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

IF 2.5 4区 医学 Q3 ONCOLOGY Cancer Management and Research Pub Date : 2024-07-09 DOI:10.2147/cmar.s469132
Yuexi Liu, Qiuying Gu, Yao Xiao, Xing Wei, Jinlong Wang, Xiaolan Huang, Hua Linghu
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Kaplan-Meier analysis, the Log rank test, and Cox regression analysis were carried out to analyze survival.<br/><strong>Results:</strong> 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 &gt; 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. 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引用次数: 0

摘要

目的:评估晚期上皮性卵巢癌(EOC)新辅助化疗(NACT)期间Ki67的表达和预后价值。患者和方法:95例晚期EOC患者在接受NACT化疗后接受间期剥除手术(IDS),其组织样本来自治疗前和治疗后的匹配标本。用免疫组化方法评估 Ki-67 的表达,并按染色细胞的百分比进行分类。Ki67的最佳临界值通过接收器操作特征分析进行评估。采用卡普兰-梅耶尔分析、对数秩检验和考克斯回归分析来分析生存率:通过单变量(HR:1.8,95% CI:1.1- 3.0,P值:0.023)和多变量(HR:1.88,95% CI:1.08- 3.26,P值:0.025)分析,NACT后Ki67是复发的独立预后因素。在多变量分析中,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%是无进展生存期的独立危险因素,但基线Ki67和Ki67变化并不提示预后意义。在CA125高的患者中,与低Ki67后患者(中位PFS:30.0个月,95% CI:13.5- 46.5个月)相比,高Ki67后患者的中位PFS(中位PFS:15.0个月,95% CI:13.4- 16.6个月)明显较差(P值:0.013):结论:NACT后Ki67≥20%是晚期EOC患者接受NACT后再接受IDS的PFS较差的一个独立相关因素。NACT后Ki67和治疗前CA125的组合可以更好地识别NACT治疗患者中PFS较差的患者。
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Prognostic Value of Ki67 in Epithelial Ovarian Cancer: Post-Neoadjuvant Chemotherapy Ki67 Combined with CA125 Predicting Recurrence
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.

Keywords: interval debulking surgery, progression-free survival, overall survival, tumor marker
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来源期刊
Cancer Management and Research
Cancer Management and Research Medicine-Oncology
CiteScore
7.40
自引率
0.00%
发文量
448
审稿时长
16 weeks
期刊介绍: Cancer Management and Research is an international, peer reviewed, open access journal focusing on cancer research and the optimal use of preventative and integrated treatment interventions to achieve improved outcomes, enhanced survival, and quality of life for cancer patients. Specific topics covered in the journal include: ◦Epidemiology, detection and screening ◦Cellular research and biomarkers ◦Identification of biotargets and agents with novel mechanisms of action ◦Optimal clinical use of existing anticancer agents, including combination therapies ◦Radiation and surgery ◦Palliative care ◦Patient adherence, quality of life, satisfaction The journal welcomes submitted papers covering original research, basic science, clinical & epidemiological studies, reviews & evaluations, guidelines, expert opinion and commentary, and case series that shed novel insights on a disease or disease subtype.
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