CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
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).
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).
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。
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。
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.
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