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

被引:1
作者
Gyurkocza, Boglarka [1 ]
Nath, Rajneesh [2 ]
Seropian, Stuart [3 ]
Choe, Hannah [4 ]
Litzow, Mark R. [5 ]
Abboud, Camille [6 ]
Koshy, Nebu [7 ]
Stiff, Patrick [8 ]
Tomlinson, Benjamin [9 ]
Abhyankar, Sunil [10 ]
Foran, James [11 ]
Hari, Parameswaran [12 ]
Chen, George [13 ,14 ]
Al-Kadhimi, Zaid [15 ]
Kebriaei, Partow [14 ]
Sabloff, Mitchell [16 ]
Orozco, Johnnie J. [17 ]
Jamieson, Katarzyna [18 ]
Silverman, Margarida [19 ]
Van Besien, Koen [20 ]
Schuster, Michael [21 ]
Law, Arjun Datt [22 ]
Larkin, Karilyn [23 ]
Pandit-Taskar, Neeta [24 ]
Rowley, Scott D. [25 ]
Munshi, Pashna [26 ]
Cook, Rachel [27 ]
Levy, Moshe Y. [28 ]
Lazarus, Hillard M. [29 ]
Sandmaier, Brenda M. [17 ]
Pagel, John M. [30 ]
Reddy, Vijay [31 ]
Macdougall, James [32 ]
Mcnamara, Kathleen
Spross, Jennifer
Haeuber, Elaina
Vusirikala, Madhuri
Nahar, Akash
Desai, Avinash
Giralt, Sergio [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, David H Koch Ctr Canc Care, New York, NY 10021 USA
[2] Banner MD Anderson Canc Ctr, Gilbert, AZ USA
[3] Yale Univ, Sch Med, Yale Canc Ctr, New Haven, CT USA
[4] Ohio State Univ, Columbus, OH USA
[5] Mayo Clin, Rochester, MN USA
[6] Washington Univ, Sch Med, St Louis, MO USA
[7] Texas Oncol Baylor A Charles Sammons Canc Ctr, Dallas, TX USA
[8] Loyola Univ, Med Ctr, Maywood, IL USA
[9] Univ Hosp Cleveland Med Ctr, Cleveland, OH USA
[10] Univ Kansas, Canc Ctr, Kansas City, KS USA
[11] Mayo Clin, Jacksonville, FL USA
[12] Froedtert Hosp, Med Coll Wisconsin, Milwaukee, WI USA
[13] Roswell Pk Comprehens Canc Ctr, Buffalo, NY USA
[14] MD Anderson Canc Ctr, Houston, TX USA
[15] Univ Nebraska Med Ctr, Omaha, NE USA
[16] Univ Ottawa, Ottawa Hosp Res Inst, Ottawa, ON, Canada
[17] Univ Washington, Fred Hutchinson Canc Ctr, Sch Med, Seattle, WA USA
[18] Univ North Carolina UNC, Chapel Hill, NC USA
[19] Univ Iowa, Iowa City, IA USA
[20] Weill Cornell Med Coll, New York, NY USA
[21] SUNY Stony Brook, Canc Ctr, Stony Brook, NY USA
[22] Princess Margaret Canc Ctr, Hans Messner Allogene Blood & Marrow Transplant Pr, Toronto, ON, Canada
[23] Ohio State Univ, Arthur G James Canc Hosp, Ctr Comprehens Canc, Richard J Solove Res Inst, Columbus, OH 43210 USA
[24] Mem Sloan Kettering, Dept Radiol, New York, NY USA
[25] Hackensack Univ, Med Ctr, Hackensack, NJ USA
[26] Medstar Georgetown Univ Hosp, Washington, DC USA
[27] Oregon Hlth & Sci Univ, Portland, OR USA
[28] Baylor Scott & White Hlth, Dallas, TX USA
[29] Case Western Reserve Univ, Cleveland, OH USA
[30] Loxo Oncol Lilly, Stamford, CT USA
[31] D2V Clin, Durham, NC USA
[32] Actinium Pharmaceut, New York, NY USA
关键词
ACUTE MYELOID-LEUKEMIA; OLDER PATIENTS; ANTIBODIES; OUTCOMES; TISSUE;
D O I
10.1200/JCO.23.02018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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 131I-apamistamab with conventional care. METHODSSIERRA (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 131I-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 131I-apamistamab group and 28-42 days after salvage chemotherapy initiation; patients without CR/CRp or with AML progression could cross over to receive 131I-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 (131I-apamistamab [n = 76]; conventional care [n = 77]). In total, 44/77 conventional care arm patients crossed over and 40/77 (52%) received 131I-apamistamab and alloHCT, with six patients (13.6%) experiencing a dCR. In the ITT population, the dCR rate was significantly higher with 131I-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 131I-apamistamab. Grade >= 3 treatment-related adverse events occurred in 59.7% and 59.2% of the 131I-apamistamab and conventional care groups, respectively. CONCLUSION The 131I-apamistamab-led regimen was associated with a higher dCR rate than conventional care in older patients with RR AML. 131I-apamistamab was well tolerated and could address an unmet need in this population.
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收藏
页码:201 / 213
页数:16
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