Crabb Simon J, Martin Karen, Abab Julia, Ratcliffe Ian, Thornton Roger, Lineton Ben, Ellis Mary, Moody Ronald, Stanton Louise, Galanopoulou Angeliki, Maishman Tom, Geldart Thomas, Bayne Mike, Davies Joe, Lamb Carolynn, Popat Sanjay, Joffe Johnathan K, Nutting Chris, Chester John, Hartley Andrew, Thomas Gareth, Ottensmeier Christian, Huddart Robert, King Emma
Cancer Sciences Unit, University of Southampton, Southampton, United Kingdom.
Southampton Clinical Trials Unit, University of Southampton, Southampton, United Kingdom.
Eur J Cancer. 2017 Dec;87:75-83. doi: 10.1016/j.ejca.2017.09.033. Epub 2017 Nov 10.
Cisplatin is one of the most ototoxic chemotherapy drugs, resulting in a permanent and irreversible hearing loss in up to 50% of patients. Cisplatin and gentamicin are thought to damage hearing through a common mechanism, involving reactive oxygen species in the inner ear. Aspirin has been shown to minimise gentamicin-induced ototoxicity. We, therefore, tested the hypothesis that aspirin could also reduce ototoxicity from cisplatin-based chemotherapy.
A total of 94 patients receiving cisplatin-based chemotherapy for multiple cancer types were recruited into a phase II, double-blind, placebo-controlled trial and randomised in a ratio of 1:1 to receive aspirin 975 mg tid and omeprazole 20 mg od, or matched placebos from the day before, to 2 days after, their cisplatin dose(s), for each treatment cycle. Patients underwent pure tone audiometry before and at 7 and 90 days after their final cisplatin dose. The primary end-point was combined hearing loss (cHL), the summed hearing loss at 6 kHz and 8 kHz, in both ears.
Although aspirin was well tolerated, it did not protect hearing in patients receiving cisplatin (p-value = 0.233, 20% one-sided level of significance). In the aspirin arm, patients demonstrated mean cHL of 49 dB (standard deviation [SD] 61.41) following cisplatin compared with placebo patients who demonstrated mean cHL of 36 dB (SD 50.85). Women had greater average hearing loss than men, and patients treated for head and neck malignancy experienced the greatest cHL.
Aspirin did not protect from cisplatin-related ototoxicity. Cisplatin and gentamicin may therefore have distinct ototoxic mechanisms, or cisplatin-induced ototoxicity may be refractory to the aspirin regimen used here.
顺铂是最具耳毒性的化疗药物之一,高达50%的患者会因此出现永久性、不可逆的听力丧失。顺铂和庆大霉素被认为通过一种共同机制损害听力,该机制涉及内耳中的活性氧。已有研究表明阿司匹林可将庆大霉素引起的耳毒性降至最低。因此,我们检验了阿司匹林也可降低基于顺铂的化疗所致耳毒性这一假设。
总共94例因多种癌症类型接受基于顺铂化疗的患者被纳入一项II期双盲安慰剂对照试验,并按1:1的比例随机分组,在每个治疗周期中,从顺铂给药前一天至给药后2天,分别接受每日三次、每次975 mg的阿司匹林和每日一次、每次20 mg的奥美拉唑,或匹配的安慰剂。患者在最后一次顺铂给药前、给药后7天和90天接受纯音听力测定。主要终点是双耳在6 kHz和8 kHz处的听力损失总和,即综合听力损失(cHL)。
尽管阿司匹林耐受性良好,但它并未保护接受顺铂治疗患者的听力(p值 = 0.233,单侧显著性水平为20%)。在阿司匹林组中,患者顺铂治疗后的平均cHL为49 dB(标准差[SD] 61.41),而安慰剂组患者的平均cHL为36 dB(SD 50.85)。女性的平均听力损失大于男性,接受头颈部恶性肿瘤治疗的患者cHL最大。
阿司匹林不能预防顺铂相关的耳毒性。因此,顺铂和庆大霉素可能具有不同的耳毒性机制,或者顺铂诱导的耳毒性可能对本研究中使用的阿司匹林方案具有抗性。