LESS Center, University Hospital for Children and Adolescents, Department for Pediatric Oncology and Immunology, Loschgestrasse 15, 91054 Erlangen, Germany.
Trends Pharmacol Sci. 2013 Aug;34(8):458-69. doi: 10.1016/j.tips.2013.05.006. Epub 2013 Jun 13.
Childhood cancer survival rates are now nearly 80% in more developed European countries because of improved therapies and better supportive care. Platinum chemotherapy drugs, such as cisplatin and carboplatin, are the cornerstone of many effective therapeutic protocols for childhood cancer. However, the antitumor efficacy of cisplatin and carboplatin comes at the cost of ototoxicity, which affects at least 60% of pediatric patients. Although ototoxicity is not life threatening, it can have debilitating effects on patients' quality of life. Recently, many initiatives have been launched with the ultimate goal of reducing cisplatin and high-dose carboplatin ototoxicity without compromising antitumor efficacy. This review addresses the incidence of platinum ototoxicity and its clinical presentation, time course, and early diagnostic evaluation. Genetic and non-genetic risk factors for platinum-associated ototoxicity, and their predictive value, are discussed. Recent developments in the prevention of platinum ototoxicity are also summarized.
由于治疗方法的改进和更好的支持性护理,现在较为发达的欧洲国家儿童癌症的存活率已接近 80%。顺铂和卡铂等铂类化疗药物是许多儿童癌症有效治疗方案的基石。然而,顺铂和卡铂的抗肿瘤疗效是以耳毒性为代价的,至少 60%的儿科患者会受到耳毒性的影响。虽然耳毒性不会危及生命,但它会对患者的生活质量产生严重影响。最近,许多举措的最终目标都是在不影响抗肿瘤疗效的情况下降低顺铂和高剂量卡铂的耳毒性。这篇综述介绍了铂类耳毒性的发生率及其临床表现、时程和早期诊断评估。还讨论了铂类相关耳毒性的遗传和非遗传风险因素及其预测价值。总结了铂类耳毒性预防的最新进展。