Chen Ming, Yao Shuzhong, Cao Qinghua, Xia Meng, Liu Junxiu, He Mian
Department of Obstetrics and Gynecology, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Department of Pathology, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Oncotarget. 2016 Dec 23;8(64):107877-107885. doi: 10.18632/oncotarget.14112. eCollection 2017 Dec 8.
This study sought to assess the prognostic role of Ki67 in primary ovarian high-grade serous carcinoma (HGSC) and to determine whether Ki67 expression can predict responsiveness to platinum and paclitaxel chemotherapy.
A total of 318 women were included in the analysis and the median follow-up time was 48 months (range, 3-150 months). Ki67 proliferation indices ranged from 3% to 95% with a median of 40%. Using 40% as the cut-off value for the Ki67 index, we classified 141 patients as having low Ki67 expression and 177 patients as having high Ki67 expression. Low Ki67 expression was a predictor of platinum resistance (hazard ratio (HR) 2.85, 95% CI 1.43-5.98, < 0.001). In the Kaplan-Meier analysis, comparisons of patients with low versus high Ki67 expression demonstrated that low Ki67 expression was significantly associated with decreased progression-free survival (PFS) (22% vs. 34% for 5-year PFS, < 0.001) and decreased overall survival (OS) (31% vs. 55%, < 0.001). Multivariate analysis indicated that low Ki67 expression was associated with decreased PFS (HR 2.98, 95% CI 1.75-6.56, < 0.001) and decreased OS (HR 1.74, 95% CI 1.38-5.01, = 0.003).
A retrospective study of patients with stage I-IV primary ovarian HGSC was conducted from January 1, 2002, to December 31, 2012. Ki67 levels were measured via immunohistochemistry (IHC) and analyzed with respect to clinicopathological factors, and a survival analysis was performed.
HGSC appears to be a heterogeneous disease with different clinical outcomes. Low Ki67 expression (< 40%) in HGSC is significantly associated with platinum resistance and decreased survival.
本研究旨在评估Ki67在原发性卵巢高级别浆液性癌(HGSC)中的预后作用,并确定Ki67表达是否可预测对铂类和紫杉醇化疗的反应性。
共有318名女性纳入分析,中位随访时间为48个月(范围3 - 150个月)。Ki67增殖指数范围为3%至95%,中位数为40%。以40%作为Ki67指数的临界值,我们将141例患者分类为低Ki67表达,177例患者分类为高Ki67表达。低Ki67表达是铂类耐药的预测指标(风险比(HR)2.85,95%置信区间1.43 - 5.98,P < 0.001)。在Kaplan-Meier分析中,低Ki67表达与高Ki67表达患者的比较表明,低Ki67表达与无进展生存期(PFS)降低显著相关(5年PFS分别为22%和34%,P < 0.001)以及总生存期(OS)降低(分别为31%和55%,P < 0.001)。多变量分析表明,低Ki67表达与PFS降低(HR 2.98,95%置信区间1.75 - 6.56,P < 0.001)和OS降低(HR 1.74,95%置信区间1.38 - 5.01,P = 0.003)相关。
对2002年1月1日至2012年12月31日期间I - IV期原发性卵巢HGSC患者进行回顾性研究。通过免疫组织化学(IHC)测量Ki67水平,并就临床病理因素进行分析,同时进行生存分析。
HGSC似乎是一种具有不同临床结局的异质性疾病。HGSC中低Ki67表达(< 40%)与铂类耐药及生存期降低显著相关。