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A prospective cohort study on the safety of checkpoint inhibitors in older cancer patients – the ELDERS study

OBJECTIVE: Older cancer patients are underrepresented in the pivotal trials of checkpoint inhibitors (CPIs). This study aimed to investigate the impact of an ageing immune system on CPI-related toxicity and provide evidence for the role of geriatric assessments with CPI. METHODS: The ELDERS study is...

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Autores principales: Gomes, F., Lorigan, P., Woolley, S., Foden, P., Burns, K., Yorke, J., Blackhall, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844568/
https://www.ncbi.nlm.nih.gov/pubmed/33516147
http://dx.doi.org/10.1016/j.esmoop.2020.100042
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author Gomes, F.
Lorigan, P.
Woolley, S.
Foden, P.
Burns, K.
Yorke, J.
Blackhall, F.
author_facet Gomes, F.
Lorigan, P.
Woolley, S.
Foden, P.
Burns, K.
Yorke, J.
Blackhall, F.
author_sort Gomes, F.
collection PubMed
description OBJECTIVE: Older cancer patients are underrepresented in the pivotal trials of checkpoint inhibitors (CPIs). This study aimed to investigate the impact of an ageing immune system on CPI-related toxicity and provide evidence for the role of geriatric assessments with CPI. METHODS: The ELDERS study is a prospective observational study with two cohorts: older (70+ years of age) and younger (<70 years of age). Patients with advanced/metastatic non-small-cell lung cancer or melanoma starting single-agent CPI were eligible. The older cohort was assessed for frailty with Geriatric-8 (G8) screening, which when positive (<15 points) was followed by a holistic set of geriatric assessments. Primary endpoint was the incidence of grade 3-5 immune-related adverse events (irAEs). RESULTS: One hundred and forty patients were enrolled with 43% being pretreated and pembrolizumab represented 92% of treatments on study. The older cohort had a significantly higher comorbidity burden (P < 0.001) and polypharmacy (P = 0.004). While 50% of older patients had a positive G8 screening, 60% on this frail subgroup had a performance status score of 0 or 1. There was no significant difference in the incidence of irAEs grade 3-5 between older and younger cohorts (18.6% versus 12.9%; odds ratio 1.55, confidence interval 95% 0.61-3.89; P = 0.353). Exposure to systemic steroids due to irAEs was numerically longer for older patients (22 versus 8 weeks; P = 0.208). A positive G8 screening predicted hospital admissions (P = 0.031) and risk of death (P = 0.01). CONCLUSIONS: The use of CPI in older patients was not associated with more high-grade toxicity. The G8 screening identified a subgroup with higher risk of AEs and its implementation should be considered in the context of CPI.
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spelling pubmed-78445682021-02-04 A prospective cohort study on the safety of checkpoint inhibitors in older cancer patients – the ELDERS study Gomes, F. Lorigan, P. Woolley, S. Foden, P. Burns, K. Yorke, J. Blackhall, F. ESMO Open Original Research OBJECTIVE: Older cancer patients are underrepresented in the pivotal trials of checkpoint inhibitors (CPIs). This study aimed to investigate the impact of an ageing immune system on CPI-related toxicity and provide evidence for the role of geriatric assessments with CPI. METHODS: The ELDERS study is a prospective observational study with two cohorts: older (70+ years of age) and younger (<70 years of age). Patients with advanced/metastatic non-small-cell lung cancer or melanoma starting single-agent CPI were eligible. The older cohort was assessed for frailty with Geriatric-8 (G8) screening, which when positive (<15 points) was followed by a holistic set of geriatric assessments. Primary endpoint was the incidence of grade 3-5 immune-related adverse events (irAEs). RESULTS: One hundred and forty patients were enrolled with 43% being pretreated and pembrolizumab represented 92% of treatments on study. The older cohort had a significantly higher comorbidity burden (P < 0.001) and polypharmacy (P = 0.004). While 50% of older patients had a positive G8 screening, 60% on this frail subgroup had a performance status score of 0 or 1. There was no significant difference in the incidence of irAEs grade 3-5 between older and younger cohorts (18.6% versus 12.9%; odds ratio 1.55, confidence interval 95% 0.61-3.89; P = 0.353). Exposure to systemic steroids due to irAEs was numerically longer for older patients (22 versus 8 weeks; P = 0.208). A positive G8 screening predicted hospital admissions (P = 0.031) and risk of death (P = 0.01). CONCLUSIONS: The use of CPI in older patients was not associated with more high-grade toxicity. The G8 screening identified a subgroup with higher risk of AEs and its implementation should be considered in the context of CPI. Elsevier 2021-01-27 /pmc/articles/PMC7844568/ /pubmed/33516147 http://dx.doi.org/10.1016/j.esmoop.2020.100042 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Gomes, F.
Lorigan, P.
Woolley, S.
Foden, P.
Burns, K.
Yorke, J.
Blackhall, F.
A prospective cohort study on the safety of checkpoint inhibitors in older cancer patients – the ELDERS study
title A prospective cohort study on the safety of checkpoint inhibitors in older cancer patients – the ELDERS study
title_full A prospective cohort study on the safety of checkpoint inhibitors in older cancer patients – the ELDERS study
title_fullStr A prospective cohort study on the safety of checkpoint inhibitors in older cancer patients – the ELDERS study
title_full_unstemmed A prospective cohort study on the safety of checkpoint inhibitors in older cancer patients – the ELDERS study
title_short A prospective cohort study on the safety of checkpoint inhibitors in older cancer patients – the ELDERS study
title_sort prospective cohort study on the safety of checkpoint inhibitors in older cancer patients – the elders study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844568/
https://www.ncbi.nlm.nih.gov/pubmed/33516147
http://dx.doi.org/10.1016/j.esmoop.2020.100042
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