上皮性卵巢癌的复发时间和总生存期:10年回顾性回顾

K. Okunade, A. Soibi-Harry, T. Onyeka, John Ogunyemi, Olufemi Thomas-Ogodo, A. Adejimi, Austin C Okoro, Benedetto Osunwusi, Sunusi Garba, R. Anorlu
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引用次数: 0

摘要

背景:上皮性卵巢癌(EOC)在标准初次治疗后复发的时间是肿瘤对治疗反应程度的重要指标。然而,尚不清楚复发的时间是否能预测生存结果。目的:本研究探讨标准初始治疗后复发时间对EOC患者总生存期(OS)的影响。方法:数据取自2011年1月至2020年12月期间诊断为EOC后接受标准初级治疗和随访的患者记录。使用Kaplan-Meier生存估计和Cox比例风险模型校正协变量进行分析。结果:初始治疗开始后,EOC的复发风险随时间的增加而稳步增加,从6个月时的13.6%增加到12个月后的71.0%。在最后的多因素分析中,治疗6个月内的复发是EOC患者生存不良的重要独立预测因子(风险比=7.23,95%CI: 3.87-13.51, P<0.01)。结论:我们的研究表明6个月内的复发是EOC预后不良的重要预测因素。早期肿瘤复发可能是一个有用的OS替代指标,因此在设计未来量身定制的随机对照试验时应考虑这一信息。未来提高EOC患者OS的策略应侧重于寻找有效的措施来预防早期肿瘤复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Timing of recurrence and overall survival in epithelial ovarian cancer: A 10-year retrospective review
Background: The timing of recurrence of epithelial ovarian cancer (EOC) after a standard primary treatment is an important indicator of the degree of response of the tumour to treatment. It, however, remains unclear if the timing of recurrence will predict survival outcomes. Aim: This study explored the impact of timing of recurrence after an initial response to standard primary treatment on the overall survival (OS) of patients with EOC. Methods: Data was extracted from the records of patients who underwent standard primary treatment and follow-up after EOC diagnosis between January 2011 and December 2020. The Kaplan-Meier survival estimates and Cox proportional hazards model adjusted for covariates were used for analyses. Results: The risks of recurrence of EOC increased steadily with increasing time from the start of primary treatment from 13.6% in 6-months to 71.0% after 12-months. In the final multivariate analyses, recurrence within 6 months of treatment was a significant independent predictor of poor OS in EOC patients (hazard ratio=7.23, 95%CI: 3.87–13.51, P<0.01). Conclusion: Our study suggests that recurrence within 6-months is an important prognostic predictor of poor OS in EOC. Early tumour recurrence may be a useful surrogate of OS and thus this information should be considered in the design of future tailored randomized controlled trials. Future strategies to improve OS in EOC patients should focus on identifying effective measures to prevent early tumour recurrence.
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