PMID- 38066907 OWN - NLM STAT- MEDLINE DCOM- 20231216 LR - 20240215 IS - 1520-4383 (Electronic) IS - 1520-4391 (Print) IS - 1520-4383 (Linking) VI - 2023 IP - 1 DP - 2023 Dec 8 TI - Selection of bispecific antibody therapies or CAR-T cell therapy in relapsed lymphomas. PG - 370-381 LID - 10.1182/hematology.2023000438 [doi] AB - Patients with relapsed and refractory (R/R) aggressive B-cell non-Hodgkin lymphomas have historically poor survival outcomes, with chimeric antigen receptor T-cell (CAR-T) therapy now presenting a curative option for a subset of those patients. However, with the approval of several novel bispecific monoclonal antibody (BsAb) therapies with considerable activity in R/R aggressive large B-cell lymphomas (LBCL), patients and oncologists will be faced with decisions regarding how to sequence CAR-T and BsAb therapies based on patient- and disease-related factors. In this review, we compare CAR-T and BsAb therapies for R/R LBCL, highlighting data on the efficacy and toxicity of each treatment paradigm, and provide a roadmap for sequencing these highly effective therapies. CI - Copyright (c) 2023 by The American Society of Hematology. FAU - Major, Ajay AU - Major A AD - Division of Hematology, Department of Medicine, University of Colorado School of Medicine, Aurora, CO. FAU - Kamdar, Manali AU - Kamdar M AD - Division of Hematology, Department of Medicine, University of Colorado School of Medicine, Aurora, CO. LA - eng PT - Journal Article PT - Review PL - United States TA - Hematology Am Soc Hematol Educ Program JT - Hematology. American Society of Hematology. Education Program JID - 100890099 RN - 0 (Receptors, Chimeric Antigen) RN - 0 (Antibodies, Bispecific) SB - IM MH - Humans MH - *Receptors, Chimeric Antigen/therapeutic use MH - Immunotherapy, Adoptive MH - *Lymphoma, Large B-Cell, Diffuse/pathology MH - *Antibodies, Bispecific/therapeutic use MH - Cell- and Tissue-Based Therapy PMC - PMC10727048 COIS- Ajay Major: no competing financial interests to declare. Manali Kamdar declares research support from Novartis; consultancy from AbbVie, AstraZeneca, Celgene/Bristol-Myers Squibb, Adaptive Biotechnologies, ADC Therapeutics, Beigene, Genentech, Impact Bio, Syncopation, and Caribou Biosciences; speaker's bureau from SeaGen; and data monitoring committee from Celgene and Genentech. EDAT- 2023/12/09 10:45 MHDA- 2023/12/17 09:43 PMCR- 2024/12/08 CRDT- 2023/12/09 01:01 PHST- 2024/12/08 00:00 [pmc-release] PHST- 2023/12/17 09:43 [medline] PHST- 2023/12/09 10:45 [pubmed] PHST- 2023/12/09 01:01 [entrez] AID - 506455 [pii] AID - 2023000438 [pii] AID - 10.1182/hematology.2023000438 [doi] PST - ppublish SO - Hematology Am Soc Hematol Educ Program. 2023 Dec 8;2023(1):370-381. doi: 10.1182/hematology.2023000438.