Kurtz J E, Deplanque G, Duclos B, Eichler F, Giron C, Limacher J M, Herbrecht R, Maloisel F, Oberling F, Bergerat J P, Dufour P
Department of Onco-Hematology, Hôpitaux Universitaires, Strasbourg, 67098, France.
Gynecol Oncol. 1998 Sep;70(3):414-7. doi: 10.1006/gyno.1998.5099.
Despite high response rates with platinum-based front-line chemotherapy, the prognosis for advanced ovarian carcinoma (AOC) is poor. Salvage chemotherapy for recurrent AOC was of little benefit before paclitaxel as single-agent therapy showed appreciable efficacy. Anthracyclines are effective, but are not often part of first-line therapy. In this pilot study, we investigated the feasibility of an anthracycline plus paclitaxel combination therapy for recurrent AOC. Twenty-four patients received 150 mg/m2 paclitaxel on day 1, with either 50 mg/m2 doxorubicin on day 1 or 75 mg/m2 epirubicin on day 1 every 3 weeks. A 27% overall response rate was obtained. Myelosuppression was the major toxicity, but was manageable. No myocardiac toxicity was observed. We conclude that paclitaxel-anthracyclines is a promising salvage combination therapy in AOC that should be investigated further.
尽管铂类一线化疗的缓解率较高,但晚期卵巢癌(AOC)的预后仍然很差。在紫杉醇单药治疗显示出显著疗效之前,复发性AOC的挽救性化疗获益甚微。蒽环类药物有效,但并不常作为一线治疗的一部分。在这项前瞻性研究中,我们探讨了蒽环类药物联合紫杉醇治疗复发性AOC的可行性。24例患者在第1天接受150mg/m²紫杉醇治疗,每3周一次,同时在第1天联合50mg/m²阿霉素或75mg/m²表阿霉素。总缓解率为27%。骨髓抑制是主要的毒性反应,但可控制。未观察到心脏毒性。我们得出结论,紫杉醇-蒽环类药物是一种有前景的AOC挽救性联合治疗方案,值得进一步研究。