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库潘尼西联合利妥昔单抗和苯达莫司汀治疗不适合移植的复发/难治性弥漫大 B 细胞淋巴瘤患者:来自 Fondazione Italiana Linfomi (FIL) 的 II 期多中心 FIL Copa-BR 试验结果

英文原题:Copanlisib in combination with rituximab and bendamustine for transplant-ineligible relapsed/refractory diffuse large B-cell lymphoma patients: Results from the phase II multicentre FIL Copa-BR trial from Fondazione Italiana Linfomi (FIL).

查看英文原题

Copanlisib in combination with rituximab and bendamustine for transplant-ineligible relapsed/refractory diffuse large B-cell lymphoma patients: Results from the phase II multicentre FIL Copa-BR trial from Fondazione Italiana Linfomi (FIL).

PubMed 2025/06/10(内容时间) Br J Haematol Q2 · IF 3.6(JCR 2025)

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中文摘要

不适合接受自体造血干细胞移植(ASCT)或嵌合抗原受体(CAR)T细胞疗法的复发/难治性(R/R)弥漫性大B细胞淋巴瘤(DLBCL)患者,治疗选择仍有限。PI3K抑制剂可潘利塞已显示单药治疗DLBCL的活性。本项II期、单臂、多中心试验评估可潘利塞联合利妥昔单抗和苯达莫司汀(copa-BR),用于不适合ASCT和CAR-T 的R/R DLBCL患者。患者接受6周期copa-BR治疗,随后最多接受12周期可潘利塞维持治疗。主要终点为12个月无进展生存期(PFS)。共纳入37例患者,年龄68–87岁,既往接受1–2线治疗后复发或难治。总缓解率为24.3%,完全缓解率为13.5%。中位随访20个月后,12个月PFS率和总生存率分别为25.1%和44.5%。3级毒性包括中性粒细胞减少(56.8%)、感染(27.0%,其中6例死于COVID-19感染,病死率25%)和血小板减少(16.2%)。由于疗效有限、耐受性较差且出现替代疗法,本试验提前终止。copa-BR活性有限且安全性不佳,不支持在不适合ASCT和CAR-T 的R/R DLBCL患者中进一步研究这一联合方案。

展开英文摘要原文

Treatment options for relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) patients ineligible for autologous stem cell transplant (ASCT) or chimeric antigen receptor (CAR)-T-cell therapy remain limited. The PI3K inhibitor copanlisib has shown activity as a single agent in DLBCL. This phase II, single-arm, multicentre trial evaluated copanlisib with rituximab and bendamustine (copa-BR) in ASCT- and CAR-T-ineligible R/R DLBCL. Patients received six cycles of copa-BR, followed by up to 12 cycles of copanlisib maintenance. The primary end-point was 12-month progression-free survival (PFS). Thirty-seven patients (aged 68-87 years, R/R after 1-2 prior lines) were enrolled.

The overall response rate was 24. 3%, with complete responses in 13. 5%. After a median follow-up of 20 months, the 12-month PFS and overall survival rates were 25. 1% and 44. 5% respectively. Grade 3 toxicities included neutropenia (56. 8%), infections (27. 0%, including 6 death due to COVID-19 infection with 25% fatality) and thrombocytopenia (16.

2%). Due to limited efficacy, poor tolerability and emerging alternative treatments, the trial was terminated prematurely. Copa-BR showed limited activity and an unfavourable safety profile, discouraging further investigation of this combination in ASCT- and CAR-T-ineligible R/R DLBCL.

论文信息

作者
Novo M、Frascione PMM、Castellino A、Marcheselli L、Dattoli SD、Vannucchi M、Rota-Scalabrini D、Tucci A
第一作者单位
SC Ematologia, AOU Città della Salute e della Scienza di Torino, Torino, Italy.Italy
通讯作者单位
Candiolo Cancer Institute, FPO-IRCCS, Candiolo (Torino), Italy.Italy
文献类型
II 期临床试验 · 多中心研究
期刊
British journal of haematology2025 Aug
原文标识
PubMed 40495420 · DOI 10.1111/bjh.20204