Study Identifies Factors Associated With Platinum-induced Ototoxicity in Pediatric Cancer Survivors
Researchers sought to assess ototoxicity frequency in a cross-sectional cohort of pediatric cancer survivors.
Treatment with a higher total cumulative dose of cisplatin, young age, and concomitant furosemide administration are associated with an increased risk of ototoxicity in childhood cancer survivors treated with platinum-based therapy, according to a study published in the European Journal of Cancer.1
Platinum-containing chemotherapeutic agents are efficacious for the treatment of various pediatric malignancies; however, these drugs, particularly cisplatin, can induce ototoxicity.
Because large cohort data on the ototoxicity of childhood cancer survivors who received platinum agents without cranial irradiation are limited, researchers sought to assess the frequency of, and factors associated with, ototoxicity in a multicenter, cross sectional cohort of pediatric cancer survivors.
For the study, investigators analyzed treatment data and audiograms from 451 childhood cancer survivors who received platinum agents but not cranial irradiation.
Results showed that 42% of patients overall reported ototoxicity. Researchers observed ototoxicity in 45% of cisplatin-treated patients, in 17% of carboplatin-treated patients, and in 75% of those who received both agents.
After adjusting for confounding factors, the study demonstrated that younger age at diagnosis (odds ratio [OR], 0.6; 95% CI, 0.5-0.6 per 5 year increase), higher total cumulative cisplatin dose (OR, 1.2; 95% CI, 1.2-1.5 per 100 mg/m2 increase), and concomitant treatment with furosemide (OR, 2.3; 95% CI, 1.4-3.9) were significantly associated with an increased risk for developing ototoxicity.
Future studies are warranted to confirm the additive risk of simultaneous administration of furosemide on the development of ototoxicity.
1. Clemens E, de Vries AC, Pluijm SF, et al. Determinants of ototoxicity in 451 platinum-treated Dutch survivors of childhood cancer: A DCOG late-effects study. Eur J Cancer. 2016;69:77-85.