Chiara De Sio , Laura Ballisat , Lana Beck , Susanna Guatelli , Dousatsu Sakata , Yuyao Shi , Jinyan Duan , Lujin Abu Sabah , Jaap Velthuis , Anatoly Rosenfeld
{"title":"靶向α疗法使用2111at:剂量和DNA损伤的Geant4模拟。","authors":"Chiara De Sio , Laura Ballisat , Lana Beck , Susanna Guatelli , Dousatsu Sakata , Yuyao Shi , Jinyan Duan , Lujin Abu Sabah , Jaap Velthuis , Anatoly Rosenfeld","doi":"10.1016/j.ejmp.2024.104860","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>:Targeted alpha therapies show great potential for cancer treatment due to their high linear energy transfer (LET) and low range. <sup>211</sup>At is currently employed in clinical trials. Targeted alpha therapies (TAT) are effective as an adjuvant treatment for cancer or to treat micrometastases and diffuse cancers. A deeper understanding of the induced initial damage is crucial to enhance treatment planning.</div></div><div><h3>Methods:</h3><div>This study shows Geant4(-DNA)-based simulations to calculate absorbed dose profiles and DNA damaging potential in intravenously administered TAT with <sup>211</sup>At. It assumes radionuclide decay on the blood vessel wall, and calculates the DNA damage in the surrounding tissue.</div></div><div><h3>Results:</h3><div>The calculated dosimetric quantities show that the effect of such treatment is mainly due to the emitted alpha particles, and is localised in a region of up to <span><math><mrow><mn>80</mn><mspace></mspace><mi>μ</mi><mi>m</mi></mrow></math></span> from the blood vessel. The RBE of the treatment is in the range <span><math><mrow><mn>2</mn><mo>.</mo><mn>5</mn><mo>−</mo><mn>4</mn></mrow></math></span>, and is calculated as a function of the number of double-strand breaks.</div></div><div><h3>Conclusions:</h3><div>Targeted therapies with <sup>211</sup>At are effective within the range of the emitted alpha particles. With its capacity to induce complex DNA damage in such a short range, it is very promising for localised treatment of small tumour cells or micrometastases.</div></div>","PeriodicalId":56092,"journal":{"name":"Physica Medica-European Journal of Medical Physics","volume":"129 ","pages":"Article 104860"},"PeriodicalIF":3.3000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Targeted alpha therapies using 211At: A Geant4 simulation of dose and DNA damage\",\"authors\":\"Chiara De Sio , Laura Ballisat , Lana Beck , Susanna Guatelli , Dousatsu Sakata , Yuyao Shi , Jinyan Duan , Lujin Abu Sabah , Jaap Velthuis , Anatoly Rosenfeld\",\"doi\":\"10.1016/j.ejmp.2024.104860\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><div>:Targeted alpha therapies show great potential for cancer treatment due to their high linear energy transfer (LET) and low range. <sup>211</sup>At is currently employed in clinical trials. Targeted alpha therapies (TAT) are effective as an adjuvant treatment for cancer or to treat micrometastases and diffuse cancers. A deeper understanding of the induced initial damage is crucial to enhance treatment planning.</div></div><div><h3>Methods:</h3><div>This study shows Geant4(-DNA)-based simulations to calculate absorbed dose profiles and DNA damaging potential in intravenously administered TAT with <sup>211</sup>At. It assumes radionuclide decay on the blood vessel wall, and calculates the DNA damage in the surrounding tissue.</div></div><div><h3>Results:</h3><div>The calculated dosimetric quantities show that the effect of such treatment is mainly due to the emitted alpha particles, and is localised in a region of up to <span><math><mrow><mn>80</mn><mspace></mspace><mi>μ</mi><mi>m</mi></mrow></math></span> from the blood vessel. The RBE of the treatment is in the range <span><math><mrow><mn>2</mn><mo>.</mo><mn>5</mn><mo>−</mo><mn>4</mn></mrow></math></span>, and is calculated as a function of the number of double-strand breaks.</div></div><div><h3>Conclusions:</h3><div>Targeted therapies with <sup>211</sup>At are effective within the range of the emitted alpha particles. With its capacity to induce complex DNA damage in such a short range, it is very promising for localised treatment of small tumour cells or micrometastases.</div></div>\",\"PeriodicalId\":56092,\"journal\":{\"name\":\"Physica Medica-European Journal of Medical Physics\",\"volume\":\"129 \",\"pages\":\"Article 104860\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Physica Medica-European Journal of Medical Physics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1120179724013280\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physica Medica-European Journal of Medical Physics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1120179724013280","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
Targeted alpha therapies using 211At: A Geant4 simulation of dose and DNA damage
Introduction
:Targeted alpha therapies show great potential for cancer treatment due to their high linear energy transfer (LET) and low range. 211At is currently employed in clinical trials. Targeted alpha therapies (TAT) are effective as an adjuvant treatment for cancer or to treat micrometastases and diffuse cancers. A deeper understanding of the induced initial damage is crucial to enhance treatment planning.
Methods:
This study shows Geant4(-DNA)-based simulations to calculate absorbed dose profiles and DNA damaging potential in intravenously administered TAT with 211At. It assumes radionuclide decay on the blood vessel wall, and calculates the DNA damage in the surrounding tissue.
Results:
The calculated dosimetric quantities show that the effect of such treatment is mainly due to the emitted alpha particles, and is localised in a region of up to from the blood vessel. The RBE of the treatment is in the range , and is calculated as a function of the number of double-strand breaks.
Conclusions:
Targeted therapies with 211At are effective within the range of the emitted alpha particles. With its capacity to induce complex DNA damage in such a short range, it is very promising for localised treatment of small tumour cells or micrometastases.
期刊介绍:
Physica Medica, European Journal of Medical Physics, publishing with Elsevier from 2007, provides an international forum for research and reviews on the following main topics:
Medical Imaging
Radiation Therapy
Radiation Protection
Measuring Systems and Signal Processing
Education and training in Medical Physics
Professional issues in Medical Physics.