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大剂量顺铂静脉推注给药对晚期癌症且听力正常患者的耳毒性。

Ototoxicity of high-dose cisplatin by bolus administration in patients with advanced cancers and normal hearing.

作者信息

Kopelman J, Budnick A S, Sessions R B, Kramer M B, Wong G Y

机构信息

Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY.

出版信息

Laryngoscope. 1988 Aug;98(8 Pt 1):858-64. doi: 10.1288/00005537-198808000-00014.

Abstract

Our institution undertook a phase I trial to define the toxicity of high-dose (150 to 225 mg) bolus administration (every 3 to 4 weeks) of cisplatin in patients with advanced cancers. All patients reported had baseline normal hearing. Hearing levels were measured prior to each course of chemotherapy. Audiological monitoring included conventional assessment of pure tone sensitivity at 500 to 8,000 Hz and assessment of ultra high frequencies (9,000 to 20,000 Hz). After one to two doses, 100% of patients failed to respond at 9,000 Hz and above. In the 2,000 to 8,000 Hz range, repeated administration of the drug effected successively lower frequencies with progressive loss, until a maximum threshold shift or plateau was reached at each frequency between 3,000 and 8,000 Hz. The plateau for cisplatin ototoxicity appears to fall within the moderate hearing loss range (40 to 60 dB HL) in the high frequencies. All patients complained of tinnitus and difficulty understanding speech in the presence of background noise. The pattern of pure tone audiometric alteration is consistent in all patients, all dosages, and each method of administration. The ultra high frequency alteration is prompt and dramatic.

摘要

我们机构开展了一项I期试验,以确定晚期癌症患者大剂量(150至225毫克)顺铂推注给药(每3至4周一次)的毒性。所有报告的患者听力基线正常。在每疗程化疗前测量听力水平。听力监测包括对500至8000赫兹纯音敏感度的常规评估以及超高频(9000至20000赫兹)评估。一至两剂后,100%的患者在9000赫兹及以上频率出现听力减退。在2000至8000赫兹范围内,重复给药使频率逐渐降低,听力逐渐丧失,直至在3000至8000赫兹的每个频率达到最大阈值偏移或平台期。顺铂耳毒性的平台期似乎处于高频中度听力损失范围(40至60分贝听力级)内。所有患者均抱怨有耳鸣,且在有背景噪音时难以理解言语。纯音听力测定改变模式在所有患者、所有剂量及每种给药方法中均一致。超高频改变迅速且显著。

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