Division of Hematology and Oncology Medicine, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan.
Department of Neurology, Changhua Christian Hospital, Changhua 500, Taiwan.
Curr Oncol. 2022 Jun 14;29(6):4245-4259. doi: 10.3390/curroncol29060339.
Chronic lymphocytic leukemia (CLL) is the most common lymphoproliferative disease in adults. Despite durable responses and sustained remission rates to frontline therapy, CLL is still incurable within standard therapy and eventually relapses. Maintenance therapies aim to achieve deep remission. However, the efficacy and safety of lenalidomide maintenance are still debated. Randomized controlled trials published before March 2022 were retrieved from databases. Primary outcomes were progression-free survival (PFS) and overall survival (OS). Trial sequential analysis examined analytical power in primary outcomes. Secondary outcomes were Grade 3-4 neutropenia, treatment discontinuation (TD), serious adverse events (SAE), and fatal adverse events (FAE). Hazard (HR) and odds ratios (ORs) with 95% confidence intervals (CIs) were calculated. Four articles (733 patients) met the selection criteria. Lenalidomide maintenance was associated with a statistically significant effect in prolonging PFS (HR, 0.43; 95% CI, 0.28-0.68; I = 57%) and higher proportion of SAE (OR 4.64; 95% CI 2.96-7.26; I = 0%) and exhibited no difference in OS (HR, 0.62; 95% CI, 0.29-1.30; I = 52%) observation/placebo. It showed no significant difference compared with observation/placebo regarding Grade 3-4 neutropenia (OR 2.30; 95% CI 0.84-6.28; I = 81%), TD (OR 0.76; 95% CI 0.29-1.99; I = 84%), and FAE (OR 0.86; 95% CI 0.28-2.63; I = 0%). Lenalidomide maintenance can prolong PFS in CLL. Further studies should verify its effect on OS.
慢性淋巴细胞白血病(CLL)是成人中最常见的淋巴增生性疾病。尽管一线治疗能够实现持久缓解和持续缓解率,但 CLL 在标准治疗下仍然无法治愈,最终会复发。维持治疗旨在实现深度缓解。然而,来那度胺维持治疗的疗效和安全性仍存在争议。从数据库中检索到 2022 年 3 月前发表的随机对照试验。主要结局是无进展生存期(PFS)和总生存期(OS)。试验序贯分析检查了主要结局的分析能力。次要结局为 3-4 级中性粒细胞减少症、治疗中断(TD)、严重不良事件(SAE)和致命不良事件(FAE)。计算了危险(HR)和 95%置信区间(CI)的优势比(ORs)。四项研究(733 例患者)符合入选标准。来那度胺维持治疗与 PFS 延长(HR,0.43;95%CI,0.28-0.68;I = 57%)和更高比例的 SAE(OR 4.64;95%CI,2.96-7.26;I = 0%)相关,并且在 OS 方面无差异(HR,0.62;95%CI,0.29-1.30;I = 52%)观察/安慰剂。与观察/安慰剂相比,它在 3-4 级中性粒细胞减少症(OR 2.30;95%CI,0.84-6.28;I = 81%)、TD(OR 0.76;95%CI,0.29-1.99;I = 84%)和 FAE(OR 0.86;95%CI,0.28-2.63;I = 0%)方面无显著差异。来那度胺维持治疗可延长 CLL 患者的 PFS。进一步的研究应该验证其对 OS 的影响。