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Mohan, Meera

0000-0002-6913-6526

Mayo Clinic

Division of Hematology/Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

Citations 3

Reassessing the Duration of Induction Therapy for Newly Diagnosed, Transplant‐Eligible Myeloma Patients in the Context of Quadruple CD38 Monoclonal Antibody‐Based Regimens: Is 24 Weeks Optimal?
Mohan, Meera, Radhakrishnan, Sabarinath, Katodritou, Eirini , Fonseca, Rafeal, Mohan, Meera , Mohan, Meera , Katodritou, Eirini , Radhakrishnan, Sabarinath Venniyil , Schinke, Carolina

American Journal of Hematology | January 27, 2026 | Volume: 101 | Issue: 5 | Pages: 1141-1147

10.1002/ajh.70215 Get It

Chimeric antigen receptor and bispecific T‐cell engager therapies in multiple myeloma patients with prior allogeneic transplantation
Hammons, Lindsay , Haider, Shabi , Portuguese, Andrew J. , Banerjee, Rahul , Pasquini, Marcelo C. , Chhabra, Saurabh , Radhakrishnan, Sabarinath Venniyil , Mohan, Meera , Narra, Ravi , Shah, Nirav N. , D’Souza, Anita , Dhakal, Binod , Pasquini, Marcelo , Chhabra, Saurabh , Mohan, Meera , Shah, Nirav N , Hamadani, Mehdi , D'Souza, Anita , Dhakal, Binod , Banerjee, Rahul , Portuguese, Andrew J , Szabó, Anikó , Dong, Jing , Janz, Siegfried , Hamadani, Mehdi , Hari, Parameswaran

British Journal of Haematology | December 6, 2023 | Volume: 204 | Issue: 3 | Pages: 887-891

10.1111/bjh.19244 Get It

Summary Chimeric antigen receptor T‐cell (CAR‐T) therapy and bispecific T‐cell engagers (BsAb) have emerged as promising immunotherapeutic modalities in patients with relapsed and/or refractory multiple myeloma (RRMM). However, there is limited data on the safety and efficacy of CAR‐T and BsAb therapies in MM patients with a prior history of allogeneic transplantation (allo‐HCT). Thirty‐three MM patients with prior allo‐HCT received CAR‐T ( n = 24) or BsAb ( n = 9) therapy. CAR‐T therapy demonstrated an ORR of 92% (67% ≥ CR), and 73% were MRD negative. BsAb therapy resulted in an ORR of 44% (44% ≥ CR) and 44% MRD negative. Safety analysis showed grade ≥3 AEs in 92% of CAR‐T and 56% of BsAb patients. Cytokine release syndrome (CRS) occurred in 83% of CAR‐T and 78% of BsAb recipients, while immune effector cell‐associated neurotoxicity syndrome (ICANS) was observed in three CAR‐T patients. Infections of grade ≥3 were reported in 50% of CAR‐T and 44% of BsAb recipients. No exacerbation of graft‐versus‐host disease occurred except in one BsAb recipient. CAR‐T and BsAb therapies appear to be feasible, safe and provide deep and durable responses in MM patients with prior allo‐HCT.