Concomitant Medications and Risk of Chemotherapy-Induced Peripheral Neuropathy.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
08 2019
Historique:
received: 17 07 2018
accepted: 16 10 2018
pubmed: 25 11 2018
medline: 1 8 2020
entrez: 25 11 2018
Statut: ppublish

Résumé

Peripheral neuropathy is the dose-limiting toxicity of many oncology drugs, including paclitaxel. There is large interindividual variability in the neuropathy, and several risk factors have been proposed; however, many have not been replicated. Here we present a comprehensive study aimed at identifying treatment and physiopathology-related paclitaxel-induced neuropathy risk factors in a large cohort of well-characterized patients. Analyses included 503 patients with breast or ovarian cancer who received paclitaxel treatment. Paclitaxel dose modifications caused by the neuropathy were extracted from medical records and patients self-reported neuropathy symptoms were collected. Multivariate logistic regression analyses were performed to identify concomitant medications and comorbidities associated with paclitaxel-induced neuropathy. Older patients had higher neuropathy: for each increase of 1 year of age, the risk of dose modifications and grade 3 neuropathy increased 4% and 5%, respectively. Cardiovascular drugs increased the risk of paclitaxel dose reductions (odds ratio [OR], 2.51; Baseline characteristics of the patients, including age and concomitant medications, could be used to identify individuals at high risk of neuropathy, personalizing chemotherapy treatment and reducing the risk of severe neuropathy. Peripheral neuropathy is a common adverse effect of many cancer drugs, including chemotherapeutics, targeted therapies, and immune checkpoint inhibitors. About 40% of survivors of cancer have functional deficits caused by this toxicity, some of them irreversible. Currently, there are no effective treatments to prevent or treat this neuropathy. This study, performed in a large cohort of well-characterized patients homogenously treated with paclitaxel, identified concomitant medications, comorbidities, and demographic factors associated with peripheral neuropathy. These factors could serve to identify patients at high risk of severe neuropathy for whom alternative non-neurotoxic alternatives may be considered.

Sections du résumé

BACKGROUND
Peripheral neuropathy is the dose-limiting toxicity of many oncology drugs, including paclitaxel. There is large interindividual variability in the neuropathy, and several risk factors have been proposed; however, many have not been replicated. Here we present a comprehensive study aimed at identifying treatment and physiopathology-related paclitaxel-induced neuropathy risk factors in a large cohort of well-characterized patients.
PATIENTS AND METHODS
Analyses included 503 patients with breast or ovarian cancer who received paclitaxel treatment. Paclitaxel dose modifications caused by the neuropathy were extracted from medical records and patients self-reported neuropathy symptoms were collected. Multivariate logistic regression analyses were performed to identify concomitant medications and comorbidities associated with paclitaxel-induced neuropathy.
RESULTS
Older patients had higher neuropathy: for each increase of 1 year of age, the risk of dose modifications and grade 3 neuropathy increased 4% and 5%, respectively. Cardiovascular drugs increased the risk of paclitaxel dose reductions (odds ratio [OR], 2.51;
CONCLUSION
Baseline characteristics of the patients, including age and concomitant medications, could be used to identify individuals at high risk of neuropathy, personalizing chemotherapy treatment and reducing the risk of severe neuropathy.
IMPLICATIONS FOR PRACTICE
Peripheral neuropathy is a common adverse effect of many cancer drugs, including chemotherapeutics, targeted therapies, and immune checkpoint inhibitors. About 40% of survivors of cancer have functional deficits caused by this toxicity, some of them irreversible. Currently, there are no effective treatments to prevent or treat this neuropathy. This study, performed in a large cohort of well-characterized patients homogenously treated with paclitaxel, identified concomitant medications, comorbidities, and demographic factors associated with peripheral neuropathy. These factors could serve to identify patients at high risk of severe neuropathy for whom alternative non-neurotoxic alternatives may be considered.

Identifiants

pubmed: 30470691
pii: theoncologist.2018-0418
doi: 10.1634/theoncologist.2018-0418
pmc: PMC6693699
doi:

Substances chimiques

Antineoplastic Agents, Phytogenic 0
Paclitaxel P88XT4IS4D

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e784-e792

Informations de copyright

© AlphaMed Press 2018.

Déclaration de conflit d'intérêts

Disclosures of potential conflicts of interest may be found at the end of this article.

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Auteurs

Lara Sánchez-Barroso (L)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Faculty of Biomedical and Health Sciences, Universidad Europea de Madrid, Madrid, Spain.

Maria Apellaniz-Ruiz (M)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.

Gerardo Gutiérrez-Gutiérrez (G)

Neurology Section, Hospital Universitario Infanta Sofía, Madrid, Spain.

María Santos (M)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.

Juan M Roldán-Romero (JM)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.

Maria Curras (M)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.

Laura Remacha (L)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.

Bruna Calsina (B)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.

Isabel Calvo (I)

Medical Oncology Department, Hospital Montepríncipe, Madrid, Spain.
Medical Oncology Department, Centro Integral Oncológico Clara Campal, Madrid, Spain.

María Sereno (M)

Medical Oncology Department, Hospital Universitario Infanta Sofía, Madrid, Spain.

María Merino (M)

Medical Oncology Department, Hospital Universitario Infanta Sofía, Madrid, Spain.

Jesús García-Donas (J)

Genitourinary Tumors Programme, Centro Integral Oncológico Clara Campal, Madrid, Spain.

Beatriz Castelo (B)

Medical Oncology Department, Hospital Universitario La Paz, Madrid, Spain.

Eva Guerra (E)

Medical Oncology Department, Hospital Universitario Ramon y Cajal, Madrid, Spain.

Rocio Letón (R)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.

Cristina Montero-Conde (C)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.

Alberto Cascón (A)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Madrid, Spain.

Lucía Inglada-Pérez (L)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Madrid, Spain.

Mercedes Robledo (M)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Madrid, Spain.

Cristina Rodríguez-Antona (C)

Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain crodriguez@cnio.es.
ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Madrid, Spain.

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Classifications MeSH