Comparative effectiveness of CAR-T cell therapy and BiTE therapy in relapsed/refractory diffuse large B-cell lymphoma: A propensity score matching analysis using real-world data from the US collaborative network database.

e19020 Background: Diffuse Large B-cell lymphoma is the most common form of non-Hodgkin lymphoma. Relapsed/refractory Diffuse Large B-cell Lymphoma (DLBCL) presents significant treatment challenges. CAR-T cell therapy and BiTE therapies have emerged as promising options. This study aims to compare their effectiveness using propensity score matching, leveraging real-world data from the TriNetX network to assess clinical outcomes and guide treatment decisions for DLBCL. Methods: This retrospective cohort study utilized the TriNetX database, a global health research network, to identify adult patients with relapsed/refractory Diffuse Large B-cell Lymphoma (DLBCL) who received CAR-T cell therapy or BiTE therapy. The CAR-T cell therapy included axicabtagene, lisocabtagene, tisagenlecleucel) or BiTE therapy included Epcoritamab and Glofitamab. A propensity score matching (PSM) approach was used to balance baseline characteristics between the two treatment groups, minimizing confounding biases. Key covariates such as age, sex, comorbidities, model. 1:1 matching was performed using nearest-neighbour matching without replacement, ensuring comparability between the CAR-T and BiTE groups. Results: Before PSM, there were 1,533 patients in the CAR-T cohort and 142 patients in the BITE therapy cohort; however, after PSM, there were 133 patients in both cohorts. Mean age (59.4 vs 57.9 years), male (60.53% vs 57.04%), white (76.69% vs 72.18%). Compared to BITE therapy, CAR-T therapy demonstrated improved overall survival (OS) (hazard ratio [HR] 0.45 (95% CI 0.32-0.61, p < 0.95). BITE therapy also had a higher risk for pancytopenia (odds ratio [OR] 4.663 [2.35-9.26], p < 0.01). The risk of diarrhoea and fatigue was, however, not statistically significant. Conclusions: This study provides valuable real-world insights into the comparative effectiveness of CAR-T cell therapy and BiTE therapy for relapsed/refractory DLBCL. The results, derived from propensity score-matched cohorts, offer far-reaching help to guide the holistic management of this patient population.

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Publication Details

Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.e19020
Primary Topic
CAR-T cell therapy research
Type
article
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article

Comparative effectiveness of CAR-T cell therapy and BiTE therapy in relapsed/refractory diffuse large B-cell lymphoma: A propensity score matching analysis using real-world data from the US collaborative network database.

Ayobami Gbenga Olafimihan, Oboseh John Ogedegbe, Shakirat Gold‐Olufadi, Chiamaka Elsie Nwachukwu et al.
Journal of Clinical Oncology
CAR-T cell therapy research
article

Comparative effectiveness of CAR-T cell therapy and BiTE therapy in relapsed/refractory diffuse large B-cell lymphoma: A propensity score matching analysis using real-world data from the US collaborative network database.

Ayobami Gbenga Olafimihan, Oboseh John Ogedegbe, Shakirat Gold‐Olufadi, Chiamaka Elsie Nwachukwu, Olanipekun Lanny Ntukidem, Neharika Shrestha, Dosbai Saparov, Henry Becerra, Asfand Yar Cheema, Duresha Malik, Sakshi Bai, Stanley Ntow Atencah
article en

Abstract

e19020 Background: Diffuse Large B-cell lymphoma is the most common form of non-Hodgkin lymphoma. Relapsed/refractory Diffuse Large B-cell Lymphoma (DLBCL) presents significant treatment challenges. CAR-T cell therapy and BiTE therapies have emerged as promising options. This study aims to compare their effectiveness using propensity score matching, leveraging real-world data from the TriNetX network to assess clinical outcomes and guide treatment decisions for DLBCL. Methods: This retrospective cohort study utilized the TriNetX database, a global health research network, to identify adult patients with relapsed/refractory Diffuse Large B-cell Lymphoma (DLBCL) who received CAR-T cell therapy or BiTE therapy. The CAR-T cell therapy included axicabtagene, lisocabtagene, tisagenlecleucel) or BiTE therapy included Epcoritamab and Glofitamab. A propensity score matching (PSM) approach was used to balance baseline characteristics between the two treatment groups, minimizing confounding biases. Key covariates such as age, sex, comorbidities, model. 1:1 matching was performed using nearest-neighbour matching without replacement, ensuring comparability between the CAR-T and BiTE groups. Results: Before PSM, there were 1,533 patients in the CAR-T cohort and 142 patients in the BITE therapy cohort; however, after PSM, there were 133 patients in both cohorts. Mean age (59.4 vs 57.9 years), male (60.53% vs 57.04%), white (76.69% vs 72.18%). Compared to BITE therapy, CAR-T therapy demonstrated improved overall survival (OS) (hazard ratio [HR] 0.45 (95% CI 0.32-0.61, p < 0.95). BITE therapy also had a higher risk for pancytopenia (odds ratio [OR] 4.663 [2.35-9.26], p < 0.01). The risk of diarrhoea and fatigue was, however, not statistically significant. Conclusions: This study provides valuable real-world insights into the comparative effectiveness of CAR-T cell therapy and BiTE therapy for relapsed/refractory DLBCL. The results, derived from propensity score-matched cohorts, offer far-reaching help to guide the holistic management of this patient population.

Journal of Clinical OncologyVol. 43(16_suppl)
Tulane University (US), Piedmont Athens Regional (US), Trinity Health (US), Cleveland Clinic (US), John H. Stroger, Jr. Hospital of Cook County (US), Brookdale University Hospital and Medical Center (US), Jackson Memorial Hospital (US)
Openalex Percentile: Top 81%
CAR-T cell therapy research
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