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2159 131I-Apamistamab Effectively Achieved Durable Responses in Patients with R/R AML Irrespective of the Presence of Multiple High-Risk Factors

Program: Oral and Poster Abstracts
Session: 721. Allogeneic Transplantation: Conditioning Regimens, Engraftment and Acute Toxicities: Poster I
Hematology Disease Topics & Pathways:
clinical trials, Research, Acute Myeloid Malignancies, AML, Biological therapies, elderly, Non-Biological therapies, Clinical Research, Diseases, Therapies, Myeloid Malignancies, Monoclonal Antibody Therapy, Human, Radiation Therapy, Study Population
Saturday, December 9, 2023, 5:30 PM-7:30 PM

Stuart Seropian, MD1, James M. Foran, MD2, Boglarka Gyurkocza, MD3, Rajneesh Nath4*, Hannah Choe, MD5, Mark R. Litzow, MD6, Nebu Koshy, MD7*, Patrick J. Stiff, MD8, Ben K. Tomlinson, MD9, Sunil Abhyankar, MD10, Sameem Abedin, MD11, George Chen, MD12,13, Zaid Al-Kadhimi, MD14,15*, Partow Kebriaei, MD16, Mitchell Sabloff, MSc, MD, FRCPC17, Johnnie J. Orozco, MD, PhD18, Katarzyna Joanna Jamieson, MD19*, Margarida Magalhaes-Silverman, MD20, Koen Van Besien, MD, PhD21,22, Michael W. Schuster, MD23, Arjun D. Law, MD24*, Sebastian A. Mayer, MD25, Hillard M. Lazarus, MD26, Jennifer Spross27*, Kate L Li, PhD27*, Elaina Haeuber, MS27*, Madhuri Vusirikala28*, Akash Nahar, MD, MPH27*, Brenda M. Sandmaier, MD29, John Pagel, MD, PhD30, Sergio A. Giralt, MD, FACP31, Avinash Desai, M.D27* and Camille N. Abboud, MD32

1Yale Univ. School of Med., New Haven, CT
2Hematology/Oncology, Mayo Clinic, Jacksonville, FL
3Adult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY
4Banner MD Anderson Cancer Center, Scottsdale, AZ
5The James Cancer Hospital Solove Research Institute and The Ohio State University Wexner Medical Center, Columbus, OH
6Division of Hematology, Mayo Clinic, Rochester, MN
7Texas Oncology Baylor Charles A. Sammons Cancer Center, Dallas, TX
8Division of Hematology and Oncology, Loyola University Medical Center, Maywood, IL
9University Hospitals Seidman Cancer Center, Cleveland, OH
10University of Kansas Medical Center, Westwood, KS
11Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, WI
12MD Anderson Cancer Center, Houston, TX
13Roswell Park Comprehensive Cancer Center, Buffalo, NY
14University of Alabama at Birmingham, Birmingham, AL
15University of Nebraska Medical Center, Omaha, NE
16Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX
17Ottawa Hospital, Ottawa, ON, CAN
18Translational Science and Therapeutics Division, Fred Hutch Cancer Research Center, Seattle, WA
19University of North Carolina, Chapel Hill, NC
20Holden Comprehensive Cancer Center, University of Iowa Hospital and Clinics, Iowa City, IA
21Division of Hematology and Oncology, Weill Cornell Medical College, New York, NY
22Weill Cornell Medical College, New York, NY
23Stony Brook University Cancer Center, Stony Brook, NY
24Hans Messner Allogenic Transplant Program, Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Canada
25Weill Cornell Medical Center, New York, NY
26Case Western Reserve University, Cleveland, OH
27Actinium Pharmaceuticals, New York, NY
28Actinium Pharmaceuticals, New York
29Fred Hutchinson Cancer Center, Clinical Research Division; University of Washington School of Medicine, Seattle, WA
30Loxo Oncology at Lilly, Stamford, CT
31Weill Cornell Medical College, Memorial Sloan Kettering Cancer Center, New York, NY
32Washington University School of Medicine, Saint Louis, MO

Background:

Most older patients (pts) with relapsed or refractory (R/R) AML cannot tolerate intensive treatment and are not eligible for curative allogeneic hematopoietic cell transplant (alloHCT). 131I-apamistamab, an anti-CD45 radioimmunoconjugate, delivers high dose targeted radiation to hematopoietic cells, allowing for myeloablation and eradication of leukemic cells while sparing toxicity to healthy organs. 131I-apamistamab led induction and conditioning can thus provide these pts with access to alloHCT.

Methods:

The SIERRA trial (NCT02665065) is a multi-center, randomized, controlled Phase 3 study comparing the rate of durable complete remission (dCR) lasting >6 months (mos) after complete remission with/without platelet recovery (CR/CRp) between two groups: 131I-apamistamab led induction and conditioning followed by alloHCT vs physician’s choice of conventional care (CC). Pts were randomized (1:1) to CC or 131I-apamistamab with fludarabine and total body irradiation (2 Gy) followed by alloHCT. CR/CRp assessment was 28-56 days post alloHCT or 28-42 days post initiation of therapy on the CC group. Pts in the CC group not achieving leukemia-free state could crossover (CO) to 131I-apamistamab. Here we report the results of a post hoc analysis to determine if the presence of various risk factors (i.e., Karnofsky Performance Status (KPS) <90, HCT Comorbidity Index >3, age >65, adverse-risk cytogenetics, venetoclax failure prior to randomization) influenced achievement of dCR in pts treated with 131I-apamistamab.

Results:

In total, 153 pts were randomized (CC, n=76; 131I-apamistamab, n=77). All pts who received the therapeutic dose of 131I-apamistamab (n=66) underwent alloHCT vs 14 (18.2%) in the CC group. Of evaluable pts, dCR rates at 6 mos were 22% in the 131I-apamistamab group vs 0% in the CC group (95% CI;12.29, 34.73; p<0.0001). A total of 19 pts (13,131I-apamistamab group; 6, CO) achieved dCR. Table 1 shows the pt, disease, and transplant characteristics of dCR vs. non-dCR pts. Eight of the 19 pts (42.1%) had primary induction failure and the median time to randomization from diagnosis was 5.4 mos. Approximately 50% of pts (9/19) had adverse-risk cytogenetics. Over 35% (7/19) of the pts had failed prior venetoclax and the median number of prior treatments was 3 (range 1-5). A total of 10/19 (52%) pts had KPS of <90% and a comorbidity index of >3. There was no difference in the rate of dCR when stratifying by number of risk factors for a given pt (0 to 5) with 27% for pts with 0-1 risk factors, 14% for pts with 2-3 risk factors, and 11% for pts with 4-5 risk factors (p=0.251).

Conclusion:

Pts with R/R AML who have multiple risk factors such as adverse risk cytogenetics, age >65, venetoclax failure, high comorbidity index or poor KPS are typically not considered for alloHCT due to high transplant-related mortality and post-transplant relapse rates. 131I-apamistamab was effective in achieving durable responses in R/R AML pts irrespective of the presence of multiple risk factors and successfully enabled alloHCT in such pts due to its targeted mechanism of action.

Disclosures: Foran: BeiGene: Membership on an entity's Board of Directors or advisory committees; BMS: Membership on an entity's Board of Directors or advisory committees; Actinium: Research Funding; Kura: Research Funding; Sellas: Research Funding; Roivant: Research Funding; Novartis: Research Funding; Celgene: Research Funding; Astellas: Research Funding; NCI: Membership on an entity's Board of Directors or advisory committees; CTI: Membership on an entity's Board of Directors or advisory committees. Gyurkocza: Actinium Pharmaceuticals, Inc: Research Funding. Nath: AlloVir: Membership on an entity's Board of Directors or advisory committees; Pfizer: Current equity holder in publicly-traded company; ADC Therapeutics: Membership on an entity's Board of Directors or advisory committees; Actinium Pharmaceuticals: Consultancy, Honoraria, Research Funding; Incyte: Consultancy, Honoraria. Choe: Actinium Pharmaceuticals: Other: Support for attending meetings and/or travel; MJH Life Sciences: Honoraria; Incyte: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: Receipt of equipment, materials, drugs to institution; Opna: Other: Receipt of equipment, materials, drugs to institution, Research Funding; NIH National Cancer Institute: Research Funding. Stiff: CRISPR: Consultancy; Amgen: Research Funding; AtaraBiotherapeutics: Research Funding; Eisai: Research Funding; Gamida Cell: Research Funding; Incyte Corp: Research Funding; Macrogenics: Research Funding; Takeda: Research Funding. Abedin: Incyte: Research Funding; AltruBio: Research Funding; Actinium Pharmaceutical: Research Funding; AbbVie: Consultancy, Honoraria; Daichii Sankyo: Consultancy, Honoraria; Servier: Consultancy, Honoraria. Kebriaei: Pfizer: Consultancy, Honoraria; Jazz: Consultancy, Honoraria. Sabloff: Pfizer: Membership on an entity's Board of Directors or advisory committees; Celgene: Membership on an entity's Board of Directors or advisory committees; Taiho Pharma: Membership on an entity's Board of Directors or advisory committees, Research Funding; Novartis: Membership on an entity's Board of Directors or advisory committees; Abbvie: Membership on an entity's Board of Directors or advisory committees; Actinium: Membership on an entity's Board of Directors or advisory committees, Research Funding; Astellas Pharma: Membership on an entity's Board of Directors or advisory committees, Research Funding; Roche: Membership on an entity's Board of Directors or advisory committees; BMS: Membership on an entity's Board of Directors or advisory committees; Jazz: Membership on an entity's Board of Directors or advisory committees. Orozco: Actinium Pharmaceuticals: Other: Site PI for clinical trials sponsored by Actinium, Research Funding. Jamieson: Actinium Pharmaceuticals: Other: Principal Investigator, SIERRA Trial, Research Funding. Van Besien: Orca: Research Funding; Precision Biosciences: Research Funding; Avertix: Current equity holder in private company; Calibr: Research Funding; BMS: Research Funding; Actinium: Research Funding; Moprhosys: Consultancy; Intellia: Consultancy; Hemogenyx: Consultancy, Current equity holder in publicly-traded company; SNIPR: Consultancy; Incyte: Consultancy. Schuster: Abbvie: Consultancy, Speakers Bureau; Actinium: Research Funding; AlloVir: Research Funding; Amgen: Other: Stock, Speakers Bureau; Astellas: Speakers Bureau; Beigene: Speakers Bureau; BMS: Consultancy, Speakers Bureau; Celgene: Speakers Bureau; Epizyme: Speakers Bureau; Genentech: Speakers Bureau; GSK: Research Funding; Incyte: Research Funding; Janssen: Consultancy, Speakers Bureau; MorphSys: Research Funding, Speakers Bureau; Pharmacyclics: Research Funding, Speakers Bureau; Rafael: Research Funding; Seattle Genetics: Speakers Bureau; Takeda: Research Funding, Speakers Bureau; ADC Therapeutics: Other; CTI Biopharma Corp: Speakers Bureau; Karyopharm: Research Funding, Speakers Bureau; Macrogenomics: Research Funding; Pfizer: Consultancy, Research Funding; Sanofi: Speakers Bureau; Syndax Pharmaceuticals: Research Funding. Law: Actinium Pharmaceuticals: Research Funding. Mayer: Omeros: Consultancy. Lazarus: Bristol Myers Squibb: Membership on an entity's Board of Directors or advisory committees. Spross: Actinium Pharmaceuticals: Current Employment. Li: Actinium Pharmaceuticals: Current Employment. Haeuber: Actinium Pharmaceuticals: Current Employment, Current equity holder in publicly-traded company, Current holder of stock options in a privately-held company. Vusirikala: Actinium Pharmaceuticals: Current Employment. Nahar: Actinium Pharmaceuticals: Current Employment, Current equity holder in publicly-traded company, Current holder of stock options in a privately-held company. Sandmaier: Actinium Pharmaceuticals: Membership on an entity's Board of Directors or advisory committees. Pagel: Loxo Oncology at Lilly: Current Employment. Giralt: Amgen, Actinuum, Celgene/BMS, Omeros, Johnson & Johnson, Miltenyi, Takeda: Research Funding; Amgen, Actinuum, Celgene/BMS, Kite Pharma, Janssen, Jazz Pharmaceuticals, Johnson & Johnson, Novartis, Spectrum Pharma, Takeda: Membership on an entity's Board of Directors or advisory committees. Desai: Actinium Pharmaceuticals: Current Employment, Current equity holder in publicly-traded company, Current holder of stock options in a privately-held company.

*signifies non-member of ASH