US20080269539A1 - Brachytherapy Device Having an Alignment and Seal Adaptor - Google Patents

Abstract

A brachytherapy device for treating tissue within a cavity of a body. The device may include a first set of tubes configured to be inserted into the cavity through an opening at the surface of the body. Each of the tubes may have an external end and an interior channel beginning at the external end that is configured to receive radioactive material. The external ends of the tubes may be bundled together. The tubes may be of a length that causes the external ends to be near the opening in the surface of the body while the tubes are in the cavity. A seal may be configured to prevent fluid that originates from the cavity from entering into the external ends of the tubes while they are near the opening in the surface of the body. The seal may include a gasket that is pressed against the external ends of the tubes. The gasket may have openings that align with channels within the external ends of the tubes.

Description

BACKGROUND
• 1. Field
• This disclosure relates to brachytherapy devices for treating cancerous tissue surrounding a cavity of a body with radiation.
• 2. Description of Related Art
• Brachytherapy devices may include a set of tubes. Examples are described in U.S. patent application Ser. No. 11/737,028, entitled “Expandable Brachytherapy Device with Constant Radiation Source Spacing,” filed Apr. 18, 2007, attorney docket no. 63344-050; U.S. patent application Ser. No. 11/379,739, entitled “Brachytherapy Apparatus for Asymmetrical Cavities,” filed Apr. 21, 2006, attorney docket no. 63344-023; and U.S. patent application Ser. No. 11/305,437, entitled “Brachytherapy Apparatus,” filed Dec. 16, 2005, attorney docket no. 63344-021 (hereinafter collectively “Prior Brachytherapy Patent Applications”). The entire content of all three of these applications is incorporated herein by reference.
• The tubes may be inserted into the cavity of a body through an opening on the surface of the body, such as through an incision or a natural opening. The tubes within the cavity may be expanded. Radioactive material may be inserted within an interior channel in one or more of the tubes and allowed to remain for a prescribed period of time.
• The tubes may have external ends that are bundled together. A device known as an afterloader may be coupled to the external ends of the tubes and used to insert radioactive material into one or more of the tubes. Radioactive material may instead be inserted manually.
• The external ends of the tubes may be near the opening in the surface of the body, such as protruding slightly beyond the opening. The external ends of the tubes may not be coupled to the afterloader or otherwise accessed for several hours or even days after the tubes are inserted within the cavity. During this period, fluid, such as seroma, may seep from the cavity through spacing between or surrounding the tubes towards the external ends of the tubes. This fluid may enter the interior channels of the tubes and solidify. This may impede the insertion of radioactive material into the interior channels of the tubes and/or its removal.
SUMMARY
• A brachytherapy device for treating tissue within a cavity of a body may include a first set of tubes configured to be inserted into the cavity through an opening at the surface of the body. Each of the tubes may have an external end and an interior channel beginning at the external end that is configured to receive radioactive material, the external ends of the tubes being bundled together. The tubes may be of a length that causes the external ends to be near the opening in the surface of the body while the tubes are in the cavity. A seal may be configured to prevent fluid that originates from the cavity from entering into the external ends of the tubes while they are near the opening in the surface of the body.
• The external ends of the tubes may lie in substantially the same plane and the seal may include a substantially flat gasket that is pressed against the external ends of the tubes.
• The gasket may include a plurality of openings, each of which may be aligned with one of the channels in the tubes so as to allow radioactive material to be inserted into the channel of the tube while preventing fluid that originates from the cavity from entering into the external end of the tube.
• The external end of each tube may have a cross-section having an outer perimeter. The opening in the gasket that may be pressed against each external end may not at any point extend beyond the outer perimeter of the external end of the tube.
• The brachytherapy device may include an alignment mechanism configured to cause each opening in the gasket that may be pressed against one of the external ends of the tubes to align with the channel in the external end of the tube.
• The brachytherapy device may include a cover configured to controllably cover the openings in the gasket.
• The cover may be configured to move from a closed position that covers the openings in the gasket to an open position that exposes the openings in the gasket.
• The cover may include openings through which radioactive material may be inserted that align with openings in the gasket when the cover is in the open position.
• The openings in the cover may not align with the openings in the gasket when the cover is in the closed position.
• The cover may include an alignment mechanism that is configured to facilitate alignment of the cover with an afterloader. The alignment mechanism may include a plurality of indentations within a surface of the cover.
• The cover may be configured to rotate about an axis while moving between the open and closed positions.
• The brachytherapy device may include a fastener configured to fasten the gasket to the tubes.
• The brachytherapy device may include a hollow tube surrounded by the ends of the first set of tubes. The gasket may include a central opening. The fastener may include a screw having a shaft that passes through the central opening in the gasket and into the hollow tube.
• The brachytherapy device may include a sleeve around the external ends of the tubes.
• The brachytherapy device may include a second set of tubes configured to be inserted into the cavity through the opening at the surface of the body along with the first set of tubes. Each of the second set of tubes may have an external end configured to be near the opening in the surface of the body while the first and second sets of tubes are inserted into the cavity. The external ends of the second set of tubes may be bundled together with the external ends of the first set of tubes, and the external ends of the first and second sets of tubes may lie in substantially the same plane. The seal may include a substantially flat gasket that is pressed against the external ends of the first and second sets of tubes.
• At least some of the second set of tubes may have an interior channel beginning at the external end of the tube. The gasket may have a plurality of openings, some of which are aligned with channels in the first set of tubes and some of which are aligned with channels in the second set of tubes.
• The brachytherapy device may include an alignment mechanism configured to align some of the openings in the gasket with the channels in the first set of tubes. The alignment mechanism may include at least one pin configured to pass through one of the openings in the gasket that aligns with a channel in one of the second sets of tubes and through the corresponding channel in one of the second sets of tubes.
• The alignment mechanism may include a plurality of pins, each configured to pass through one of the openings in the gasket that aligns with a channel in one of the second sets of tubes and through the corresponding channel in one of the second sets of tubes.
• The second set of tubes may surround the first set of tubes.
• A seal may be provided for a brachytherapy device that has tubes configured to be inserted into a cavity through an opening at a surface of a body. The seal may include a substantially flat gasket that is configured to be pressed against the external ends of the tubes. The gasket may have a plurality of openings oriented so as to be aligned with the channels in the tubes when pressed against the external ends of the tubes so as to allow radioactive material to be inserted into the channels of the tubes, while preventing fluid that originates from the cavity from entering into the external ends of the tubes.
• A brachytherapy process for treating tissue within a cavity of a body may include inserting a hollow set of tubes into the cavity through an opening at the surface of the body. A cover may be from a closed position that covers entryways to the tubes to an open position that opens the entryway to the tubes. Radioactive material may be inserted into at least one of the tubes while the cover is in the open position. Radioactive material may be removed from the tubes. The cover may be rotated to the closed position.
• These, as well as other components, steps, features, objects, benefits, and advantages, will now become clear from a review of the following detailed description of illustrative embodiments, the accompanying drawings, and the claims.
BRIEF DESCRIPTION OF DRAWINGS
• The drawings disclose illustrative embodiments. They do not set forth all embodiments. Other embodiments may be used in addition or instead. Details that may be apparent or unnecessary may be omitted to save space or for more effective illustration. When the same numeral appears in different drawings, it is intended to refer to the same or like components or steps.
• FIG. 1 illustrates a brachytherapy device after being inserted into a breast and expanded.
• FIG. 2 is an enlarged view of the expanded portion of the brachytherapy device illustrated inFIG. 1.
• FIG. 3 is an enlarged view of the external end of the brachytherapy device illustrated inFIG. 1 without a center tube.
• FIG. 4 illustrates an exploded view of a seal and alignment adapter having a gasket, alignment disk, cover and screw.
• FIG. 5 illustrates an assembled view of the seal and alignment adapter illustrated inFIG. 4 with the alignment disk being transparent and the cover in a closed position.
• FIG. 6 illustrates an assembled view of the seal and alignment adapter illustrated inFIG. 4 with the cover in a closed position.
DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS
• Illustrative embodiments are now discussed. Other embodiments may be used in addition or instead. Details that may be apparent or unnecessary may be omitted to save space or for a more effective presentation.
• FIG. 1 illustrates a brachytherapy device after being inserted into a breast and being expanded. As shown inFIG. 1, abrachytherapy device101 may be inserted into acavity103 in abreast105. Thebrachytherapy device101 may include a set of expandedinner tubes107 and a set of expandedouter tubes109. Theinner tubes107 and theouter tubes109 may haveexternal ends111 that are bundled together. Asleeve113 may be used to bundle the external ends111 together. Aclamp115 may be used in addition or instead to bundle the external ends111 together. Theclamp115 may or may not be integral with thesleeve113.
• The length of theinner tubes107 and theouter tubes109 may be such as to cause the external ends111 to be near asurface117 of thebreast105, such as slightly protruding from it.
• Although having illustrated and discussed one particular type of brachytherapy device, any type of brachytherapy device may be used. More details about the device that has been illustrated and described and processes for causing it to be in the configuration shown inFIG. 1, as well as other types of usable brachytherapy devices, are set forth in the Prior Brachytherapy Patent Applications identified and incorporated by reference above.
• Thecavity103 may result from the resection of a tumor. Thecavity103 may in addition or instead be a naturally occurring cavity within the body, such as a cavity within a bladder, vagina, rectum, colon, subglottic region, stomach, bronchial tubes, nasopharynx region, and the like.
• FIG. 2 is an enlarged view of the expanded portion of the brachytherapy device illustrated inFIG. 1. It reveals details about theinner tubes107 and theouter tubes109 shown inFIG. 1.FIG. 2 also illustrates acenter tube201 that may run through the center of theinner tubes107 and theouter tubes109.
• FIG. 3 is an enlarged view of the external ends111 of thebrachytherapy device101 illustrated inFIG. 1 without a center tube. As illustrated inFIG. 3, each of theinner tubes107 may have anexternal end301, and each of theouter tubes109 may have anexternal end303. The external ends301 and303 may all lie in substantially the same plane.
• Each of theinner tubes107 may have aninterior channel305 beginning at itsexternal end301 that may or may not be configured to receive radioactive material. Similarly, each of theouter tubes109 may have aninterior channel307 beginning at itsexternal end303 that may or may not be configured to receive radioactive material.
• During use of thebrachytherapy device101, fluid, such as seroma, may have seeped through spacing between theinner tubes107 and theouter tubes109, through or around thecenter tube201 and/or between the outer perimeter of theouter tubes109 and the tissue that surrounds them. Unless stopped, this fluid may seep into theinterior channels305 and/or307. In turn, this may impede the insertion of radioactive material within one or more of these channels and/or its removal, particularly after the seroma hardens.
• FIG. 4 illustrates an exploded view of a seal and alignment adaptor. As shown inFIG. 4, the seal and alignment adaptor may include agasket401, analignment disk403, acover405, and a fastener, such as ascrew407.
• Thegasket401 may include a set ofinner openings409, a set ofouter openings411, and acentral opening413.
• Theinner openings409 may be configured so as to align with the external ends of thechannels305 in theinner tubes107 when placed against theinner tubes107. Similarly, theouter openings411 may be configured to align with the external ends of some of thechannels307 in theouter tubes109. Similarly, thecentral opening413 may be configured to align with the opening in thecenter tube201 at the external ends111.
• Theopenings409 and/or411 may be sized so as to permit radioactive material to be inserted into thechannels305 and/or307, respectively. Theopenings409 and/or411 may also be sized so as not at any point to exceed the perimeter of the cross section of any of theinner tubes107 and/or theouter tubes109 at their external ends111. When so sized and configured, and when thegasket401 is pressed against the external ends111 and its openings are aligned with the corresponding channels in theinner tubes107 and/or theouter tubes109, radioactive material may be inserted into one or more of these channels. Yet, fluid that may have seeped toward the external ends111 from within thecavity103 may be unable to enter any of thechannels305 and/or307 due to the sealing effect provided by thegasket401.
• Thealignment disk403 may includeopenings414, which may be configured to align with theinner openings409 in thegasket401. Thealignment disk403 may include agasket recess415 sized to house thegasket401. Thealignment disk403 may include acentral opening417 configured to align with thecentral opening413 in thegasket401.
• Thealignment disk403 may include acover recess418 configured to house thecover405. Thealignment disk403 may include anaccess port429 that may be configured to provide user access to atab421 on thecover405 when thecover405 is placed within thecover recess418 of thealignment disk403.
• Thecover405 may haveopenings419 that are configured to align with theopenings414 in thealignment disk403 and theinner openings409 in thegasket401. The cover may include acentral opening423 that is configured to align with thecentral opening417 in thealignment disk403 and thecentral opening413 in thegasket401.
• Thecover405 my include an alignment mechanism to facilitate alignment of the cover with an afterloader, such asdepressions425.Depressions425 may or may not go through the entire thickness of thecover405.
• Thescrew407 may be a threaded, self-tapping screw. It may be configured to extend through acentral opening423 in the cover, thecentral opening417 in the alignment disk, and thecentral opening413 in the gasket, and to then screw into and engage a center bore of thecenter tube201 in thebrachytherapy device101. Thescrew407 may be tightened so as to ultimately press thegasket401 against the external ends111 of thebrachytherapy device101 in an amount that is sufficient to prevent fluid that has seeped toward the external ends111 from further seeping into thechannels305 of theinner tubes107 and/or thechannels307 of theouter tubes109.
• In an alternate configuration, a mechanism may be used to hold thegasket401, thealignment disk403, and thecover405 together and to press thegasket401 against the external ends111 that does not occupy thecentral openings413,417 and423. This may leave these central openings available for radioactive material to be inserted therein and intocenter tube201.
• FIG. 5 illustrates an assembled view of the seal and alignment adaptor illustrated inFIG. 4 with the alignment disk being transparent and the cover in a closed position. As shown inFIG. 5, thealignment disk403 may include a plurality ofpins501 that protrude from thegasket recess415 in which thegasket401 may reside. As shown inFIG. 5, thepins501 may be configured so as to align with several of theouter openings411 in thegasket401 when thegasket401 is within thegasket recess415.
• Thepins501 may be configured to pass through theseouter openings411 and into some or all of thechannels307 of theouter tubes109. Thepins501 may have a taper that makes assembly easier. The taper of thepins501 may be selected so as to cause thepins501 to fit snugly within theopenings411 of thegasket401 when the gasket is fully seated within thegasket recess415 and to fit snugly within thechannels307 of theouter tubes109 when the external ends111 of theouter tubes109 are pressed fully against thegasket401.
• This snug fitting of thepins501 may contribute to more precise alignment between thechannels305 in theinner tubes107 and theinner openings409 in thegasket401, theopenings414 in thealignment disk403, and theopenings419 in thecover405. An alignment mechanism other than thepins501 may be used in addition or instead. For example, thepins501 could instead be integral with thegasket401, in which case there might not be anyouter openings411 in thegasket401.
• FIG. 6 illustrates an assembled view of the seal and alignment adaptor illustrated inFIG. 4 with the cover in a closed position. When thecover405 is in the position shown inFIG. 6, thetab421 may be pushed against the uppermost portion of the access port427. While in this closed position, theopenings419 in thecover405 may not align with theopenings414 in thealignment disk403 and theinner openings409 in thegasket401. This may effectively block thechannels305 in theinner tubes107 from being loaded with radioactive material and from otherwise being contaminated. When thecover405 is rotated counterclockwise by pushing thetab421 toward the bottom portion of the access port427 in thealignment disk403, theopenings419 in thecover405 may become fully aligned with theopenings414 in thealignment disk403 and theinner openings409 in thegasket401. In this position, thechannels305 in theinner tubes107 may be loaded with radioactive material inserted through theopenings419 in thecover405.
• The brachytherapy devices that have thus-far been described may be used in a variety of applications.
• For example, a tumor may be resected from thebreast105 shown inFIG. 1. A balloon may be inserted into the cavity that is created as a result and inflated. Later, the balloon may be deflated and removed. The cavity may instead be a naturally occurring cavity, such as a cavity in a bladder, vagina, rectum, colon, subglottic region, stomach, bronchial tubes, nasopharynx region, or the like.
• Thesleeve113 may be inserted into the cavity. Theinner tubes107 and theouter tubes109, while in an elongated and collapsed state, may be threaded through thesleeve113 and into thecavity103 of thebreast105. Theinner tubes107 and theouter tubes109 may then be expanded to the positions illustrated inFIGS. 1 and 2. Apparatus for accomplishing this may include any of the devices disclosed in the Prior Brachytherapy Patent Applications identified and incorporated by reference above.
• Theclamp115 may be tightened and portions of theinner tubes107 and theouter tubes109 that extend substantially beyond theclamp115 may be cut off. The seal and alignment adaptor illustrated inFIG. 4 may be coupled to the external ends111 of thebrachytherapy device101 by aligning thepins501 that protrude from the rear of thealignment disk403 and that protrude through thegasket401 with the correspondingchannels307 in theouter tubes109. Thescrew407 may be inserted into thecentral opening423 of the cover, thecentral opening417 of the alignment disk, thecentral opening413 of the gasket, and into the opening of thecenter tube201. Thescrew407 may be tightened until thegasket401 is pressed against the external ends111 of thebrachytherapy device101 with sufficient force to prevent fluid from entering thechannels305 in theinner tubes107 and/or thechannels307 in theouter tubes109. Thetab421 may be moved to the closed position, if not already in this position.
• When ready for treatment, thetab421 may be moved to the open position. The alignment depressions425 may be aligned with an afterloader. The afterloader may be directed to insert radioactive material into one or more of thechannels305 in theinner tubes107 through theopenings419. The radioactive material may instead be inserted manually.
• The radioactive material may include or consist of any type of radioactive material, including material that is itself radioactive, such as radioactive pellets, radioactive seeds, radioactive liquid, and/or radioactive wires, and/or radioactive sources that contain radioactive material, such as encapsulated radioactive pellets or seeds, radioactive particles suspended in liquid, and/or radioactive seeds or pellets embedded in wires of other types of strands. When multiple units of radioactive material are inserted into a channel, the units may be spaced apart. The radioactive material may be left within one or more of thechannels305, following which it may be removed.
• In some cases, a unit of radioactive material may be allowed to dwell at different locations within the same channel. In some cases, a unit of radioactive material may be removed from one channel and placed within another channel.
• When a radioactive treatment session is complete, the radioactive material may be removed from all of the channels and thecover405 may be closed by rotating thetab421 clockwise.
• During a subsequent treatment, thecover405 may again be opened by rotating thetab421 counterclockwise to the open position and by repeating this or a different treatment regimen.
• When all of the radiation treatments have been completed, theclamp115 may be released and removed. Theinner tubes107 and theouter tubes109 may be allowed to collapse and elongate. Theinner tubes107 and theouter tubes109 may be completely removed from thecavity103, along with thesleeve113.
• Theopenings419 in thecover405, theopenings414 in thealignment disk403, and theinner openings409 in thegasket401 may be of any size. In one embodiment, theopenings419 in thecover405 may be larger than theopenings414 in thealignment disk403, which may be larger than theinner openings409 in thegasket401, thereby making it easier for the afterloader to insert radioactive material into thechannels305 or for this material to be inserted manually. In one embodiment, theopenings419 in thecover405 may be approximately 70 thousandths of an inch, theopenings414 in thealignment disk403 may be approximately 50 thousandths of an inch, theinner openings409 in thegasket401 may be slightly larger than approximately 40 thousandths of an inch, and thechannels305 in theinner tubes107 may be approximately 40 thousandths of an inch. These openings may be tapered from wide to narrow so as to further facilitate the smooth entry of radioactive material from the afterloader or by manual means into thechannels305 in theinner tubes107.
• The components of the seal and alignment adaptor that is shown inFIG. 4 may be made of any material. For example, the gasket may be made of a flexible material, such as silicone, and other components, such as the alignment disk, may be made from an acrylic or a polycarbonate-like material, such as Lexan.
• The components, steps, features, objects, benefits and advantages that have been discussed are merely illustrative. None of them, nor the discussions relating to them, are intended to limit the scope of protection in any way. Numerous other embodiments are also contemplated, including embodiments that have fewer, additional, and/or different components, steps, features, objects, benefits and advantages. The components and steps may also be arranged and ordered differently.
• For example, the seal that is used may not necessarily be a gasket, as illustrated inFIG. 4. Instead, a powerful clamp may be used that pinches closed the external ends111 of thechannels305. The seal might in addition or instead be material, such as silicone, that is inserted temporarily into thechannels305.
• The bundledexternal ends111 may also not necessarily be in a circular arrangement, such as is illustrated inFIG. 3. The bundle may instead have rectangular shape or any other shape.
• Although inner and outer tubes have thus-far been illustrated, the brachytherapy device may have only one level of tubes. The number of the inner or outer tubes or of only single-level tubes may be greater or less.
• Although radioactive material has thus-far been described as being inserted into the inner tubes, radioactive material may in addition or instead be inserted into one or more of the outer tubes, either at the same time or times as radioactive material is inserted into one or more of the inner tubes, or at one or more different times.
• The phrase “means for” when used in a claim embraces the corresponding structures and materials that have been described and their equivalents. Similarly, the phrase “step for” when used in a claim embraces the corresponding acts that have been described and their equivalents. The absence of these phrases means that the claim is not limited to any of the corresponding structures, materials, or acts or to their equivalents.
• Nothing that has been stated or illustrated is intended to cause a dedication of any component, step, feature, object, benefit, advantage, or equivalent to the public, regardless of whether it is recited in the claims.
• In short, the scope of protection is limited solely by the claims that now follow. That scope is intended to be as broad as is reasonably consistent with the language that is used in the claims and to encompass all structural and functional equivalents.

Claims (22)

1. A brachytherapy device for treating tissue within a cavity of a body comprising:

a first set of tubes configured to be inserted into the cavity through an opening at the surface of the body, each of the tubes having an external end and an interior channel beginning at the external end that is configured to receive radioactive material, the external ends of the tubes being bundled together, the tubes being of a length that causes the external ends to be near the opening in the surface of the body while the tubes are in the cavity; and

a seal configured to prevent fluid that originates from the cavity from entering into the external ends of the tubes while they are near the opening in the surface of the body.

2. The brachytherapy device ofclaim 1 wherein the external ends of the tubes lie in substantially the same plane and wherein the seal includes a substantially flat gasket that is pressed against the external ends of the tubes.

3. The brachytherapy device ofclaim 2 wherein the gasket includes a plurality of openings, each of which is aligned with one of the channels in the tubes so as to allow radioactive material to be inserted into the channel of the tube while preventing fluid that originates from the cavity from entering into the external end of the tube.

4. The brachytherapy device ofclaim 3 wherein the external end of each tube has a cross-section having an outer perimeter and wherein the opening in the gasket that is pressed against each external end does not at any point extend beyond the outer perimeter of the external end of the tube.

5. The brachytherapy device ofclaim 4 further comprising an alignment mechanism configured to cause each opening in the gasket that is pressed against one of the external ends of the tubes to align with the channel in the external end of the tube.

6. The brachytherapy device ofclaim 3 further comprising a cover configured to cover the openings in the gasket.

7. The brachytherapy device ofclaim 6 wherein the cover is configured to move from a closed position that covers the openings in the gasket to an open position that exposes the openings in the gasket.

8. The brachytherapy device ofclaim 7 wherein the cover includes openings through which radioactive material may be inserted that align with openings in the gasket when the cover is in the open position.

9. The brachytherapy device ofclaim 8 wherein the openings in the cover do not align with the openings in the gasket when the cover is in the closed position.

10. The brachytherapy device ofclaim 8 wherein the cover includes an alignment mechanism that is configured to facilitate alignment of the cover with an afterloader.

11. The brachytherapy device ofclaim 10 wherein the alignment mechanism includes a plurality of indentations within a surface of the cover.

12. The brachytherapy device ofclaim 7 wherein the cover is configured to rotate about an axis while moving between the open and closed positions.

13. The brachytherapy device ofclaim 2 further comprising a fastener configured to fasten the gasket to the tubes.

14. The brachytherapy device ofclaim 13 further comprising a hollow tube surrounded by the ends of the first set of tubes, wherein the gasket includes a central opening and the fastener includes a screw having a shaft that passes through the central opening in the gasket and into the hollow tube.

15. The brachytherapy device ofclaim 2 further comprising a sleeve around the external ends of the tubes.

16. The brachytherapy device ofclaim 1 further comprising a second set of tubes configured to be inserted into the cavity through the opening at the surface of the body along with the first set of tubes, each of the second set of tubes having an external end configured to be near the opening in the surface of the body while the first and second sets of tubes are inserted into the cavity, the external ends of the second set of tubes being bundled together with the external ends of the first set of tubes, wherein the external ends of the first and second sets of tubes lie in substantially the same plane and wherein the seal includes a substantially flat gasket that is pressed against the external ends of the first and second sets of tubes.

17. The brachytherapy device ofclaim 16 wherein at least some of the second set of tubes have an interior channel beginning at the external end of the tube, and wherein the gasket has a plurality of openings, some of which are aligned with channels in the first set of tubes and some of which are aligned with channels in the second set of tubes.

18. The brachytherapy device ofclaim 17 further including an alignment mechanism configured to align some of the openings in the gasket with the channels in the first set of tubes, the alignment mechanism including at least one pin configured to pass through one of the openings in the gasket that aligns with a channel in one of the second sets of tubes and through the corresponding channel in one of the second sets of tubes.

19. The brachytherapy device ofclaim 18 wherein the alignment mechanism includes a plurality of pins, each configured to pass through one of the openings in the gasket that aligns with a channel in one of the second sets of tubes and through the corresponding channel in one of the second sets of tubes.

20. The brachytherapy device ofclaim 16 wherein the second set of tubes surround the first set of tubes.

21. A seal for a brachytherapy device that has tubes configured to be inserted into a cavity through an opening at a surface of a body, each of the tubes having an external end and an interior channel beginning at the external end that is configured to receive radioactive material, the external ends of the tubes being bundled together and lying in substantially the same plane, the tubes being of a length that causes the external ends to be near the opening in the surface of the body when the tubes are in the cavity, the seal comprising:

a substantially flat gasket that is configured to be pressed against the external ends of the tubes, the gasket having a plurality of openings oriented so as to be aligned with the channels in the tubes when pressed against the external ends of the tubes so as to allow radioactive material to be inserted into the channels of the tubes while preventing fluid that originates from the cavity from entering into the external ends of the tubes.

22. A brachytherapy process for treating tissue within a cavity of a body comprising in the order recited:

inserting a hollow set of tubes into the cavity through an opening at the surface of the body;

rotating a cover from a closed position that covers entryways to the tubes to an open position that opens the entryway to the tubes;

inserting radioactive material into at least one of the tubes while the cover is in the open position;

removing the radioactive material from the tubes; and

rotating the cover to the closed position.

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