Department of Surgery, Division of Gynecologic Oncology, City of Hope National Medical Center (COH), Duarte, CA, United States of America.
Biostatistics Core, City of Hope National Medical Center (COH), Duarte, CA, United States of America.
Gynecol Oncol. 2024 Oct;189:41-48. doi: 10.1016/j.ygyno.2024.06.024. Epub 2024 Jul 14.
Efforts have been made to better risk stratify patients given the rise in incidence of endometrial cancer (EC). The 2023 FIGO staging now incorporates histologic subtype and molecular classification into determination of EC stage. We sought to elucidate if the new staging system demonstrated prognostic differences compared to the 2009 staging system.
A retrospective chart review was performed on women treated for EC at our institution from September 2013 to May 2023 and combined with the publicly available TCGA Nature 2013 dataset. Detailed clinical information was captured. Patients were restaged according to the 2023 guidelines. Survival estimates were obtained using Kaplan-Meier method, and the log-rank test was used to compare survival curves for progression-free survival (PFS).
919 patients were included in our analysis. The datasets were comparable regarding histologic grade, stage, and age at diagnosis. 175 (31.5%) of patients in the institution dataset and 115 (31.6%) patients in the TCGA dataset experienced a stage change. Most patients whose stage changed were upstaged (275/290; 94.8%). 3-year PFS estimates for stage IA patients with no stage change versus those upstaged were 92.3% (95% CI: 87.2, 95.4) v. 72.0% (95% CI: 68.4, 84.9), p = 0.002. No significant differences in survival difference were seen in other stage subsets.
Modest survival differences exist in patients with EC originally staged as IA who underwent upstaging. No significant survival difference is observed in patients who are restaged to stage II or III subsets. Improved risk stratification is needed in assessing prognosis and adjuvant therapy for patients with endometrial cancer.
由于子宫内膜癌(EC)发病率的上升,人们一直在努力更好地对患者进行风险分层。2023 年 FIGO 分期现在将组织学亚型和分子分类纳入 EC 分期的确定中。我们试图阐明新的分期系统与 2009 年分期系统相比是否显示出预后差异。
对我院 2013 年 9 月至 2023 年 5 月治疗的 EC 女性进行回顾性病历审查,并与公开的 TCGA Nature 2013 数据集相结合。详细的临床信息被捕获。根据 2023 年指南对患者进行重新分期。使用 Kaplan-Meier 方法获得生存估计,对数秩检验用于比较无进展生存期(PFS)的生存曲线。
我们的分析共纳入 919 例患者。在组织学分级、分期和诊断时的年龄方面,两个数据集具有可比性。在机构数据集的 175 例(31.5%)和 TCGA 数据集的 115 例(31.6%)患者经历了分期变化。分期改变的大多数患者都是升级(275/290;94.8%)。无分期变化的 IA 期患者与升级患者的 3 年 PFS 估计分别为 92.3%(95%CI:87.2,95.4)和 72.0%(95%CI:68.4,84.9),p=0.002。在其他分期亚组中,未观察到生存差异的显著差异。
在最初分期为 IA 但进行升级的 EC 患者中,存在适度的生存差异。在重新分期为 II 期或 III 期亚组的患者中,未观察到生存差异。需要改进风险分层,以评估子宫内膜癌患者的预后和辅助治疗。