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Renin-Angiotensin-System Inhibitors for the Prevention of Chemotherapy-Induced Peripheral Neuropathy: OncoToxSRA, a Preliminary Cohort Study

Chemotherapy-induced peripheral neuropathy (CIPN) is a frequent and dose-limiting adverse side effect of treatment. CIPN affects the oncological prognosis of patients, as well as their quality of life. To date, no specific pharmacological therapy has demonstrated effectiveness in preventing CIPN. Ac...

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Autores principales: Frachet, Simon, Danigo, Aurore, Labriffe, Marc, Bessaguet, Flavien, Quinchard, Bianca, Deny, Nicolas, Baffert, Kim-Arthur, Deluche, Elise, Sturtz, Franck, Demiot, Claire, Magy, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9144468/
https://www.ncbi.nlm.nih.gov/pubmed/35629066
http://dx.doi.org/10.3390/jcm11102939
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author Frachet, Simon
Danigo, Aurore
Labriffe, Marc
Bessaguet, Flavien
Quinchard, Bianca
Deny, Nicolas
Baffert, Kim-Arthur
Deluche, Elise
Sturtz, Franck
Demiot, Claire
Magy, Laurent
author_facet Frachet, Simon
Danigo, Aurore
Labriffe, Marc
Bessaguet, Flavien
Quinchard, Bianca
Deny, Nicolas
Baffert, Kim-Arthur
Deluche, Elise
Sturtz, Franck
Demiot, Claire
Magy, Laurent
author_sort Frachet, Simon
collection PubMed
description Chemotherapy-induced peripheral neuropathy (CIPN) is a frequent and dose-limiting adverse side effect of treatment. CIPN affects the oncological prognosis of patients, as well as their quality of life. To date, no specific pharmacological therapy has demonstrated effectiveness in preventing CIPN. Accumulating preclinical evidence suggests that renin-angiotensin system (RAS) inhibitors may have neuroprotective effects. One hundred and twenty patients were included in this observational study and were followed from the beginning of their neurotoxic chemotherapy schedule until their final assessment, at least one month after its cessation. The National Cancer Institute’s common toxicity criteria 4.0 (NCI-CTC 4.0) were used to grade the severity of adverse events. Follow-ups also included electrochemical skin conductance and scales for pain, quality of life and disability. Among patients receiving a platinum-based regimen, the mean grade of sensory neuropathy (NCI-CTC 4.0) was significantly lower in the RAS inhibitor group after the end of their anticancer treatment schedule. Because of the observational design of the study, patients in the RAS inhibitor group cumulated comorbidities at risk of developing CIPN. Randomized controlled trials in platinum-based regimens would be worth conducting in the future to confirm the neuroprotective potential of RAS inhibitors during chemotherapy.
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spelling pubmed-91444682022-05-29 Renin-Angiotensin-System Inhibitors for the Prevention of Chemotherapy-Induced Peripheral Neuropathy: OncoToxSRA, a Preliminary Cohort Study Frachet, Simon Danigo, Aurore Labriffe, Marc Bessaguet, Flavien Quinchard, Bianca Deny, Nicolas Baffert, Kim-Arthur Deluche, Elise Sturtz, Franck Demiot, Claire Magy, Laurent J Clin Med Article Chemotherapy-induced peripheral neuropathy (CIPN) is a frequent and dose-limiting adverse side effect of treatment. CIPN affects the oncological prognosis of patients, as well as their quality of life. To date, no specific pharmacological therapy has demonstrated effectiveness in preventing CIPN. Accumulating preclinical evidence suggests that renin-angiotensin system (RAS) inhibitors may have neuroprotective effects. One hundred and twenty patients were included in this observational study and were followed from the beginning of their neurotoxic chemotherapy schedule until their final assessment, at least one month after its cessation. The National Cancer Institute’s common toxicity criteria 4.0 (NCI-CTC 4.0) were used to grade the severity of adverse events. Follow-ups also included electrochemical skin conductance and scales for pain, quality of life and disability. Among patients receiving a platinum-based regimen, the mean grade of sensory neuropathy (NCI-CTC 4.0) was significantly lower in the RAS inhibitor group after the end of their anticancer treatment schedule. Because of the observational design of the study, patients in the RAS inhibitor group cumulated comorbidities at risk of developing CIPN. Randomized controlled trials in platinum-based regimens would be worth conducting in the future to confirm the neuroprotective potential of RAS inhibitors during chemotherapy. MDPI 2022-05-23 /pmc/articles/PMC9144468/ /pubmed/35629066 http://dx.doi.org/10.3390/jcm11102939 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Frachet, Simon
Danigo, Aurore
Labriffe, Marc
Bessaguet, Flavien
Quinchard, Bianca
Deny, Nicolas
Baffert, Kim-Arthur
Deluche, Elise
Sturtz, Franck
Demiot, Claire
Magy, Laurent
Renin-Angiotensin-System Inhibitors for the Prevention of Chemotherapy-Induced Peripheral Neuropathy: OncoToxSRA, a Preliminary Cohort Study
title Renin-Angiotensin-System Inhibitors for the Prevention of Chemotherapy-Induced Peripheral Neuropathy: OncoToxSRA, a Preliminary Cohort Study
title_full Renin-Angiotensin-System Inhibitors for the Prevention of Chemotherapy-Induced Peripheral Neuropathy: OncoToxSRA, a Preliminary Cohort Study
title_fullStr Renin-Angiotensin-System Inhibitors for the Prevention of Chemotherapy-Induced Peripheral Neuropathy: OncoToxSRA, a Preliminary Cohort Study
title_full_unstemmed Renin-Angiotensin-System Inhibitors for the Prevention of Chemotherapy-Induced Peripheral Neuropathy: OncoToxSRA, a Preliminary Cohort Study
title_short Renin-Angiotensin-System Inhibitors for the Prevention of Chemotherapy-Induced Peripheral Neuropathy: OncoToxSRA, a Preliminary Cohort Study
title_sort renin-angiotensin-system inhibitors for the prevention of chemotherapy-induced peripheral neuropathy: oncotoxsra, a preliminary cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9144468/
https://www.ncbi.nlm.nih.gov/pubmed/35629066
http://dx.doi.org/10.3390/jcm11102939
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