Jennifer L Crombie, Monika Jun, Tongsheng Wang, Alex Mutebi, Anthony Wang, Anindit Chhibber, Rajesh Kamalakar, Jon Ukropec, Julie Blaedel, Anupama Kalsekar
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引用次数: 0
摘要
这项研究使用了美国患者的 COTA 去标识化数据(2010-2021 年),以探讨新型疗法在真实世界中治疗复发/难治性弥漫大 B 细胞淋巴瘤 (DLBCL) 的疗效。我们评估了接受新型疗法(包括嵌合抗原受体T细胞(CAR T)疗法和基于他法西单抗或泊拉珠单抗的疗法)的复发性/难治性弥漫性大B细胞淋巴瘤患者的人口统计学特征、临床特征和临床疗效。总共分析了175名R/R DLBCL患者,其中73人、69人和27人分别接受了CAR T疗法、基于泊拉珠单抗的疗法和基于他法西塔单抗的疗法。在既往接受过≥1线治疗的患者中(即开始接受二线或以后的治疗;2 L+),CAR T、基于泊拉珠单抗的方案和基于他法西他单抗的方案的中位总生存期分别为26.5个月、7.8个月和6.3个月。CAR T治疗后复发患者的疗效尤其差,这表明基于泊拉珠单抗和他法西他单抗的2 L + R/R DLBCL治疗方案在现实世界中的疗效并不理想。我们需要更多的治疗方案。
Real-world outcomes with novel therapies in relapsed/refractory diffuse large B-cell lymphoma.
This study used COTA de-identified data (2010-2021) of patients in the US to explore outcomes of novel therapies in relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) in real-world settings. Demographics, clinical characteristics, and clinical outcomes of patients with R/R DLBCL who received novel treatments including chimeric antigen receptor T-cell (CAR T) therapy and tafasitamab- or polatuzumab-based therapies were evaluated. Overall, 175 patients with R/R DLBCL were analyzed; 73, 69, and 27 received CAR T therapy, polatuzumab-based regimens, and tafasitamab-based regimens, respectively. In patients who had ≥1 prior lines of therapy (i.e. starting second-line or later therapy; 2 L+), CAR T, polatuzumab-based regimens, and tafasitamab-based regimens achieved a median overall survival of 26.5, 7.8, and 6.3 months, respectively. Outcomes were particularly poor for patients with relapse following CAR T, indicating that polatuzumab- and tafasitamab-based regimens in 2 L + R/R DLBCL have suboptimal outcomes in the real world. Additional treatment options are needed.
期刊介绍:
Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor