Deciphering response dynamics and treatment resistance from circulating tumor DNA after CAR T-cells in multiple myeloma

Despite advances in treatments, multiple myeloma (MM) remains an incurable cancer where relapse is common. We developed a circulating tumor DNA (ctDNA) approach in order to characterize tumor genomics, monitor treatment response, and detect early relapse in MM. By sequencing 412 specimens from 64 patients with newly diagnosed or relapsed/refractory disease, we demonstrate the correlation between ctDNA and key clinical biomarkers, as well as patient outcomes. We further extend our approach to simultaneously track CAR-specific cell-free DNA (CAR-cfDNA) in patients undergoing anti-BCMA CAR T-cell (BCMA-CAR) therapy. We demonstrate that ctDNA levels following BCMA-CAR inversely correlate with relative time to progression (TTP), and that measurable residual disease (MRD) quantified by peripheral blood ctDNA (ctDNA-MRD) was concordant with clinical bone marrow MRD. Finally, we show that ctDNA-MRD can anticipate clinical relapse and identify the emergence of genomically-defined therapy-resistant clones. These findings suggest multiple clinical uses of ctDNA for MM in molecular characterization and disease surveillance.

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Publication Details

Journal
Nature Communications
Published
2025-02-20
DOI
https://doi.org/10.1038/s41467-025-56486-6
Citations
9
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
9.41

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article

Deciphering response dynamics and treatment resistance from circulating tumor DNA after CAR T-cells in multiple myeloma

Oscar Silva, Surbhi Sidana, Hitomi Hosoya, David Iberri et al.
9 citations
Nature Communications
CAR-T cell therapy research
9.41
article

Deciphering response dynamics and treatment resistance from circulating tumor DNA after CAR T-cells in multiple myeloma

Oscar Silva, Surbhi Sidana, Hitomi Hosoya, David Iberri, Sally Arai, Vanna Hovanky, George E. Durán, Henning Stehr, Michael S. Khodadoust, Mia Carleton, Alisha M. Birk, Bita Sahaf, Brian J. Sworder, David M. Kurtz, Shriya Syal, David B. Miklos, Kailee Tanaka, Michaela Liedtke, Tian Zhang
article en
9 citations

Abstract

Despite advances in treatments, multiple myeloma (MM) remains an incurable cancer where relapse is common. We developed a circulating tumor DNA (ctDNA) approach in order to characterize tumor genomics, monitor treatment response, and detect early relapse in MM. By sequencing 412 specimens from 64 patients with newly diagnosed or relapsed/refractory disease, we demonstrate the correlation between ctDNA and key clinical biomarkers, as well as patient outcomes. We further extend our approach to simultaneously track CAR-specific cell-free DNA (CAR-cfDNA) in patients undergoing anti-BCMA CAR T-cell (BCMA-CAR) therapy. We demonstrate that ctDNA levels following BCMA-CAR inversely correlate with relative time to progression (TTP), and that measurable residual disease (MRD) quantified by peripheral blood ctDNA (ctDNA-MRD) was concordant with clinical bone marrow MRD. Finally, we show that ctDNA-MRD can anticipate clinical relapse and identify the emergence of genomically-defined therapy-resistant clones. These findings suggest multiple clinical uses of ctDNA for MM in molecular characterization and disease surveillance.

Nature CommunicationsVol. 16(1)
University of California, Irvine (US), Stanford Blood Center (US), Stanford Medicine (US), Stanford University (US)
Society for Immunotherapy of Cancer, National Cancer Institute, Stanford Cancer Institute
Openalex Percentile: Top 2%
CAR-T cell therapy research
9.41
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