Cargando…

Colorectal Cancer Survivors Suffering From Sensory Chemotherapy-Induced Peripheral Neuropathy Are Not a Homogenous Group: Secondary Analysis of Patients’ Profiles With Oxaliplatin-Induced Peripheral Neuropathy

Oxaliplatin, a pivotal drug in the management of colorectal cancer, causes chemotherapy-induced peripheral neuropathy (CIPN) in a third of cancer survivors. Based on a previous cross-sectional study assessing oxaliplatin-related sensory CIPN in colorectal cancer survivors, a secondary analysis was d...

Descripción completa

Detalles Bibliográficos
Autores principales: Kerckhove, Nicolas, Selvy, Marie, Lambert, Céline, Gonneau, Coralie, Feydel, Gabrielle, Pétorin, Caroline, Vimal-Baguet, Agnès, Melnikov, Sergey, Kullab, Sharif, Hebbar, Mohamed, Bouché, Olivier, Slimano, Florian, Bourgeois, Vincent, Lebrun-Ly, Valérie, Thuillier, Frédéric, Mazard, Thibault, Tavan, David, Benmammar, Kheir Eddine, Monange, Brigitte, Ramdani, Mohamed, Péré-Vergé, Denis, Huet-Penz, Floriane, Bedjaoui, Ahmed, Genty, Florent, Leyronnas, Cécile, Busserolles, Jérôme, Trévis, Sophie, Pinon, Vincent, Pezet, Denis, Balayssac, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599933/
https://www.ncbi.nlm.nih.gov/pubmed/34803689
http://dx.doi.org/10.3389/fphar.2021.744085
Descripción
Sumario:Oxaliplatin, a pivotal drug in the management of colorectal cancer, causes chemotherapy-induced peripheral neuropathy (CIPN) in a third of cancer survivors. Based on a previous cross-sectional study assessing oxaliplatin-related sensory CIPN in colorectal cancer survivors, a secondary analysis was designed to explore the possibility that different clusters of patients may co-exist among a cohort of patients with oxaliplatin-related CIPN. Other objectives were to characterize these clusters considering CIPN severity, anxiety, depression, health-related quality of life (HRQOL), patients’ characteristics and oxaliplatin treatments. Among the 96 patients analyzed, three clusters were identified (cluster 1: 52, cluster 2: 34, and cluster 3: 10 patients). Clusters were significantly different according to CIPN severity and the proportion of neuropathic pain (cluster 1: low, cluster 2: intermediate, and cluster 3: high). Anxiety, depressive disorders and HRQOL alteration were lower in cluster 1 in comparison to clusters 2 and 3, but not different between clusters 2 and 3. This study underlines that patients with CIPN are not a homogenous group, and that CIPN severity is associated with psychological distress and a decline of HRQOL. Further studies are needed to explore the relation between clusters and CIPN management.