit, and resiliently closing to an airtight
seal when the needles or probes are removed. Thus, the valve allows
for insertion of various instruments and elongate medical devices
while maintaining the seal necessary to provide sufficient suction
to hold the tumor. A stopper or cap 15 is provided for insertion
into the slit when the valve is not occupied by a needle or probe
to positively seal the valve. A backup valve, such as ball valve
which opens to form a clear and straight lumen, may be placed in
line before the valve 12 in place of the stopper. The cannula is
made of an acceptable biological material such as Teflon.TM.
(polytetrafluoroethylene (PTFE) or expanded polytetrafluoroethylene
(ePTFE)), carbon fiber, metal or metal composite for maximum
strength with minimal wall thickness. The self-sealing valve is
comprised of silicone or other material of similar resilience and
conformability. An additional valve 16 may be added on the proximal
handle, controlling a port 17 communicating between the vacuum
lumen and the exterior of the cannula. The valve illustrated is
merely a thumbslide mounted in a recess 18. This valve may be used
to break the vacuum established in the vacuum lumen to release a
lesion from the distal tip of the device, or to bleed the vacuum
from the lumen to lessen the suction on a lesion.
[0017] FIG. 2 illustrates the cannula in use with a biopsy needle
20 in place within the lumen. A biopsy needle 20 fits within the
lumen of the cannula and passes through the valve 12. The valve
deforms and opens enough to allow the needle to pass through, yet
still maintains a sufficiently airtight seal to maintain the vacuum
within the cannula lumen. The needle has a sharp distal tip 21
which can pierce the tumor 4. The distal tip is shaped with a
coring edge to collect tissue within the lumen 22 of the needle. As
depicted in FIG. 2, suction has been applied to the cannula lumen
through the vacuum hose 11 and connection 10, thus drawing the
tumor to the distal edge of the cannula and securely holding it in
place. The biopsy needle has been inserted through the self-sealing
valve and through the cannula lumen into and through the tumor. A
small core of tumor tissue 23 has been forced into the lumen of the
needle. The needle may now be removed and the core of tumor tissue
extracted and analyzed for the presence of cancer cells. When the
needle is removed, the suction is maintained on the cannula lumen
and the tumor remains securely engaged with the cannula distal
edge. The biopsy needle (or another) can then be inserted through
the cannula and into the tumor without having to relocate and
reengage the tumor with the cannula. After all necessary biopsies
have been taken, the sample tissue may be analyzed for the presence
of cancer cells or other undesirable tissue for which ablation is
indicated.
[0018] FIG. 3 illustrates a multiple coring needle 24 for use with
the system. This needle includes several coring lumens 25 opening
at the distal end of the needle into coring edges 26. The coring
lumens are spaced in a circle about the circumference of the
needle, and extend from the distal tip 21 of the needle proximally
to the proximal end of the needle. It may be used in place of the
single biopsy coring needle as illustrated in FIG. 2. By providing
suction to one or more of the lumens, the tumor is secured to the
coring needle.
[0019] FIG. 4 illustrates the use of an ablative device, such as
cryoprobe, with the cannula. The cryoprobe 27 fits within the lumen
of the cannula and passes through the valve 12, and the distal tip
of the cryoprobe is forced into the tumor until the active freezing
portion of the probe resides within the tumor. During placement of
the cryoprobe, the vacuum is maintained within the lumen so that
the tumor is securely engaged by the cannula. With the tumor
secured by the vacuum, the cryoprobe may be easily forced into the
tumor. The cryoprobe may be operated to ablate the tumor with
cryogenic freezing as required to destroy the tumor. To operate the
cryoprobe, liquid or gas cryogenic fluids (such as liquid nitrogen,
or gaseous argon in combination with a Joule-Thomson cryostat in
the probe tip) are passed through the probe, supplied from a
cryosurgical control system (not shown). The operation of the
cryoprobe creates an iceball 28 which encompasses the lesion 4, and
cools the lesion to lethal cryogenic temperatures. Any ablation
device may be used in place of the cryoprobe, including RF ablation
probes, microwave ablation probes, laser ablation probes, or
focused ultrasound energy probes. Temperature sensors 29 may be
mounted on the skin over the lesion in order to monitor skin
temperature, so that the surgeon may avoid ablating the skin.
[0020] In use, the devices described above are used in place of
traditional biopsy, coring and ablation devices. Prior to use, the
patient is prepared and the breast is appropriately prepped and
draped. The site is prepared using local anesthesia and,
optionally, intravenous sedation. The patient is positioned on an
operating table in the supine position, with the patient on her
back. (If the procedure is accomplished under stereotactic
guidance, the patient may be prone on a stereotactic table,
exposing the breast below the table.) The breast is imaged, if not
previously imaged, to determine the location of lesions. A small
incision is made in the breast to allow the cannula to be easily
inserted into the skin. The surgeon inserts the cannula into the
patient's breast through the incision, pushes it into the breast
until the distal edge of the cannula is proximate to the boundary
of the tumor. An ultrasound scanner, MRI, stereotactic,
mammographic, infrared or other imaging device is used to obtain an
image of the breast, including the tumor and any device inserted
into the breast, and the surgeon uses the display from the imaging
device to assist in guidance of the cannula to the tumor. With the
cannula distal edge in position near the tumor, the surgeon applies
vacuum to the cannula through the side port on the cannula. The
vacuum draws the tumor toward the cannula, and the cannula securely
engages the tumor until the suction is broken at the end of the
procedure. The surgical biopsy needle can be inserted through the
cannula and into the tumor to retrieve a sample of tissue for
analysis. Because coring can be accomplished without removing the
portion of the tumor engaged by the cannula, or otherwise
disrupting the suction between the cannula and the tumor, several
biopsy samples may be taken without having to relocate and
re-engage the tumor.
[0021] Depending on the analysis of the biopsy (whether or not the
samples obtained contain cancerous cells or other conditions),
treatment of the tumor may be required. If analysis can be
accomplished intra-operatively (that is, during a period of time in
which it is feasible to keep the patient in the operating room and
maintain the tumor engaged with the cannula), and indicates the
presence of cancerous cells or other condition for which ablation
is indicated, an ablation instrument can be inserted through the
cannula and into the tumor. If so, the surgeon inserts an ablation
instrument, such as a small caliber cryoprobe, into the tumor.
Preferably, the surgeon inserts a cryoprobe through the valve and
cannula and into the tumor, while maintaining suction on the
cannula. The surgeon initiates cooling of the cryoprobe, and cools
the tumor through one or more cycles of cooling to cryogenic
temperatures and subsequent warming and thawing. A double
freeze-thaw cycle is currently recommended. Each cycle consists of
a 6 to 15 minute freeze followed by thawing until the internal
cryoprobe temperature reaches 0.degree. C. (approximately 6 to 15
minutes). The device may also be used without regard to biopsy
results. Patients prefer to have these lesions treated, even if
they prove to be benign. In current practice, should biopsy results
indicate the presence of cancer, the patient must return to the
operating room shortly after the biopsy, undergo preparation,
anesthesia, relocation of the lesion and ablation. Instead, the
lesions may be ablated intraoperatively with the biopsy,
immediately after biopsy and without interrupting the procedure to
await the biopsy results. Should the biopsy prove negative for the
presence of cancer, the patient will have received a substantially
cosmetic treatment. Should the biopsy prove positive, the patient
will have received a necessary therapeutic procedure. In addition
to the ablative procedure, the positive biopsy may indicate the
need for additional monitoring and treatment.
[0022] For lesions deeper than 1 cm from the skin surface, the
cryoprobe is advanced until the distal tip is located approximately
in the center of the lesion or just beyond the lesion. For smaller
lesions (<2 cm diameter) the ice ball may grow beyond the
margins of the tumor, while for larger lesions, the ice ball may
remain within the confines of the tumor. The cryoprobe tip
temperatures and skin mounted thermocouple readings are monitored
throughout the ablation procedure. If the temperature of the skin
overlying the cryoprobe measures below freezing, freezing operation
of the cryoprobes should be paused until it returns to 10.degree.
C. (the temperature at the edge of the ice ball edge is 0.degree.
C. and exposure to such a temperature for the few minutes will not
harm the skin, but caution should always be employed).
[0023] The procedure may be augmented with additional steps. Just
prior to ablation treatment, prophylactic antibiotics can be
administered at the surgeon's discretion. Just prior to
cryosurgical ablation, cryogenic enhancement agents may be injected
directly into the tumor through a hypodermic needle inserted
through the valve and cannula and into the tumor while it is
secured by suction to the cannula. During cooling operation of the
cryoprobes, warm saline may be washed over the skin overlying the
tumor and iceball to prevent freezing of the skin.
[0024] If the lesion being treated is close to the skin such that
cryoablation of the lesion entails a danger of cryoablation of the
overlying skin, several milliliters of a resorbable material such
as sterile saline may be injected or inserted into the subcutaneous
tissue between the skin and the lesion. This will create a
thermally protective mass or barrier layer between the tumor and
the skin. Thermal protection may arise from insulative effect of
the thermally protective mass or merely by the distension or
separation of the skin away from the tumor and thus away from the
iceball. As illustrated in FIG. 5, where the tumor 4 is close to
the skin 3, the thermally protective mass 30 is injected between
the skin 3 and the subcutaneous fat 31 of the breast. When the
cryoprobe 27 is operated to create the iceball, the ice-ball 32
either grows into the thermally protective mass or is inhibited in
growth in the direction of the thermally protective mass (as
illustrated by the non-spherical shape of the iceball in this
illustration). This method basically distends the skin away from
the iceball. This may also be accomplished by dissecting the skin
away from the tumor with a balloon inserted between the skin and
fat in the area overlying the tumor. Balloon dissection can be
accomplished as illustrated in FIG. 6. Here, a balloon 33 has been
inserted subcutaneously between the tumor 4 and the overlying skin
3. The balloon is inflated with air or other sterile gas, through
inflation tube 34, creating a good layer of insulation between the
cryoprobe and the overlying skin.
[0025] FIG. 7 illustrates an adaptation of the cannula to provide
additional protection to the skin. The cryoprobe 27 is inserted
through a side lumen 35 provided on the cannula 5. The breast
lesion 4 is drawn by vacuum to the tip of the cannula. The
cryoprobe is advanced distally out of the side lumen until the
freezing region underlies the lesion, and it operated to create the
iceball 36. The iceball extends superficially toward the skin and
to encompass the lesion, and also extends posteriorly into the
breast, where some healthy breast tissue is ablated but the
overlying skin is not. This system and procedure also has the
advantage that the lesion itself is not punctured, limiting the
potential for seeding due to the release of cancerous cells from
the disruption of the tissue of the tumor.
[0026] The cannula illustrated above is preferably 10 to 20 cm in
length and about 3 mm in diameter with an internal diameter of 2.8
mm, and a clearance of about 0.25 mm between the inner bore of the
cannula and any device inserted through the cannula during suction.
The cryoprobes may be Joule-Thomson probes, liquid cryogen probes,
or probes of other designs. Various other ablative devices may be
used in place of the cryoprobe, including laser ablation devices,
RF ablation devices, chemical ablation catheters and any other
ablative technology proposed for use to destroy tumors and lesions.
The vacuum applied is preferably in the range of 14 to 21 inches of
mercury vacuum.
[0027] The devices and methods illustrated above have been
illustrated in relation to the treatment of tumors and lesions
within the breast. However, they may be used to treat tumors and
lesions throughout the body wherever the tumors which are difficult
to secure and locate are encountered, and wherever nearby tissue
must be protected from freezing. Thus the devices and methods may
be used for tumors and lesions of the uterine tube (such as uterine
fibroids), kidney, liver, prostate or brain.
[0028] Thus, while the preferred embodiments of the devices and
methods have been described in reference to the environment in
which they were developed, they are merely illustrative of the
principles of the inventions. Other embodiments and configurations
may be devised without departing from the spirit of the inventions
and the scope of the appended claims.
* * * * *