-Author name in bold denotes the presenting author
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5165 Meaningful Change in Patient-Reported Outcomes after CAR T-Cell Therapy for Relapsed/Refractory Multiple Myeloma in Standard of Care: Differences By Race and Ethnicity

Program: Oral and Poster Abstracts
Session: 907. Outcomes Research: Plasma Cell Disorders: Poster III
Hematology Disease Topics & Pathways:
Research, Clinical Research, Health disparities research, Patient-reported outcomes, Real-world evidence, Survivorship
Monday, December 9, 2024, 6:00 PM-8:00 PM

Carina E. Ferraris1*, Xiaoyin Li2*, Gabriel De Avila3*, Lisa M. Gudenkauf4*, Aasha I. Hoogland2*, Oanh Nguyen4*, Yvelise Rodriguez2*, Sylvia L. Crowder4*, Nathan Parker, PhD, MPH2*, Tiffany L. Carson4*, Rachid C. Baz5, Kenneth H. Shain, MD, PhD6, Brandon Blue3, Ariel Grajales-Cruz, MD7, Melissa Alsina, MD7, Ciara Louise Freeman, PhD, MSc, FRCPC, MRCP8, Omar Castaneda, MD8, Taiga Nishihori, MD9, Hien Liu, MD7, Frederick L. Locke, MD10, Heather S.L. Jim, PhD2*, Doris K. Hansen, MD8, Lauren C. Peres, PhD, MPH11* and Laura B. Oswald, PhD2*

1College of Allopathic Medicine, Nova Southeastern University, Fort Lauderdale
2Department of Health Outcomes and Behavior, Moffitt Cancer Center, Tampa, FL
3H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL
4Department of Health Outcomes and Behavior, Moffitt Cancer Center, Tampa
5Department of Malignant Hematology, Moffitt Cancer Center, Tampa, FL
6H. Lee Moffitt Cancer Center, Tampa, FL
7Moffitt Cancer Center, Tampa, FL
8Department of Blood and Marrow Transplantation and Cellular Immunotherapy, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL
9Department of Blood and Marrow Transplantation and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL
10Department of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL
11Department of Cancer Epidemiology, Moffitt Cancer Center, Tampa, FL

Background: Chimeric antigen receptor T-cell therapies (CAR Ts) have revolutionized treatment of relapsed/refractory multiple myeloma (RRMM), with remarkable improvements in progression free and overall survival in both clinical trials and standard of care settings. Clinical trials also show meaningful improvements in patient-reported outcomes (PROs) such as health-related quality of life (HRQOL) and patient-reported symptom burden, but PROs from RRMM patients treated in standard of care are limited. Moreover, racial and ethnic minority patients are underrepresented in key RRMM CAR T clinical trials, despite RRMM disproportionately affecting non-Hispanic Black (NHB) individuals compared to non-Hispanic White individuals (NHW). To address this gap, we assessed meaningful changes in PROs after CAR T and explored differences by race/ethnicity in a cohort of RRMM patients treated with CAR T in standard of care. We hypothesized that the majority of patients would show stable or meaningfully improved PROs from pre-CAR T to day 90 post-infusion.

Methods: Patients with RRMM scheduled to receive CAR T as standard of care at Moffitt Cancer Center were recruited between September 2022 and June 2024. PROs were assessed at baseline (pre-lymphodepleting chemotherapy) and day 90 post-CAR T. Participants completed the Functional Assessment of Cancer Therapy – General (FACT-G), which assesses overall HRQOL as well as physical, social, emotional, and functional well-being. Minimally important differences (MIDs) were defined as a ±4-point change for overall HRQOL and ±2-point change for all other FACT-G domains. Participants also completed PRO Measurement Information System (PROMIS) measures of depression, anxiety, fatigue, sleep disturbance, pain interference, global pain, physical function, cognitive function, and social function. MIDs were defined as a ±2-point change for global pain and ±5 for all other PROMIS measures. For each participant, MIDs were used to determine whether changes from baseline to day 90 were clinically meaningful (i.e., meaningful improvement, stable/no meaningful change, or meaningful deterioration). Chi-square analyses and Fisher’s exact tests were used to compare differences between racial/ethnic groups.

Results: Participants (N=99) were treated with idecabtagene-vicleucel (n=49) and ciltacabtagene-autoleucel (n=50). Most participants were male (61%), and median age was 66 years (range 46-84). Most self-identified as NHW (68%), followed by NHB (16%), Hispanic (15%), and other (1%). Racial/ethnic minority participants (32%) were less likely than NHW participants to be retired (50% vs. 67%) and more likely to be working (31% vs. 9%; p=0.019). There were no other differences in demographics and no differences in PROs between NHW and racial/ethnic minority participants at baseline (p-values>0.05). Across all PROs, most participants reported meaningful improvement (16-48%) or stable/no meaningful change (25-66%) from baseline to day 90. Physical well-being had the largest proportion of participants with meaningful improvement (48%), followed by overall HRQOL (47%) and pain interference (46%). Analyses of differences by race/ethnicity indicated that a larger proportion of racial/ethnic minority vs. NHW participants reported meaningful improvement in global pain (54% vs. 18%; p=0.002) and fatigue (43% vs. 28%; p=0.055), though the difference in fatigue did not reach statistical significance. There were no other differences in meaningful PRO change by race/ethnicity (p-values>0.05).

Conclusions: Consistent with our hypothesis, the majority of RRMM patients treated with CAR T in standard of care reported meaningful improvement or stable/no meaningful change in PROs from pre-CAR T to day 90 post-infusion. Notably, almost half of all participants reported meaningful improvements in physical well-being, overall HRQOL, and pain interference, indicating that a substantial proportion of CAR T recipients perceive meaningful benefits for important PROs. Racial/ethnic minority participants were more likely than NHW participants to report meaningful improvement in global pain and fatigue, suggesting that racial/ethnic minority patients may uniquely benefit from CAR T. These findings should be further explored in future studies with larger cohorts of diverse RRMM patients treated with CAR T.

Disclosures: Baz: Abbvie: Research Funding; BRISTOL MYERS SQUIBB: Research Funding; Celgen: Research Funding; Cellectar: Membership on an entity's Board of Directors or advisory committees; Janssen: Membership on an entity's Board of Directors or advisory committees, Research Funding; Karyopharm Therapeutics: Research Funding; Pfizer: Membership on an entity's Board of Directors or advisory committees; Regeneron: Research Funding. Shain: Janssen: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding; Sanofi: Consultancy; Karyopharm: Research Funding; Abbvie: Research Funding; BMS: Consultancy, Research Funding; Amgen: Research Funding; Takeda: Consultancy; Glaxo Smith Kline: Consultancy, Membership on an entity's Board of Directors or advisory committees; Karyopharm, Janssen, Adaptive Biotechnologies, GlaxoSmithKline, BMS, Sanofi, and Regeneron: Honoraria; Adaptive Biotech: Consultancy. Blue: Sanofi: Speakers Bureau; Pfizer Pharmaceuticals, Oncopeptides, Takeda, Abbvie, Janssen, and Kite Pharmaceuticals: Consultancy. Grajales-Cruz: Cellectar, Janssen, Sanofi: Membership on an entity's Board of Directors or advisory committees; Amgen, Sanovi: Speakers Bureau. Alsina: BMS: Membership on an entity's Board of Directors or advisory committees, Research Funding; Janssen: Membership on an entity's Board of Directors or advisory committees; Sanofi: Membership on an entity's Board of Directors or advisory committees. Freeman: Abbvie: Consultancy; Sanofi: Consultancy; Janssen: Consultancy, Research Funding; Roche/Genentech: Research Funding; Amgen: Consultancy; Incyte: Consultancy; ONK therapeutics: Consultancy; Celgene: Consultancy; Seattle Genetics: Consultancy; BMS: Consultancy, Honoraria, Research Funding. Castaneda: Legend Biotech: Consultancy; Janssen: Consultancy; BMS: Consultancy. Nishihori: Novartis: Research Funding; ImmunoGen: Consultancy; Medexus: Membership on an entity's Board of Directors or advisory committees; Karyopharm: Other: drug only supply to the institution. Liu: BioLineRx: Consultancy, Honoraria. Locke: Aptitude Health: Honoraria; Caribou: Consultancy; Iovance: Consultancy; Cowen: Consultancy; A2: Consultancy; BioPharma: Honoraria; ASH: Honoraria, Other: Travel support; Janssen: Consultancy; Society for Immunotherapy of Cancer: Honoraria; Communications CARE Education: Honoraria; Moffit Cancer Center: Patents & Royalties: cellular immunotherapy; Emerging Therapy Solutions Gerson Lehman Group: Consultancy; ecoR1: Consultancy; Novartis: Consultancy, Research Funding; Bluebird Bio: Consultancy, Research Funding; Umoja: Consultancy; Kite, a Gilead Company: Consultancy, Other: Travel support, Research Funding; Gilead Company: Consultancy; iMedX: Honoraria; GammaDelta Therapeutics: Consultancy; Calibr: Consultancy; Cellular Biomedicine Group: Consultancy; Legend Biotech: Consultancy; Celgene: Consultancy; BMS: Consultancy, Research Funding; Allogene: Consultancy, Research Funding; Amgen: Consultancy; Sana: Consultancy; Wugen: Consultancy; Clinical Care Options Oncology: Honoraria; Gerson Lehrman Group (GLG): Consultancy; Pfizer: Consultancy; CERo Therapeutics: Research Funding; 2SeventyBio: Research Funding; National Cancer Institute: Research Funding; Leukemia and Lymphoma Society Scholar in Clinical Research: Research Funding; Aptitude Health: Honoraria. Jim: Kite Pharma: Research Funding; SBR Biosciences: Consultancy. Hansen: Pfizer: Consultancy; Karyopharm: Consultancy, Research Funding; Janssen: Consultancy; BMS: Consultancy, Research Funding. Peres: Karyopharm Therapeutics: Research Funding; Bristol Myers Squibb: Research Funding.

*signifies non-member of ASH