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Clonal Myeloid Dysplasia Following CAR T-Cell Therapy: Chicken or the Egg?

Authors :
Gatt, Vladimir Vainstein
Batia Avni
Sigal Grisariu
Shlomit Kfir-Erenfeld
Nathalie Asherie
Boaz Nachmias
Shlomtzion Auman
Revital Saban
Eran Zimran
Miri Assayag
Kalman Filanovsky
Netanel A. Horowitz
Eyal Lebel
Adir Shaulov
Michal Gur
Chaggai Rosenbluh
Svetlana Krichevsky
Polina Stepensky
Moshe E.
Source :
Cancers; Volume 15; Issue 13; Pages: 3471
Publication Year :
2023
Publisher :
Multidisciplinary Digital Publishing Institute, 2023.

Abstract

Multiple myeloma (MM) is characterized by recurrent relapses. Consequently, patients receive multiple therapy lines, including alkylating agents and immune modulators, which have been associated with secondary malignancies such as myelodysplastic syndrome (MDS). Anti-B-cell maturation antigen (BCMA) chimeric antigen receptor T cell (CART) therapy is efficacious in patients with relapsed/refractory (R/R) MM. However, the long-term complications, particularly MDS, are not well understood. Whether CART therapy causes or promotes MDS has not been thoroughly investigated. In this study, we explored the causal relationship between MDS and CART therapy. We retrospectively examined the prevalence of MDS-related morphological and mutational changes before and after administration of CART therapy in five patients. Among them, four developed MDS after CART therapy, while one had pre-existing MDS prior to CART. None of the four patients who developed post-CART MDS showed morphological MDS changes prior to CART therapy. However, all four patients exhibited molecular alterations associated with MDS in their pre-CART as well as post-CART therapy bone marrow. No new mutations were observed. Our findings provide initial evidence suggesting that anti-BCMA CART therapy in MM may promote expansion of pre-existing MDS clones rather than causing development of new clones.

Details

Language :
English
ISSN :
20726694
Database :
OpenAIRE
Journal :
Cancers; Volume 15; Issue 13; Pages: 3471
Accession number :
edsair.multidiscipl..4262f7cb072d966e64b71a11cb9dc62a
Full Text :
https://doi.org/10.3390/cancers15133471