Perspectives on T-cell engaging therapies in relapsed/refractory indolent non-Hodgkin lymphoma

Max Bakker, Maria T. Kuipers, Marie Jose Kersten, Sanne H. Tonino, Yasmina I. M. Serroukh*

*Corresponding author for this work

Research output: Contribution to journalReview articleAcademicpeer-review

Abstract

Purpose of review Follicular lymphoma (FL) and marginal zone lymphoma (MZL) are indolent subtypes of non-Hodgkin lymphoma (iNHL) characterized by a relapsing-remitting disease course. A promising novel therapeutic class emerges with T-cell engaging therapies, which include CD19 directed chimeric antigen receptor T-cell (CAR-T) therapy and CD3xCD20 directed bispecific antibodies (BsABs). This review provides a comprehensive evaluation of their efficacy and safety along with logistical considerations in relapsed/refractory (r/r) iNHL. Recent findings Several pivotal CAR-T trials have presented impressive response rates and durable remissions in r/r FL, while data in MZL is scarce. CAR-T is given as a single infusion, but requires a complex logistical infrastructure. Different BsAbs have shown favorable efficacy with a lower rate of acute toxicities. Off-the-shelve availability favors its usability, although prolonged administration of BsAbs might impose a substantial burden for patients. Long-term infection risk is a concern for both treatments. Clinical studies that directly compare CAR-T and BsAbs are still lacking. Summary Both CAR-T and BsAbs have demonstrated promising efficacy as treatment modalities in iNHL. Decision making for T-cell engaging therapies should be tailored to patient specific factors and availability. Maturation of follow-up data will further guide evidence-based treatment choices in FL and MZL.
Original languageEnglish
Article number10.1097/CCO.0000000000001160
Pages (from-to)393-400
Number of pages8
JournalCurrent opinion in oncology
Volume37
Issue number5
Early online date2025
DOIs
Publication statusPublished - 1 Sept 2025

Keywords

  • T-cell engaging therapies
  • bispecific antibodies
  • chimeric antigen receptor T-cell therapy
  • follicular lymphoma
  • marginal zone lymphoma

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