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儿童顺铂耳毒性的实用分级系统。

Practical grading system for evaluating cisplatin ototoxicity in children.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

J Clin Oncol. 2010 Apr 1;28(10):1788-95. doi: 10.1200/JCO.2009.24.4228. Epub 2010 Mar 1.

Abstract

PURPOSE

We present a new ototoxicity grading system that has clearly defined and frequency-specific audiometric criteria. The purpose of this study was to validate this grading system by assessing its correspondence to audiology treatment recommendations and comparing it with the currently utilized Common Terminology Criteria for Adverse Events (CTCAE).

PATIENTS AND METHODS

A retrospective chart review was conducted using audiologic, demographic, and clinical data from 134 children receiving 149 courses of chemotherapy consisting of cisplatin and/or carboplatin. Pure-tone audiograms were evaluated using both our proposed grading criteria and the CTCAE criteria. The resulting grades were then compared with charted audiologic interventions and a number of clinical parameters to assess the clinical validity of the grading scale.

RESULTS

Chang grade 2a or higher predicted audiologic intervention. Although both the Chang and CTCAE ototoxicity grades were significantly related to audiologist recommendations for assistive devices such as hearing aids and/or frequency modulated systems (P < .0001), the Chang scale was more specific, with the CTCAE scale diverging from clinical recommendation at higher grades. As expected, patients receiving cisplatin had more severe hearing loss with concurrent carboplatin administration, radiation therapy exposure, younger age, smaller body-surface area, longer treatment exposure, and more severe disease.

CONCLUSION

This grading system provides robust and clinically useful criteria to represent clinical hearing loss induced by ototoxicity with regard to the impact on speech and language and the need for assistive hearing devices. It is both more specific and more sensitive than the traditional CTCAE criteria for identifying clinically significant ototoxicity.

摘要

目的

我们提出了一种新的耳毒性分级系统,该系统具有明确界定和频率特异性的听力学标准。本研究的目的是通过评估其与听力学治疗建议的一致性,并与当前使用的不良事件常用术语标准(CTCAE)进行比较,来验证该分级系统。

患者和方法

使用来自 134 名儿童的听力学、人口统计学和临床数据进行回顾性图表审查,这些儿童接受了 149 个顺铂和/或卡铂化疗疗程。使用我们提出的分级标准和 CTCAE 标准评估纯音听力图。然后将得出的等级与图表听力干预和许多临床参数进行比较,以评估分级量表的临床有效性。

结果

Chang 分级 2a 或更高预测听力干预。尽管 Chang 和 CTCAE 耳毒性分级均与听力学家对助听器和/或调频系统等辅助设备的建议显著相关(P<.0001),但 Chang 分级更具特异性,CTCAE 分级在较高分级时与临床建议不符。正如预期的那样,同时接受卡铂治疗、接受放射治疗、年龄较小、体表面积较小、治疗暴露时间较长和疾病更严重的患者,顺铂的听力损失更严重。

结论

该分级系统提供了强大且具有临床意义的标准,可代表耳毒性引起的临床听力损失对言语和语言的影响以及对辅助听力设备的需求。与传统的 CTCAE 标准相比,它在识别临床上有意义的耳毒性方面更具特异性和敏感性。

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