嵌合抗原受体 T 细胞疗法成功治疗一名心脏移植受者的难治性移植后淋巴组织增生性疾病

IF 1.3 Q4 HEMATOLOGY
Katherine Hickmann, Ryan Sweeney, Chelsea Peterson, Kathleen Faringer, Madeline Riley, Mark Bunker, A. Hadi, Cyrus Khan, Y. Samhouri
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引用次数: 0

摘要

移植后淋巴增生性疾病(PTLDs)是一种机会性恶性肿瘤,使造血干细胞或实体器官移植的成功变得复杂。这些疾病通常在移植后出现,原因是移植后需要进行免疫抑制,以尽量降低供体组织排斥的风险。这些疾病的一线治疗包括在允许的情况下限制免疫抑制。后续治疗包括使用单克隆抗 CD20 抗体(利妥昔单抗)和/或联合化疗。嵌合抗原受体(CAR)T细胞疗法彻底改变了许多淋巴恶性肿瘤的治疗模式。由于PTLD患者被排除在关键临床试验之外,该疗法尚未获准用于PTLD。此外,该疗法在移植后的应用可能非常复杂,多学科护理对于成功实施这种可能治愈疾病的疗法至关重要。我们为大家介绍一位68岁的患者,她曾因非缺血性心肌病接受过心脏移植手术,被诊断为PTLD,在成功接受CAR T细胞疗法之前,她一直对现行指南中的治疗方法感到难治。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful Treatment of Refractory Post-Transplant Lymphoproliferative Disorder With Chimeric Antigen Receptor T-Cell Therapy in a Heart Transplant Recipient
Post-transplant lymphoproliferative disorders (PTLDs) are opportunistic malignancies that complicate the success of hematopoietic stem cell or solid organ transplantation. These disorders often arise post-transplant due to the immunosuppression required for minimizing the risk of rejection of donor tissue. First-line treatment of these disorders includes limiting immunosuppression when permissible. Subsequent treatment includes the use of monoclonal anti-CD20 antibody (rituximab), and/or combination chemotherapy. Chimeric antigen receptor (CAR) T-cell therapy has revolutionized the treatment paradigm in many lymphoid malignancies. It is not approved for PTLD due to exclusion of PTLD patients from pivotal clinical trials. Also, its utilization post-transplant can be complex and multidisciplinary care is of utmost importance for successful administration of a potentially curative treatment. We present a 68-year-old patient with history of heart transplant for non-ischemic cardiomyopathy, diagnosed with PTLD that was refractory to treatment using current guidelines until successfully receiving CAR T-cell therapy.
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来源期刊
Journal of hematology
Journal of hematology HEMATOLOGY-
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