Please use this identifier to cite or link to this item: http://hdl.handle.net/11434/2322
Title: An evaluation of odronextamab for the treatment of multiple subtypes of relapsed/refractory B-cell non- Hodgkin lymphoma.
Epworth Authors: Bayly-McCredie, Elena
Prince, Henry Miles
Yannakou, Costas Kleanthes
Fiorenza, Salvatore
Keywords: Relapsed/Refactory B-Cell non Hodgkin lumphoma
Odronextamab
CD20×CD3
Bispecific Antibody
Diffuse large B-cell lymphoma
Follicular Lymphoma
Drug Evaluation
Cancer Services Clinical Institute, Epworth HealthCare, Victoria, Australia
Issue Date: Mar-2025
Publisher: Taylor and Francis
Citation: Expert Opin Biol Ther . 2025 Mar 24:1-13. doi: 10.1080/14712598.2025.2479631.
Abstract: Introduction: Patients with relapsed/refractory B-cell non-Hodgkin lymphoma (B-NHL) have a poor median survival rate when treated with traditional salvage therapies. Bispecific antibodies (BsAbs) are an emerging class of 'off-the-shelf' immunotherapies that show promising efficacy in this population. Odronextamab is a CD20×CD3 targeting bispecific antibody that is being investigated in multiple subtypes of relapsed/refractory B-NHL. Areas covered: This article describes the development of odronextamab from pre-clinical work through to ongoing clinical trials in relapsed/refractory B-NHL. The structure, safety, efficacy, and administration of odronextamab are discussed. Studies were selected for inclusion by performing a search in PubMed, EMBASE, Cochrane Library, and relevant conference abstracts from 2014 to 2024. The clinicaltrials.gov website and reference lists of the included studies were also reviewed. Expert opinion: Odronextamab has demonstrated manageable safety and promising efficacy in multiple subtypes of relapsed/refractory B-NHL. The low rates of immune effector cell-associated neurotoxicity syndrome (ICANS) and high response rates in rare aggressive subtypes of B-NHL are particularly noteworthy. High rates of severe infections remain a challenge with BsAbs, with further prophylactic efforts required to reduce the risk. Clinical trials of combination therapies with odronextamab are required to improve the utility of this BsAb across a wider range of settings and subtypes of B-NHL.
URI: http://hdl.handle.net/11434/2322
DOI: https://doi.org/10.1080/14712598.2025.2479631
PubMed URL: https://pubmed.ncbi.nlm.nih.gov/40106587/
ISSN: 1471-2598
Journal Title: Expert Opinion on Biological Therapy
Type: Journal Article
Affiliated Organisations: The University of Melbourne, Melbourne, Australia.
Monash University, Melbourne, Australia.
Sir Peter MacCallum Cancer Centre, Melbourne, Australia.
Department of Clinical Haematology, Alfred Health, Melbourne, Australia.
Faculty of Medicine and Health, University of Sydney, Camperdown, Australia.
Type of Clinical Study or Trial: N/A
Appears in Collections:Cancer Services

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