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Circulating Activin A predicts survival in cancer patients

BACKGROUND: Several experimental evidences pinpoint the possible role of Activin A (ActA) as a driver of cancer cachexia. Supporting this hypothesis, we showed recently that human cancer cachexia is associated with high ActA levels. Moreover, ActA levels were correlated with body weight loss and ske...

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Autores principales: Loumaye, Audrey, de Barsy, Marie, Nachit, Maxime, Lause, Pascale, van Maanen, Aline, Trefois, Pierre, Gruson, Damien, Thissen, Jean‐Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659049/
https://www.ncbi.nlm.nih.gov/pubmed/28712119
http://dx.doi.org/10.1002/jcsm.12209
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author Loumaye, Audrey
de Barsy, Marie
Nachit, Maxime
Lause, Pascale
van Maanen, Aline
Trefois, Pierre
Gruson, Damien
Thissen, Jean‐Paul
author_facet Loumaye, Audrey
de Barsy, Marie
Nachit, Maxime
Lause, Pascale
van Maanen, Aline
Trefois, Pierre
Gruson, Damien
Thissen, Jean‐Paul
author_sort Loumaye, Audrey
collection PubMed
description BACKGROUND: Several experimental evidences pinpoint the possible role of Activin A (ActA) as a driver of cancer cachexia. Supporting this hypothesis, we showed recently that human cancer cachexia is associated with high ActA levels. Moreover, ActA levels were correlated with body weight loss and skeletal muscle density, two prognostic factors in cancer patients. Our goal was therefore to investigate the value of ActA to predict survival in cancer patients. METHODS: Patients with colorectal or lung cancer were prospectively enrolled at the time of diagnosis or relapse between January 2012 and March 2014. At baseline, patients had clinical, nutritional, and functional assessment. Body composition and skeletal muscle density were measured by CT scan, and plasma ActA concentrations were determined. Overall survival (OS) was analysed since inclusion to 24 months later. RESULTS: Survival data were available for 149 patients out of 152. Patients with high ActA (≥408 pg/mL) had lower OS than those with low levels, regardless the type of cancer (OS in colorectal cancer, 50% vs. 79%, P < 0.05; and in lung cancer, 27% vs. 67%, P = 0.001). The multivariable analysis confirmed the prognostic value of ActA independently of tumour stage or inflammatory markers, particularly in lung cancer. Low muscularity was also an independent prognostic factor. CONCLUSIONS: Our study demonstrates that high ActA level is an independent prognosis factor of survival in cancer patients. More than a basic marker of the severity of the neoplastic disease or of the inflammatory process, ActA seems to influence survival by contributing to the development of cachexia and loss of skeletal muscle mass.
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spelling pubmed-56590492017-11-01 Circulating Activin A predicts survival in cancer patients Loumaye, Audrey de Barsy, Marie Nachit, Maxime Lause, Pascale van Maanen, Aline Trefois, Pierre Gruson, Damien Thissen, Jean‐Paul J Cachexia Sarcopenia Muscle Original Articles BACKGROUND: Several experimental evidences pinpoint the possible role of Activin A (ActA) as a driver of cancer cachexia. Supporting this hypothesis, we showed recently that human cancer cachexia is associated with high ActA levels. Moreover, ActA levels were correlated with body weight loss and skeletal muscle density, two prognostic factors in cancer patients. Our goal was therefore to investigate the value of ActA to predict survival in cancer patients. METHODS: Patients with colorectal or lung cancer were prospectively enrolled at the time of diagnosis or relapse between January 2012 and March 2014. At baseline, patients had clinical, nutritional, and functional assessment. Body composition and skeletal muscle density were measured by CT scan, and plasma ActA concentrations were determined. Overall survival (OS) was analysed since inclusion to 24 months later. RESULTS: Survival data were available for 149 patients out of 152. Patients with high ActA (≥408 pg/mL) had lower OS than those with low levels, regardless the type of cancer (OS in colorectal cancer, 50% vs. 79%, P < 0.05; and in lung cancer, 27% vs. 67%, P = 0.001). The multivariable analysis confirmed the prognostic value of ActA independently of tumour stage or inflammatory markers, particularly in lung cancer. Low muscularity was also an independent prognostic factor. CONCLUSIONS: Our study demonstrates that high ActA level is an independent prognosis factor of survival in cancer patients. More than a basic marker of the severity of the neoplastic disease or of the inflammatory process, ActA seems to influence survival by contributing to the development of cachexia and loss of skeletal muscle mass. John Wiley and Sons Inc. 2017-07-15 2017-10 /pmc/articles/PMC5659049/ /pubmed/28712119 http://dx.doi.org/10.1002/jcsm.12209 Text en © 2017 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of the Society on Sarcopenia, Cachexia and Wasting Disorders This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Loumaye, Audrey
de Barsy, Marie
Nachit, Maxime
Lause, Pascale
van Maanen, Aline
Trefois, Pierre
Gruson, Damien
Thissen, Jean‐Paul
Circulating Activin A predicts survival in cancer patients
title Circulating Activin A predicts survival in cancer patients
title_full Circulating Activin A predicts survival in cancer patients
title_fullStr Circulating Activin A predicts survival in cancer patients
title_full_unstemmed Circulating Activin A predicts survival in cancer patients
title_short Circulating Activin A predicts survival in cancer patients
title_sort circulating activin a predicts survival in cancer patients
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659049/
https://www.ncbi.nlm.nih.gov/pubmed/28712119
http://dx.doi.org/10.1002/jcsm.12209
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