Yasui Naoko, Adachi Nodoka, Kato Motohiro, Koh Katsuyoshi, Asanuma Satoshi, Sakata Hideaki, Hanada Ryoji
*Division of Pediatric Oncology, National Cancer Center Hospital, Tsukiji, Chuo-ku Departments of ‡Hematology/Oncology †Otolaryngology, Saitama Children's Medical Center, Saitama §Department of Speech, Language and Hearing Therapy, Faculty of Health Sciences, Mejiro University Clinic, Tokyo, Japan.
J Pediatr Hematol Oncol. 2014 May;36(4):e241-5. doi: 10.1097/MPH.0000000000000028.
Cisplatin is an effective chemotherapeutic agent against pediatric cancers; however, ototoxicity is a concern. This study describes the frequency, severity, and clinical course of hearing loss in Japanese pediatric patients treated with cisplatin-based multimodal therapy. A total of 55 children who received cisplatin-based therapy from 1983 to 2012 underwent audiologic evaluations. Data were analyzed to determine the onset, time-to-progression, and severity of hearing loss. Thirty-five patients, 12 of 16 older patients (4 y or older), and 23 of 39 younger patients (under 4 y), including 7 of 8 patients treated with cisplatin, carboplatin, and radiotherapy, developed hearing loss. Ten of 18 patients who received a cumulative cisplatin dose of <360 mg/m developed hearing loss at a minimum dose of 200 mg/m. Median time to onset after the last cisplatin dose was 71 days; 6 patients developed hearing loss after ≥2 years. Four patients required hearing aids, 6 patients developed progressive hearing loss with time, and 4 patients exhibited persistent hearing failure at low frequencies. Risk factors for acquired hearing loss and its severity may be associated with a combination of factors such as cisplatin and carboplatin therapy, radiotherapy, age at diagnosis, and genetic background. Our results suggested that all pediatric patients treated with cisplatin would have their hearing evaluated regularly, irrespective of the cumulative cisplatin dose as a suggestion, and that further prospective studies regarding ototoxicity including genetic polymorphisms analysis were required.
顺铂是一种治疗儿童癌症的有效化疗药物;然而,耳毒性是一个令人担忧的问题。本研究描述了接受基于顺铂的多模式治疗的日本儿童患者听力损失的频率、严重程度和临床过程。共有55名在1983年至2012年期间接受基于顺铂治疗的儿童接受了听力评估。对数据进行分析以确定听力损失的发作、进展时间和严重程度。35名患者出现听力损失,其中16名年龄较大的患者(4岁或以上)中有12名,39名年龄较小的患者(4岁以下)中有23名,包括8名接受顺铂、卡铂和放疗的患者中的7名。在累积顺铂剂量<360mg/m²的18名患者中,有10名在最低剂量200mg/m²时出现听力损失。最后一剂顺铂后听力损失发作的中位时间为71天;6名患者在≥2年后出现听力损失。4名患者需要佩戴助听器,6名患者随着时间的推移出现渐进性听力损失,4名患者在低频出现持续性听力障碍。获得性听力损失及其严重程度的危险因素可能与顺铂和卡铂治疗、放疗、诊断时的年龄和遗传背景等多种因素的组合有关。我们的结果表明,作为一项建议,所有接受顺铂治疗的儿童患者都应定期进行听力评估,无论顺铂的累积剂量如何,并且需要进行包括基因多态性分析在内的关于耳毒性的进一步前瞻性研究。