Department of Urology, Seoul National University Bundang Hospital, Seongnam, Korea.
PLoS One. 2019 Nov 7;14(11):e0224671. doi: 10.1371/journal.pone.0224671. eCollection 2019.
Ki-67 is known to be useful in estimating the fraction of proliferation tumor cells in various malignancies. We tried to investigate clinical association of Ki-67 (MIB-1) expression with the oncological outcomes in patients with localized prostate cancer (PCa) after the radical prostatectomy (RP).
We retrospectively analyzed the data of 1,561 patients who underwent RP for localized PCa. According to the propensity score having Ki-67 expression, 183 patients with positive Ki-67 expression were matched to 549 patients without Ki-67 expression. By using multivariate Cox-proportional hazards models and logistic regression tests, the prognostic value of each variable was tested.
After propensity score matching, positive Ki-67 group showed significant worse clinical characteristics and pathologic outcomes than negative Ki-67 group. The multivariate analysis showed that the Ki-67 expression was significantly associated with several adverse pathologic outcomes including higher pathologic stage (p = 0.006), higher grade group (p = 0.005), seminal vesicle invasion (p = 0.036), and positive surgical margin (p = 0.025). The group with Ki-67 expression showed significant worse biochemical recurrence-free survival (p<0.001) than negative Ki-67 group. Subsequent multivariate Cox analyses showed that Ki-67 was independent predictor for BCR after RP (HR 1.549, 95% CI 1.187-2.021, p = 0.001).
In our study, high Ki-67 expression was significantly related with adverse pathological and finally with worse biochemical recurrence-free survival. Further studies are needed to validate the prognostic value of Ki-67 more exactly in PCa patients.
Ki-67 已被证明可用于估计各种恶性肿瘤中增殖肿瘤细胞的比例。我们试图研究 Ki-67(MIB-1)表达与接受根治性前列腺切除术(RP)后的局限性前列腺癌(PCa)患者的肿瘤学结果之间的临床关联。
我们回顾性分析了 1561 名接受 RP 治疗局限性 PCa 的患者的数据。根据 Ki-67 表达的倾向评分,将 183 例 Ki-67 阳性患者与 549 例 Ki-67 阴性患者进行匹配。通过使用多变量 Cox 比例风险模型和逻辑回归检验,测试了每个变量的预后价值。
在倾向评分匹配后,Ki-67 阳性组的临床特征和病理结果明显比 Ki-67 阴性组差。多变量分析显示,Ki-67 表达与几个不良病理结果显著相关,包括更高的病理分期(p = 0.006)、更高的分级组(p = 0.005)、精囊侵犯(p = 0.036)和阳性切缘(p = 0.025)。Ki-67 表达组的生化无复发生存率明显低于 Ki-67 阴性组(p<0.001)。随后的多变量 Cox 分析显示,Ki-67 是 RP 后 BCR 的独立预测因子(HR 1.549,95%CI 1.187-2.021,p = 0.001)。
在我们的研究中,高 Ki-67 表达与不良的病理结果显著相关,最终与生化无复发生存率较差相关。需要进一步的研究来更准确地验证 Ki-67 在 PCa 患者中的预后价值。