Recommendations on the use of azole antifungals in hematology-oncology patients
- PMID: 37017117
- PMCID: PMC10238801
- DOI: 10.37201/req/013.2023
Recommendations on the use of azole antifungals in hematology-oncology patients
Abstract
The administration of antifungals for therapeutic and, especially, prophylactic purposes is virtually a constant in patients requiring hematology-oncology treatment. Any attempt to prevent or treat Aspergillus or Mucor infections requires the administration of some drugs in the azole group, which include voriconazole, posaconazole and isavuconazole, noted for their activity against these pathogens. One very relevant aspect is the potential risk of interaction when associated with one of the antineoplastic drugs used to treat hematologic tumors, with serious complications. In this regard, acalabrutinib, bortezomib, bosutinib, carfilzomib, cyclophosphamide, cyclosporine A, dasatinib, duvelisib, gilteritinib, glasdegib, ibrutinib, imatinib, nilotinib, ponatinib, prednisone, ruxolitinib, tacrolimus, all-transretinoic acid, arsenic trioxide, venetoclax, or any of the vinca alkaloids, are very clear examples of risk, in some cases because their clearance is reduced and in others because of increased risk of QTc prolongation, which is particularly evident when the drug of choice is voriconazole or posaconazole.
La administración de antifúngicos con fines terapéuticos y especialmente, profilácticos es casi un constante en el paciente que precisa tratamiento oncohematológico. El intento de evitar o de tratar infecciones por Aspergillus o por Mucor exige la administración de algunos fármacos pertenecientes al grupo de los azoles, entre los que destacan por su actividad frente a estos patógenos, voriconazol, posaconazol e isavuconazol. Un aspecto de gran importancia es el riesgo potencial de interacciones cuando se asocian a alguno de los fármacos antineoplásico utilizados en el tratamiento de los tumores hematológicos, dando lugar a graves complicaciones. En este sentido, acalabrutinib, bortezomid, bosutinib, carfizolid, ciclofosfamida, ciscloporina A, dasatinib, duvelisib, gilteritinib, glasdegib, ibrutinib, imatinib, nilotinib, ponatinib, prednisona, ruxolitinib, tacrolimus, trans-retinoico, trióxido de Arsenio, venetoclax, o cualquiera de los alcaloides de la vinca, representan ejemplos muy evidentes de riesgos en unos casos porque su aclaramiento resulta reducido, en otros porque que se potencia el riesgo de prolongación del QTc, especialmente evidentes cuando el fármaco elegido es voriconazol o posaconazol.
Keywords: Azoles; drug-drug interactions; hematology patients.
©The Author 2023. Published by Sociedad Española de Quimioterapia. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)(https://creativecommons.org/licenses/by-nc/4.0/).
Conflict of interest statement
JRA has received honoraria for talks on behalf of Pfizer, GSK, Menarini, Shionogi and MSD.
JB has received honoraria for talks on behalf of Pfizer, Gilead, Shionogi, and MSD.
LV has received honoraria for talks on behalf of Astellas, Gilead, MSD, Pfizer, Janssen, Astra Zeneca and GSK, and has received honoraria for consulting from Astellas, Gilead, Pfizer, and GSK
MK has received honoraria for lectures and consulting from Gilead, Jazz, Pfizer
LY has received honoraria for talks on behalf of Janssen, Abbvie, Gilead-Kite, Roche, Novartis, MSD, Pfizer, AstraZeneca, Novartis, Beigene, Lilly, has received honoraria for advisory board from Janssen, Abbvie, Gilead-Kite, Roche, Jazz, Sandoz, Celgene, MSD, Pfizer, AstraZeneca, BeiGene, Lilly, Alexion, and research funds from Janssen
JMA has been a consultant to and on the speakers bureau for Pfizer, Gilead, Merck Sharp and Dohme, and United Medical-Biotoscana.
IRC has received honoraria for talks on behalf of MSD, gilead, Astra Zeneca, Pfizer, GSK, Jansenn, and BMS and has received honoraria for advisory board from Pfizer, GSK, Astra Zeneca, and Gilead
JF has participated in scientific events or received remuneration in the form of research support or oral presentations from Merck, Pfizer, Gilead, MSD, Astellas, Novartis, and Roche.
MS has participated in advisory board or received honoraria for talks on behalf of Gilead, Menarini, MSD, Pfizer and Shionogi
CG received research support from Merck and Pfizer and honoraria for talks sponsored by Merck, Gilead, and Pfizer, and Shionogi.
CG-V has received honoraria for talks on behalf of Gilead Science, MSD, Novartis, Pfizer, Janssen, Menarini, GSK and Sanofi, as well as a grant from Gilead Science, Pfizer, and GSK.
PG-S has participated in advisory board or received honoraria for talks on behalf of Pfizer, MSD, Gilead, Astellas, and Abbvie.
CDG has participated in advisory board or received honoraria for talks on behalf of MSD, Pfizer, Shionogi, Menarini, Gilead, Janssen, ViiV, Roche and GSK
Rest of authors have no conflict of interest.
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