Ingrith Crenguța Miron, Mirabela Alecsa, Ileana Ioniuc, Otilia Elena Frăsinariu, Raluca Olariu, Andreea Iațentiuc, Iustin Mihai Iațentiuc, Sebastian Romică Cozma, Oana Roxana Bitere-Popa, Luminița Mihaela Rădulescu, Magdalena Cuciureanu, Constantin Guma
Journal: International journal of molecular sciences 2025;26(10):
PMID: 40429930
There is significant inter-individual variability in the prevalence and severity of cisplatin-induced ototoxicity, which is greatly influenced by genetic and non-genetic factors that predispose the patient to the development of hearing loss. Currently, the focus should be on identifying patients who are more likely to develop ototoxicity based on genetic and non-genetic factors, as therapies to combat ototoxicity are limited or still under study. The severity of hearing loss and the time of its onset may be influenced by certain genetic polymorphisms or the dose administered, age, sex, diet, the administration of other drugs with ototoxic potential, and association with radiotherapy of the head and neck. Knowing the risk factors allows the doctor to manage each case in a personalized manner, preventing hearing damage, especially in the long term. With the help of PubMed and Scopus, we searched for relevant studies documenting the genetic and non-genetic risk in patients treated with cisplatin. This review article is a synthesis of the literature that points out the importance of these factors, encouraging genetic screening and improving quality of life in patients treated with cisplatin.
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