Randomized Phase III SIERRA Trial of 131I-Apamistamab Before Allogeneic Hematopoietic Cell Transplantation Versus Conventional Care for Relapsed/Refractory AML

医学 移植 危险系数 内科学 养生 外科 人口 耐火材料(行星科学) 临床终点 挽救疗法 造血干细胞移植 化疗方案 胃肠病学 化疗 随机对照试验 置信区间 物理 环境卫生 天体生物学
作者
Boglarka Gyurkocza,Rajneesh Nath,Stuart Seropian,Hannah Choe,Mark R. Litzow,Camille N. Abboud,Nebu Koshy,Patrick J. Stiff,Benjamin Tomlinson,Sunil Abhyankar,James M. Foran,Parameswaran Hari,George L. Chen,Zaid Al‐Kadhimi,Partow Kebriaei,Mitchell Sabloff,Johnnie J. Orozco,Katarzyna Jamieson,Margarida Silverman,Koen van Besien
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
被引量:9
标识
DOI:10.1200/jco.23.02018
摘要

PURPOSE Older patients with relapsed or refractory AML (RR AML) have dismal prognoses without allogeneic hematopoietic cell transplantation (alloHCT). SIERRA compared a targeted pretransplant regimen involving the anti-CD45 radioconjugate 131 I-apamistamab with conventional care. METHODS SIERRA (ClinicalTrials.gov identifier: NCT02665065 ) was a phase III open-label trial. Patients age ≥55 years with active RR AML were randomly assigned 1:1 to either an 131 I-apamistamab–led regimen before alloHCT or conventional care followed by alloHCT if initial complete remission (CR)/CR with incomplete platelet recovery (CRp) occurred. Initial response was assessed 28-56 days after alloHCT in the 131 I-apamistamab group and 28-42 days after salvage chemotherapy initiation; patients without CR/CRp or with AML progression could cross over to receive 131 I-apamistamab followed by alloHCT. The primary end point was durable complete remission (dCR) lasting 180 days after initial CR/CRp. Secondary end points were overall survival (OS) and event-free survival (EFS), assessed hierarchically in the intention-to-treat (ITT) population. RESULTS The ITT population included 153 patients ( 131 I-apamistamab [n = 76]; conventional care [n = 77]). In total, 44/77 conventional care arm patients crossed over and 40/77 (52%) received 131 I-apamistamab and alloHCT, with six patients (13.6%) experiencing a dCR. In the ITT population, the dCR rate was significantly higher with 131 I-apamistamab (17.1% [95% CI, 9.4 to 27.5]) than conventional care (0% [95% CI, 0 to 4.7]; P < .0001). The OS hazard ratio (HR) was 0.99 (95% CI, 0.70 to 1.41; P = .96), and the EFS HR was 0.23 (95% CI, 0.15 to 0.34), with HR <1 favoring 131 I-apamistamab. Grade ≥3 treatment-related adverse events occurred in 59.7% and 59.2% of the 131 I-apamistamab and conventional care groups, respectively. CONCLUSION The 131 I-apamistamab–led regimen was associated with a higher dCR rate than conventional care in older patients with RR AML. 131 I-apamistamab was well tolerated and could address an unmet need in this population.
最长约 10秒,即可获得该文献文件

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
starleo完成签到,获得积分10
刚刚
小蘑菇应助jingxuan采纳,获得10
刚刚
科研通AI6.2应助羊羊采纳,获得30
1秒前
777完成签到,获得积分10
2秒前
成成发布了新的文献求助10
2秒前
烟花应助呆呆茹采纳,获得10
2秒前
3秒前
zhangyiyang完成签到,获得积分10
4秒前
科研搬砖应助dy采纳,获得10
4秒前
4秒前
allen发布了新的文献求助10
4秒前
orixero应助yc采纳,获得10
5秒前
XXJ完成签到,获得积分10
5秒前
5秒前
学术底层发布了新的文献求助10
5秒前
6秒前
烟花应助Alice采纳,获得10
6秒前
完美世界应助Wang采纳,获得10
7秒前
Li应助starleo采纳,获得50
7秒前
活着完成签到,获得积分10
7秒前
sffsv发布了新的文献求助10
8秒前
丘比特应助shsheng采纳,获得10
8秒前
9秒前
9秒前
9秒前
杨榆藤完成签到,获得积分10
9秒前
认真的山兰完成签到,获得积分20
11秒前
11秒前
1111应助左欣岳采纳,获得10
11秒前
善学以致用应助sffsv采纳,获得10
12秒前
13秒前
刘俊彤发布了新的文献求助10
13秒前
寞本轩昂发布了新的文献求助10
13秒前
lilili发布了新的文献求助10
13秒前
共享精神应助认真的山兰采纳,获得30
14秒前
14秒前
ding应助漫漫采纳,获得10
14秒前
lshl2000完成签到,获得积分10
15秒前
15秒前
搜集达人应助小万采纳,获得10
15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
Modern Epidemiology, Fourth Edition 5000
Handbook of pharmaceutical excipients, Ninth edition 5000
Digital Twins of Advanced Materials Processing 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 生物化学 化学工程 物理 计算机科学 复合材料 内科学 催化作用 物理化学 光电子学 电极 冶金 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6022608
求助须知:如何正确求助?哪些是违规求助? 7643263
关于积分的说明 16169884
捐赠科研通 5170921
什么是DOI,文献DOI怎么找? 2766913
邀请新用户注册赠送积分活动 1750251
关于科研通互助平台的介绍 1636941