Pierre Loap , Justine Decroocq , Rudy Birsen , Natacha Johnson , Didier Bouscary , Youlia Kirova
{"title":"Car-T细胞桥接放疗期间暴露于免疫系统","authors":"Pierre Loap , Justine Decroocq , Rudy Birsen , Natacha Johnson , Didier Bouscary , Youlia Kirova","doi":"10.1016/j.canrad.2025.104595","DOIUrl":null,"url":null,"abstract":"<div><h3>Purpose</h3><div>The objective of this study was to quantify how much dose from bridging radiotherapy is being delivered to non-lymphoma immune cells.</div></div><div><h3>Material and methods</h3><div>All patients who underwent bridging radiotherapy between January 2023 and April 2024 at the institut Curie (Paris, France) surrounding the infusion of chimeric antigen receptor (Car)-T cells, were identified. The effective dose to the immune cells was calculated for each of them.</div></div><div><h3>Results</h3><div>Nine patients were included, with a mean follow-up time of 6<!--> <!-->months; one patient experienced a recurrence. No grade 2+ toxicity was reported. Median effective dose to the immune cells was 0.56<!--> <!-->Gy (range: 0.039–2.72<!--> <!-->Gy) and varied between patients. The main contribution came from the integral dose (0.43<!--> <!-->Gy, range: 0.039–1.42<!--> <!-->Gy).</div></div><div><h3>Conclusions</h3><div>The doses received by the immune system when undergoing bridging radiotherapy for Car-T cells can vary considerably from one patient to another, and the integral dose represents the primary part of this exposure of the immune system. Prospective solid data is needed in this context to evaluate the role of choice of radiotherapy techniques in bridging radiotherapy.</div></div>","PeriodicalId":9504,"journal":{"name":"Cancer Radiotherapie","volume":"29 2","pages":"Article 104595"},"PeriodicalIF":1.5000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Exposure to the immune system during bridging radiotherapy for Car-T cells\",\"authors\":\"Pierre Loap , Justine Decroocq , Rudy Birsen , Natacha Johnson , Didier Bouscary , Youlia Kirova\",\"doi\":\"10.1016/j.canrad.2025.104595\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Purpose</h3><div>The objective of this study was to quantify how much dose from bridging radiotherapy is being delivered to non-lymphoma immune cells.</div></div><div><h3>Material and methods</h3><div>All patients who underwent bridging radiotherapy between January 2023 and April 2024 at the institut Curie (Paris, France) surrounding the infusion of chimeric antigen receptor (Car)-T cells, were identified. The effective dose to the immune cells was calculated for each of them.</div></div><div><h3>Results</h3><div>Nine patients were included, with a mean follow-up time of 6<!--> <!-->months; one patient experienced a recurrence. No grade 2+ toxicity was reported. Median effective dose to the immune cells was 0.56<!--> <!-->Gy (range: 0.039–2.72<!--> <!-->Gy) and varied between patients. The main contribution came from the integral dose (0.43<!--> <!-->Gy, range: 0.039–1.42<!--> <!-->Gy).</div></div><div><h3>Conclusions</h3><div>The doses received by the immune system when undergoing bridging radiotherapy for Car-T cells can vary considerably from one patient to another, and the integral dose represents the primary part of this exposure of the immune system. Prospective solid data is needed in this context to evaluate the role of choice of radiotherapy techniques in bridging radiotherapy.</div></div>\",\"PeriodicalId\":9504,\"journal\":{\"name\":\"Cancer Radiotherapie\",\"volume\":\"29 2\",\"pages\":\"Article 104595\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2025-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer Radiotherapie\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1278321825000113\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer Radiotherapie","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1278321825000113","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
Exposure to the immune system during bridging radiotherapy for Car-T cells
Purpose
The objective of this study was to quantify how much dose from bridging radiotherapy is being delivered to non-lymphoma immune cells.
Material and methods
All patients who underwent bridging radiotherapy between January 2023 and April 2024 at the institut Curie (Paris, France) surrounding the infusion of chimeric antigen receptor (Car)-T cells, were identified. The effective dose to the immune cells was calculated for each of them.
Results
Nine patients were included, with a mean follow-up time of 6 months; one patient experienced a recurrence. No grade 2+ toxicity was reported. Median effective dose to the immune cells was 0.56 Gy (range: 0.039–2.72 Gy) and varied between patients. The main contribution came from the integral dose (0.43 Gy, range: 0.039–1.42 Gy).
Conclusions
The doses received by the immune system when undergoing bridging radiotherapy for Car-T cells can vary considerably from one patient to another, and the integral dose represents the primary part of this exposure of the immune system. Prospective solid data is needed in this context to evaluate the role of choice of radiotherapy techniques in bridging radiotherapy.
期刊介绍:
Cancer/radiothérapie se veut d''abord et avant tout un organe francophone de publication des travaux de recherche en radiothérapie. La revue a pour objectif de diffuser les informations majeures sur les travaux de recherche en cancérologie et tout ce qui touche de près ou de loin au traitement du cancer par les radiations : technologie, radiophysique, radiobiologie et radiothérapie clinique.