Int J Gynecol Cancer. 2018 Mar;28(3):505-513. doi: 10.1097/IGC.0000000000001191.
The aim of this study was to evaluate the immunohistochemical (IHC) expression of Ki-67, estrogen receptors α (ERsα), and progesterone receptors (PRs) in high-risk endometrial cancer patients and to assess their prognostic impact.
METHODS/MATERIALS: Immunohistochemical expression of Ki-67, ERsα, and PRs was evaluated in primary untreated endometrial cancer. The correlation among IHC staining and risk factors of recurrence such as age, Federation International of Gynecology and Obstetrics stage, grading, depth of invasion, and metastatic spread was assessed.
Eighty-two patients were available for the analysis. Mean ± SD age was 65.05 ± 10.48 years. The IHC assessment revealed a lack of ERα in 46.3% and of PR in 48.7% as well as a high Ki-67 in 31.7%. Loss of ERα and PR was associated with a significant higher rate of advanced stage of disease, a higher frequency of G3 tumors, and a myometrial invasion greater than 50%. A strong Ki-67 expression correlated with a deeper myometrial invasion. Analysis of the interrelationship between receptor immunonegativity revealed a relevant association of ERα immunolocalization with PR and with a high Ki-67 expression. The present study also showed that loss of ERα (P = 0.003), advanced Federation International of Gynecology and Obstetrics stage (P < 0.001), and high Ki-67 (P = 0.004) were independent prognostic factors of a shorter disease-free survival. Importantly, loss of ERα, loss of PR, and a high Ki-67 were correlated with a higher incidence of distant recurrence.
A systematic immunohistochemistry should be a key step in the therapeutic algorithm and could contribute to the identification of high-risk tumors.
本研究旨在评估 Ki-67、雌激素受体α(ERsα)和孕激素受体(PRs)在高危型子宫内膜癌患者中的免疫组织化学(IHC)表达,并评估其预后影响。
方法/材料:对未经治疗的原发性子宫内膜癌进行 Ki-67、ERsα 和 PRs 的免疫组织化学表达评估。评估 IHC 染色与复发风险因素(如年龄、国际妇产科联合会分期、分级、浸润深度和转移扩散)之间的相关性。
82 例患者可用于分析。平均年龄±标准差为 65.05±10.48 岁。IHC 评估显示,46.3%的患者缺乏 ERα,48.7%的患者缺乏 PR,31.7%的患者 Ki-67 高表达。ERα 和 PR 的缺失与疾病的晚期阶段、G3 肿瘤的高发生率以及大于 50%的肌层浸润显著相关。Ki-67 强表达与更深的肌层浸润相关。受体免疫阴性的相互关系分析显示,ERα 免疫定位与 PR 和高 Ki-67 表达存在显著相关性。本研究还表明,ERα 缺失(P=0.003)、国际妇产科联合会晚期分期(P<0.001)和 Ki-67 高表达(P=0.004)是无病生存时间较短的独立预后因素。重要的是,ERα 缺失、PR 缺失和 Ki-67 高表达与远处复发的发生率升高相关。
系统的免疫组织化学检查应成为治疗算法中的关键步骤,并有助于识别高危型肿瘤。