Sequencing of Novel Therapies for Mantle Cell Lymphoma.


Journal

Current treatment options in oncology
ISSN: 1534-6277
Titre abrégé: Curr Treat Options Oncol
Pays: United States
ID NLM: 100900946

Informations de publication

Date de publication:
23 11 2021
Historique:
accepted: 28 05 2021
entrez: 23 11 2021
pubmed: 24 11 2021
medline: 17 3 2022
Statut: epublish

Résumé

There is no standard approach to sequencing novel therapies in mantle cell lymphoma (MCL). For initial treatment, intensive induction chemotherapy followed by autologous stem cell transplant and rituximab maintenance remains our preferred approach in young, fit patients. We consider bendamustine plus rituximab or lenalidomide plus rituximab in patients who are ineligible for intensive chemotherapy-based approaches. Bruton's tyrosine kinase inhibitors are our preferred class of agents to use in the second-line setting. When patients inevitably relapse on one of these agents, we proceed with chimeric antigen receptor T-cell (CAR T) therapy in eligible patients, often with the use of bridging therapy with corticosteroids, lenalidomide, or venetoclax. We treat patients who are ineligible for CAR T or clinic trial with venetoclax, lenalidomide, or proteosome inhibitor-based regimens, although efficacy is expected to be limited in this setting with a shortened duration of response to each subsequent line of therapy. Allogeneic stem cell transplant remains an option for carefully selected patients who progress after autologous stem cell transplant and CAR T. Clinical trials involving combinations of novel agents in early lines of therapy are ongoing, and new compounds with unique mechanisms of action are in development. The results of ongoing clinical trials with novel agents will further change the treatment landscape for patients with MCL in the coming years.

Identifiants

pubmed: 34812968
doi: 10.1007/s11864-021-00907-3
pii: 10.1007/s11864-021-00907-3
doi:

Substances chimiques

Antineoplastic Agents 0
Bridged Bicyclo Compounds, Heterocyclic 0
Glucocorticoids 0
Proteasome Inhibitors 0
Protein Kinase Inhibitors 0
Receptors, Chimeric Antigen 0
Sulfonamides 0
Rituximab 4F4X42SYQ6
Bendamustine Hydrochloride 981Y8SX18M
Agammaglobulinaemia Tyrosine Kinase EC 2.7.10.2
Lenalidomide F0P408N6V4
venetoclax N54AIC43PW

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

118

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Auteurs

Jason T Romancik (JT)

Department of Hematology and Medical Oncology, Winship Cancer Institute At Emory University, Atlanta, GA, USA.

Jonathon B Cohen (JB)

Department of Hematology and Medical Oncology, Winship Cancer Institute At Emory University, Atlanta, GA, USA. jonathon.cohen@emory.edu.

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Classifications MeSH