| Literature DB >> 31279751 |
Michael Byrne1, Olalekan O Oluwole1, Bipin Savani1, Navneet S Majhail2, Brian T Hill2, Fredrick L Locke3.
Abstract
Most patients with large cell lymphoma are cured with frontline chemoimmunotherapy. For individuals with refractory disease and those who relapse after conventional therapies, chimeric antigen receptor (CAR) T cells are an important treatment option and have led to remissions in otherwise refractory patients. In the pivotal trials, durable responses were achieved in approximately 40% to 50% of patients treated with axicabtagene ciloleucel, tisagenlecleucel, or lisocabtagene maraleucel, indicating that many patients will require subsequent treatment. Failure after CAR T cell therapy is caused by a variety of factors that can be divided into 3 broad categories: tumor intrinsic factors, other host factors, and inadequacies of the CAR T cells. Within this framework, this article reviews possible mechanisms of treatment failures and, based on the timing of relapse, considers potential salvage therapies and opportunities for future clinical studies.Entities:
Keywords: CAR T cell; Diffuse large B cell lymphoma; Relapse
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Year: 2019 PMID: 31279751 PMCID: PMC7800228 DOI: 10.1016/j.bbmt.2019.06.036
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742