Cleveland Clinic, Cleveland, OH, USA.
The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Br J Haematol. 2019 Feb;184(4):524-535. doi: 10.1111/bjh.15720. Epub 2018 Dec 21.
Bendamustine (B) with rituximab (R) is a standard frontline treatment for medically fit follicular lymphoma (FL) patients. The safety and efficacy of maintenance rituximab (MR) after BR induction has not been formally compared to observation for FL, resulting in disparate practice patterns. Prospective trials have shown benefit of MR after R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) or R-CVP (rituximab, cyclophosphamide, vincristine, prednisone), yet recent data from the GALLIUM study comparing outcomes of patients treated with chemotherapy with R or obinutuzumab (G) showed higher than anticipated fatal adverse events with BR/BG. In order to assess the efficacy and tolerability of MR after BR, we retrospectively collected data on 640 newly diagnosed patients treated with FL. We found that patients who achieved partial remission (PR) after ≥4 cycles of BR had improved duration of response (DOR) with MR vs. no maintenance, whereas those in complete remission did not. These findings were confirmed in a validation cohort. In the entire study population, the known fatal adverse event rate after BR was 2·5% and did not significantly differ in those receiving MR versus no maintenance. [Correction added on 14 January 2019, after online publication: The preceding sentence has been corrected in this current version.] Within the limitations inherent to retrospective analysis, these data suggest that FL patients with a PR to BR experience prolongation of remission with MR with an acceptable safety profile.
苯达莫司汀(B)联合利妥昔单抗(R)是适合医学治疗的滤泡性淋巴瘤(FL)患者的标准一线治疗方案。BR 诱导后维持利妥昔单抗(MR)的安全性和疗效尚未与 FL 的观察进行正式比较,导致实践模式存在差异。前瞻性试验表明,在 R-CHOP(利妥昔单抗、环磷酰胺、多柔比星、长春新碱、泼尼松)或 R-CVP(利妥昔单抗、环磷酰胺、长春新碱、泼尼松)后使用 MR 有益,但最近来自 GALLIUM 研究的数据比较了接受化疗联合 R 或奥滨尤妥珠单抗(G)治疗的患者的结果,显示 BR/BG 治疗的致命不良事件发生率高于预期。为了评估 BR 后 MR 的疗效和耐受性,我们回顾性地收集了 640 例新诊断为 FL 的患者的数据。我们发现,在 BR 治疗后≥4 个周期达到部分缓解(PR)的患者与不维持治疗相比,MR 治疗具有更长的缓解持续时间(DOR),而完全缓解的患者则没有。这些发现在验证队列中得到了证实。在整个研究人群中,BR 后的已知致命不良事件发生率为 2.5%,在接受 MR 治疗与不维持治疗的患者中没有显著差异。