Department of Internal Medicine, Division of Hematology/Oncology, Mayo Clinic, Phoenix, Arizona.
Evidence-Based Practice Center, Mayo Clinic, Rochester, Minnesota.
Am J Hematol. 2018 Oct;93(10):1220-1226. doi: 10.1002/ajh.25226. Epub 2018 Sep 3.
Mantle cell lymphoma is characterized by relapse and progressive disease, despite initial response to chemoimmunotherapy. We conducted a systematic review and meta-analysis to determine the efficacy of rituximab maintenance (RM) therapy in patients with mantle cell lymphoma. We searched PubMed, Embase and Cochrane Central Register of Controlled Trials from database inception through November 1, 2017. Only full-text articles were included. Prespecified data elements were extracted from each trial. Outcomes of interest included progression-free survival (PFS) and overall survival (OS). The overall effect was pooled using the Der Simonian-Laird random effects model. Three randomized controlled trials and four observational studies met our inclusion criteria and were identified in the analyses. Six studies compared RM therapy to observation, and one compared RM therapy to interferon alfa. Meta-analysis evaluating outcomes of patients treated after ASCT revealed that RM improved for both PFS (HR = 0.33, 95% CI = 0.23-0.49) and OS (HR of death = 0.35, 95% CI = 0.17-0.69). A second meta-analysis of studies evaluating outcomes of patients who are ASCT-ineligible treated with anthracycline-based induction therapy revealed that RM improved PFS (HR = 0.38, 95% CI = 0.25-0.58). There is a paucity of data on the role of RM in ASCT-ineligible patients and those with relapsed disease. Overall, RM therapy appears to improve PFS and OS in previously untreated patients with mantle cell lymphoma who undergo induction chemoimmunotherapy followed by ASCT.
套细胞淋巴瘤的特点是尽管初始化疗免疫治疗有效,但仍会复发和进展。我们进行了系统评价和荟萃分析,以确定利妥昔单抗维持(RM)治疗套细胞淋巴瘤患者的疗效。我们检索了从数据库建立到 2017 年 11 月 1 日的 PubMed、Embase 和 Cochrane 中央对照试验注册库。仅纳入全文文章。从每个试验中提取预定的数据元素。主要观察终点为无进展生存期(PFS)和总生存期(OS)。采用 Der Simonian-Laird 随机效应模型对总效应进行汇总。纳入的分析中,有 3 项随机对照试验和 4 项观察性研究符合纳入标准。其中 6 项研究比较了 RM 治疗与观察,1 项研究比较了 RM 治疗与干扰素 alfa。评估 ASCT 后患者治疗结局的荟萃分析显示,RM 改善了 PFS(HR=0.33,95%CI=0.23-0.49)和 OS(HR 死亡=0.35,95%CI=0.17-0.69)。另一项评估接受基于蒽环类药物诱导治疗的不适合 ASCT 的患者结局的研究荟萃分析显示,RM 改善了 PFS(HR=0.38,95%CI=0.25-0.58)。关于 RM 在不适合 ASCT 的患者和复发患者中的作用的数据有限。总体而言,RM 治疗似乎可改善接受诱导化疗免疫治疗后行 ASCT 的初治套细胞淋巴瘤患者的 PFS 和 OS。