A system for directly producing yttrium-90 for cancer treatment

Abstract

To provide a system and method including a substance for emitting beta particles of high energy to destroy cancer cells included in a cancerous tumor or a cancer tissue.SOLUTION: An electronic neutron generator generates neutrons having energy with high probability of interacting with yttrium 89 and generating yttrium 90. Yttrium 90 emits beta-rays with maximum energy of about 2.25 MeV and a half life of about 64 hours, which decays to stable zirconium. Stable yttrium 89 is disposed directly in the cancer tissue or its periphery and neutrons in the energy range of 0.1-15 keV are radiated so that yttrium 90 in a significant amount can be generated. The beta-rays emitted from yttrium 90 destroy cancer cells more sensitive to a radioactive ray mainly within the range of beta particles. The resultant zirconium isotope is not radioactive so that no further radioactive ray is released.SELECTED DRAWING: None

Description

[Technical Field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority under 35 U.S.C. §119(e) to U.S. Provisional Patent Application No. 62 / 631,737, filed February 17, 2018, entitled "SYSTEM FOR THE DIRECT PRODUCTION OF THERAPEUTIC YTTRIUM-90 FOR CANCER TREATMENT," which is incorporated herein by reference. The present invention relates generally to cancer treatment, and specifically to the treatment of highly localized cancer cells. [Background technology]

[0002] Treatment of highly localized cancer cells, such as tumors, in the human body with ionizing radiation has proven highly effective. However, when ionizing radiation is applied to the human body, it typically passes through normal tissue before reaching the intended target site, causing damage to normal tissue. Therefore, attempts to reduce tumor damage from a single radiation dose necessitate multiple treatments, resulting in cumulative, potentially harmful biological effects and increased treatment costs. If treatment is insufficient and repair of normal cell damage cannot keep up with tumor growth and / or metastasis, patients are likely to die from their cancer. Therefore, new therapies that attack cancerous tissue while minimizing damage to surrounding normal tissue are desirable.

[0003] Boron neutron capture therapy (BNCT) has been investigated as a potential treatment to address these needs, but to date, it has proven ineffective due to the narrow therapeutic range of the radiation it emits. A problem to be solved, therefore, is how to better utilize the neutron generation and implantation technique of boron neutron capture therapy to expand the therapeutic range of the radiation it emits. Therefore, there is a need in the art to design and develop devices based on BNCT that can emit radiation in the therapeutic range, and methods for using such devices to effectively treat localized cancer cells in animals (e.g., patients). Summary of the Invention

[0004] The present invention overcomes the harmful effects of cancer radiation therapy by providing a method for treating localized cancer cells in an animal body. The method includes placing a therapeutic radiation source in the body near cancer cells, the therapeutic radiation source being substantially non-radioactive when not exposed to a neutron source or in a neutron irradiation field below a given intensity, but providing a source of highly ionizing but poorly penetrating radiation in a neutron irradiation field above a given intensity. The step of placing the therapeutic radiation source preferably involves surgically implanting the therapeutic radiation source material in contact with the cancer cells. The therapeutic radiation source is irradiated from outside the body with a neutron field above a given intensity for a prescribed period of time, and this irradiating step is repeated at prescribed intervals. The present invention focuses on the design and operation of a therapeutic radiation source that acts as an irradiation target to expand the energy and range of emitted radiation to achieve a range of therapeutic levels.

[0005] In a preferred embodiment, a therapeutic source of highly ionizing but poorly penetrating radiation comprises a thin layer of yttrium metal in which, upon absorption of neutrons, yttrium-89 is converted to the medically important yttrium isotope yttrium-90, which emits beta rays with a maximum energy of approximately 2.25 MeV and a relatively short half-life of 64.1 hours. The yttrium metal layer is insoluble in water and non-toxic to the body.

[0006] The therapeutic radiation source, which emits highly ionizing but poorly penetrating radiation, is configured to irradiate substantially only the cancer cells. To achieve this, a radiation shield is formed on the surface of the therapeutic radiation source opposite the cancer cells. Preferably, the step of irradiating the therapeutic radiation source with neutrons includes using a radiation source (e.g., an electric neutron generator such as a Neutristor) to irradiate the therapeutic radiation source with neutrons. One such embodiment uses multiple electric neutron generators positioned around the body to irradiate the therapeutic radiation source with neutrons from various angles.

[0007] The method may also include using a neutron moderator between the electric neutron generator and the therapeutic radiation source to adjust the neutron energy or neutron field to optimize the highly ionizing but poorly penetrating radiation generated by the therapeutic radiation source. The neutron moderator may be deuterium oxide (DO), carbon (C), or other material with similar moderating properties. The neutron moderator is placed outside the body between the electric neutron generator and the body.

[0008] In certain embodiments, the therapeutic radiation source remains in the body between treatments of the localized cancer cells (e.g., for an interval). The therapeutic radiation source is removed from the body after treatment is completed. The therapeutic radiation source is comprised of one or more very thin disks or plates having a thickness on the order of microns, and the combined surface area of ​​the one or more disks or plates is large enough that when placed around the cancer cells and exposed to a neutron irradiation field, the highly ionizing but poorly penetrating radiation affects the entire mass or area of ​​the localized cancer cells.

[0009] The method may also include monitoring the intensity of gamma rays emitted as a by-product of neutron irradiation of the therapeutic source material with a gamma ray spectrometer, thereby monitoring the rate of production of charged particles during the neutron irradiation. The monitored gamma ray intensity and the neutron intensity of the neutron field may be used to determine the radiation dose received by the body. The method may also control the strength of the neutron irradiation field based on the monitored gamma ray intensity and the radiation dose. [Brief explanation of the drawings]

[0010] The invention will now be described in detail by way of example of a preferred embodiment with reference to the accompanying drawings, in which: FIG.

[0011] [Figure 1] 1 is a schematic diagram of an apparatus that can be used to practice the present invention, according to some embodiments.

[0012] [Figure 2] 2 is a schematic diagram showing details of the therapeutic radiation source 10 of FIG. 1 according to an embodiment. DETAILED DESCRIPTION OF THE INVENTION

[0013] The present invention includes systems and methods, including a therapeutic and irradiation / neutron source, for treating localized cancer cells, e.g., cancerous tumors and / or cancerous tissues, that form and grow within the body of an animal, including a human subject, human being, or patient (these terms are used interchangeably herein). The therapeutic source is placed or implanted within the patient, more particularly at or near the location of the cancer cells. In certain embodiments, the therapeutic source is placed on or adjacent to the cancer cells. The therapeutic source comprises one or more devices having disk(s), plate(s), or needle(s) approximately 1 micron thick. The one or more disks, plates, or needles each have a surface area sufficient to, alone or in concert, impact the entire mass of localized cancer cells with the radiation they emit. The therapeutic source should be composed of or consist of a material (e.g., a metal) that generates high-energy alpha or beta particles but does not generate gamma rays or generates low-energy gamma rays. Suitable materials are insoluble in water and non-toxic. The neutron reaction products of this material must also be non-toxic to the patient and have a very short half-life.

[0014] The disk or plates or needles may be at least substantially composed of yttrium, e.g., in the form of a thin layer or sheet approximately 1 mm thick. Natural yttrium is composed of the yttrium-89 isotope. When yttrium-89 absorbs neutrons, it is converted to yttrium-90, a medically important isotope useful in cancer radiotherapy. Typically, stable yttrium-89 is placed in, on, or around localized cancer cells and irradiated with neutrons in the energy range of 0.1-15 keV to produce significant amounts of yttrium-90, which emits beta rays that can destroy radiation-sensitive cancer cells within the beta particle range. Upon absorbing a neutron, yttrium-89 emits beta rays with a maximum energy of approximately 2.25 MeV. These beta rays primarily destroy more radiation-sensitive cancer cells within the beta particle range. The resulting zirconium isotope is not radioactive and does not emit any further radiation. Not only do the beta rays damage the cancerous tumor or tissue, but the small percentage of gamma rays produced also help destroy the cancer cells.

[0015] The therapeutic radiation source may further include radiation shielding. The metal (e.g., yttrium) layer and the radiation shielding may be in a laminated configuration. The therapeutic radiation source is positioned so that the yttrium metal surface faces the cancer cells and the radiation shielding surface faces the opposite side, i.e., the side of the therapeutic radiation source away from the cancer cells. The radiation shielding is composed or configured of a material that is substantially transparent to neutrons but can shield at least a portion of the normal tissue surrounding the cancer cells from highly ionizing particles. Suitable materials include light metals such as aluminum, magnesium, and their alloys, as well as similar substances with relatively low density and similar shielding properties. The presence of the therapeutic shielding and the configuration / positioning of the therapeutic radiation source are effective in ensuring that only cancer cells are irradiated and normal tissue is not irradiated.

[0016] Therapeutic sources, or irradiation targets, can be formed into many shapes and sizes using commercially available fabrication techniques for placement directly within or adjacent to cancer cells, carcinomas, and tissue. Because the source material is not radioactive unless irradiated with neutrons, placing the source material in or around a patient does not expose the human body to radiation.

[0017] The irradiation neutron source includes an electric neutron generator, such as a Neutristor, and is located outside the patient's body. Generally, a suitable irradiation source produces neutrons with an energy that is likely to interact with yttrium-89 to produce yttrium-90. Neutrons emitted from the electric neutron generator irradiate a therapeutic source inside the patient, resulting in radiation emitted from this therapeutic source at a certain radioactivity level within the therapeutic range. Irradiation continues even when the electronic neutron generator system is turned off. However, the short range and short decay half-life of 64 hours of emitted beta radiation easily limit personnel exposure until the irradiated target decays to a safe level. One or more irradiation sources can be used over a period of time and repeated at predetermined intervals. Multiple irradiation sources can be arranged so that neutrons are directed at the patient from various angles. Miniature neutron generators can be configured in an array to provide neutron energy and dose distributions at the therapeutic source, i.e., the irradiation target.

[0018] In certain embodiments, the compact, fast electrical neutron generator array, similar in configuration to the "Neutristor" design developed by Sandia National Laboratories and described in a Snowmass 2013 white paper entitled "Novel Compact Accelerator Based Neuron and Gamma Sources for FutureDetector Calibration" by G. Jennings, C. Sanzeni, and D.R. Winn (Fairfield University, Fairfield, CT 06824), can be used to irradiate a neutron field onto a therapeutic source material after the source material is implanted in a patient. The array is preferably configured to provide sufficient neutron intensity at the therapeutic source location to maximize neutron reaction rates without excessive neutron exposure to other parts of the patient's body.

[0019] In certain embodiments, the therapeutic radiation source is implanted in the patient's body and remains there during repeated radiation treatments. Between treatments, the therapeutic radiation source is not exposed to any radiation or to therapeutic levels of radiation, and is therefore substantially non-radioactive. Thus, the therapeutic radiation source is controlled to treat cancer cells only as prescribed or desired. Once the prescribed number of treatments has been reached, the therapeutic radiation source is removed from the patient's body.

[0020] Between the radiation source and the patient's body containing the implanted therapeutic radiation source, a neutron moderator device can be placed, which contains a sufficient amount of a neutron moderator, such as deuterium oxide (DO), carbon (C), or any similar material with similar moderating properties, as its composition or material of construction. Neutron moderator devices can be placed between each neutron generator and the therapeutic radiation source, and each can be individually adjusted to achieve the goal of maximizing the number of neutrons with optimal energy for generating charged particles through neutron interactions with the targeted therapeutic radiation source material. In certain embodiments, a combination of distance from the patient and a flexible neutron moderator achieves a selected neutron energy and / or dose distribution. Such a neutron moderator can be, for example, a hydrogen-rich material or variable-shape chunks of deuterium with varying amounts, contained in a specially shaped plastic container.

[0021] In certain embodiments, the neutron generator array is geometrically configured so that neutrons from each generator are incident on the carcinoma at different angles to maximize the number of fully thermalized neutrons reaching the target, i.e., the location of the therapeutic source. This is achieved by varying the geometric configuration of the irradiation / neutron source array as well as the thickness of the material used in the neutron moderator placed between the neutron source array and the therapeutic source, i.e., the irradiation target. The calculations required to establish optimal conditions can be performed by one skilled in the art using many different commercially available neutron transport calculation products, such as the Monte Carlo N-Particle (MCNP) transport code provided by Los Alamos National Laboratory.

[0022] The present invention can also include a gamma ray spectrometer that measures the intensity of gamma rays emitted from the target isotope produced by the neutron reaction so that the rate of charged particle production during neutron irradiation can be monitored. This can be accomplished with a number of commercially available devices.

[0023] The present invention may also include a computer control system used to determine the radiation dose delivered to the patient from the measured gamma ray intensity and neutron generator operating conditions and compare it to a target dose, the control system having the ability to increase or decrease the intensity of the neutron radiation provided by any or all of the neutron generators in the array based on the gamma ray intensity and dose measurements.

[0024] FIG. 1 is a schematic diagram illustrating one particular embodiment of a system for treating localized cancer cells 22 forming cancerous tumors or cancerous tissue within a patient's body 12. FIG. 1 includes a therapeutic radiation source 10 implanted in proximity to, and preferably adjacent to, the cancer cells 22 within the patient's body 12. An irradiation / neutron source 14 includes an array of, possibly small, neutron generators 32 (e.g., multiple neutron generators 32) positioned outside the patient's body 12, e.g., spaced apart from the patient's body 12, that emits neutrons 30 toward the patient's body 12. The neutron generators 32 and the neutrons 30 emitted therefrom can be configured to provide a neutron energy and dose distribution at the location of the therapeutic radiation source 10, i.e., the irradiation target. A neutron moderator device 16 is geometrically configured between the array of neutron generators 32 and the patient's body 12. 1 , e.g., spaced apart from the patient's body 12. Gamma ray spectrometer 18 measures the intensity of gamma rays emitted from therapeutic radiation source 10 when neutrons react with the yttrium isotopes. Computer control system 20 determines the radiation dose delivered to patient's body 12, compares it to a dose target, and can increase or decrease the intensity of the neutron rays provided by any or all of neutron generators 32 based on the gamma ray intensity and dose measurements.

[0025] The field plate 24 can be provided to accelerate the emitted electrons to a certain penetration depth and / or a preferred irradiation direction within the patient's body 12. Because beta rays have electrical properties similar to electrons, the effects of emitted beta rays can be further controlled by applying an electric and / or magnetic field. This method also allows for improved control of the dose delivered to the patient by manipulating an external electric and / or magnetic field, for example, with the field plate 24, to change the kinetic energy and primary direction of movement of electrons emitted from the irradiation target. As an example, applying an oscillating electric field can accelerate the emitted electrons beyond or constrain them within a range defined by the kinetic energy imparted by gamma photon collisions with electrons from gold or platinum. Applying an external magnetic field can concentrate the emitted electrons closer to or farther from the emitter element.

[0026] FIG. 2 is a schematic diagram showing details of the therapeutic radiation source 10 of FIG. 1 according to one embodiment. FIG. 2 includes a first material 26 and a second material 28. The first material 26 is at least substantially composed of yttrium, which is the yttrium-89 isotope, and the second material 28 represents radiation shielding, which is substantially composed of aluminum. The first material 26 has the second material 28 attached to one side or surface thereof, and the other / opposite side or surface thereof faces the cancer cells 22. The second material 28 has the first material 26 attached to one side or surface thereof, and the other / opposite side or surface thereof faces a neutron field 30 generated by a neutron generator 32 (shown in FIG. 1) that interacts with the therapeutic radiation source 10.

[0027] Yttrium-90 beta-emitter targets (BERTs) can be configured into a number of shapes, such as needles and disks, allowing for great flexibility in treatment.

[0028] The cancer treatment method and system described herein differ from existing radiation therapy methods in that, rather than injecting compounds that form limited amounts of radiotherapeutic deposits in the desired area, non-radioactive targets are created and implanted in or around the tumor. The system's ability to activate inherently non-radioactive materials with neutrons, for example, in a hospital setting, maximizes the benefits of charged particle cancer treatment while minimizing unwanted expenses and radiation exposure for patients and caregivers. The methods and systems of the present invention allow for highly precise and efficient destruction of cancer cells. Furthermore, the targeted source can remain implanted in the body until the tumor is completely eliminated without increasing the patient's total body radiation dose. Multiple doses can be administered relatively easily. The use of Neutristor-type neutron generators allows treatment to be performed in a hospital environment rather than at the site of a nuclear reactor or a very large neutron source. This significantly reduces treatment costs (or significantly increases treatment profitability) compared to existing radiation therapy methods.

[0029] While specific embodiments of the present invention have been described in detail, those skilled in the art will be able to develop various modifications and alternatives to these detailed embodiments in light of the teachings of this disclosure as a whole. Accordingly, the specific embodiments disclosed herein are for illustrative purposes only and do not limit the scope of the present invention, which encompasses the full scope of the appended claims and all equivalents thereof.

Claims

1. An electric neutron generator (32) disposed outside the patient's body (12) and generating a neutron field that irradiates neutrons in the energy range of 0.1 to 15 keV toward the patient's body (12); a therapeutic radiation source (10) implantable on or adjacent to cancer cells (22) within the patient's body (12); A system comprising: The therapeutic radiation source (10) has a first surface and a second surface opposite to the first surface, the first surface is provided with yttrium 89, which is converted to yttrium 90 when exposed to the neutron field and emits beta rays that destroy the cancer cells, and the second surface is provided with radiation shielding that prevents beta rays from the therapeutic radiation source (10) from being emitted from the second surface. system.

2. An electric neutron generator (32) disposed outside the patient's body (12) and generating a neutron field that irradiates neutrons in the energy range of 0.1 to 15 keV toward the patient's body (12); a therapeutic radiation source (10) implantable on or adjacent to cancer cells (22) within the patient's body (12); A system comprising: the therapeutic radiation source (10) has a first surface and a second surface opposite to the first surface, the first surface is provided with yttrium 89, which is converted to yttrium 90 when exposed to the neutron field and emits beta rays that destroy the cancer cells, and the second surface is provided with radiation shielding that prevents beta rays from the therapeutic radiation source (10) from being emitted from the second surface; The system further includes a field plate (24) disposed external to the patient's body (12), the field plate (24) generating a second field for manipulating the direction or energy of the beta rays emitted by the therapeutic radiation source (10). system.

3. The system of claim 2 , wherein the second field comprises an electric field, a magnetic field, or a combination thereof.

4. 10. The system of claim 1, further comprising a neutron moderator device (16) disposed between the electric neutron generator (32) and the body (12), the neutron moderator device (16) including a neutron moderator material for adjusting the energy of the neutrons in the neutron field.

5. The system of claim 4, wherein the neutron moderator comprises deuterium oxide or carbon.

6. The system of claim 1 , wherein the radiation shield is transparent to at least a portion of the neutrons.

7. The system of claim 6 , wherein the radiation shielding is made of aluminum, magnesium, or an alloy thereof.

8. An electric neutron generator (32) positioned outside the patient's body (12) and generating a neutron field that irradiates neutrons in the energy range of 0.1 to 15 keV toward the patient's body (12); a therapeutic radiation source (10) implantable on or adjacent to cancer cells (22) within the patient's body (12); A system comprising: the therapeutic radiation source (10) has a first surface and a second surface opposite to the first surface, the first surface is provided with yttrium 89, which is converted to yttrium 90 when exposed to the neutron field and emits beta rays that destroy the cancer cells, and the second surface is provided with radiation shielding that prevents beta rays from the therapeutic radiation source (10) from being emitted from the second surface; The therapeutic radiation source is a disk or plate having a laminated structure of a first layer and a second layer, the first layer comprising the first surface of the therapeutic radiation source, and the second layer comprising the second surface of the therapeutic radiation source. system.

9. 9. The system of claim 8, wherein the first layer has a thickness of 1 mm.

10. The system of claim 8 , wherein the first layer has a thickness of 1 micrometer.

11. The system of claim 1 , wherein the therapeutic radiation source is a needle.

12. 2. The system of claim 1, wherein the maximum energy of the beta rays is 2.25 MeV.

13. 2. The system of claim 1, wherein the neutron generator repeats generating the neutron field at prescribed intervals when the therapeutic radiation source is implanted in the patient's body.

14. 2. The system of claim 1, wherein the electric neutron generator comprises a plurality of electric neutron generators arranged external to and around the patient's body, such that the neutrons are irradiated from various angles toward the therapeutic radiation source.

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