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Early experience using salvage radiotherapy for relapsed/refractory non-Hodgkin lymphomas after CD19 chimeric antigen receptor (CAR) T cell therapy.
British Journal of Haematology ( IF 5.1 ) Pub Date : 2020-03-05 , DOI: 10.1111/bjh.16541
Brandon S Imber 1 , Michel Sadelain 2 , Carl DeSelm 3 , Connie Batlevi 4, 5 , Renier J Brentjens 5 , Parastoo B Dahi 6 , Sergio Giralt 6 , Jae H Park 5 , Craig Sauter 6 , Michael Scordo 6 , Gunjan Shah 6 , Miguel-Angel Perales 6 , M Lia Palomba 4, 5 , Joachim Yahalom 1
Affiliation  

Radiotherapy is potentially an important salvage strategy post‐chimeric antigen receptor T cell therapy (CART), but limited data exist. We reviewed 14 patients treated with salvage radiation post‐CART progression (SRT). Most received SRT for first post‐CART relapse (71%) to sites previously PET‐avid pre‐CART (79%). Median overall survival (OS) post‐SRT was 10 months. Post‐SRT, six localized relapses achieved 100% response (3 = complete, 3 = partial), with improved freedom from subsequent relapse (P  = 0·001) and OS (P  = 0·004) compared to advanced stage relapses. Three were bridged to allogeneic transplantation; at analysis, all were alive/NED. SRT has diverse utility and can integrate with novel agents or transplantation to attempt durable remissions.

中文翻译:

CD19嵌合抗原受体(CAR)T细胞治疗后复发/难治性非霍奇金淋巴瘤使用挽救性放疗的早期经验。

放射疗法可能是嵌合抗原受体T细胞疗法(CART)后的一项重要挽救策略,但数据有限。我们回顾了14例接受CART后加急放疗治疗的患者。多数接受首次CART复发的SRT(71%)到先前PET-avid进行CART的部位(79%)。SRT后的总生存期(OS)中位数为10个月。SRT后, 与晚期复发相比,六次局部复发实现了100%的响应(3 =完全,3 =部分),与随后的复发(P  = 0·001)和OS(P = 0·004)的自由度得到了提高。三个被移植到同种异体移植中。经过分析,所有患者都还活着。SRT具有多种用途,可以与新型药物或移植药物整合以尝试持久缓解。
更新日期:2020-03-05
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