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McNamara, Kathleen

https://orcid.org/0000-0002-7020-1663

Mayo Clinic

Actinium Pharmaceuticals (United States)

Citations 2

Randomized Phase III SIERRA Trial of 131 I-Apamistamab Before Allogeneic Hematopoietic Cell Transplantation Versus Conventional Care for Relapsed/Refractory AML
Gyurkocza, Boglarka , Nath, Rajneesh , Seropian, Stuart , Choe, Hannah , Litzow, Mark R. , Abboud, Camille N. , Koshy, Nebu , Stiff, Patrick J. , Tomlinson, Benjamin , Abhyankar, Sunil , Foran, James M. , Al‐Kadhimi, Zaid , Kebriaei, Partow, Orozco, Johnnie J. , Jamieson, Katarzyna , Silverman, Margarida, Law, Arjun , Munshi, Pashna N. , Cook, Rachel J. , Levy, Moshe , Pagel, John M. , Reddy, Vijay , MacDougall, James A., McNamara, Kathleen , Spross, Jennifer , Haeuber, Elaina, Vusirikala, Madhuri , Nahar, Akash, Desai, Avinash, Magalhaes‐Silverman, Margarida , Abboud, Camille N , Stiff, Patrick J , Foran, James M , Hari, Parameswaran , Chen, George , Al-Kadhimi, Zaid , Sabloff, Mitchell , Orozco, Johnnie J , Besien, Koen van , Larkin, Karilyn , Rowley, Scott D , Lazarus, Hillard M , Sandmaier, Brenda M , Pagel, John M , Spross, Jennifer , Giralt, Sergio , Magalhaes-Silverman, Margarida , Hari, Parameswaran , Chen, George L. , Kebriaei, Partow , Sabloff, Mitchell , Schuster, Michael K. , Pandit-Taskar, Neeta D. , Lazarus, Hillard M. , MacDougall, James, McNamara, Kathleen, Giralt, Sergio

Journal of Clinical Oncology | September 19, 2024 | Volume: 43 | Issue: 2 | Pages: 201-213

10.1200/jco.23.02018 Get It

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.