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Early cisplatin induced ototoxicity profile may predict the need for hearing support in children with medulloblastoma

机译:早期顺铂诱导的耳毒性谱可能预示了髓母细胞瘤儿童需要听力支持

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Background: Cisplatin (CDDP) ototoxicity is a significant side effect of the current treatment of medulloblastoma (MB). Cumulative dose of CDDP and age are recognized risk factors for hearing loss, but inter-individual susceptibility limits our ability to identify patients at risk for hearing loss. We describe the kinetics of early audiometric changes during therapy and identify profiles associated with a higher risk of needing hearing aids. Procedure: Serial audiometric evaluations were performed during and after completion of therapy in children with average risk (AR) and high-risk (HR) MB. Each audiogram was scored according to five grading systems. Variations of pure tone thresholds were analyzed at each frequency for each consecutive audiogram. CDDP dose modifications and hearing outcome were recorded. Results: A total of 258 audiograms from 35 patients (22 AR, 13 HR) were analyzed. Eighteen AR patients (81.3%) required dose reduction and the median cumulative dose of CDDP administered was 412.5mg/m2 (150-600), corresponding to 68% of the intended dose. Three HR patients (23.0%) required dose reduction. At a median follow-up of 67 months (11-117), nine patients (25.7%) required hearing support: After two cycles of CDDP (150mg/m2), the average hearing loss at 8,000Hz was twice higher in the group that eventually required hearing support. Conclusion: Early alteration of high-frequency thresholds may help identify individuals who will require hearing support. In the MB population, alternative strategies should be developed to limit the cumulative dose of CDDP to prevent significant ototoxicity.
机译:背景:顺铂(CDDP)的耳毒性是目前治疗髓母细胞瘤(MB)的重要副作用。 CDDP的累积剂量和年龄是公认的听力损失的危险因素,但是个体间的易感性限制了我们识别有听力损失风险的患者的能力。我们描述了治疗期间早期听力测验变化的动力学,并确定了与需要助听器的较高风险相关的配置文件。程序:对平均风险(AR)和高风险(HR)MB的儿童,在治疗过程中和治疗结束后进行串行测听评估。每个听力图根据五个评分系统评分。对于每个连续的听力图,在每个频率上分析纯音阈值的变化。记录CDDP剂量变化和听力结果。结果:分析了来自35位患者(22 AR,13 HR)的258个听力图。 18名AR患者(81.3%)需要降低剂量,并且CDDP的中位累积剂量为412.5mg / m2(150-600),相当于预期剂量的68%。三名HR患者(23.0%)需要减少剂量。在67个月的中位随访(11-117)中,有9名患者(25.7%)需要听力支持:经过两个周期的CDDP(150mg / m2),该组在8,000Hz处的平均听力损失要高出两倍。最终需要听力支持。结论:高频阈值的早期改变可能有助于识别需要听力支持的个体。在MB人群中,应制定替代策略以限制CDDP的累积剂量,以防止明显的耳毒性。

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