Fan Bo, Zhang Hongshuo, Jin Huidan, Gai Yu, Wang Honglong, Zong Huafeng, Jin Mingyu, Yang Hao, Wan Shuping, Zhu Jiabin, Xu Siyao, Wang Jianbo, Yang Deyong, Song Xishuang
Graduate School, Dalian Medical University, Dalian, Liaoning, P.R. China.
Cell Physiol Biochem. 2016;40(6):1613-1625. doi: 10.1159/000453211. Epub 2016 Dec 23.
Upper tract urinary carcinoma (UTUC) is a relatively uncommon but aggressive disease. The Ki-67 antigen is a classic marker of cellular proliferation, but there is still controversy regarding the significance and importance of Ki-67 in tumor progression.
In this study, we first detected Ki-67 expression in UTUC patients by immunohistochemistry (IHC). Subsequently, we quantitatively combined the results with those from the published literature in a meta-analysis after searching several databases.
IHC results demonstrated that patients with muscle-invasive tumors (T2-T4) had higher Ki-67 expression than those with non-muscle-invasive tumors (Tis-T1), suggesting that high Ki-67 expression may be associated with the aggressive form of UTUC. Kaplan-Meier curves showed that patients with high Ki-67 expression had significantly poorer cancer-specific survival (CSS) and disease-free survival (DFS). Furthermore, multivariate analysis suggested that Ki-67 expression was an independent prognostic factor for CSS (hazard ratio, HR=3.196) and DFS (HR=3.517) in UTUC patients. Then, a meta-analysis of the published literature investigating Ki-67 expression and its effects on UTUC prognosis was conducted. After searching the PubMed, Medline, Embase, Cochrane Library and Scopus databases, 12 articles met the eligibility criteria for this analysis. The eligible studies included a total of 1740 patients with a mean number of 82 patients per study (range, 38-475). The combined results showed that increased Ki-67 levels were associated with poor survival and disease progression, with a pooled HR estimate of 2.081 and 2.791, respectively. In subgroup analysis, the pooled HR was statistically significant for cancer-specific survival (HR=2.276), metastasis-free survival (HR=3.008) and disease-free survival (HR=6.336).
In conclusion, high Ki-67 expression was associated with poor survival in patients with UTUC, as well as a high risk of disease progression, although these findings need to be interpreted with caution. Large-scale, adequately designed, prospective trials are needed to further confirm the value of Ki-67 in prognosis of UTUC patients.
上尿路尿路上皮癌(UTUC)是一种相对罕见但侵袭性较强的疾病。Ki-67抗原是细胞增殖的经典标志物,但关于Ki-67在肿瘤进展中的意义和重要性仍存在争议。
在本研究中,我们首先通过免疫组织化学(IHC)检测UTUC患者的Ki-67表达。随后,在检索多个数据库后,我们将结果与已发表文献中的结果进行定量合并,进行荟萃分析。
免疫组化结果显示,肌层浸润性肿瘤(T2-T4)患者的Ki-67表达高于非肌层浸润性肿瘤(Tis-T1)患者,这表明高Ki-67表达可能与UTUC的侵袭性形式有关。Kaplan-Meier曲线显示,Ki-67高表达的患者癌症特异性生存率(CSS)和无病生存率(DFS)明显较差。此外,多因素分析表明,Ki-67表达是UTUC患者CSS(风险比,HR=3.196)和DFS(HR=3.517)的独立预后因素。然后,对已发表的关于Ki-67表达及其对UTUC预后影响的文献进行了荟萃分析。在检索PubMed、Medline、Embase、Cochrane图书馆和Scopus数据库后,有12篇文章符合本分析的纳入标准。符合条件的研究共纳入1740例患者,每项研究平均82例(范围38-475例)。合并结果显示,Ki-67水平升高与生存率降低和疾病进展相关,合并HR估计值分别为2.081和2.791。在亚组分析中,合并HR对癌症特异性生存率(HR=2.276)、无转移生存率(HR=3.008)和无病生存率(HR=6.336)具有统计学意义。
总之,高Ki-67表达与UTUC患者的低生存率以及疾病进展的高风险相关,尽管这些发现需要谨慎解读。需要大规模、设计充分的前瞻性试验来进一步证实Ki-67在UTUC患者预后中的价值。