医学
彭布罗利珠单抗
自体干细胞移植
临床终点
内科学
肿瘤科
移植
临床研究阶段
淋巴瘤
外科
临床试验
免疫疗法
癌症
作者
Mwanasha Merrill,Parastoo B. Dahi,Robert Redd,Mikaela M. McDonough,Yi‐Bin Chen,Zachariah DeFilipp,Alex F. Herrera,David C. Fisher,Ann S. LaCasce,Oreofe O. Odejide,Samuel Y. Ng,Caron A. Jacobson,Reid W. Merryman,Austin I. Kim,Yago Nieto,Craig S. Sauter,Gunjan L. Shah,Jasmine Zain,Philippe Armand,Eric Jacobsen
出处
期刊:Blood
[American Society of Hematology]
日期:2023-08-17
卷期号:142 (7): 621-628
被引量:4
标识
DOI:10.1182/blood.2023020244
摘要
Abstract Autologous stem cell transplantation (ASCT) is often used as consolidation for several subtypes of peripheral T-cell lymphoma (PTCL) in first remission. However, many patients relapse after ASCT and have a very poor prognosis. There are no approved treatment options for posttransplantation maintenance or consolidation in PTCL. PD-1 blockade has demonstrated some efficacy for patients with PTCL. We, therefore, conducted a phase 2 multicenter study of the anti–PD-1 monoclonal antibody pembrolizumab after ASCT in patients with PTCL in first remission. Pembrolizumab was administered at 200 mg IV every 3 weeks for up to 8 cycles within 21 days from post-ASCT discharge (and within 60 days of stem cell infusion). The primary end point was progression-free survival (PFS) at 18 months after ASCT. Twenty-one patients were treated in this study and 67% (n = 14) completed 8 cycles of treatment. Among all patients who were evaluable, 13 of 21 were alive and achieved PFS at 18 months after ASCT, meeting the study’s primary end point. The estimated 18-month PFS was 83.6% (95% confidence interval [CI], 68-100), and overall survival 94.4% (95% CI, 84-100). The toxicity profile was consistent with the known toxicity profile of pembrolizumab, with no grade 5 toxicities. In conclusion, PD-1 blockade after ASCT with pembrolizumab is feasible with a favorable safety profile and promising activity, supporting further confirmatory studies. This trial was registered at www.clinicaltrials.gov as #NCT02362997.
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