Cargando…
Predictive Value of Skeletal Muscle Mass in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma Patients Treated With Immune Checkpoint Inhibitors
BACKGROUND: Reduced muscle mass has been associated with increased treatment complications in several tumor types. We evaluated the impact of skeletal muscle index (SMI) on prognosis and immune-related adverse events (IrAEs) in a cohort of recurrent/metastatic (R/M) head and neck squamous cell carci...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267860/ https://www.ncbi.nlm.nih.gov/pubmed/34249760 http://dx.doi.org/10.3389/fonc.2021.699668 |
_version_ | 1783720235873861632 |
---|---|
author | Arribas, Lorena Plana, Maria Taberna, Miren Sospedra, Maria Vilariño, Noelia Oliva, Marc Pallarés, Natalia González Tampán, Ana Regina Del Rio, Luis Miguel Mesia, Ricard Baracos, Vickie |
author_facet | Arribas, Lorena Plana, Maria Taberna, Miren Sospedra, Maria Vilariño, Noelia Oliva, Marc Pallarés, Natalia González Tampán, Ana Regina Del Rio, Luis Miguel Mesia, Ricard Baracos, Vickie |
author_sort | Arribas, Lorena |
collection | PubMed |
description | BACKGROUND: Reduced muscle mass has been associated with increased treatment complications in several tumor types. We evaluated the impact of skeletal muscle index (SMI) on prognosis and immune-related adverse events (IrAEs) in a cohort of recurrent/metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) treated with immune checkpoints inhibitors (ICI). METHODS: A single-institutional, retrospective study was performed including 61 consecutive patients of R/M HNSCC diagnosed between July 2015 and December 2018. SMI was quantified using a CT scan at L3 to evaluate body composition. Median baseline SMI was used to dichotomize patients in low and high SMI. Kaplan-Meier estimations were used to detect overall survival (OS) and progression-free survival (PFS). Toxicity was recorded using Common Terminology Criteria for Adverse Event v4.3. RESULTS: Patients were 52 men (85.2%) with mean of age 57.7 years (SD 9.62), mainly oral cavity (n = 21; 34.4%). Low SMI was an independent factor for OS in the univariate (HR, 2.06; 95% CI, 1.14–3.73, p = 0.017) and multivariate Cox analyses (HR, 2.99; 95% CI, 1.29–6.94; p = 0.011). PFS was also reduced in patients with low SMI (PFS HR, 1.84; 95% CI, 1.08–3.12; p = 0.025). IrAEs occurred in 29 (47.5%) patients. There was no association between low SMI and IrAEs at any grade (OR, 0.56; 95% CI, 0.20–1.54; p = 0.261). However, grades 3 to 4 IrAEs were developed in seven patients of whom three had low SMI. CONCLUSIONS: Low SMI before ICI treatment in R/M HNSCC patients had a negative impact on OS and PFS. Further prospective research is needed to confirm the role of body composition as a predictive biomarker in ICI treatment. |
format | Online Article Text |
id | pubmed-8267860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82678602021-07-10 Predictive Value of Skeletal Muscle Mass in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma Patients Treated With Immune Checkpoint Inhibitors Arribas, Lorena Plana, Maria Taberna, Miren Sospedra, Maria Vilariño, Noelia Oliva, Marc Pallarés, Natalia González Tampán, Ana Regina Del Rio, Luis Miguel Mesia, Ricard Baracos, Vickie Front Oncol Oncology BACKGROUND: Reduced muscle mass has been associated with increased treatment complications in several tumor types. We evaluated the impact of skeletal muscle index (SMI) on prognosis and immune-related adverse events (IrAEs) in a cohort of recurrent/metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) treated with immune checkpoints inhibitors (ICI). METHODS: A single-institutional, retrospective study was performed including 61 consecutive patients of R/M HNSCC diagnosed between July 2015 and December 2018. SMI was quantified using a CT scan at L3 to evaluate body composition. Median baseline SMI was used to dichotomize patients in low and high SMI. Kaplan-Meier estimations were used to detect overall survival (OS) and progression-free survival (PFS). Toxicity was recorded using Common Terminology Criteria for Adverse Event v4.3. RESULTS: Patients were 52 men (85.2%) with mean of age 57.7 years (SD 9.62), mainly oral cavity (n = 21; 34.4%). Low SMI was an independent factor for OS in the univariate (HR, 2.06; 95% CI, 1.14–3.73, p = 0.017) and multivariate Cox analyses (HR, 2.99; 95% CI, 1.29–6.94; p = 0.011). PFS was also reduced in patients with low SMI (PFS HR, 1.84; 95% CI, 1.08–3.12; p = 0.025). IrAEs occurred in 29 (47.5%) patients. There was no association between low SMI and IrAEs at any grade (OR, 0.56; 95% CI, 0.20–1.54; p = 0.261). However, grades 3 to 4 IrAEs were developed in seven patients of whom three had low SMI. CONCLUSIONS: Low SMI before ICI treatment in R/M HNSCC patients had a negative impact on OS and PFS. Further prospective research is needed to confirm the role of body composition as a predictive biomarker in ICI treatment. Frontiers Media S.A. 2021-06-25 /pmc/articles/PMC8267860/ /pubmed/34249760 http://dx.doi.org/10.3389/fonc.2021.699668 Text en Copyright © 2021 Arribas, Plana, Taberna, Sospedra, Vilariño, Oliva, Pallarés, González Tampán, Del Rio, Mesia and Baracos https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Arribas, Lorena Plana, Maria Taberna, Miren Sospedra, Maria Vilariño, Noelia Oliva, Marc Pallarés, Natalia González Tampán, Ana Regina Del Rio, Luis Miguel Mesia, Ricard Baracos, Vickie Predictive Value of Skeletal Muscle Mass in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma Patients Treated With Immune Checkpoint Inhibitors |
title | Predictive Value of Skeletal Muscle Mass in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma Patients Treated With Immune Checkpoint Inhibitors |
title_full | Predictive Value of Skeletal Muscle Mass in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma Patients Treated With Immune Checkpoint Inhibitors |
title_fullStr | Predictive Value of Skeletal Muscle Mass in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma Patients Treated With Immune Checkpoint Inhibitors |
title_full_unstemmed | Predictive Value of Skeletal Muscle Mass in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma Patients Treated With Immune Checkpoint Inhibitors |
title_short | Predictive Value of Skeletal Muscle Mass in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma Patients Treated With Immune Checkpoint Inhibitors |
title_sort | predictive value of skeletal muscle mass in recurrent/metastatic head and neck squamous cell carcinoma patients treated with immune checkpoint inhibitors |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267860/ https://www.ncbi.nlm.nih.gov/pubmed/34249760 http://dx.doi.org/10.3389/fonc.2021.699668 |
work_keys_str_mv | AT arribaslorena predictivevalueofskeletalmusclemassinrecurrentmetastaticheadandnecksquamouscellcarcinomapatientstreatedwithimmunecheckpointinhibitors AT planamaria predictivevalueofskeletalmusclemassinrecurrentmetastaticheadandnecksquamouscellcarcinomapatientstreatedwithimmunecheckpointinhibitors AT tabernamiren predictivevalueofskeletalmusclemassinrecurrentmetastaticheadandnecksquamouscellcarcinomapatientstreatedwithimmunecheckpointinhibitors AT sospedramaria predictivevalueofskeletalmusclemassinrecurrentmetastaticheadandnecksquamouscellcarcinomapatientstreatedwithimmunecheckpointinhibitors AT vilarinonoelia predictivevalueofskeletalmusclemassinrecurrentmetastaticheadandnecksquamouscellcarcinomapatientstreatedwithimmunecheckpointinhibitors AT olivamarc predictivevalueofskeletalmusclemassinrecurrentmetastaticheadandnecksquamouscellcarcinomapatientstreatedwithimmunecheckpointinhibitors AT pallaresnatalia predictivevalueofskeletalmusclemassinrecurrentmetastaticheadandnecksquamouscellcarcinomapatientstreatedwithimmunecheckpointinhibitors AT gonzaleztampananaregina predictivevalueofskeletalmusclemassinrecurrentmetastaticheadandnecksquamouscellcarcinomapatientstreatedwithimmunecheckpointinhibitors AT delrioluismiguel predictivevalueofskeletalmusclemassinrecurrentmetastaticheadandnecksquamouscellcarcinomapatientstreatedwithimmunecheckpointinhibitors AT mesiaricard predictivevalueofskeletalmusclemassinrecurrentmetastaticheadandnecksquamouscellcarcinomapatientstreatedwithimmunecheckpointinhibitors AT baracosvickie predictivevalueofskeletalmusclemassinrecurrentmetastaticheadandnecksquamouscellcarcinomapatientstreatedwithimmunecheckpointinhibitors |