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Understanding and Managing Large B Cell Lymphoma Relapses after Chimeric Antigen Receptor T Cell Therapy.
Biology of Blood and Marrow Transplantation ( IF 5.609 ) Pub Date : 2019-07-04 , DOI: 10.1016/j.bbmt.2019.06.036
Michael Byrne 1 , Olalekan O Oluwole 1 , Bipin Savani 1 , Navneet S Majhail 2 , Brian T Hill 2 , Fredrick L Locke 3
Affiliation  

Most patients with large cell lymphoma are cured with frontline chemoimmunotherapy. For individuals with refractory disease and those who relapse after conventional therapies, chimeric antigen receptor (CAR) T cells are an important treatment option and have led to remissions in otherwise refractory patients. In the pivotal trials, durable responses were achieved in approximately 40% to 50% of patients treated with axicabtagene ciloleucel, tisagenlecleucel, or lisocabtagene maraleucel, indicating that many patients will require subsequent treatment. Failure after CAR T cell therapy is caused by a variety of factors that can be divided into 3 broad categories: tumor intrinsic factors, other host factors, and inadequacies of the CAR T cells. Within this framework, this article reviews possible mechanisms of treatment failures and, based on the timing of relapse, considers potential salvage therapies and opportunities for future clinical studies.

中文翻译:

嵌合抗原受体T细胞治疗后理解和管理大B细胞淋巴瘤复发。

大多数大细胞淋巴瘤患者可通过一线化学免疫疗法治愈。对于患有难治性疾病的患者以及常规治疗后复发的患者,嵌合抗原受体(CAR)T细胞是一种重要的治疗选择,可导致原本难治的患者缓解。在关键试验中,大约40%至50%的接受阿昔单抗基因环丙沙星,替沙可根微核素或可瑞可卡培因maraleucel治疗的患者获得了持久的反应,表明许多患者将需要后续治疗。CAR T细胞治疗后的失败是由多种因素引起的,这些因素可分为3大类:肿瘤内在因素,其他宿主因素和CAR T细胞的不足。在此框架内,本文回顾了治疗失败的可能机制,
更新日期:2019-07-04
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