Hernádi Z, Juhász B, Póka R, Lampé L G
Department of Obstetrics and Gynecology, University Medical School, Debrecen, Hungary.
Int J Gynaecol Obstet. 1988 Oct;27(2):199-204. doi: 10.1016/0020-7292(88)90008-2.
Forty-eight patients with FIGO stage III and IV epithelial carcinomas of the ovary were entered in this randomised trial. Radical surgery was performed and no residual tumor with a diameter greater than 2 cm was left behind. Of these patients 62.5% (10/16) had a complete or partial response on cyclophosphamide + cisplatin (CP) 87.5% (14/16) on cyclophosphamide + doxorubicin + cisplatin (CAP) and cyclophosphamide + 4'-epi-doxorubicin + cisplatin (CEP). The median time to progression was 3.5 months on CP, 12.5 months on CAP and 11.0 months on CEP. Patients treated with CAP combination chemotherapy had generally longer progression-free survival (log rank chi 2 = 5.4; P = 0.04). No significant difference was found, however, between patients on CAP and CEP. The median survival times were 12.5 months on CP, 26.5 months on CAP and 14.0 months on CEP. Patients treated with CAP combination chemotherapy had generally longer survival (logrank chi 2 = 9.08; P = 0.0099). No significant difference was found, however, between patients on CAP and CEP in terms of survival. Asymptomatic mild-to-moderate laboratory test toxicity occurred in 6-12% of patients on CP, 6-12% on CAP and no toxicity of this type and grade on CEP. Nausea and vomiting were also less severe and less frequent in the CEP group. Cardiotoxicity was seen in 12.5% (2/16) only in the CAP group.
48例国际妇产科联盟(FIGO)III期和IV期卵巢上皮癌患者进入了这项随机试验。患者均接受了根治性手术,术后未残留直径大于2 cm的肿瘤。这些患者中,62.5%(10/16)对环磷酰胺+顺铂(CP)有完全或部分反应,87.5%(14/16)对环磷酰胺+阿霉素+顺铂(CAP)以及环磷酰胺+4'-表阿霉素+顺铂(CEP)有反应。CP组的疾病进展中位时间为3.5个月,CAP组为12.5个月,CEP组为11.0个月。接受CAP联合化疗的患者总体无进展生存期更长(对数秩检验χ2 = 5.4;P = 0.04)。然而,CAP组和CEP组患者之间未发现显著差异。CP组的中位生存时间为12.5个月,CAP组为26.5个月,CEP组为14.0个月。接受CAP联合化疗的患者总体生存期更长(对数秩检验χ2 = 9.08;P = 0.0099)。然而,在生存方面,CAP组和CEP组患者之间未发现显著差异。CP组6 - 12%的患者出现无症状的轻至中度实验室检查毒性,CAP组为6 - 12%,CEP组未出现此类及该级别的毒性。CEP组恶心和呕吐的严重程度及频率也较低。仅CAP组有12.5%(2/16)的患者出现心脏毒性。