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Development of Compendium for Esophageal Squamous Cell Carcinoma
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The prognostic value of TP53 mutations in oesophageal adenocarcinoma: a systematic review and meta-analysis
Oliver M Fisher1, Sarah J Lord1,2,3, Dan Falkenback1,4
1Gastroesophageal Cancer Program, St Vincent's Centre for Applied Medical Research University of New South Wales, Sydney, New South Wales, Australia.
Gut
|January 7, 2016
Summary
Tumour protein 53 (TP53) gene mutations are linked to poorer survival in oesophageal adenocarcinoma (OAC) patients. This finding is independent of cancer stage, highlighting TP53 as a potential prognostic biomarker for OAC management.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Oesophageal adenocarcinoma (OAC) requires reliable prognostic biomarkers to guide patient management.
- Tumour protein 53 (TP53) mutations are frequently observed in various cancers, but their specific prognostic role in OAC needs clarification.
Purpose of the Study:
- To systematically evaluate the prognostic significance of TP53 mutations in patients diagnosed with OAC.
- To determine if TP53 mutation status can predict survival outcomes in OAC.
Main Methods:
- A systematic review of studies published between 1990 and 2015 was performed using multiple databases (MEDLINE, Embase, PubMed, Current Contents Connect).
- Studies included populations with at least 50% OAC diagnoses, reporting TP53 status and survival data (hazard ratios).
- Risk of bias was assessed, and a pooled hazard ratio was calculated using a random-effects model.
Main Results:
- Sixteen studies comprising 888 patients were analyzed.
- TP53 mutations were significantly associated with reduced overall survival in OAC patients (HR 1.48, 95% CI 1.16-1.90).
- A stronger negative prognostic effect was observed in a sensitivity analysis of high-quality, OAC-only studies (HR 2.11, 95% CI 1.35-3.31).
Conclusions:
- TP53 gene mutations are associated with diminished overall survival in oesophageal adenocarcinoma.
- The prognostic impact of TP53 mutations on survival is independent of the tumour stage in OAC patients.
- TP53 mutation status represents a valuable prognostic biomarker for OAC.
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