首页> 外文期刊>The journal of obstetrics and gynaecology research >Long-term survival in patients with clear cell adenocarcinoma of ovary treated with irinotecan hydrochloride plus cisplatin therapy as first-line chemotherapy.
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Long-term survival in patients with clear cell adenocarcinoma of ovary treated with irinotecan hydrochloride plus cisplatin therapy as first-line chemotherapy.

机译:盐酸伊立替康联合顺铂作为一线化疗治疗卵巢透明细胞腺癌患者的长期生存。

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摘要

Several previous reports showed that irinotecan hydrochloride plus cisplatin (CPT-P) was a candidate first-line chemotherapy regimen for clear cell adenocarcinoma of the ovary (CCC). However, long-term survival in CCC patients treated with CPT-P as first-line chemotherapy remains to be determined. The aim of the present study was to evaluate the long-term results of CPT-P as first-line chemotherapy for CCC.We performed a retrospective review of 31 patients with CCC who were treated with CPT-P between 1996 and 2004.The median follow-up period was 91 months. The estimated 8-year overall survival (OS) rate in all patients was 64.5%, while the rate in 18 stage I, 21 stage I/II, and 10 stage III/IV patients was 88.9%, 85.7%, and 20.0%, respectively. The estimated 8-year OS rate in patients with pT1/pT2 disease was 87.0%, while the 3-year OS rate in patients with pT3 disease was 0%. Univariate analysis using the log-rank test revealed that Eastern Cooperative Oncology Group performance-status 1, pT3 stage, and presence of residual disease (stage II-IV) were significantly correlated with shortened patient survival. Multiple regression analysis revealed that pT3 predicted worse OS in patients with CCC than pT1 (P<0.001) or pT2 disease (P?
机译:先前的一些报道表明,盐酸伊立替康加顺铂(CPT-P)是卵巢透明细胞腺癌(CCC)的候选一线化疗方案。然而,作为一线化疗的CPT-P治疗的CCC患者的长期存活率尚待确定。本研究的目的是评估CPT-P作为CCC一线化疗的长期结果。我们回顾性回顾了1996年至2004年间接受CPT-P治疗的31例CCC患者。随访时间为91个月。估计所有患者的8年总生存率(OS)为64.5%,而I期18例,I / II期21例和III / IV期10例的8年总生存率分别为88.9%,85.7%和20.0%,分别。 pT1 / pT2疾病患者的8年OS估计率为87.0%,而pT3疾病患者3年的OS为0%。使用对数秩检验的单变量分析显示,东部合作肿瘤小组的表现状态1,pT3阶段和残留疾病的存在(II-IV阶段)与患者生存期缩短显着相关。多元回归分析显示,pT3预测的CCC患者的OS较pT1(P <0.001)或pT2疾病(P?<?0.005)更差。长期结果表明CPT-P可作为CCC一线化疗的候选药物不仅在I期患者,而且在pT1 / pT2疾病的最佳减退II-IV期患者中也是如此。

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