← 返回

利妥昔单抗时代复发/难治性弥漫大 B 细胞淋巴瘤的真实世界临床结局:STRIDER 研究

英文原题:Real life clinical outcomes of relapsed/refractory diffuse large B cell lymphoma in the rituximab era: The STRIDER study.

查看英文原题

Real life clinical outcomes of relapsed/refractory diffuse large B cell lymphoma in the rituximab era: The STRIDER study.

PubMed 2024/07/01(内容时间) Cancer Med Q2 · IF 3.5(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

我们的发现证实,在利妥昔单抗时代 R/R DLBCL 的结局极差。

中文摘要

弥漫大B细胞淋巴瘤一线R-CHOP后约40%复发、约15%难治。本研究回顾意大利都灵两家大型血液中心403例患者的真实世界结局。

中位随访50个月时,确诊后5年总生存率为66.5%,2年无进展生存率为68%。134例患者对R-CHOP复发或难治。常用挽救治疗包括含铂方案和来那度胺。复发或进展后的中位总生存期和无进展生存期分别仅为6.7和5.1个月;含铂方案与其他方案在总体缓解率及生存方面无显著差异。多变量分析中,60至80岁、来源于生发中心B细胞及结外受累部位少于2处与复发后的较好总生存期相关。讨论:研究证实利妥昔单抗时代复发/难治患者结局仍很差,亟待国家药监机构广泛批准CAR-T 和双特异性抗体等新疗法作为二线方案以改善结局。

展开英文摘要原文

Relapse and refractory (R/R) rates after first-line R-CHOP in diffuse large B cell lymphomas (DLBCL) are ~40% and ~15% respectively. AIMS: We conducted a retrospective real-world analysis aimed at evaluating clinical outcomes of R/R DLBCL patients. MATERIAL AND METHODS: Overall, 403 consecutive DLBCL patients treated in two large hematological centers in Torino, Italy were reviewed.

At a median follow up of 50 months, 5-year overall survival from diagnosis (OS-1) was 66.5%, and 2-year progression free survival (PFS-1) was 68%. 134 (34.4%) patients relapsed (n = 46, 11.8%) or were refractory (n = 88, 22.6%) to R-CHOP. Most employed salvage treatments included platinum salt-based regimens in 38/134 (28.4%), lenalidomide in 14 (10.4%). Median OS and PFS after disease relapse or progression (OS-2 and PFS-2) were 6.7 and 5.1 months respectively. No significant difference in overall response rate, OS-2 or PFS-2 in patients treated with platinum-based regimens versus other regimens was observed. By multivariate analysis, age between 60 and 80 years, germinal center B cell type cell of origin and extranodal involvement of <2 sites were associated with better OS-2. DISCUSSION: Our findings confirm very poor outcomes of R/R DLBCL in the rituximab era. Widespread approval by national Medicine Agencies of novel treatments such as CAR-T cells and bispecific antibodies as second-line is eagerly awaited to improve these outcomes.

论文信息

作者
Dogliotti I、Peri V、Clerico M、Vassallo F、Musto D、Mercadante S、Ragaini S、Botto B
单位
Division of Hematology, University Hospital A.O.U. "Citt&#xe0; della Salute e della Scienza", Turin, Italy.Italy
文献类型
多中心研究 · 非美国政府资助研究
期刊
Cancer medicine2024 Jul
原文标识
PubMed 39030982 · DOI 10.1002/cam4.7448