Langer C J, Nash S, Catalano R, Rosenblum N G, Hogan W M, Comis R L, O'Dwyer P J
Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
Gynecol Oncol. 1991 Dec;43(3):242-6. doi: 10.1016/0090-8258(91)90028-4.
On the basis of a Phase I reevaluation of thio-TEPA in which 3 of 9 patients with ovarian carcinoma responded, we instituted a Phase II study at high doses. Fourteen patients with a histologic diagnosis of epithelial carcinoma of the ovary, who had received at least one prior cisplatin-based regimen, were entered. Thio-TEPA was initially administered intravenously at a dose of 65 mg/m2 every 4 weeks, but was reduced to 50 mg/m2 after severe myelotoxicity developed in the first 5 patients. In 4 patients stable disease lasted 3, 4, 5, and 9 months; 10 patients progressed. There were no objective responses. At this dose and schedule, thio-TEPA has a response rate less than 20% in ovarian cancer patients previously treated with cisplatin.
基于硫代替派的I期重新评估(9例卵巢癌患者中有3例有反应),我们开展了高剂量的II期研究。纳入了14例经组织学诊断为卵巢上皮癌、此前至少接受过一种含顺铂方案治疗的患者。硫代替派最初静脉给药,剂量为65mg/m²,每4周一次,但在前5例患者出现严重骨髓毒性后,剂量减至50mg/m²。4例患者病情稳定持续了3、4、5和9个月;10例患者病情进展。无客观缓解。在此剂量和给药方案下,硫代替派在先前接受过顺铂治疗的卵巢癌患者中的缓解率低于20%。