Athanassiou A E, Bafaloukos D, Pectasides D, Dimitriadis M, Varthalitis I, Barbounis V
Department of Medical Oncology, Metaxas Memorial Cancer Hospital, Piraeus, Greece.
Br J Cancer. 1989 Nov;60(5):755-8. doi: 10.1038/bjc.1989.353.
Thirty-one consecutive patients with advanced epithelial ovarian cancer entered a phase II study with cisplatin and etoposide combination chemotherapy. None of them had received prior chemotherapy or radiotherapy. Most patients had advanced (88%) or far advanced (61%) disease. All 31 patients are evaluable for toxicity which was significant and led to removal of five (16%) patients from the study. Of the 23 patients evaluable for response there were four clinical complete (CR) and eight partial (PR) responders for a total clinical response rate of 52% of evaluable patients and 39% of all patients. Eight patients (four clinical CR and four good PR) have undergone second look laparotomy with pathological CR in one of the clinical CR patients. Median survival time for responders and non-responders is 19 and 8 months respectively. The results obtained appear to be inferior to other cisplatin based combinations. Although this could be attributed to the unusually high proportion of patients with bulky disease and stage IV patients, we feel that the study suggests that etoposide did not add any benefits for this patient population to cisplatin as a single agent.
31例连续的晚期上皮性卵巢癌患者进入了一项使用顺铂和依托泊苷联合化疗的II期研究。他们均未接受过先前的化疗或放疗。大多数患者患有晚期(88%)或极晚期(61%)疾病。所有31例患者均可评估毒性,毒性显著,导致5例(16%)患者退出研究。在可评估疗效的23例患者中,有4例临床完全缓解(CR),8例部分缓解(PR),可评估患者的总临床缓解率为52%,所有患者的总临床缓解率为39%。8例患者(4例临床CR和4例良好PR)接受了二次剖腹探查,其中1例临床CR患者出现病理CR。缓解者和未缓解者的中位生存时间分别为19个月和8个月。获得的结果似乎不如其他基于顺铂的联合方案。虽然这可能归因于肿块较大的患者和IV期患者比例异常高,但我们认为该研究表明,对于该患者群体,依托泊苷作为单一药物并未给顺铂带来任何益处。