Novel Immune-Based treatments for Diffuse Large B-Cell Lymphoma: The Post-CAR T Cell Era
- PMID: 35720352
- PMCID: PMC9198279
- DOI: 10.3389/fimmu.2022.901365
Novel Immune-Based treatments for Diffuse Large B-Cell Lymphoma: The Post-CAR T Cell Era
Abstract
Prognosis for patients with refractory/relapsed (R/R) diffuse large B-cell lymphoma (DLBCL) is poor. Immune-based therapeutic treatments such as CD19 Chimeric Antigen Receptor (CAR) T cell therapies have dramatically changed the treatment landscape for R/R DLBCL leading to durable remissions in ~ 50% of patients. However, there remains an unmet need for developing novel therapies to improve clinical outcomes of patients not responding or relapsing after CAR T cell therapies. Lack of suitable immunotherapeutic targets and disease heterogeneity represent the foremost challenges in this emerging field. In this review, we discuss the recently approved and emerging novel immunotherapies for patients with R/R DLBCL in the post-CAR T era and the cell surface targets currently used.
Keywords: chimeric antigen receptor T-cell therapy; diffuse large B-cell lymphoma; discovery; high-risk; immunotherapy; target.
Copyright © 2022 Atallah-Yunes, Robertson, Davé, Ghione and Perna.
Conflict of interest statement
PG participated in advisory boards for Astra Zeneca, Daiichi Sanyo, Secura Bio and Kyowa Hakko Kirin. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
-
- Sarkozy C, Sehn LHJAL. New Drugs for the Management of Relapsed or Refractory Diffuse Large B-Cell Lymphoma. Annals Lymphoma (2019) 3(10).
-
- Gutiérrez-García G, Cardesa-Salzmann T, Climent F, González-Barca E, Mercadal S, Mate JL, et al. . Gene-Expression Profiling and Not Immunophenotypic Algorithms Predicts Prognosis in Patients With Diffuse Large B-Cell Lymphoma Treated With Immunochemotherapy. Blood (2011) 117(18):4836–43. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
