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Integrated analysis of next generation sequencing minimal residual disease (MRD) and PET scan in transplant eligible myeloma patients
Minimal residual disease (MRD) assays allow response assessment in patients with multiple myeloma (MM), and negativity is associated with improved survival outcomes. The role of highly sensitive next generation sequencing (NGS) MRD in combination with functional imaging remains to be validated. We p...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988896/ https://www.ncbi.nlm.nih.gov/pubmed/36878906 http://dx.doi.org/10.1038/s41408-023-00794-x |
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author | Fonseca, Rodrigo Arribas, Mariano Wiedmeier-Nutor, Julia E. Kusne, Yael N. González Vélez, Miguel Kosiorek, Heidi E. Butterfield, Richard (Duke) J. Kirsch, Ilan R. Mikhael, Joseph R. Stewart, A. Keith Reeder, Craig Larsen, Jeremy Bergsagel, P. Leif Fonseca, Rafael |
author_facet | Fonseca, Rodrigo Arribas, Mariano Wiedmeier-Nutor, Julia E. Kusne, Yael N. González Vélez, Miguel Kosiorek, Heidi E. Butterfield, Richard (Duke) J. Kirsch, Ilan R. Mikhael, Joseph R. Stewart, A. Keith Reeder, Craig Larsen, Jeremy Bergsagel, P. Leif Fonseca, Rafael |
author_sort | Fonseca, Rodrigo |
collection | PubMed |
description | Minimal residual disease (MRD) assays allow response assessment in patients with multiple myeloma (MM), and negativity is associated with improved survival outcomes. The role of highly sensitive next generation sequencing (NGS) MRD in combination with functional imaging remains to be validated. We performed a retrospective analysis on MM patients who underwent frontline autologous stem cell transplant (ASCT). Patients were evaluated at day 100 post-ASCT with NGS-MRD and positron emission tomography (PET-CT). Patients with ≥ 2 MRD measurements were included in a secondary analysis for sequential measurements. 186 patients were included. At day 100, 45 (24.2%) patients achieved MRD negativity at a sensitivity threshold of 10(−6). MRD negativity was the most predictive factor for longer time to next treatment (TTNT). Negativity rates did not differ according to MM subtype, R-ISS Stage nor cytogenetic risk. PET-CT and MRD had poor agreement, with high rates of PET-CT negativity in MRD-positive patients. Patients with sustained MRD negativity had longer TTNT, regardless of baseline risk characteristics. Our results show that the ability to measure deeper and sustainable responses distinguishes patients with better outcomes. Achieving MRD negativity was the strongest prognostic marker and could help guide therapy-related decisions and serve as a response marker for clinical trials. |
format | Online Article Text |
id | pubmed-9988896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99888962023-03-08 Integrated analysis of next generation sequencing minimal residual disease (MRD) and PET scan in transplant eligible myeloma patients Fonseca, Rodrigo Arribas, Mariano Wiedmeier-Nutor, Julia E. Kusne, Yael N. González Vélez, Miguel Kosiorek, Heidi E. Butterfield, Richard (Duke) J. Kirsch, Ilan R. Mikhael, Joseph R. Stewart, A. Keith Reeder, Craig Larsen, Jeremy Bergsagel, P. Leif Fonseca, Rafael Blood Cancer J Article Minimal residual disease (MRD) assays allow response assessment in patients with multiple myeloma (MM), and negativity is associated with improved survival outcomes. The role of highly sensitive next generation sequencing (NGS) MRD in combination with functional imaging remains to be validated. We performed a retrospective analysis on MM patients who underwent frontline autologous stem cell transplant (ASCT). Patients were evaluated at day 100 post-ASCT with NGS-MRD and positron emission tomography (PET-CT). Patients with ≥ 2 MRD measurements were included in a secondary analysis for sequential measurements. 186 patients were included. At day 100, 45 (24.2%) patients achieved MRD negativity at a sensitivity threshold of 10(−6). MRD negativity was the most predictive factor for longer time to next treatment (TTNT). Negativity rates did not differ according to MM subtype, R-ISS Stage nor cytogenetic risk. PET-CT and MRD had poor agreement, with high rates of PET-CT negativity in MRD-positive patients. Patients with sustained MRD negativity had longer TTNT, regardless of baseline risk characteristics. Our results show that the ability to measure deeper and sustainable responses distinguishes patients with better outcomes. Achieving MRD negativity was the strongest prognostic marker and could help guide therapy-related decisions and serve as a response marker for clinical trials. Nature Publishing Group UK 2023-03-06 /pmc/articles/PMC9988896/ /pubmed/36878906 http://dx.doi.org/10.1038/s41408-023-00794-x Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fonseca, Rodrigo Arribas, Mariano Wiedmeier-Nutor, Julia E. Kusne, Yael N. González Vélez, Miguel Kosiorek, Heidi E. Butterfield, Richard (Duke) J. Kirsch, Ilan R. Mikhael, Joseph R. Stewart, A. Keith Reeder, Craig Larsen, Jeremy Bergsagel, P. Leif Fonseca, Rafael Integrated analysis of next generation sequencing minimal residual disease (MRD) and PET scan in transplant eligible myeloma patients |
title | Integrated analysis of next generation sequencing minimal residual disease (MRD) and PET scan in transplant eligible myeloma patients |
title_full | Integrated analysis of next generation sequencing minimal residual disease (MRD) and PET scan in transplant eligible myeloma patients |
title_fullStr | Integrated analysis of next generation sequencing minimal residual disease (MRD) and PET scan in transplant eligible myeloma patients |
title_full_unstemmed | Integrated analysis of next generation sequencing minimal residual disease (MRD) and PET scan in transplant eligible myeloma patients |
title_short | Integrated analysis of next generation sequencing minimal residual disease (MRD) and PET scan in transplant eligible myeloma patients |
title_sort | integrated analysis of next generation sequencing minimal residual disease (mrd) and pet scan in transplant eligible myeloma patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988896/ https://www.ncbi.nlm.nih.gov/pubmed/36878906 http://dx.doi.org/10.1038/s41408-023-00794-x |
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