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Peripheral Absolute Lymphocyte Count: An Economical and Clinical Available Immune-Related Prognostic Marker for Newly Diagnosed Multiple Myeloma
BACKGROUND: To find economical and clinically available immune-related prognostic markers that could predict the overall survival (OS) of newly diagnosed multiple myeloma (NDMM) in the new drug era. MATERIAL/METHODS: Absolute lymphocyte count (ALC) and absolute monocyte count (AMC) were measured in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418483/ https://www.ncbi.nlm.nih.gov/pubmed/32732863 http://dx.doi.org/10.12659/MSM.923716 |
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author | Yang, Ying Liu, Zhuogang Wang, Hongtao |
author_facet | Yang, Ying Liu, Zhuogang Wang, Hongtao |
author_sort | Yang, Ying |
collection | PubMed |
description | BACKGROUND: To find economical and clinically available immune-related prognostic markers that could predict the overall survival (OS) of newly diagnosed multiple myeloma (NDMM) in the new drug era. MATERIAL/METHODS: Absolute lymphocyte count (ALC) and absolute monocyte count (AMC) were measured in routine blood samples from 102 patients with NDMM, and the lymphocyte-monocyte ratio (LMR) was derived. All the patients were receiving bortezomib-based chemotherapy as induction treatment. Log-rank testing was used for comparing the differences between groups. Univariate and multivariate tests were used to identify prognostic markers. RESULTS: The median ALC and LMR values at diagnosis were 1.43×10(9)/L and 3.7, respectively, and served as the cutoff point. As prognostic factors, ALC, LMR, and a new staging system combining ALC and the ISS staging system (L-ISS) were expected to have a significant impact on predicting OS. Furthermore, multivariate analysis showed that ALC ≥1.43×10(9)/L (hazard ratio [HR]: 0.223; 95% confidence interval [CI]: 0.071–0.705; P=0.011), LMR ≥3.7 (HR: 0.363; 95% CI: 0.139–0.947; P=0.038), and L-ISS late stage (HR: 1.619; 95% CI: 1.065–2.743; P=0.027) were independent predictors for OS. CONCLUSIONS: ALC and LMR can serve as surrogate markers for patients’ antitumor immunity at the initial diagnosis of multiple myeloma. A new immune-related staging system, L-ISS, which combines ALC and the ISS staging system, can predict clinical outcomes in patients who are receiving bortezomib-based chemotherapy. |
format | Online Article Text |
id | pubmed-7418483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74184832020-08-20 Peripheral Absolute Lymphocyte Count: An Economical and Clinical Available Immune-Related Prognostic Marker for Newly Diagnosed Multiple Myeloma Yang, Ying Liu, Zhuogang Wang, Hongtao Med Sci Monit Clinical Research BACKGROUND: To find economical and clinically available immune-related prognostic markers that could predict the overall survival (OS) of newly diagnosed multiple myeloma (NDMM) in the new drug era. MATERIAL/METHODS: Absolute lymphocyte count (ALC) and absolute monocyte count (AMC) were measured in routine blood samples from 102 patients with NDMM, and the lymphocyte-monocyte ratio (LMR) was derived. All the patients were receiving bortezomib-based chemotherapy as induction treatment. Log-rank testing was used for comparing the differences between groups. Univariate and multivariate tests were used to identify prognostic markers. RESULTS: The median ALC and LMR values at diagnosis were 1.43×10(9)/L and 3.7, respectively, and served as the cutoff point. As prognostic factors, ALC, LMR, and a new staging system combining ALC and the ISS staging system (L-ISS) were expected to have a significant impact on predicting OS. Furthermore, multivariate analysis showed that ALC ≥1.43×10(9)/L (hazard ratio [HR]: 0.223; 95% confidence interval [CI]: 0.071–0.705; P=0.011), LMR ≥3.7 (HR: 0.363; 95% CI: 0.139–0.947; P=0.038), and L-ISS late stage (HR: 1.619; 95% CI: 1.065–2.743; P=0.027) were independent predictors for OS. CONCLUSIONS: ALC and LMR can serve as surrogate markers for patients’ antitumor immunity at the initial diagnosis of multiple myeloma. A new immune-related staging system, L-ISS, which combines ALC and the ISS staging system, can predict clinical outcomes in patients who are receiving bortezomib-based chemotherapy. International Scientific Literature, Inc. 2020-07-31 /pmc/articles/PMC7418483/ /pubmed/32732863 http://dx.doi.org/10.12659/MSM.923716 Text en © Med Sci Monit, 2020 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Clinical Research Yang, Ying Liu, Zhuogang Wang, Hongtao Peripheral Absolute Lymphocyte Count: An Economical and Clinical Available Immune-Related Prognostic Marker for Newly Diagnosed Multiple Myeloma |
title | Peripheral Absolute Lymphocyte Count: An Economical and Clinical Available Immune-Related Prognostic Marker for Newly Diagnosed Multiple Myeloma |
title_full | Peripheral Absolute Lymphocyte Count: An Economical and Clinical Available Immune-Related Prognostic Marker for Newly Diagnosed Multiple Myeloma |
title_fullStr | Peripheral Absolute Lymphocyte Count: An Economical and Clinical Available Immune-Related Prognostic Marker for Newly Diagnosed Multiple Myeloma |
title_full_unstemmed | Peripheral Absolute Lymphocyte Count: An Economical and Clinical Available Immune-Related Prognostic Marker for Newly Diagnosed Multiple Myeloma |
title_short | Peripheral Absolute Lymphocyte Count: An Economical and Clinical Available Immune-Related Prognostic Marker for Newly Diagnosed Multiple Myeloma |
title_sort | peripheral absolute lymphocyte count: an economical and clinical available immune-related prognostic marker for newly diagnosed multiple myeloma |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418483/ https://www.ncbi.nlm.nih.gov/pubmed/32732863 http://dx.doi.org/10.12659/MSM.923716 |
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