Surgery – Radioactive substance applied to body for therapy – Radioactive substance placed within body
Reexamination Certificate
2000-10-30
2003-03-25
Winakur, Eric F. (Department: 3736)
Surgery
Radioactive substance applied to body for therapy
Radioactive substance placed within body
C604S891100, C600S008000
Reexamination Certificate
active
06537193
ABSTRACT:
TECHNICAL FIELD
This invention relates generally to the field of brachytherapy. In particular, this invention relates to brachytherapy in combination with an adjunctive therapy for the treatment of malignancy in solid organs.
BACKGROUND
Brachytherapy is a form of radiation treatment in which a radiation source is placed into or adjacent to a malignant tumor. There are two general categories of brachytherapy: high dose rate (HDR); and low dose rate (LDR). HDR brachytherapy involves the placement of a radiation source with high activity adjacent to or into the malignant tumor for a limited period of time. LDR brachytherapy involves the placement of a low activity radiation source adjacent to or into the malignant tumor for an indefinite period of time.
The radiation sources used in LDR brachytherapy are radioactive isotopes. The most common isotopes used in LDR brachytherapy are
103
Pd (Palladium),
125
I (Iodine),
198
Au (Gold), and
192
Ir (Iridium). These isotopes are packaged in a cylindrical titanium housing and are commonly referred to as isotope seeds. The typical dimensions of the seeds are 0.5 mm in diameter and 0.5-1.0 cm in length. The isotopes used in LDR brachytherapy are chosen for their low energy and short half life. Low energy provides for limited penetration of the radiation so that the radiation effect is limited to the tumor without affecting adjacent normal tissue. A short half life is desirable so that the radiation dose can be delivered in a reasonably short time frame.
For
103
Pd and
125
I, the zone of therapeutic effect is limited to about a 1 cm diameter sphere about the seed, so typically, a three-dimensional array of seeds is used to treat a tumor. In LDR brachytherapy of prostate cancer, over 100 seeds are typically used. Because solid tumors, such as those found in prostate cancer, are perceived to be diffuse, the entire organ is targeted.
To place multiple seeds into a three dimensional array, seeds can be delivered by needles using a two dimensional grid pattern, and longitudinal spacing. The two dimensional grid is usually defined by a needle guide, called a template. The template consists of a matrix of holes that guide the longitudinal advancement of the needles to insure their proper two dimensional position in the tumor. Once the two dimensional array of needles is established in the tumor, the seeds are deposited along the longitudinal axis of each needle. The spacing of the seeds along the longitudinal axis of the needle is accomplished by using biocompatible spacers between the seeds. The spacers and seeds are alternately inserted into the needle prior to placement of the needle into the tumor. Once the needle is placed into the tumor, a mandrel is used to maintain the position of the line of seeds and spacers as the needle is withdrawn. This leaves a line of seeds in their proper longitudinal position. This process is then repeated at the other two dimensional grid coordinates forming the desired three dimensional array of seeds.
LDR brachytherapy is an effective modality for treating localized malignancies, however, it is not always successful in eradicating the malignancy. Some tumors are resistant to the effect of radiation, and sometimes the placement of seeds is not optimal, leaving spaces that are under treated. To enhance the effectiveness of brachytherapy, adjunctive treatments are often used. These adjunctive treatments include external beam radiation therapy, hyperthermia, systemic chemotherapy, systemic hormonal therapy, and immunotherapy.
Often there is a synergistic effect between brachytherapy and the adjunctive therapy. Brachytherapy can destroy the majority of the malignant cells and injured the remaining malignant cells. The adjunctive therapy can eradicate the remaining injured cells. Alternatively, the adjunctive therapy can make the malignant cells vulnerable to the radioactive isotope from the brachytherapy, for example, by holding the cells in the radiosensitive part of the cell cycle (e.g., G2M, late G2 or G2/S). Examples of radiosensitizing agents include butyrate, gemcitabine, 5-fluorouracil, catalase, paclitaxel, and misonidazole.
SUMMARY OF THE INVENTION
This invention primarily relates to LDR brachytherapy, also referred to as permanent seed implant brachytherapy, in combination with an adjunctive therapy. In addition, the device and methods of this invention also relate to HDR brachytherapy in combination with an adjunctive therapy. As used herein, the term adjunctive therapeutic is meant to embrace materials and/or compounds that can be used to effectuate an adjunctive therapy. As used herein, the term therapeutic is meant to embrace both curative and palliative treatments.
More specifically, the invention relates to radiation therapy using methods and devices that sensitizes target pathologies to radiation without sensitizing normal non-target tissue to radiation. In this aspect, the invention involves the placement of devices containing radiation sensitizing agents into a target pathology concurrent with a radiation therapy. This invention is not specific to a particular radiation sensitizing agent. Also, the sensitizing agent can have beneficial properties in addition to sensitizing the target pathology to radiation.
In one aspect, the invention features an implantable cancer therapy device including adjacent segments of a radioactive therapeutic and an adjunctive therapeutic. The segments of radioactive therapeutic and adjunctive therapeutic can be alternatively disposed in a predetermined spatial array. The implantation can be permanent or temporary. The device can be a substantially cylindrical filament, a mesh patch, or plurality of spaced radioactive seeds overlaid with an adjunctive therapeutic.
The device can also be a monofilament comprising an adjunctive therapeutic and a radioactive therapeutic. The monofilament has spaced depressions for indicating length and facilitating cutting. The depressions can be evenly or unevenly spaced.
In another aspect, the invention features a method of treating cancer comprising the steps of placing adjacent segments of a radioactive therapeutic and an adjunctive cancer therapeutic into or adjacent to a malignant tumor. The segments can be in the form of a substantially cylindrical filament with a diameter that is smaller than the inner diameter of a brachytherapy seed placement device.
The foregoing and other objects, aspects, features, and advantages of the invention will become more apparent from the following description and from the claims.
REFERENCES:
patent: 6159143 (2000-12-01), Lennox
Sci-Med Life Systems, Inc.
Testa Hurwitz & Thibeault LLP
Veniaminov Nikita R
Winakur Eric F.
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