Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/201424
Title: Sex differences on multikinase inhibitors toxicity in patients with advanced gastroenteropancreatic neuroendocrine tumours
Author: Hernando, Jorge
Roca Herrera, Maria
García Álvarez, Alejandro
Raymond, Eric
Ruszniewski, Philippe
Kulke, Matthew H.
Grande, Enrique
García Carbonero, Rocío
Castellano, Daniel
Salazar, Ramón
Ibrahim, Toni
Teulé Vega, Àlex
Alonso, Vicente
Fazio, Nicola
Valle, Juan W.
Tafuto, Salvatore
Carmona, Ana
Navarro, Victor
Capdevila, Jaume
Keywords: Neuroendocrinologia
Tumors
Factors sexuals en les malalties
Neuroendocrinology
Tumors
Sex factors in disease
Issue Date: 1-Jul-2023
Publisher: Elsevier BV
Abstract: Purpose: There is an increasing interest in the role of sex and gender in cancer pa-tients. The impact of sex differences in oncological systemic therapies is still unknown, and there is a lack of evidence specially in uncommon neoplasms like neuroendocrine tumours (NET). In the present study, we combine the differential toxicities by sex in five published clinical trials with multikinase inhibitors (MKI) in gastroenteropancreatic (GEP) NET.Methods: We performed a pooled univariate analysis of reported toxicity in patients treated in five phase 2 and phase 3 clinical trials with MKI in the GEP NET setting: sunitinib (SU11248, SUN1111), Pazopanib (PAZONET), sorafenib-bevacizumab (GETNE0801) and Lenvatinib (TALENT). Differential toxicities between male and female patients were evaluated considering relationship with study drug and different weights of each trial by random effect adjustment.Results: We found nine toxicities which were more frequent in female patients (leukopenia, alopecia, vomiting, headache, bleeding, nausea, dysgeusia, neutrophil count decreased and dry mouth) and two toxicities being more frequent in male patients (Anal Symptoms and Insomnia). Asthenia and diarrhoea were the only severe (Grade 3-4) toxicities more frequent in female pa-tients.Conclusions: Sex-related differences in toxicity with the MKI treatment require targeted in-formation and individualised management of patients with NET. Differential reporting of toxicity should be promoted when clinical trials are published.(c) 2023 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY -NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Note: Reproducció del document publicat a: https://doi.org/10.1016/j.ejca.2023.04.013
It is part of: European Journal of Cancer, 2023, vol. 188, p. 39-48
URI: http://hdl.handle.net/2445/201424
Related resource: https://doi.org/10.1016/j.ejca.2023.04.013
ISSN: 0959-8049
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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