TP53 Mutations and Survival in Osteosarcoma Patients: A Meta-Analysis of Published Data
- PMID: 27239089
- PMCID: PMC4863100
- DOI: 10.1155/2016/4639575
TP53 Mutations and Survival in Osteosarcoma Patients: A Meta-Analysis of Published Data
Abstract
Several research groups have examined the association between TP53 mutations and prognosis in human osteosarcoma. However, the results were controversial. The purpose of this study was to evaluate the prognostic value of TP53 mutations in osteosarcoma patients. A meta-analysis was conducted with all eligible studies which quantitatively evaluated the relationship between TP53 mutations and clinical outcome of osteosarcoma patients. Eight studies with a total of 210 patients with osteosarcoma were included in this meta-analysis. The risk ratio (RR) with a 95% confidence interval (95% CI) was calculated to assess the effect of TP53 mutations on 2-year overall survival. The quantitative synthesis of 8 published studies showed that TP53 mutations were associated with 2-year overall survival in osteosarcoma patients. These data suggested that TP53 mutations had an unfavorable impact on 2-year overall survival when compared to the counterparts with wild type (WT) TP53 (RR: 1.79; 95% CI: 1.12 to 2.84; P = 0.01; I (2) = 0%). There was no between-study heterogeneity. TP53 mutations are an effective prognostic marker for survival of patients with osteosarcoma. However, further large-scale prospective trials should be performed to clarify the prognostic value of TP53 mutations on 3- or 5-year survival in osteosarcoma patients.
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References
-
- Geller D. S., Revskaya E., Khan M., Morris J., Gorlick R., Dadachova E. Abstract 1798: targeted therapy of osteosarcoma with radiolabeled monoclonal antibody to an insulin-like growth factor-2 receptor. Cancer Research. 2015;75(15, supplement):1798–1798. doi: 10.1158/1538-7445.am2015-1798. - DOI - PubMed
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