Evidence map›Paper›PMID 41859580›Full record

ArticleCureus2026

Myelodysplastic Syndrome Secondary to Chimeric Antigen Receptor T-cell (CAR-T) Therapy for the Treatment of Relapsed/Refractory Multiple Myeloma.

Waqqas Tai, Daniel Kim, Joe Dib, Jessica Thomas, Swathi Gopishetty, Precious Idogun, Afoma Anyadibe, Anuoluwa Ayetoran, Syed Zaidi, Savitha Balaraman and 1 more

Abstract readCase Reports
In one paragraph

Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Waqqas TaiHematology and Oncology, Corewell Health William Beaumont University Hospital, Royal Oak, USA.
Daniel KimHematology and Oncology, Kansas City University, Kansas City, USA.
Joe DibHematology and Oncology, Corewell Health William Beaumont University Hospital, Royal Oak, USA.
Jessica ThomasHematology and Oncology, Corewell Health William Beaumont University Hospital, Royal Oak, USA.
Swathi GopishettyHematology and Oncology, Corewell Health William Beaumont University Hospital, Royal Oak, USA.
Precious IdogunHematology and Oncology, Corewell Health William Beaumont University Hospital, Royal Oak, USA.
Afoma AnyadibeHematology and Oncology, Corewell Health William Beaumont University Hospital, Royal Oak, USA.
Anuoluwa AyetoranHematology and Oncology, Corewell Health William Beaumont University Hospital, Royal Oak, USA.
Syed ZaidiPathology, Corewell Health William Beaumont University Hospital, Royal Oak, USA.
Savitha BalaramanHematology and Oncology, Corewell Health William Beaumont University Hospital, Royal Oak, USA.
Ishmael JaiyesimiHematology and Oncology, Corewell Health William Beaumont University Hospital, Royal Oak, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

car-t cells in hematological malignanciesidecabtagene vicleucelide-celmyelodysplastic syndrome (mds)plasma cell dyscrasiasrelapsed/refractory multiple myelomatherapy-related mds

Identifiers

PMID41859580
PMCPMC12998396

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.