...
首页> 外文期刊>Gynecologic Oncology: An International Journal >Randomized trial of pegylated liposomal doxorubicin (PLD) plus carboplatin versus carboplatin in platinum-sensitive (PS) patients with recurrent epithelial ovarian or peritoneal carcinoma after failure of initial platinum-based chemotherapy (Southwes
【24h】

Randomized trial of pegylated liposomal doxorubicin (PLD) plus carboplatin versus carboplatin in platinum-sensitive (PS) patients with recurrent epithelial ovarian or peritoneal carcinoma after failure of initial platinum-based chemotherapy (Southwes

机译:聚铂脂质体阿霉素(PLD)联合卡铂与卡铂在铂类初始化疗失败后对铂敏感性(PS)复发性上皮性卵巢或腹膜癌患者中的随机试验(Southwes

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

OBJECTIVE: Because debate continues over the role of combination, platinum-based chemotherapy for platinum-sensitive (PS), recurrent ovarian cancer (OC), we compared overall survival (OS), progression-free survival (PFS), confirmed complete response rate and time to treatment failure in this population. METHODS: Patients with recurrent stage III or IV OC, a progression-free and platinum-free interval of 6-24 months after first-line platinum-based chemotherapy and up to 12 courses of a non-platinum containing consolidation treatment were eligible. Patients were randomized to i.v. pegylated liposomal doxorubicin (PLD) (30 mg/m2) plus i.v. carboplatin (AUC=5 mg/mL min) once every 4 weeks (PLD arm) or i.v. carboplatin alone (AUC=5 mg/mL min) once every 4 weeks. RESULTS: The PLD arm enrolled 31 patients and the carboplatin alone arm 30 for a total of 61 patients out of 900 planned. Response rates were 67% for the PLD arm and 32% for the carboplatin only arm (Fisher's exact p=0.02). The estimated median PFS was 12 and 8 months for PLD versus carboplatin alone. The estimated median OS on the PLD arm was 26 months and 18 months on the carboplatin only arm (p=0.02). Twenty-six percent of the patients on the PLD arm reported grade 4 toxicities, all hematological in nature. CONCLUSION: This study was closed early because of slow patient accrual. The response rate, median PFS and OS results are intriguing. These data suggest that there may be an advantage to the PLD plus carboplatin combination treatment in patients with PS, recurrent OC. The regimen should be further tested.
机译:目的:由于关于联合用药,铂类敏感性化疗(PS),复发性卵巢癌(OC)的作用的争论仍在继续,我们比较了总生存期(OS),无进展生存期(PFS),确诊完全缓解率和该人群治疗失败的时间。方法:患有复发性III或IV期OC,一线铂类化学疗法后6-24个月无进展和无铂间隔以及最多12个疗程的非铂类巩固治疗的患者是合格的。患者被随机分为静脉注射。聚乙二醇化脂质体阿霉素(PLD)(30 mg / m2)加上i.v.卡铂(AUC = 5 mg / mL min)每4周一次(PLD组)或i.v.每4周一次单独使用卡铂(AUC = 5 mg / mL min)。结果:PLD组招募了31名患者,仅卡铂组招募了30名患者,总共计划的900名患者中有61名患者。 PLD组的响应率为67%,仅卡铂组的响应率为32%(Fisher的确切p = 0.02)。与仅使用卡铂相比,PLD的估计中位PFS为12和8个月。 PLD组的估计中位OS为26个月,仅卡铂组的OS为18个月(p = 0.02)。 PLD组有26%的患者报告了4级毒性,全部属于血液学性质。结论:该研究因患者预后缓慢而提前关闭。响应率,中位PFS和OS结果令人感兴趣。这些数据表明,PS,复发性OC患者,PLD加卡铂联合治疗可能有优势。该方案应进一步测试。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号