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利妥昔单抗时代复发/难治性弥漫性大 B 细胞淋巴瘤的真实临床结局:STRIDER 研究。

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

机构信息

Division of Hematology, University Hospital A.O.U. "Città della Salute e della Scienza", Turin, Italy.

Division of Hematology U, Department of Molecular Biotechnologies and Health Sciences, University of Turin, Turin, Italy.

出版信息

Cancer Med. 2024 Jul;13(14):e7448. doi: 10.1002/cam4.7448.

Abstract

BACKGROUND

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.

RESULTS

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.

摘要

背景

弥漫性大 B 细胞淋巴瘤(DLBCL)患者一线 R-CHOP 治疗后的复发和难治(R/R)率分别约为 40%和 15%。

目的

我们进行了一项回顾性真实世界分析,旨在评估 R/R DLBCL 患者的临床结局。

材料和方法

总体上,回顾了意大利都灵的两个大型血液学中心治疗的 403 例连续 DLBCL 患者。

结果

在中位随访 50 个月时,从诊断开始的 5 年总生存率(OS-1)为 66.5%,2 年无进展生存率(PFS-1)为 68%。134 例(34.4%)患者对 R-CHOP 复发(n=46,11.8%)或难治(n=88,22.6%)。大多数采用的挽救治疗包括 38/134 例(28.4%)患者使用铂类药物方案,14 例(10.4%)患者使用来那度胺。疾病复发或进展后的中位 OS 和 PFS(OS-2 和 PFS-2)分别为 6.7 和 5.1 个月。未观察到接受铂类药物方案与其他方案治疗的患者在总体缓解率、OS-2 或 PFS-2 方面有显著差异。多变量分析显示,年龄在 60 至 80 岁之间、生发中心 B 细胞型细胞起源和<2 个部位的结外累及与更好的 OS-2 相关。

讨论

我们的发现证实了在利妥昔单抗时代 R/R DLBCL 的预后非常差。迫切需要国家药品管理局批准新型治疗方法,如 CAR-T 细胞和双特异性抗体作为二线治疗方法,以改善这些结局。

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