Identification of the Distinct Immune Microenvironment Features Associated with Progression Following High-Dose Melphalan and Autologous Stem Cell Transplant in Multiple Myeloma

A key treatment for patients with multiple myeloma is high-dose melphalan followed by autologous stem cell transplant (ASCT). It can provide a deep response with long-term remission. However, some patients progress quickly, and it is not clear why. In this study, we performed single-cell RNA and T-cell receptor sequencing of the immune microenvironment of 40 patients before and after ASCT to determine if differences in the immune composition could define those who would progress. Clear differences in cell populations were identified in progressors, including increased T-cell infiltration, decreased T-cell receptor diversity, and decreased frequency of monocytes and CD56bright NK cells. We identified cell interactions that predicted progression, including increased frequency of CD8+ exhausted T cells and stromal cells and decreased frequency of CD56bright NK cells and plasmacytoid dendritic cells. We propose and validate a model of progression that can also be determined by flow cytometry. Together, these data highlight the importance of the immune microenvironment in understanding responses to ASCT.

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Publication Details

Journal
Cancer Immunology Research
Published
2025-05-08
DOI
https://doi.org/10.1158/2326-6066.cir-25-0019
Primary Topic
Multiple Myeloma Research and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Identification of the Distinct Immune Microenvironment Features Associated with Progression Following High-Dose Melphalan and Autologous Stem Cell Transplant in Multiple Myeloma

Mohammad Abu Zaid, Faiza Zafar, Brian A. Walker, Vivek S. Chopra et al.
Cancer Immunology Research
Multiple Myeloma Research and Treatments
article

Identification of the Distinct Immune Microenvironment Features Associated with Progression Following High-Dose Melphalan and Autologous Stem Cell Transplant in Multiple Myeloma

Mohammad Abu Zaid, Faiza Zafar, Brian A. Walker, Vivek S. Chopra, Magdalena Czader, Rafat Abonour, Parvathi Sudha, Kelvin P. Lee, Attaya Suvannasankha, Enze Liu, Sherif S. Farag, Travis S. Johnson, Habib Hamidi, Ola Landgren, Gareth J. Morgan, Michael Nixon, Ke Yang, Brad Smith
article en

Abstract

A key treatment for patients with multiple myeloma is high-dose melphalan followed by autologous stem cell transplant (ASCT). It can provide a deep response with long-term remission. However, some patients progress quickly, and it is not clear why. In this study, we performed single-cell RNA and T-cell receptor sequencing of the immune microenvironment of 40 patients before and after ASCT to determine if differences in the immune composition could define those who would progress. Clear differences in cell populations were identified in progressors, including increased T-cell infiltration, decreased T-cell receptor diversity, and decreased frequency of monocytes and CD56bright NK cells. We identified cell interactions that predicted progression, including increased frequency of CD8+ exhausted T cells and stromal cells and decreased frequency of CD56bright NK cells and plasmacytoid dendritic cells. We propose and validate a model of progression that can also be determined by flow cytometry. Together, these data highlight the importance of the immune microenvironment in understanding responses to ASCT.

Cancer Immunology ResearchVol. 13(7)
Roche (Switzerland) (CH), Indiana University Health (US), Amgen (United States) (US), University of Indianapolis (US), University of Miami (US), NYU Langone Health (US), Indiana Cancer Consortium (US), Sylvester Comprehensive Cancer Center (US), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US), Indiana University (US)
Multiple Myeloma Research Foundation, Eli Lilly and Company, Lilly Endowment, Genentech, School of Medicine, Indiana University, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 87%
Multiple Myeloma Research and Treatments
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