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Pharmacogenet Genomics ; 26(5): 243-7, 2016 May.
Artigo em Inglês | MEDLINE | ID: mdl-26928270

RESUMO

OBJECTIVE: Irreversible hearing loss is a frequent side effect of the chemotherapeutic agent cisplatin and shows considerable interpatient variability. The variant rs1872328 in the ACYP2 gene was recently identified as a risk factor for the development of cisplatin-induced ototoxicity in children with brain tumors. We aimed to replicate this finding in patients with osteosarcoma. METHODS: An independent cohort of 156 patients was genotyped for the rs1872328 variant and evaluated for the presence of cisplatin-induced ototoxicity. RESULTS: A significant association was observed between carriership of the A allele and cisplatin-induced ototoxicity after the end of treatment (P=0.027). CONCLUSION: This is the first study replicating the association of ACYP2 variant rs1872328 with cisplatin-induced ototoxicity in patients with osteosarcoma who did not receive potentially ototoxic cranial irradiation. Hence, the ACYP2 variant should be considered a predictive pharmacogenetic marker for hearing loss, which may be used to guide therapies for patients treated with cisplatin.


Assuntos
Hidrolases Anidrido Ácido/genética , Antineoplásicos/efeitos adversos , Neoplasias Ósseas/tratamento farmacológico , Cisplatino/efeitos adversos , Perda Auditiva/induzido quimicamente , Osteossarcoma/tratamento farmacológico , Polimorfismo de Nucleotídeo Único , Adolescente , Adulto , Antineoplásicos/uso terapêutico , Neoplasias Ósseas/genética , Criança , Cisplatino/uso terapêutico , Feminino , Perda Auditiva/genética , Humanos , Masculino , Osteossarcoma/genética , Adulto Jovem , Acilfosfatase
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