van der Gaast A, Splinter T A
Department of Medical Oncology, University Hospital, Rotterdam-Dijkzigt, The Netherlands.
Semin Oncol. 1992 Apr;19(2 Suppl 6):95-7.
Relatively few patients with gynecologic malignancies have been included in trials with teniposide given as a single agent. For 109 patients with advanced ovarian cancer treated with various doses and schedules, an overall response rate of 12% was reported. Most patients were heavily pretreated and presumably had resistant disease. Information about teniposide's activity in combination with other cytotoxic agents, as well as its efficacy in other gynecologic malignancies, is limited. In view of the favorable pharmacologic and toxicity profiles of teniposide and its possible synergism with cisplatin and carboplatin, new treatment strategies are discussed that may have implications for further investigation of the usefulness of teniposide in advanced ovarian cancer.
相对较少的妇科恶性肿瘤患者被纳入以替尼泊苷作为单一药物的试验。对于109例接受不同剂量和给药方案治疗的晚期卵巢癌患者,报告的总体缓解率为12%。大多数患者此前接受过大量治疗,推测患有耐药性疾病。关于替尼泊苷与其他细胞毒性药物联合使用时的活性以及其在其他妇科恶性肿瘤中的疗效的信息有限。鉴于替尼泊苷良好的药理学和毒性特征及其与顺铂和卡铂可能存在的协同作用,讨论了新的治疗策略,这些策略可能对进一步研究替尼泊苷在晚期卵巢癌中的效用具有启示意义。