Session: 906. Outcomes Research: Lymphoid Malignancies Excluding Plasma Cell Disorders: Poster II
Hematology Disease Topics & Pathways:
Research, Clinical Practice (Health Services and Quality), Clinical Research, Diseases, Lymphoid Malignancies
Methods: Hematology/oncology specialists treating R/R DLBCL in EU4, the UK, and Japan participated in a retrospective cross-sectional study from April to June and October to December of 2022 and 2023 as part of IQVIA CAR T-Cell Monitor. Pts with CAR T ongoing were reported by a panel of physicians from CAR T-accredited sites, while pts receiving non-CAR T treatments were reported by physicians from both accredited and non-accredited sites. Physicians reported on pt diagnoses, clinical characteristics, and ongoing and prior treatment regimens for pts treated in the previous 6 months. Findings were stratified by region (EU4/UK or Japan) and by reported CAR T treatment status (eligible but not planned, planned, or ongoing).
Results: 377 hematology/oncology specialists provided data on 986 pts with R/R DLBCL who were eligible for or currently receiving CAR T. Of these pts, 169 total (147 EU4/UK, 22 Japan) were eligible but not planned for CAR T; 156 total (120 EU4/UK, 36 Japan) were planned for CAR T, and 661 total had CAR T ongoing (587 EU4/UK, 74 Japan). More pts were eligible but not planned for CAR T vs planned or ongoing, respectively, who were >65 years old (EU4/UK: 50% vs 42% and 28%; Japan: 73% vs 28% and 16%) and considered frail (EU4/UK: 26% vs 14% and 11%; Japan: 50% vs 8% and 16%). The proportion of pts with Eastern Cooperative Oncology Group (ECOG) performance status 0-1 was similar across the eligible but not planned, planned, and ongoing CAR T groups in EU4/UK (83%, 86%, and 83%, respectively); however, in Japan, a lower percentage of pts eligible but not planned for CAR T had ECOG status 0-1 (64%) vs those with CAR T planned (86%) or ongoing (92%). In the EU4/UK, 42% of CAR T eligible but not planned, 50% of CAR T planned, and 41% of CAR T ongoing pts had no preexisting comorbidities. In Japan, a slightly smaller proportion (45%) of CAR T eligible but not planned pts had no preexisting comorbidities vs 56% of CAR T planned and 58% of CAR T ongoing pts. Stem cell therapy (SCT) eligibility status varied by CAR T status and region: in EU4/UK, 24% of CAR T eligible but not planned, 21% of CAR T planned, and 22% of CAR T ongoing pts were ineligible for SCT; in Japan, these values were 50%, 25%, and 58%, respectively. Previous treatments received also varied by CAR T status and region. In EU4/UK, the proportion of pts who had received second-line (2L) immunotherapy was similar among those who were CAR T eligible but not planned (7%), planned (6%), and ongoing (9%). In Japan, a larger proportion of CAR T eligible but not planned pts were treated with 2L immunotherapy (20%) vs CAR T planned (3%) and ongoing (10%) pts. In the EU4/UK, 55%, 70%, and 54% of pts in the CAR T eligible but not planned, planned, and ongoing groups, respectively, were treated with chemotherapy and rituximab-based regimens in 2L; in Japan, these proportions were 55%, 53%, and 51%.
Conclusion: CAR T utilization remains hampered by limitations in access for pts. Results of this study suggest physicians select pts for CAR T with better fitness, lower ECOG performance status, younger age, and fewer comorbidities. These findings highlight a persistent unmet need in the European Union, the UK, and Japan for novel treatment options, particularly for pts who may be eligible for CAR T but are not selected to receive treatment.
Disclosures: Park: AbbVie: Current Employment, Other: Shareholder. Cooper: AbbVie: Current Employment, Other: Shareholder. Liede: AbbVie: Current Employment, Other: Shareholder.