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网络荟萃分析在慢性淋巴细胞白血病中的维持治疗。

A network meta-analysis of maintenance therapy in chronic lymphocytic leukemia.

机构信息

Division of Hematology and Oncology Medicine, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, ROC.

School of Public Health, National Defense Medical Center, Taipei, Taiwan, ROC.

出版信息

PLoS One. 2020 Jan 29;15(1):e0226879. doi: 10.1371/journal.pone.0226879. eCollection 2020.

Abstract

BACKGROUND

Chronic lymphocytic leukemia (CLL) is incurable through conventional chemoimmunotherapy regimens. Despite durable responses to front-line therapy and sustained remission rates in patients with CLL, a majority of patients eventually relapse in 5 years of initial treatment. The depth of the response may affect the length of response. Maintenance therapies were aimed to deep remissions and extend the period of disease quiescence. Lenalidomide, rituximab and ofatumumab had demonstrated some efficacy as a maintenance therapy compared to no intervention for CLL patients. The relative effect on disease control and safety between different maintenance therapies were unclear.

METHODS

We performed a systematic literature review and network meta-analysis to evaluate relative effect on disease control and safety of current available maintenance therapies. We searched PubMed, Embase and Cochrane database up to March 6, 2019. Relevant reference of review article and conference abstract including European Hematology Association Annual Meeting (EHA 2018), American Society of Hematology Annual Meeting (ASH 2018) and American Society of Clinical Oncology Annual Meeting (ASCO 2018) were searched. Randomized controlled trials (RCT) involving current available maintenance therapy including "Lenalidomide", "Rituximab", "Ofatumumab", "Ibrutinib", "Idelalisib", "Venetoclax"and "Obinutuzumab"were eligible. Outcomes of interest included progression-free survival (PFS), overall survival (OS) and serious adverse events (SAE) in CLL patients received subsequent maintenance therapy. Two authors CHL and CL) independently assessed eligibility for all identified citations and extracted data from the original trial reports. The selected studies' risk of bias was assessed following the guidelines of Cochrane Collaboration Handbook.

RESULTS

In total, six phase III RCTs with total 1,615 CLL patients were identified. Maintenance therapy using lenalidomide, rituximab, and ofatumumab demonstrated a statistically significant effect in prolongation of progression-free survival (HR:0.37, 95% CI: 0.27-0.50 of lenalidomide; HR:0.50, 95% CI: 0.38-0.66 of rituximab; HR:0.52, 95% CI:0.41-0.66 of ofatumumab, separately) compared with no intervention; however, for overall survival, the effect of maintenance therapy showed no significant difference versus no intervention (HR: 0.89, 95% CI: 0.70-1.14). Lenalidomide showed the best efficacy for PFS (HR: 0.37, 95% CI: 0.27-0.50, Probability of being best treatment: 96%).

CONCLUSIONS

Our network meta-analysis provided an integrated overview of relative efficacy and safety of different maintenance therapies in CLL. All maintenance therapies were effective in reducing the risk of disease progression versus no intervention. Based on current best evidence, maintenance therapy with lenalidomide is the most efficacious option.

摘要

背景

慢性淋巴细胞白血病(CLL)通过常规化疗免疫疗法方案无法治愈。尽管 CLL 患者在前线治疗中有持久的反应和持续的缓解率,但大多数患者在最初治疗的 5 年内最终会复发。反应的深度可能会影响反应的持续时间。维持治疗旨在达到深度缓解并延长疾病静止期。来那度胺、利妥昔单抗和奥法妥珠单抗与 CLL 患者不干预相比,已显示出作为维持治疗的一些疗效。不同维持治疗在疾病控制和安全性方面的相对效果尚不清楚。

方法

我们进行了系统的文献综述和网络荟萃分析,以评估当前可用的维持治疗在疾病控制和安全性方面的相对效果。我们检索了 PubMed、Embase 和 Cochrane 数据库,检索时间截至 2019 年 3 月 6 日。还检索了相关综述文章的参考文献和会议摘要,包括欧洲血液学协会年会(EHA 2018)、美国血液学会年会(ASH 2018)和美国临床肿瘤学会年会(ASCO 2018)。纳入了涉及当前可用维持治疗的随机对照试验(RCT),包括“来那度胺”、“利妥昔单抗”、“奥法妥珠单抗”、“依鲁替尼”、“idelalisib”、“venetoclax”和“obinutuzumab”。感兴趣的结局包括接受后续维持治疗的 CLL 患者的无进展生存期(PFS)、总生存期(OS)和严重不良事件(SAE)。两位作者(CHL 和 CL)独立评估了所有确定引用的入选标准,并从原始试验报告中提取数据。按照 Cochrane 协作手册的指南评估了所选研究的偏倚风险。

结果

共确定了 6 项 III 期 RCT,共纳入 1615 例 CLL 患者。与不干预相比,来那度胺、利妥昔单抗和奥法妥珠单抗维持治疗在延长无进展生存期方面表现出统计学上的显著效果(来那度胺 HR:0.37,95%CI:0.27-0.50;利妥昔单抗 HR:0.50,95%CI:0.38-0.66;奥法妥珠单抗 HR:0.52,95%CI:0.41-0.66);然而,对于总生存期,维持治疗的效果与不干预相比无显著差异(HR:0.89,95%CI:0.70-1.14)。来那度胺在 PFS 方面表现出最佳疗效(HR:0.37,95%CI:0.27-0.50,成为最佳治疗的概率:96%)。

结论

我们的网络荟萃分析提供了 CLL 中不同维持治疗的相对疗效和安全性的综合概述。所有维持治疗在降低疾病进展风险方面均优于不干预。基于当前最佳证据,来那度胺维持治疗是最有效的选择。

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