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Improving Access to Chimeric Antigen Receptor T-cells for Refractory or Relapsing Diffuse Large B Cell Lymphoma Therapy in Asia

Overview
Journal Discov Oncol
Publisher Springer
Specialty Oncology
Date 2025 Feb 14
PMID 39951161
Authors
Affiliations
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Abstract

Chimeric antigen receptor T-cell (CAR-T)-mediated therapies have shown promising clinical benefit in patients with refractory or relapsing (R/R) diffuse large B-cell lymphoma (DLBCL). However, CAR-T treatment presents challenges such as lack of drug accessibility, financial barriers, variable physician preference or experience, and risk assessment based on patient-specific characteristics. This article thus aims to provide an overview of the CAR-T landscape for R/R DLBCL in Asia, with a focus on identifying barriers to access, from the perspective of Asian and international lymphoma experts. Presently, existing clinical data indicate that CAR-T therapy is a potentially curative strategy for R/R DLBCL in addition to stem cell transplantation, provided the patient's disease profile and treatment history have been thoroughly considered. However, longer-term follow-up data from large-scale studies are needed to confirm curative potential and define optimal sequencing of CAR-T in the context of novel emerging treatments, such as bi-specific antibodies, in the management of R/R DLBCL. Consequently, further research into CAR-T would benefit from collaboration between institutions. Furthermore, there is a wide disparity in CAR-T accessibility across regions due to complicated logistics and cost, which represent a significant barrier to patients in Asia. Hence, there is a need to increase representation and engagement across different stakeholders such as policymakers, payers, and the industry to arrive at a consensus on patient selection, establish clear guidelines, and develop strategies to lower CAR-T costs. Ultimately, data can support a multi-stakeholder approach when devising strategies to make CAR-T feasible and sustainable for patients.

References
1.
Maziarz R, Zhang J, Yang H, Chai X, Yuan C, Schwarz E . Indirect comparison of tisagenlecleucel and historical treatments for relapsed/refractory diffuse large B-cell lymphoma. Blood Adv. 2022; 6(8):2536-2547. PMC: 9043930. DOI: 10.1182/bloodadvances.2021006280. View

2.
Xu H, Li N, Wang G, Cao Y . Predictive short/long-term efficacy biomarkers and resistance mechanisms of CD19-directed CAR-T immunotherapy in relapsed/refractory B-cell lymphomas. Front Immunol. 2023; 14:1110028. PMC: 10083339. DOI: 10.3389/fimmu.2023.1110028. View

3.
Thieblemont C, Phillips T, Ghesquieres H, Cheah C, Clausen M, Cunningham D . Epcoritamab, a Novel, Subcutaneous CD3xCD20 Bispecific T-Cell-Engaging Antibody, in Relapsed or Refractory Large B-Cell Lymphoma: Dose Expansion in a Phase I/II Trial. J Clin Oncol. 2022; 41(12):2238-2247. PMC: 10115554. DOI: 10.1200/JCO.22.01725. View

4.
Assayag J, Kim C, Chu H, Webster J . The prognostic value of Eastern Cooperative Oncology Group performance status on overall survival among patients with metastatic prostate cancer: a systematic review and meta-analysis. Front Oncol. 2024; 13:1194718. PMC: 10757350. DOI: 10.3389/fonc.2023.1194718. View

4.
Kim H, Jang M, Kim H, Kim S, Kim W, Kim S . Clinical impact of CD5 expression in Korean patients with diffuse large B-cell lymphoma. Blood Res. 2017; 52(3):193-199. PMC: 5641511. DOI: 10.5045/br.2017.52.3.193. View