Myelodysplastic Syndrome Secondary to Chimeric Antigen Receptor T-cell (CAR-T) Therapy for the Treatment of Relapsed/Refractory Multiple Myeloma
We present the case of a 65-year-old man with relapsed/refractory multiple myeloma (RRMM) who developed therapy-related myelodysplastic syndrome (MDS) following chimeric antigen receptor T-cell (CAR-T) therapy with idecabtagene vicleucel (ide-cel). The patient, initially diagnosed in 2019, underwent multiple lines of therapy, including high-dose melphalan with autologous stem cell transplantation, before receiving ide-cel for progressive disease. Despite initial remission, a day 100 bone marrow biopsy revealed MDS with a 7q deletion, a cytogenetic abnormality not present on prior marrow evaluations. While CAR-T therapy has revolutionized RRMM treatment, long-term complications such as therapy-related hematologic malignancy remain under-recognized. The temporal relationship between CAR-T infusion and the emergence of a new therapy-induced cytogenetic abnormality raises concern for either CAR-T stress revealing a pre-existing myeloid clone or acceleration of therapy-induced myeloid neoplasia in a heavily pretreated patient. This case illustrates the need for standardized guidelines for malignancy screenings and long-term monitoring in CAR-T recipients. Further studies are essential to delineate the timing, mechanisms, and risk factors for secondary malignancies in CAR-T recipients.
Authors
- Precious Idogun
- Swathi Gopishetty
- Savitha Balaraman
- Ishmael A. Jaiyesimi (ORCID: https://orcid.org/0000-0002-6352-9054)
- Afoma Anyadibe
- Daniel Kim
- Jessica Thomas
- Anuoluwa Ayetoran
- Syed Zaidi
- Waqqas Tai
- Joe Dib
Institutions
- The University of Kansas Health System (US)
- Beaumont Hospital, Royal Oak (US)
- Beaumont Hospital, Troy (US)
- University of Missouri–Kansas City (US)
Publication Details
- Journal
- Cureus
- Published
- 2026-02-16
- DOI
- https://doi.org/10.7759/cureus.103706
- Primary Topic
- CAR-T cell therapy research
- Type
- article
- Field-Weighted Citation Impact
- 0.00