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

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.

Authors

Institutions

Publication Details

Journal
Blood
Published
2024-11-05
DOI
https://doi.org/10.1182/blood-2024-208529
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Laura B. Oswald, Yvelise Rodriguez, Frederick Lundry Locke, Gabriel De Avila et al.
Blood
CAR-T cell therapy research
article

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

Laura B. Oswald, Yvelise Rodriguez, Frederick Lundry Locke, Gabriel De Avila, Tiffany L. Carson, C. Ferraris, Heather S.L. Jim, Doris K. Hansen, Xiaoyin Li, Kenneth H. Shain, Hien D. Liu, Omar Castaneda, Sylvia L. Crowder, Ciara L. Freeman, Taiga Nishihori, Nathan H. Parker, Lisa M. Gudenkauf, Rachid Baz, Lauren Cole Peres, Ariel Felipe Grajales-Cruz, Aasha I. Hoogland, Brandon Jamaal Blue, Melissa Alsina, Oanh Kieu Nguyen
article en

Abstract

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.

BloodVol. 144(Supplement 1)
Nova Southeastern University (US), Moffitt Cancer Center (US)
Openalex Percentile: Top 61%
CAR-T cell therapy research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.