Binder M, Winkler A, Dorffner R, Glebowski E, Wolff K, Pehamberger H
Department of Dermatology I, University of Vienna, Austria.
Eur J Cancer. 1992;28A(11):1814-6. doi: 10.1016/0959-8049(92)90010-y.
19 patients with advanced malignant melanoma were treated with fotemustine and dacarbazine. Data recorded and available for evaluation in all patients included clinical and histopathological parameters of the primary melanoma, blood chemistry, blood cell count, chest X-ray, ultrasound and bone scan for initial staging of the site of metastases and follow-up during treatment. Dosage was fotemustine 100 mg/m2 and dacarbazine 200 mg/m2 intravenously twice monthly on days 1 and 8, repeated for a maximum of six courses. There were two complete and three partial responses in 5/19 patients (26%), and 8 patients (42%) had stable disease. 6 (32%) patients had no response. Median length of complete and partial responses was 3.9 months, and that of stable disease 4.2 months. The main side-effects were thrombocytopenia in 10 patients (53%) and nausea in 6 (32%); the nausea was easily suppressed by ondasetron. Thus, fotemustine-dacarbazine may be new treatment in advanced melanoma.
19例晚期恶性黑色素瘤患者接受了福莫司汀和达卡巴嗪治疗。记录并可用于所有患者评估的数据包括原发性黑色素瘤的临床和组织病理学参数、血液化学、血细胞计数、胸部X线、超声以及用于转移部位初始分期和治疗期间随访的骨扫描。剂量为福莫司汀100mg/m²,达卡巴嗪200mg/m²,于第1天和第8天每月静脉注射两次,最多重复六个疗程。19例患者中有5例(26%)出现2例完全缓解和3例部分缓解,8例(42%)病情稳定。6例(32%)患者无反应。完全缓解和部分缓解的中位持续时间为3.9个月,病情稳定的中位持续时间为4.2个月。主要副作用为10例患者(53%)出现血小板减少,6例(32%)出现恶心;昂丹司琼可轻松抑制恶心。因此,福莫司汀 - 达卡巴嗪可能是晚期黑色素瘤的新治疗方法。