Outcomes of Relapsed or Refractory Diffuse Large B‐Cell Lymphoma Treated With R‐GemOx: A Multicenter Cohort Study

医学 弥漫性大B细胞淋巴瘤 奥沙利铂 化学免疫疗法 美罗华 内科学 胃肠病学 吉西他滨 淋巴瘤 肿瘤科 外科 化疗 癌症 结直肠癌
作者
Samuel Yamshon,Jean L. Koff,Melissa C. Larson,Brad S. Kahl,Carla Casulo,Izidore S. Lossos,Sara Haddadi,Michele Stanchina,Dai Chihara,Amy Ayers,Thomas M. Habermann,Yucai Wang,Arushi Khurana,Grzegorz S. Nowakowski,Tanner W. Reicks,Umar Farooq,Brian K. Link,Jonathon B. Cohen,Peter Martin,Jia Li
出处
期刊:American Journal of Hematology [Wiley]
卷期号:100 (4): 606-615 被引量:6
标识
DOI:10.1002/ajh.27630
摘要

ABSTRACT Rituximab, gemcitabine, and oxaliplatin (R‐GemOx) is a commonly used chemoimmunotherapy regimen for relapsed or refractory (R/R) diffuse large B‐cell lymphoma (DLBCL), but there are limited real‐world data. In a multicenter retrospective study from a cohort of eight US academic centers (LEO CReWE), we evaluated 183 patients with R/R DLBCL and high‐grade B cell lymphoma treated with R‐GemOx, including subgroups treated without intent for consolidation with autologous stem cell transplant (ASCT) or chimeric antigen receptor (CAR) T cell therapy ( n = 100), those utilizing R‐GemOx as a bridge to ASCT or CAR T ( n = 83), and those aged 70 and older ( n = 71). Overall response rates (ORRs) for all patients treated with R‐GemOx were 45% with a complete response (CR) rate of 29%. The median event‐free survival (EFS) was 2.3 months, and the median overall survival (OS) was 13.5 months. Patients receiving R‐GemOx without intent for ASCT or CAR T had ORR and CR rates of 33% and 18%, respectively, with median EFS and OS of 2.0 and 9.5 months, respectively. Patients receiving R‐GemOx as a bridge to ASCT or CAR T had ORR and CR rates of 57% and 36%, respectively, with median EFS and OS of 3.5 and 17.4 months, respectively. Patients receiving R‐GemOx aged 70 and older had ORR and CR rates of 53% and 33%, respectively, with median EFS and OS of 2.2 and 13.9 months, respectively. These data provide a benchmark for R‐GemOx in the rapidly evolving landscape of R/R DLBCL therapies.
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