The shifting therapeutic paradigm for relapsed/refractory mantle cell lymphoma.
BTK inhibitor
Bispecific antibodies
CAR-T
Mantle cell lymphoma
Targeted therapies
Journal
Leukemia research
ISSN: 1873-5835
Titre abrégé: Leuk Res
Pays: England
ID NLM: 7706787
Informations de publication
Date de publication:
11 2023
11 2023
Historique:
received:
26
06
2023
revised:
28
08
2023
accepted:
29
08
2023
medline:
3
11
2023
pubmed:
7
9
2023
entrez:
6
9
2023
Statut:
ppublish
Résumé
Mantle cell lymphoma (MCL) is a heterogeneous subtype of non-Hodgkin lymphoma that has been historically associated with poor 5-year overall survival rates, especially for aggressive variants. Traditional cytotoxic chemotherapy had been a mainstay of therapy for relapsed/refractory (R/R) MCL for many years until the advent of molecularly targeted therapies and cell-based approaches. However, a significant concern is the lack of definitive consensus guidelines for management of R/R MCL. The managerial conundrum partly stems from the absence of head-to-head comparisons of novel therapies, with conclusions drawn from cross-trial comparisons. In this evidence-based review, we discuss the current therapeutic options for R/R MCL, including the most recent data from the BRUIN study that led to the approval of the first-in-class non-covalent reversible Bruton's tyrosine kinase (BTK) inhibitor pirtobrutinib in 2023, as well as the recent removal of ibrutinib from the market. We discuss outlooks for targeted therapy and tolerability considerations for novel agents, including unique considerations for the elderly population. We highlight emerging data that support the curative potential of chimeric antigen receptor-T (CAR-T) therapy from ZUMA-2, relative to other promising investigational agents in the pipeline, including glofitamab, epcoritamab, and zilovertamab vedotin. We summarize management recommendations based upon the most rigorous clinical evidence to date.
Identifiants
pubmed: 37672954
pii: S0145-2126(23)00650-1
doi: 10.1016/j.leukres.2023.107385
pii:
doi:
Substances chimiques
glofitamab
06P3KLK2J8
pirtobrutinib
0
Antineoplastic Agents
0
Antibodies, Bispecific
0
Types de publication
Journal Article
Review
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
107385Subventions
Organisme : NCATS NIH HHS
ID : UL1 TR001453
Pays : United States
Informations de copyright
Copyright © 2023 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest SAP served on the Multiple Myeloma advisory board for Pfizer, the COMMANDS trial advisory board for Bristol Myers Squibb, and the Acute Myeloid Leukemia advisory board for Bristol Myers Squibb. SAK and JG have no conflicts of interest.