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Skeletal muscle mass predicts the outcome of nivolumab treatment for non-small cell lung cancer

Nivolumab, a monoclonal antibody targeting programmed cell death-1, significantly prolongs survival for patients with advanced non-small-cell lung cancer (NSCLC). However, little is known about the value of predictive biomarkers. Hence, we investigated the impact of skeletal muscle (SM) mass loss on...

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Autores principales: Tsukagoshi, Mariko, Yokobori, Takehiko, Yajima, Toshiki, Maeno, Toshitaka, Shimizu, Kimihiro, Mogi, Akira, Araki, Kenichiro, Harimoto, Norifumi, Shirabe, Ken, Kaira, Kyoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035054/
https://www.ncbi.nlm.nih.gov/pubmed/32049805
http://dx.doi.org/10.1097/MD.0000000000019059
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author Tsukagoshi, Mariko
Yokobori, Takehiko
Yajima, Toshiki
Maeno, Toshitaka
Shimizu, Kimihiro
Mogi, Akira
Araki, Kenichiro
Harimoto, Norifumi
Shirabe, Ken
Kaira, Kyoichi
author_facet Tsukagoshi, Mariko
Yokobori, Takehiko
Yajima, Toshiki
Maeno, Toshitaka
Shimizu, Kimihiro
Mogi, Akira
Araki, Kenichiro
Harimoto, Norifumi
Shirabe, Ken
Kaira, Kyoichi
author_sort Tsukagoshi, Mariko
collection PubMed
description Nivolumab, a monoclonal antibody targeting programmed cell death-1, significantly prolongs survival for patients with advanced non-small-cell lung cancer (NSCLC). However, little is known about the value of predictive biomarkers. Hence, we investigated the impact of skeletal muscle (SM) mass loss on clinical outcomes in NSCLC patients undergoing nivolumab treatment. Thirty patients with histologically confirmed NSCLC treated with nivolumab were included in this study. Computed tomography was used to determine SM loss based on the SM index (SMI). The SMI is the cross-sectional area of the bilateral psoas muscles at the third lumbar vertebra, divided by height squared. The cut-off values were defined as 6.36 cm(2)/m(2) for men and 3.92 cm(2)/m(2) for women. Among the 30 patients, 13 (43%) had SM loss. There was no significant association between SM loss and immune-related adverse events. The SM loss group had undergone significantly more prior chemotherapy cycles (P = .04). SM loss was significantly associated with fewer nivolumab cycles (P = .01). No patients in the SM loss group achieved a partial response. Patients with SM loss had a significantly shorter progression-free survival period (P = .008) and median overall survival than those with normal SM mass (10 vs 25 months, respectively, P = .03). SM loss was an independent prognostic factor of poor survival. In conclusion, SM loss may be a predictive factor of poor outcomes in NSCLS patients undergoing nivolumab therapy.
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spelling pubmed-70350542020-03-10 Skeletal muscle mass predicts the outcome of nivolumab treatment for non-small cell lung cancer Tsukagoshi, Mariko Yokobori, Takehiko Yajima, Toshiki Maeno, Toshitaka Shimizu, Kimihiro Mogi, Akira Araki, Kenichiro Harimoto, Norifumi Shirabe, Ken Kaira, Kyoichi Medicine (Baltimore) 5700 Nivolumab, a monoclonal antibody targeting programmed cell death-1, significantly prolongs survival for patients with advanced non-small-cell lung cancer (NSCLC). However, little is known about the value of predictive biomarkers. Hence, we investigated the impact of skeletal muscle (SM) mass loss on clinical outcomes in NSCLC patients undergoing nivolumab treatment. Thirty patients with histologically confirmed NSCLC treated with nivolumab were included in this study. Computed tomography was used to determine SM loss based on the SM index (SMI). The SMI is the cross-sectional area of the bilateral psoas muscles at the third lumbar vertebra, divided by height squared. The cut-off values were defined as 6.36 cm(2)/m(2) for men and 3.92 cm(2)/m(2) for women. Among the 30 patients, 13 (43%) had SM loss. There was no significant association between SM loss and immune-related adverse events. The SM loss group had undergone significantly more prior chemotherapy cycles (P = .04). SM loss was significantly associated with fewer nivolumab cycles (P = .01). No patients in the SM loss group achieved a partial response. Patients with SM loss had a significantly shorter progression-free survival period (P = .008) and median overall survival than those with normal SM mass (10 vs 25 months, respectively, P = .03). SM loss was an independent prognostic factor of poor survival. In conclusion, SM loss may be a predictive factor of poor outcomes in NSCLS patients undergoing nivolumab therapy. Wolters Kluwer Health 2020-02-14 /pmc/articles/PMC7035054/ /pubmed/32049805 http://dx.doi.org/10.1097/MD.0000000000019059 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 5700
Tsukagoshi, Mariko
Yokobori, Takehiko
Yajima, Toshiki
Maeno, Toshitaka
Shimizu, Kimihiro
Mogi, Akira
Araki, Kenichiro
Harimoto, Norifumi
Shirabe, Ken
Kaira, Kyoichi
Skeletal muscle mass predicts the outcome of nivolumab treatment for non-small cell lung cancer
title Skeletal muscle mass predicts the outcome of nivolumab treatment for non-small cell lung cancer
title_full Skeletal muscle mass predicts the outcome of nivolumab treatment for non-small cell lung cancer
title_fullStr Skeletal muscle mass predicts the outcome of nivolumab treatment for non-small cell lung cancer
title_full_unstemmed Skeletal muscle mass predicts the outcome of nivolumab treatment for non-small cell lung cancer
title_short Skeletal muscle mass predicts the outcome of nivolumab treatment for non-small cell lung cancer
title_sort skeletal muscle mass predicts the outcome of nivolumab treatment for non-small cell lung cancer
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035054/
https://www.ncbi.nlm.nih.gov/pubmed/32049805
http://dx.doi.org/10.1097/MD.0000000000019059
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