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논문 기본 정보

자료유형
학술저널
저자정보
Lei Xin (Yantaishan Hospital) Fangrong Tang (Yantai Quanticision Diagnostics Inc. (Division of Quanticision Diagnostics Inc. of USA)) Bo Song (Yantaishan Hospital) Maozhou Yang (Yantai Quanticision Diagnostics Inc. (Division of Quanticision Diagnostics Inc. of USA)) Jiandi Zhang (Yantai Quanticision Diagnostics Inc. (Division of Quanticision Diagnostics Inc. of USA))
저널정보
대한위암학회 Journal of Gastric Cancer Journal of Gastric Cancer 제21권 제4호
발행연도
2021.12
수록면
335 - 351 (17page)
DOI
10.5230/jgc.2021.21.e32

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Purpose: An underlying factor for the failure of several clinical trials of anti-epidermal growth factor receptor (EGFR) therapies is the lack of an effective method to identify patients who overexpress EGFR protein. The quantitative dot blot method (QDB) was used to measure EGFR protein levels objectively, absolutely, and quantitatively. Its feasibility was evaluated for the prognosis of overall survival (OS) of patients with gastric cancer. Materials and Methods: Slices of 2×5 μm from formalin-fixed paraffin-embedded gastric cancer specimens were used to extract total tissue lysates for QDB measurement. Absolutely quantitated EGFR protein levels were used for the Kaplan-Meier OS analysis. Results: EGFR protein levels ranged from 0 to 772.6 pmol/g (n=246) for all gastric cancer patients. A poor correlation was observed between quantitated EGFR levels and immunohistochemistry scores with ρ=0.024 and P=0.717 in Spearman's correlation analysis. EGFR was identified as an independent negative prognostic biomarker for gastric cancer patients only through absolute quantitation, with a hazard ratio of 1.92 (95% confidence interval, 1.05?3.53; P=0.034) in multivariate Cox regression OS analysis. A cutoff of 208 pmol/g was proposed to stratify patients with a 3-year survival probability of 44% for patients with EGFR levels above the cutoff versus 68% for those below the cutoff based on Kaplan-Meier OS analysis (log rank test, P=0.002). Conclusions: A QDB-based assay was developed for gastric cancer specimens to measure EGFR protein levels absolutely, quantitatively, and objectively. This assay should facilitate clinical trials aimed at evaluation of anti-EGFR therapies retrospectively and prospectively for gastric cancer.

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