Department of Public Health, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Department of Research and Development, Netherlands Comprehensive Cancer Organisation (IKNL), Utrecht, The Netherlands.
Blood Cancer J. 2024 Sep 12;14(1):157. doi: 10.1038/s41408-024-01137-0.
First-line treatment for advanced-stage diffuse large B-cell lymphoma (DLBCL) typically involves 6x R-CHOP21 or 6x R-CHOP21 with two additional rituximab administrations (6x R-CHOP21 + 2 R). In contemporary practice, this treatment choice might be guided by interim PET scan results. This nationwide, population-based study investigates the comparative effectiveness of these treatment regimens in an era where interim PET-guided treatment decisions were not standard practice. Utilizing the Netherlands Cancer Registry, we identified 1577 adult patients diagnosed with advanced-stage DLBCL between 2014-2018 who completed either 6x R-CHOP21 (43%) or 6x R-CHOP21 + 2 R (57%). We used propensity scores to assess differences in event-free survival (EFS) and overall survival (OS). At five years, EFS (hazard ratio of 6x R-CHOP21 + 2 R versus 6x R-CHOP21 [HR] = 0.89; 95% confidence interval [CI], 0.72-1.09) and OS (HR = 0.93; 95% CI, 0.73-1.18) were not significantly different between both regimens. In exploratory risk-stratified analysis according to the International Prognostic Index (IPI), high-IPI patients (i.e., scores of 4-5) benefit most from 6x R-CHOP21 + 2 R (5-year absolute risk difference of EFS = 16.8%; 95% CI, -0.4%-34.1% and OS = 12.1%; 95% CI, -5.4-29.6%). Collectively, this analysis reveals no significant differences on average in EFS and OS between the two treatments. However, the potential benefits for high-risk patients treated with 6x R-CHOP21 + 2 R underscore the need for future research.
对于晚期弥漫性大 B 细胞淋巴瘤 (DLBCL),一线治疗通常包括 6 个周期的 R-CHOP21 或 6 个周期的 R-CHOP21 加 2 个额外的利妥昔单抗治疗(6x R-CHOP21 + 2R)。在当代实践中,这种治疗选择可能取决于中期 PET 扫描结果。本项全国性、基于人群的研究在中期 PET 指导治疗决策并非标准实践的时代,调查了这些治疗方案的比较效果。利用荷兰癌症登记处,我们确定了 2014 年至 2018 年间诊断为晚期 DLBCL 且完成 6 个周期 R-CHOP21(43%)或 6 个周期 R-CHOP21 + 2R(57%)治疗的 1577 名成年患者。我们使用倾向评分来评估无事件生存(EFS)和总生存(OS)的差异。在五年时,6x R-CHOP21 + 2R 与 6x R-CHOP21 的 EFS(6x R-CHOP21 + 2R 与 6x R-CHOP21 的风险比 [HR] = 0.89;95%置信区间 [CI],0.72-1.09)和 OS(HR = 0.93;95%CI,0.73-1.18)无显著差异。根据国际预后指数(IPI)进行的探索性风险分层分析显示,高 IPI 患者(即评分 4-5)从 6x R-CHOP21 + 2R 中获益最大(EFS 的 5 年绝对风险差异为 16.8%;95%CI,-0.4%-34.1%和 OS 为 12.1%;95%CI,-5.4%-29.6%)。总的来说,这项分析显示两种治疗方法在 EFS 和 OS 方面平均没有显著差异。然而,高危患者接受 6x R-CHOP21 + 2R 治疗的潜在获益突显了未来研究的必要性。