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Liquid biopsy and blood-based minimal residual disease evaluation in multiple myeloma
Novel drug availability has increased the depth of response and revolutionised the outcomes of multiple myeloma patients. Minimal residual disease evaluation is a surrogate for progression-free survival and overall survival and has become widely used not-only in clinical trials but also in daily pat...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tech Science Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229300/ https://www.ncbi.nlm.nih.gov/pubmed/37305387 http://dx.doi.org/10.32604/or.2023.028668 |
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author | GOZZETTI, ALESSANDRO BOCCHIA, MONICA |
author_facet | GOZZETTI, ALESSANDRO BOCCHIA, MONICA |
author_sort | GOZZETTI, ALESSANDRO |
collection | PubMed |
description | Novel drug availability has increased the depth of response and revolutionised the outcomes of multiple myeloma patients. Minimal residual disease evaluation is a surrogate for progression-free survival and overall survival and has become widely used not-only in clinical trials but also in daily patient management. Bone marrow aspiration is the gold standard for response evaluation, but due to the patchy nature of myeloma, false negatives are possible. Liquid biopsy and blood-based minimal residual disease evaluation consider circulating plasma cells, mass spectrometry or circulating tumour DNA. This approach is less invasive, can provide a more comprehensive picture of the disease and could become the future of response evaluation in multiple myeloma patients. |
format | Online Article Text |
id | pubmed-10229300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Tech Science Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102293002023-06-10 Liquid biopsy and blood-based minimal residual disease evaluation in multiple myeloma GOZZETTI, ALESSANDRO BOCCHIA, MONICA Oncol Res Viewpoint Novel drug availability has increased the depth of response and revolutionised the outcomes of multiple myeloma patients. Minimal residual disease evaluation is a surrogate for progression-free survival and overall survival and has become widely used not-only in clinical trials but also in daily patient management. Bone marrow aspiration is the gold standard for response evaluation, but due to the patchy nature of myeloma, false negatives are possible. Liquid biopsy and blood-based minimal residual disease evaluation consider circulating plasma cells, mass spectrometry or circulating tumour DNA. This approach is less invasive, can provide a more comprehensive picture of the disease and could become the future of response evaluation in multiple myeloma patients. Tech Science Press 2023-05-24 /pmc/articles/PMC10229300/ /pubmed/37305387 http://dx.doi.org/10.32604/or.2023.028668 Text en © 2023 Gozzetti and Bocchia https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Viewpoint GOZZETTI, ALESSANDRO BOCCHIA, MONICA Liquid biopsy and blood-based minimal residual disease evaluation in multiple myeloma |
title | Liquid biopsy and blood-based minimal residual disease evaluation in multiple myeloma |
title_full | Liquid biopsy and blood-based minimal residual disease evaluation in multiple myeloma |
title_fullStr | Liquid biopsy and blood-based minimal residual disease evaluation in multiple myeloma |
title_full_unstemmed | Liquid biopsy and blood-based minimal residual disease evaluation in multiple myeloma |
title_short | Liquid biopsy and blood-based minimal residual disease evaluation in multiple myeloma |
title_sort | liquid biopsy and blood-based minimal residual disease evaluation in multiple myeloma |
topic | Viewpoint |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229300/ https://www.ncbi.nlm.nih.gov/pubmed/37305387 http://dx.doi.org/10.32604/or.2023.028668 |
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