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理解和管理嵌合抗原受体 T 细胞治疗后大 B 细胞淋巴瘤的复发。

Understanding and Managing Large B Cell Lymphoma Relapses after Chimeric Antigen Receptor T Cell Therapy.

机构信息

Division of Hematology Oncology, Department of Medicine, Vanderbilt School of Medicine, Nashville, Tennessee.

Department of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.

出版信息

Biol Blood Marrow Transplant. 2019 Nov;25(11):e344-e351. doi: 10.1016/j.bbmt.2019.06.036. Epub 2019 Jul 4.

Abstract

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.

摘要

大多数大细胞淋巴瘤患者可通过一线化疗免疫治疗治愈。对于难治性疾病患者和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,已使原本难治性的患者获得缓解。在关键试验中,接受 axicabtagene ciloleucel、tisagenlecleucel 或 lisocabtagene maraleucel 治疗的患者中约有 40%至 50%获得了持久缓解,表明许多患者将需要后续治疗。CAR T 细胞治疗后失败是由多种因素引起的,可以分为 3 大类:肿瘤内在因素、其他宿主因素和 CAR T 细胞不足。基于这一框架,本文综述了治疗失败的可能机制,并根据复发时间考虑了潜在的挽救治疗和未来临床研究的机会。

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