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Meta-Analysis
. 2016 Mar 1;7(9):10023-36.
doi: 10.18632/oncotarget.7054.

CD133 expression may be useful as a prognostic indicator in colorectal cancer, a tool for optimizing therapy and supportive evidence for the cancer stem cell hypothesis: a meta-analysis

Affiliations
Meta-Analysis

CD133 expression may be useful as a prognostic indicator in colorectal cancer, a tool for optimizing therapy and supportive evidence for the cancer stem cell hypothesis: a meta-analysis

Yang Zhao et al. Oncotarget. .

Abstract

We performed a meta-analysis of CD133-related clinical data to investigate the role of cancer stem cells (CSCs) in the clinical outcomes of colorectal cancer (CRC) patients, analyzing the effectiveness of various therapeutic strategies and examining the validity of the CSC hypothesis. For 28 studies (4546 patients), the relative risk (RR) to survival outcomes associated with CD133+ CRCs were calculated using STATA 12.0 software. Pooled results showed that CD133High patients had poor 5-year overall survival (RR 0.713, 95% CI 0·616-0·826) and 5-year disease free survival (RR 0·707, 95% CI 0·602-0·831). Both associations were consistently observed across different races, research techniques and therapeutic strategies. In a subgroup receiving adjuvant therapy, CD133Low patients achieved significantly better survival than CD133High patients. The findings suggest that CD133 could serve as a predictive marker of poor prognosis and treatment failure in CRC. CD133Low patients could benefit from adjuvant treatments, while CD133High patients should be given novel treatments besides adjuvant therapy. Our results also provide evidence in support of the CSC hypothesis.

Keywords: CD133; cancer stem cell; meta-analysis; tumor genesis; tumor recurrence.

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Conflict of interest statement

CONFLICTS OF INTEREST

All authors declared that they had no conflicts of interests.

Figures

Figure 1
Figure 1. Flow chart for eligible articles identified in this meta-analysis
Figure 2
Figure 2
Begg's funnel plots to explore the possibility of publication bias in the pooled analyses of CD133 expression and OS (A) or DFS (B).
Figure 3
Figure 3. Forest plots of RRs for the association of CD133 expression with the (A) OS and (B) DFS
Figure 4
Figure 4. The stratified analysis evaluating the association of CD133 expression with (A) OS and (B) DFS in the subgroups with or without AT

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