Bridge the Gap to CAR: Bridging Therapy in CAR T-Cell Therapy for Relapsed or Refractory Diffuse Large B-Cell Lymphoma

Chimeric antigen receptor (CAR) T-cell therapy has fundamentally transformed the treatment paradigm for relapsed or refractory diffuse large B-cell lymphoma (R/R DLBCL). However, implementing this therapy faces logistical and biological hurdles, including the prolonged interval between lymphocyte apheresis, delivery of the final product and initiation of lymphodepleting chemotherapy. This waiting period, often four to eight weeks, creates a risk during which uncontrolled disease progression may render patients ineligible for the planned treatment or increase their risk of complications. Bridging therapy has become a temporary strategy to control the disease and maintain patient fitness while awaiting the return of manufactured autologous CAR T cells. This review discusses the current scientific understanding of bridging therapy in the context of CAR T-cell treatment for R/R DLBCL, including its rationale, approaches, clinical evidence and future prospects. PEER REVIEWED ARTICLE **Peer reviewers:** Prof. Dr Felicitas Hitz, Cantonal Hospital Münsterlingen, Münsterlingen, Switzerland One anonymous peer reviewer Received on November 20, 2025; accepted after peer review on February 10, 2026; published online on February 13, 2026.

Authors

Publication Details

Journal
healthbook TIMES Oncology Hematology
Published
2026-02-13
DOI
https://doi.org/10.36000/hbt.oh.2026.27.202
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00
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article

Bridge the Gap to CAR: Bridging Therapy in CAR T-Cell Therapy for Relapsed or Refractory Diffuse Large B-Cell Lymphoma

Wehrli, Holbro
healthbook TIMES Oncology Hematology
CAR-T cell therapy research
article

Bridge the Gap to CAR: Bridging Therapy in CAR T-Cell Therapy for Relapsed or Refractory Diffuse Large B-Cell Lymphoma

Wehrli, Holbro
article en

Abstract

Chimeric antigen receptor (CAR) T-cell therapy has fundamentally transformed the treatment paradigm for relapsed or refractory diffuse large B-cell lymphoma (R/R DLBCL). However, implementing this therapy faces logistical and biological hurdles, including the prolonged interval between lymphocyte apheresis, delivery of the final product and initiation of lymphodepleting chemotherapy. This waiting period, often four to eight weeks, creates a risk during which uncontrolled disease progression may render patients ineligible for the planned treatment or increase their risk of complications. Bridging therapy has become a temporary strategy to control the disease and maintain patient fitness while awaiting the return of manufactured autologous CAR T cells. This review discusses the current scientific understanding of bridging therapy in the context of CAR T-cell treatment for R/R DLBCL, including its rationale, approaches, clinical evidence and future prospects. PEER REVIEWED ARTICLE **Peer reviewers:** Prof. Dr Felicitas Hitz, Cantonal Hospital Münsterlingen, Münsterlingen, Switzerland One anonymous peer reviewer Received on November 20, 2025; accepted after peer review on February 10, 2026; published online on February 13, 2026.

healthbook TIMES Oncology Hematology
Good health and well-being
Openalex Percentile: Top 28%
CAR-T cell therapy research
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