Introduction
Colorectal carcinoma (CRC) is the fourth most common cause of death induced by carcinoma, accounting for 600,000 deaths per year [
1]. Some clinical factors, such as tumor stage, tumor necrosis, vascular invasion and differentiation, have been reported to be associated with prognosis of CRC patients [
2,
3]. However, these factors were not sufficient to accurately make risk stratification for clinical prognosis. In clinical practice, identification of patients with high risk of poor prognosis would help to optimize treatment and to improve clinical prognosis. Therefore, there is an urgent need to find reliable prognostic factors for prediction of clinical prognosis in CRC patients.
Ki-67 antigen expresses throughout the cell cycle in proliferating cells, except for quiescent (G0) cells [
4]. The correlation between Ki-67 expression and prognosis of CRC patients were still contradictory in various studies [
5‐
38]. Several studies showed that high Ki-67 expression was related with poor overall survival (OS) [
26‐
30], whereas several studies reported that high Ki-67 expression was correlated with favorable OS [
8,
15,
16]. Therefore, we performed this meta analysis to determine the prognostic value of Ki-67 expression in CRC patients.
Materials and methods
Literature search strategy
Four electronic databases, including EMBASE, PubMed, Web of Knowledge and Cochrane Library, were searched from January 1990 to July 2017 for eligible studies. We performed literature search by combined text word and MeSH strategy for PubMed with the following search strategy: (“Ki67” or “Ki-67” or “MIB-1” or “MIB1”) and (“carcinoma” or “neoplasm” or “tumor” or “cancer” or “malignancy”) and (“colorectal” or “rectal” or “colon”) and (“prognosis” or “prognostic” or “survival” or “outcome” or “mortality”).The strategies for EMBASE and other databases were similar but were adapted according to the guideline of the database. Meanwhile, expanded search of hyponym was performed. In the retrieval process, we made a manual search using the references of the including articles to supplement eligible studies. We contacted the corresponding author to get necessary study data if necessary. The search was restricted to human studies and there was no restriction in terms of language or publication time. All information investigation and collection were conducted according to the principles of Declaration of Helsinki.
Criteria for inclusion and exclusion
The inclusion criteria were defined as follows: (1) proven pathological diagnosis of CRC in humans; (2) assessment of Ki-67 expression by using immunohistochemistry (IHC) method; (3) enough survival information such as hazard ratio (HR) and 95% confidence interval (CI). Studies not directly providing hazard ratio and 95% confidence interval were included if survival information were available from survival curves or tables. Articles published in Chinese were included in the present meta analysis as English literature. For multiple studies from the same study population, only the most recently published study was included in the present analysis.
The following studies were excluded: (1) non-human experiments; (2) case reports, reviews, letters and conference abstracts without survival information; (3) lack of the necessary survival information.
Quality assessment
Two reviewers (Zhi-Qiao Zhang and Zhao-Wen Luo) independently assessed the quality of the studies included in the present meta analysis using Newcastle-Ottawa Quality Assessment Scale (NOS). The NOS comprises assessments of patient selection, study comparability, follow-up and outcomes of interest. The total scores were used to evaluate the quality of the study. Disagreements between two reviewers (Zhi-Qiao Zhang and Zhao-Wen Luo) were resolved by consultation with a third reviewer (Ming-Gu Zhu).
Two investigators (Zhi-Qiao Zhang and Zhao-Wen Luo) independently extracted the survival information of the original studies: surname of the first author, country, study sample size, publication year, disease stage, test method of Ki-67 expression, clinical parameters, and survival information (HRs and 95%CIs). All study information were extracted and recorded by using a standardized form. All included studies were coded as the surname of the first author + publish year in the standardized form. Study authors were contacted to get necessary data if necessary. Disagreements between two investigators were resolved by discussion with a third investigator (Ming-Gu Zhu).
Statistical analysis
The statistical analysis was performed according to the suggestions advised by the Meta analysis of Observational.
Studies in Epidemiology group(MOOSE) [
39]. The hazard ratios (HR) and 95% CI were used to summary the final effects of survival outcome. We pooled HR and 95% CI if the survival data were reported in the original articles. While HR and 95% CI were not directly reported in the articles, survival data was extracted from Kaplan-Meier curve and used to estimate HR. The heterogeneity among various studies was measured by the Q and
I2 tests. A probability value of
I2 value≥30% and
P value< 0.1 indicated the existence of significant heterogeneity. A random effect model (DerSimonian and Laird method) or fixed effect model(Mantel-Haenszel method) was used according to the results of heterogeneity analyses. Meta-regression analyses (Reml method) and subgroup analyses were performed to explore the sources of heterogeneity. Funnel plot, Begg’s test, Egger’s test, and trim and fill method were performed to assess publication bias. The difference was considered to be statistically significant if
P value < 0.05. The statistical analyses were performed by STATA version 12.0 software (Stata Corporation, College Station, Texas, USA).
Discussion
The present meta analysis showed that high Ki-67 expression is significantly correlated with poor prognosis in CRC patients. The pooled hazard ratios were 1.54(95% CI 1.17–2.02, P = 0.005) for overall survival and 1.43(1.12–1.83, P = 0.008) for disease free survival in univariate analysis. After adjustment of other prognostic factors, the pooled HR was 1.50(95% CI 1.02–2.22, P = 0.03) for overall survival in multivariate analysis.
Some previous studies have reported that high Ki-67 expression significantly predicted poor OS in CRC patients [
26‐
30]. The conclusion of the present meta analysis was consistent with that of these previous studies. Although the mechanism of Ki-67 expression on tumor prognosis was still uncertain, some clinical studies have provided interesting evidences for utility of Ki-67 expression as a predictive tool for clinical prognosis in patients with different tumors, for example prostate cancer, thyroid carcinoma and renal clear cell [
41‐
43]. Interestingly, there were three studies indicated that there was a negative association between the high Ki-67 expression and the overall survival of CRC patients. Salminen et al. [
8] reported that HR of high Ki-67 expression was 0.63 (95% CI 0.41–0.98) for overall survival in univariate analysis, whereas it was 1.26 (95% CI 0.67–2.39) for overall survival in multivariate analysis. Xi et al. [
15] reported that HR of high Ki-67 expression was 0.34 (95% CI 0.16–0.73) for overall survival by using a special scoring system of Ki-67 expression: The intensity of positivity was scored as follows: 0, negative; 1, weak; 2, moderate; 3, strong. The extent of positivity was scored according to the percentage of cells showing positive staining: 0, < 5%; 1, 5–25%; 2, 25–50%; 3, 50–75%; 4, > 75%. The final score was determined by multiplying the intensity of positivity and the extent of positivity scores and final score > 5 was defined as positive. Ivanecz et al. [
16] selected 98 patients for prognostic study from 406 patients by using the following criteria: first liver resection for CLM; potentially curative R0 resection; follow-up period of surviving patients > 5 years. The special inclusion criteria might influence the baseline characteristics and weaken the credibility of study conclusion.
There was significant heterogeneity in the present meta analysis. The current meta analysis might exist several potential sources of heterogeneity as follows: First, the heterogeneity caused by different cut off values of Ki-67 expression was inevitable. The subgroup analysis have revealed the influence of different cut off values on heterogeneity. Second, the subgroup analysis suggested that different treatment has a significant effect on heterogeneity and might be a potential source of heterogeneity. Third, obvious difference of the pooled HRs between rectal cancer subgroup and colorectal liver metastases subgroup suggested that further study is need to clarify the exact influence of different pathologic type on clinical prognosis.
Publication bias is an important influence factor for interpreting the conclusion. The funnel plot for OS in univariate analysis was obviously asymmetrical and Egger’s test also demonstrated significant publication bias (P = 0.008). The funnel plot asymmetry might be caused by different reasons as follows: Firstly, publication bias was one important source of funnel plot asymmetry, for example location bias, citation bias, language bias, time lag bias, multiple publication bias and outcome reporting bias. Secondly, the true heterogeneity in intervention effects might be one resource of funnel plot asymmetry. The true heterogeneity might be caused by differences in the intensity of interventions or differences in underlying risk between studies with different sizes. Thirdly, poor methodological quality was another source of funnel plot asymmetry. Smaller studies were often performed with poorer methodological quality than larger studies. Therefore, smaller studies with poorer methodological quality also tended to display larger influences than larger studies. Finally, funnel plot asymmetrical might be caused by chance. We conducted a contour-enhanced funnel plot using the trim-and-fill method to explore the potential cause of funnel plot asymmetry. Given that all 9 dummy studies were in areas of high statistical significance, the publication bias might not the major cause of funnel plot asymmetry in the present meta analysis.
Although significant heterogeneity existed in the present meta analysis, sensitivity analysis demonstrated that the relation between high Ki-67 expression and poor prognosis of CRC patients did not changed after removing any individual study. Meanwhile, cumulative meta analysis also showed that performance of high Ki-67 expression for poor prognosis in CRC patients was stable and reliable.
The present meta analysis had several strengths: Firstly, there were 34 eligible studies and 6180 CRC patients in the present study, which could significantly increase persuasiveness of the conclusion. Secondly, Ki-67 expression in 34 eligible studies was all measured with IHC method, leading to less clinical heterogeneity. Thirdly, studies published in Chinese were also included in this meta analysis as English literature, increasing the representation of the study population.
The conclusion of the present meta analysis should be interpreted cautiously for reasons as follows: Firstly, most studies defined positive status of Ki-67 expression according to different cut off values, which might result in clinical heterogeneity. Hence, it is necessary to determine an universal cut off value for future studies. Secondly, heterogeneity was inevitable due to different baseline characteristics, such as tumor stage and treatment, which might increase clinical heterogeneity and reduce the persuasiveness of the conclusion. Thirdly, some survival data were extracted from survival curves indirectly. Although the method for extracting HR and 95% CI from survival curves is widely accepted, we could not completely eliminate the sources of information inaccuracy in the process of information extraction. Fourthly, Ki-67 expression in the selected studies was measured by IHC method. This method might suffer from important variation among different studies and was not enough precise for a rigorous and precise conclusion. Fifthly, several genes have been reported to be related with the prognosis of CRC patients including KRAS, Cyclin-dependent kinase 2 (cdc2), and Cathepsin D [
5,
35,
36]. Interestingly enough, Nash reported that patients with KRAS mutant tumors that expressed high levels of Ki-67 had significantly worse DFS than patients with KRAS wild-type tumors that expressed low level of Ki-67, indicating that combined application of these predictive genes might provide more valuable prognostic information and further improve the clinical prediction of prognosis for CRC patients.
In conclusion, the present meta analysis demonstrated that high Ki-67 expression significantly predicts poor overall survival and disease free survival. High Ki-67 expression may serve as a valuable predictive biomarker for poor prognosis in CRC patients.