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 天体生物学 物理 环境卫生
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,Michael Schuster,Arjun Law,Karilyn Larkin,Neeta Pandit‐Taskar,Scott D. Rowley,Pashna N. Munshi,Rachel J. Cook,Moshe Levy,Hillard M. Lazarus,Brenda M. Sandmaier,John M. Pagel,Vijay Reddy,James A. MacDougall,Kathleen McNamara,Jennifer Spross,Elaina Haeuber,Madhuri Vusirikala,Akash Nahar,Avinash Desai,Sergio Giralt
出处
期刊:Journal of Clinical Oncology [Lippincott Williams & Wilkins]
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.
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