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Ki67在上皮性卵巢癌中的预后价值:新辅助化疗后Ki67联合CA125预测复发

Prognostic Value of Ki67 in Epithelial Ovarian Cancer: Post-Neoadjuvant Chemotherapy Ki67 Combined with CA125 Predicting Recurrence.

作者信息

Liu Yuexi, Gu Qiuying, Xiao Yao, Wei Xing, Wang Jinlong, Huang Xiaolan, Linghu Hua

机构信息

Department of Gynecology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, People's Republic of China.

出版信息

Cancer Manag Res. 2024 Jul 9;16:761-769. doi: 10.2147/CMAR.S469132. eCollection 2024.

Abstract

PURPOSE

To evaluate Ki67 expression and prognostic value during neoadjuvant chemotherapy (NACT) in advanced epithelial ovarian cancer (EOC).

PATIENTS AND METHODS

95 patients with advanced EOC receiving NACT followed by interval debulking surgery (IDS) were available for tissue samples from matched pre- and post-therapy specimens. The expression of Ki-67 was evaluated by immunohistochemistry and classified by percentage of stained cells. The optimal cutoff values of the Ki67 were assessed by receiver operating characteristic analysis. Kaplan-Meier analysis, the Log rank test, and Cox regression analysis were carried out to analyze survival.

RESULTS

Post-NACT Ki67 was an independent prognostic factor for recurrence by univariate (HR: 1.8, 95% CI: 1.1-3.0, P-value: 0.023) and multivariate (HR: 1.88, 95% CI: 1.08-3.26, P-value: 0.025) analysis. Residual disease >1cm (HR: 2.69, 95% CI: 1.31-5.54, P-value: 0.0070) and pre-treatment CA125 ≥ 1432 U/mL (HR: 2.00, 95% CI: 1.13-3.55, P-value: 0.017) were also independent risk factors for progression-free survival (PFS) in multivariate analysis. Post-NACT Ki67 ≥ 20% was an independent risk factor for PFS, however, baseline Ki67 and Ki67 change did not suggest prognostic significance. In patients with high CA125, the median PFS for patients with high postKi67 (median PFS: 15.0 months, 95% CI: 13.4-16.6 months) was significantly (P-value: 0.013) poorer compared to patients with low postKi67 (median PFS: 30.0 months, 95% CI: 13.5-46.5 months).

CONCLUSION

Post-NACT Ki67 ≥ 20% was an independent factor associated with poorer PFS in patients with advanced-stage EOC undergoing NACT followed by IDS. The combination of post-NACT Ki67 and pretreatment CA125 could better identify patients with poorer PFS in NACT-administered patients.

摘要

目的

评估新辅助化疗(NACT)期间晚期上皮性卵巢癌(EOC)中Ki67的表达及预后价值。

患者与方法

95例接受NACT后行间歇性肿瘤细胞减灭术(IDS)的晚期EOC患者,可获得治疗前和治疗后标本的配对组织样本。通过免疫组织化学评估Ki-67的表达,并根据染色细胞百分比进行分类。通过受试者工作特征分析评估Ki67的最佳临界值。采用Kaplan-Meier分析、Log秩检验和Cox回归分析来分析生存情况。

结果

NACT后Ki67是单因素(HR:1.8,95%CI:1.1 - 3.0,P值:0.023)和多因素(HR:1.88,95%CI:1.08 - 3.26,P值:0.025)分析中复发的独立预后因素。多因素分析中,残留病灶>1cm(HR:2.69,95%CI:1.31 - 5.54,P值:0.0070)和治疗前CA125≥1432 U/mL(HR:2.00,95%CI:1.13 - 3.55,P值:0.017)也是无进展生存期(PFS)的独立危险因素。NACT后Ki67≥20%是PFS的独立危险因素,然而,基线Ki67和Ki67变化并无预后意义。在CA125水平高的患者中,NACT后Ki67高的患者中位PFS(中位PFS:15.0个月,95%CI:13.4 - 16.6个月)显著(P值:0.013)低于NACT后Ki67低的患者(中位PFS:30.0个月,95%CI:13.5 - 46.5个月)。

结论

NACT后Ki67≥20%是接受NACT后行IDS的晚期EOC患者中与较差PFS相关的独立因素。NACT后Ki67与治疗前CA125联合可更好地识别接受NACT患者中PFS较差的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa65/11246084/7e2ec7c7caeb/CMAR-16-761-g0001.jpg

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