Division of Epidemiology, The Ohio State University College of Public Health, Columbus, OH, United States of America.
Department of Statistics, The Ohio State University College of Arts and Sciences, Columbus, OH, United States of America.
Gynecol Oncol. 2023 Nov;178:130-137. doi: 10.1016/j.ygyno.2023.10.004. Epub 2023 Oct 19.
Endometrial cancer stage is a strong prognostic factor; however, the current stage classification does not incorporate transtubal spread as determined by intraluminal tumor cells (ILTCs). We examined relationships between ILTCs and survival outcomes according to histological subtype and stage and examined whether identification of ILTCs improves prognostic accuracy of endometrial cancer staging.
We conducted a retrospective cohort study of women diagnosed with endometrial cancer at five academic hospitals between 2007 and 2012. Pathologists determined ILTC presence (no vs. yes) and location (free in lumen vs. attached to epithelial surface) based on pathology review of hematoxylin and eosin-stained sections of fallopian tubes. Associations between ILTCs with time to recurrence (TTR) and overall survival (OS) were examined with Cox proportional hazards models adjusted for other prognostic factors. Model discrimination metrics were used to assess the addition of ILTCs to stage for prediction of 5-year TTR and OS.
In the overall study population (N = 1303), ILTCs were not independently associated with TTR (HR = 0.95, 95% CI = 0.69-1.32) or OS (HR = 0.97, 95% CI = 0.72-1.31). Among 805 women with stage I disease, ILTCs were independently associated with worse TTR (HR = 2.31, 95% CI = 1.06-5.05) and OS (HR = 2.16, 95% CI = 1.14-4.11). Upstaging early-stage cases with ILTCs present did not increase model discrimination.
While our data do not suggest that endometrial cancer staging guidelines should be revised to include ILTCs, associations between ILTCs and reduced survival observed among stage I cases suggest this tumor feature holds clinical relevance for subgroups of endometrial cancer patients.
子宫内膜癌分期是一个强有力的预后因素;然而,目前的分期分类并未纳入腔内肿瘤细胞(ILTCs)确定的跨管扩散。我们根据组织学亚型和分期检查了 ILTCs 与生存结果之间的关系,并检查了是否确定 ILTCs 可以提高子宫内膜癌分期的预后准确性。
我们对 2007 年至 2012 年间在五所学术医院诊断为子宫内膜癌的女性进行了回顾性队列研究。病理学家根据对输卵管苏木精和伊红染色切片的病理复查,确定 ILTCs 的存在(无 vs. 有)和位置(游离在管腔中 vs. 附着在上皮表面)。使用 Cox 比例风险模型调整其他预后因素后,检查了 ILTCs 与复发时间(TTR)和总生存(OS)之间的关联。使用模型判别指标评估将 ILTCs 添加到分期中以预测 5 年 TTR 和 OS 的效果。
在整个研究人群(N=1303)中,ILTCs 与 TTR(HR=0.95,95%CI=0.69-1.32)或 OS(HR=0.97,95%CI=0.72-1.31)均无独立相关性。在 805 例 I 期疾病患者中,ILTCs 与较差的 TTR(HR=2.31,95%CI=1.06-5.05)和 OS(HR=2.16,95%CI=1.14-4.11)独立相关。对存在 ILTCs 的早期病例进行升级并不会提高模型判别力。
虽然我们的数据表明子宫内膜癌分期指南不应该修订以纳入 ILTCs,但在 I 期病例中观察到 ILTCs 与生存降低之间的关联表明,这种肿瘤特征与子宫内膜癌患者的亚组具有临床相关性。