Hilgers R D, Rivkin S E, Von Hoff D D, Alberts D S
Am J Clin Oncol. 1984 Oct;7(5):499-501. doi: 10.1097/00000421-198410000-00020.
Thirty-nine patients with advanced heavily pretreated epithelial carcinoma of the ovary were treated with mitoxantrone (dihydroxyanthracenedione hydrochloride). Twenty-five patients were started at a dose of 12 mg/m2 q 21d and 13 patients, with compromised bone marrow, at a dose of 10 mg/m2 q 21d. Two stable responses (6%) occurred in 31 fully evaluable patients. The median duration of survival was 17 weeks. The principal toxicity, hematopoietic (primarily leukopenia), was mild and well tolerated. We conclude that mitoxantrone is a relatively inactive drug in the treatment of epithelial ovarian carcinoma.
39例晚期卵巢上皮癌且接受过大量前期治疗的患者接受了米托蒽醌(盐酸二羟基蒽二酮)治疗。25例患者起始剂量为12mg/m²,每21天给药一次;13例骨髓功能受损的患者起始剂量为10mg/m²,每21天给药一次。31例可进行全面评估的患者中有2例病情稳定(6%)。中位生存期为17周。主要毒性为血液学毒性(主要是白细胞减少),程度较轻且耐受性良好。我们得出结论,米托蒽醌在治疗卵巢上皮癌方面是一种相对无效的药物。