Nitz Alexandra, Kontopantelis Evangelos, Bielack Stefan, Koscielniak Ewa, Klingebiel Thomas, Langer Thorsten, Paulides Marios
Department of Paediatric Oncology and Immunology, LESS Centre, University Hospital for Children and Adolescents, Erlangen D-91054, Germany ;
Oncol Lett. 2013 Jan;5(1):311-315. doi: 10.3892/ol.2012.997. Epub 2012 Oct 25.
Platinum-compound chemotherapy is known to have ototoxic side-effects. However, there is a paucity of literature examining hearing function prospectively and longitudinally in cohorts containing paediatric and adult patients treated within the same cisplatin- or carboplatin-containing treatment trial protocols. In Germany, Austria and Switzerland, late effects of treatment for osteosarcoma and soft tissue sarcoma have been prospectively and longitudinally registered by the Late Effects Surveillance System since 1998. The aim of this study was to analyse cisplatin- and carboplatin-induced ototoxity in a group of 129 osteosarcoma and soft tissue sarcoma patients treated within the COSS-96, CWS-96 and CWS-2002P treatment trials. The cohort consisted of 112 children and 17 adults. The median age at diagnosis was 13.56 (IQR, 10.26-16.27) years. Follow-up was 6.97 (IQR, 0.87-15.63) months. Hearing function was examined by audiometry before and after platinum treatment. A total of 108 patients were treated with cisplatin with a median cumulative dose of 360 mg/m(2). Thirteen patients received carboplatin with a median cumulative dose of 1500 mg/m(2) and 8 patients were treated with both platinum compounds (median cisplatin dose, 240 mg/m(2); IQR, 240-360 mg/m(2) and median carboplatin dose: 1200 mg/m(2); IQR, 600-3000 mg/m(2)). Following cessation of therapy, 47.3% of the patients demonstrated a hearing impairment, namely 55 children (49.1%) and 6 adults (42.1%). Out of thirteen children treated with carboplatin with a cumulative dose of 1500 mg/m(2), six revealed a significant hearing impairment. Although ototoxicity caused by platinum compounds is considered irreversible, we identified hearing improvements over time in 11 children (9.8%) and 3 adults (17.6%). None of these patients received irradiation to the head. We conclude that hearing loss is frequent in children treated with protocols containing platinum compounds and recommend prospective testing via audiometry.
已知铂类化合物化疗具有耳毒性副作用。然而,在包含接受相同含顺铂或卡铂治疗试验方案治疗的儿科和成人患者的队列中,前瞻性和纵向研究听力功能的文献较少。自1998年以来,德国、奥地利和瑞士的晚期效应监测系统对骨肉瘤和软组织肉瘤治疗的晚期效应进行了前瞻性和纵向登记。本研究的目的是分析在COSS - 96、CWS - 96和CWS - 2002P治疗试验中接受治疗的129例骨肉瘤和软组织肉瘤患者中顺铂和卡铂引起的耳毒性。该队列包括112名儿童和17名成人。诊断时的中位年龄为13.56(四分位间距,10.26 - 16.27)岁。随访时间为6.97(四分位间距,0.87 - 15.63)个月。在铂类治疗前后通过听力测定检查听力功能。共有108例患者接受顺铂治疗,中位累积剂量为360mg/m²。13例患者接受卡铂治疗,中位累积剂量为1500mg/m²,8例患者接受两种铂类化合物治疗(顺铂中位剂量,240mg/m²;四分位间距,240 - 360mg/m²;卡铂中位剂量:1200mg/m²;四分位间距,600 - 3000mg/m²)。治疗停止后,47.3%的患者出现听力障碍,即55名儿童(49.1%)和6名成人(42.1%)。在接受累积剂量为1500mg/m²卡铂治疗的13名儿童中,6名出现明显听力障碍。尽管铂类化合物引起的耳毒性被认为是不可逆的,但我们发现11名儿童(9.8%)和3名成人(17.6%)的听力随时间有所改善。这些患者均未接受头部放疗。我们得出结论,在接受含铂类化合物方案治疗的儿童中听力损失很常见,并建议通过听力测定进行前瞻性检测。