A phase 2 study of pembrolizumab after autologous stem cell transplantation in patients with T-cell non-Hodgkin lymphoma

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 H. 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 D. Jacobsen
出处
期刊:Blood [Elsevier BV]
卷期号:142 (7): 621-628 被引量:9
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.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
4秒前
阳光沛菡完成签到 ,获得积分10
5秒前
老夫子爱读书给老夫子爱读书的求助进行了留言
7秒前
懒大王完成签到 ,获得积分10
7秒前
领导范儿应助明媚采纳,获得20
8秒前
吕程校完成签到,获得积分10
11秒前
共享精神应助咕鼠采纳,获得10
11秒前
秋秋完成签到,获得积分10
11秒前
萨尔莫斯完成签到,获得积分10
11秒前
赘婿应助咕鼠采纳,获得10
11秒前
薛强完成签到,获得积分10
11秒前
14秒前
顾矜应助科研通管家采纳,获得10
14秒前
14秒前
CodeCraft应助科研通管家采纳,获得10
15秒前
DOC_XIONG应助科研通管家采纳,获得10
15秒前
脑洞疼应助科研通管家采纳,获得10
15秒前
DOC_XIONG应助科研通管家采纳,获得10
15秒前
新晋老板完成签到,获得积分10
16秒前
威哥发布了新的文献求助10
17秒前
千柳完成签到 ,获得积分10
19秒前
和谐寻云完成签到,获得积分10
20秒前
王淳完成签到 ,获得积分10
21秒前
魔术师完成签到 ,获得积分10
25秒前
橘络完成签到 ,获得积分10
27秒前
兔子吃胡萝卜完成签到,获得积分10
28秒前
藤藤菜应助小杨采纳,获得50
28秒前
胖胖橘完成签到 ,获得积分10
31秒前
南枝焙雪完成签到 ,获得积分10
32秒前
含光完成签到,获得积分10
33秒前
星空完成签到,获得积分10
34秒前
duoduozs完成签到,获得积分10
34秒前
学在大闽完成签到,获得积分10
37秒前
38秒前
善良的冰绿完成签到,获得积分10
40秒前
清淮完成签到 ,获得积分10
40秒前
BINBIN完成签到 ,获得积分10
45秒前
45秒前
奕柯完成签到,获得积分10
46秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Principles of town planning: translating concepts to applications 1000
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
核安全综合知识2024版 500
Photothermal Science and Techniques 500
Digital Displacement Hydrostatic Transmission for Rotorcraft and Distributed Propulsion 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7711544
求助须知:如何正确求助?哪些是违规求助? 9267764
关于积分的说明 20068048
捐赠科研通 7288127
什么是DOI,文献DOI怎么找? 3297250
关于科研通互助平台的介绍 2451795
邀请新用户注册赠送积分活动 2304271