Hospital clinical staging accuracy for upper gastrointestinal malignancy
Wilson Luiz da Costa1, Hop S Tran Cao2, Jorge I Portuondo3,4
1Department of Medicine, Epidemiology, and Population Sciences, Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas, USA.
Journal of Surgical Oncology
|September 25, 2020
Summary
Hospitals frequently misstage upper gastrointestinal cancers, impacting treatment decisions. This study reveals significant inaccuracies in clinical staging for esophageal, gastric, and pancreatic cancers, with poor correlation across sites.
Area of Science:
- Oncology
- Surgical Oncology
- Health Services Research
Background:
- Clinical staging is crucial for multimodality treatment planning in upper gastrointestinal malignancies.
- However, the accuracy of clinical staging at the hospital level remains largely unexamined.
Purpose of the Study:
- To evaluate hospital-level accuracy in clinical staging for esophageal, gastric, and pancreatic adenocarcinomas.
- To assess the correlation of staging accuracy across these disease sites within individual hospitals.
Main Methods:
- A national cohort study utilized data from the National Cancer Database (NCDB) from 2006-2015.
- Included patients with adenocarcinoma of the esophagus, stomach, or pancreas treated with upfront resection.
- Calculated hospital-level staging accuracy by comparing clinical stage to pathologic stage and assessed cross-site correlations.
Main Results:
- 1246 hospitals were analyzed, showing median T-staging accuracy of 77.5% (esophageal), 73.7% (gastric), and 60.8% (pancreatic).
- Median N-staging accuracy was 80.2% (esophageal), 72.9% (gastric), and 61.8% (pancreatic).
- Under-staging was most common in pancreatic cancer (36.1% T-stage, 37.4% N-stage). Correlation across sites was weak (r=0.34 for T-stage, r=0.30 for N-stage).
Conclusions:
- Hospitals inaccurately stage 20-40% of patients with upper gastrointestinal cancers.
- Clinical staging accuracy varies significantly across hospitals and disease sites.
- The low correlation across disease sites highlights a need for improved staging consistency in multimodality treatment planning.
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