{"title":"Predicting abiraterone efficacy in advanced prostate cancer: Insights from marker of proliferation Ki67","authors":"Fengnian Zhao, Jinge Zhao, Xinyuan Wei, Yifu Shi, Nanwei Xu, Sha Zhu, Junru Chen, Guangxi Sun, Jindong Dai, Zhipeng Wang, Xingming Zhang, Jiayu Liang, Xu Hu, Haoyang Liu, Junjie Zhao, Zhenhua Liu, Ling Nie, Pengfei Shen, Ni Chen, Hao Zeng","doi":"10.1002/pros.24710","DOIUrl":null,"url":null,"abstract":"BackgroundKI67 is a well‐known biomarker reflecting cell proliferation. We aim to elucidate the predictive role of KI67 in the efficacy of abiraterone for patients with advanced prostate cancer (PCa).MethodsClinicopathological data of 152 men with metastatic PCa, who received abiraterone therapy were retrospectively collected. The KI67 positivity was examined by immunohistochemistry using the prostate biopsy specimen. The predictive value of KI67 on the therapeutic efficacy of abiraterone was explored using Kaplan–Meier curve and Cox regression analysis. The endpoints included prostate‐specific antigen (PSA) progression‐free survival (PSA‐PFS), radiographic PFS (rPFS), and overall survival (OS).ResultsIn total, 85/152 (55.9%) and 67/152 (44.1%) cases, respectively, received abiraterone at metastatic hormone‐sensitive (mHSPC) and castration‐resistant PCa (mCRPC) stage. The median KI67 positivity was 20% (interquartile range: 10%–30%). Overall, KI67 rate was not correlated with PSA response. Notably, an elevated KI67‐positive rate strongly correlated with unfavorable abiraterone efficacy, with KI67 ≥ 30% and KI67 ≥ 20% identified as the optimal cutoffs for prognosis differentiation in mHSPC (median PSA‐PFS: 11.43 Mo vs. 26.43 Mo, <jats:italic>p</jats:italic> < 0.001; median rPFS: 16.63 Mo vs. 31.90 Mo, <jats:italic>p</jats:italic> = 0.003; median OS: 21.77 Mo vs. not reach, <jats:italic>p</jats:italic> = 0.005) and mCRPC (median PSA‐PFS: 7.17 Mo vs. 12.20 Mo, <jats:italic>p</jats:italic> = 0.029; median rPFS: 11.67 Mo vs. 16.47 Mo, <jats:italic>p</jats:italic> = 0.012; median OS: 21.67 Mo vs. not reach, <jats:italic>p</jats:italic> = 0.073) patients, respectively. Multivariate analysis supported the independent predictive value of KI67 on abiraterone efficacy. In subgroup analysis, an elevated KI67 expression was consistently associated with unfavorable outcomes in the majority of subgroups. Furthermore, data from another cohort of 79 PCa patients with RNA information showed that those with KI67 RNA levels above the median had a significantly shorter OS than those below the median (17.71 vs. 30.72 Mo, <jats:italic>p</jats:italic> = 0.035).ConclusionsThis study highlights KI67 positivity in prostate biopsy as a strong predictor of abiraterone efficacy in advanced PCa. These insights will assist clinicians in anticipating clinical outcomes and refining treatment decisions for PCa patients.","PeriodicalId":501684,"journal":{"name":"The Prostate","volume":"36 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Prostate","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/pros.24710","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
BackgroundKI67 is a well‐known biomarker reflecting cell proliferation. We aim to elucidate the predictive role of KI67 in the efficacy of abiraterone for patients with advanced prostate cancer (PCa).MethodsClinicopathological data of 152 men with metastatic PCa, who received abiraterone therapy were retrospectively collected. The KI67 positivity was examined by immunohistochemistry using the prostate biopsy specimen. The predictive value of KI67 on the therapeutic efficacy of abiraterone was explored using Kaplan–Meier curve and Cox regression analysis. The endpoints included prostate‐specific antigen (PSA) progression‐free survival (PSA‐PFS), radiographic PFS (rPFS), and overall survival (OS).ResultsIn total, 85/152 (55.9%) and 67/152 (44.1%) cases, respectively, received abiraterone at metastatic hormone‐sensitive (mHSPC) and castration‐resistant PCa (mCRPC) stage. The median KI67 positivity was 20% (interquartile range: 10%–30%). Overall, KI67 rate was not correlated with PSA response. Notably, an elevated KI67‐positive rate strongly correlated with unfavorable abiraterone efficacy, with KI67 ≥ 30% and KI67 ≥ 20% identified as the optimal cutoffs for prognosis differentiation in mHSPC (median PSA‐PFS: 11.43 Mo vs. 26.43 Mo, p < 0.001; median rPFS: 16.63 Mo vs. 31.90 Mo, p = 0.003; median OS: 21.77 Mo vs. not reach, p = 0.005) and mCRPC (median PSA‐PFS: 7.17 Mo vs. 12.20 Mo, p = 0.029; median rPFS: 11.67 Mo vs. 16.47 Mo, p = 0.012; median OS: 21.67 Mo vs. not reach, p = 0.073) patients, respectively. Multivariate analysis supported the independent predictive value of KI67 on abiraterone efficacy. In subgroup analysis, an elevated KI67 expression was consistently associated with unfavorable outcomes in the majority of subgroups. Furthermore, data from another cohort of 79 PCa patients with RNA information showed that those with KI67 RNA levels above the median had a significantly shorter OS than those below the median (17.71 vs. 30.72 Mo, p = 0.035).ConclusionsThis study highlights KI67 positivity in prostate biopsy as a strong predictor of abiraterone efficacy in advanced PCa. These insights will assist clinicians in anticipating clinical outcomes and refining treatment decisions for PCa patients.
背景KI67是一种众所周知的反映细胞增殖的生物标志物。我们旨在阐明 KI67 对阿比特龙治疗晚期前列腺癌(PCa)患者疗效的预测作用。方法 回顾性收集了 152 名接受阿比特龙治疗的转移性 PCa 男性患者的临床病理学数据。方法回顾性收集了152名接受阿比特龙治疗的转移性前列腺癌患者的临床病理数据,并利用前列腺活检标本通过免疫组织化学方法检测了KI67的阳性率。利用卡普兰-梅耶曲线和考克斯回归分析探讨了KI67对阿比特龙疗效的预测价值。研究终点包括前列腺特异性抗原(PSA)无进展生存期(PSA-PFS)、放射学无进展生存期(rPFS)和总生存期(OS)。结果在转移性激素敏感PCa(mHSPC)和阉割耐药PCa(mCRPC)阶段,分别有85/152(55.9%)和67/152(44.1%)例患者接受了阿比特龙治疗。KI67阳性率的中位数为20%(四分位间范围:10%-30%)。总体而言,KI67阳性率与PSA反应无关。值得注意的是,KI67阳性率升高与阿比特龙疗效不佳密切相关,KI67≥30%和KI67≥20%被确定为mHSPC预后分化的最佳临界值(中位PSA-PFS:11.43个月 vs. 26.43个月,p < 0.001;中位rPFS:16.63个月 vs. 31.90个月,p = 0.003;中位OS:21.77个月 vs. 未达标,p = 0.003):中位 PSA-PFS: 7.17 Mo vs. 12.20 Mo, p = 0.029; 中位 rPFS: 11.67 Mo vs. 16.47 Mo, p = 0.012; 中位 OS: 21.67 Mo vs. not reach, p = 0.005)和 mCRPC(中位 PSA-PFS: 7.17 Mo vs. 12.20 Mo, p = 0.029; 中位 rPFS: 11.67 Mo vs. 16.47 Mo, p = 0.012; 中位 OS:21.67月 vs. 未达到,p = 0.073)患者。多变量分析支持 KI67 对阿比特龙疗效的独立预测价值。在亚组分析中,在大多数亚组中,KI67表达升高始终与不利的预后相关。此外,来自另一个队列的79例PCa患者的RNA信息数据显示,KI67 RNA水平高于中位数的患者的OS明显短于低于中位数的患者(17.71月 vs. 30.72月,p = 0.035)。这些见解将有助于临床医生预测临床结果并改进 PCa 患者的治疗决策。