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纳武利尤单抗单药治疗失败后复发/难治性霍奇金淋巴瘤患者中纳武利尤单抗与苯达莫司汀(NB)联合治疗的安全性和疗效研究。

A Study of Safety and Efficacy of Nivolumab and Bendamustine (NB) in Patients With Relapsed/Refractory Hodgkin Lymphoma After Nivolumab Monotherapy Failure.

作者信息

Lepik Kirill V, Mikhailova Natalia B, Kondakova Elena V, Zalyalov Yuri R, Fedorova Liudmila V, Tsvetkova Luibov A, Kotselyabina Polina V, Borzenkova Evgeniya S, Babenko Elena V, Popova Marina O, Darskaya Elena I, Baykov Vadim V, Moiseev Ivan S, Afanasyev Boris V

机构信息

Raisa Gorbacheva Memorial Institute of Children Oncology Hematology and Transplantation, Pavlov First Saint Petersburg State Medical University, Saint Petersburg, Russian Federation.

出版信息

Hemasphere. 2020 Jun 8;4(3):e401. doi: 10.1097/HS9.0000000000000401. eCollection 2020 Jun.

Abstract

This single-center prospective clinical trial evaluated the combination of nivolumab plus bendamustine (NB) as a salvage regimen in classical Hodgkin lymphoma patients after failure of nivolumab monotherapy. A total of 30 patients received nivolumab (3 mg/kg) on D1,14 and bendamustine (90 mg/m) on D1, 2 of a 28-day cycle for up to 3 cycles. The ORR was 87% with 57% CR, 30% PR. With median follow-up of 25 months, the estimated 2-year OS was 96,7% (95% CI, 90.2%-100%), PFS was 23,3% (95% CI, 8.2%-38.4%) median PFS was 10.2 months (95% CI, 7.7-14.2 months) with median DOR 6.6 months (95% CI 3.9-11.6 months). Ten patients (33.3%) experienced grade 3 to 4 AE during therapy. Infections were most common AEs of the combined therapy. NB was a highly efficient salvage regimen in relapsed/refractory cHL with a manageable toxicity profile and modest potential for achievement of long-term remission. Registered at www.clinicaltrials.gov (#NCT0334365).

摘要

这项单中心前瞻性临床试验评估了纳武利尤单抗联合苯达莫司汀(NB)作为纳武利尤单抗单药治疗失败后的经典型霍奇金淋巴瘤患者挽救方案的疗效。总共30例患者在28天周期的第1天、第14天接受纳武利尤单抗(3mg/kg),在第1天、第2天接受苯达莫司汀(90mg/m²),最多进行3个周期。客观缓解率(ORR)为87%,完全缓解(CR)率为57%,部分缓解(PR)率为30%。中位随访25个月时,估计2年总生存率(OS)为96.7%(95%置信区间[CI],90.2%-100%),无进展生存期(PFS)为23.3%(95%CI,8.2%-38.4%),中位PFS为10.2个月(95%CI,7.7-14.2个月),中位缓解持续时间(DOR)为6.6个月(95%CI,3.9-11.6个月)。10例患者(33.3%)在治疗期间出现3至4级不良事件(AE)。感染是联合治疗中最常见的AE。NB是复发/难治性经典型霍奇金淋巴瘤高效的挽救方案,毒性特征可控,实现长期缓解的潜力适中。在www.clinicaltrials.gov注册(#NCT0334365)

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