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6xR-CHOP21 与 6xR-CHOP21+2R 方案治疗晚期弥漫性大 B 细胞淋巴瘤患者的疗效比较。

Comparative effectiveness of 6x R-CHOP21 versus 6x R-CHOP21 + 2 R for patients with advanced-stage diffuse large B-cell lymphoma.

机构信息

Department of Public Health, Erasmus University Medical Centre, Rotterdam, The Netherlands.

Department of Research and Development, Netherlands Comprehensive Cancer Organisation (IKNL), Utrecht, The Netherlands.

出版信息

Blood Cancer J. 2024 Sep 12;14(1):157. doi: 10.1038/s41408-024-01137-0.

DOI:10.1038/s41408-024-01137-0
PMID:39266543
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11393348/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11393348/ffe404fda779/41408_2024_1137_Fig4_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11393348/ffe404fda779/41408_2024_1137_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11393348/ebb1835f7209/41408_2024_1137_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11393348/c2e43bf3412b/41408_2024_1137_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11393348/eddb56cf6657/41408_2024_1137_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f3a/11393348/ffe404fda779/41408_2024_1137_Fig4_HTML.jpg

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