Abstract
Objective: To explore the target protein expression in separate tumors in a patient with synchronous multiple gastric carcinomas (SMGCs). Study Design: Immunohistochemistry for HER2, EGFR, and MET were performed in 282 carcinomas from 141 patients. Results: Of 141 patients with SMGCs, 11.3%, 23.4%, and 14.9% of cases showed HER2, EGFR, and MET protein overexpression, respectively. In SMGC cases with overexpression of target proteins in > 1 tumor, intertumoral heterogeneity was 81.3% (13/16) for HER2, 78.8% (26/33) for EGFR, and 90.5% (19/21) for MET protein. The concordance rate of HER2, EGFR, and MET expression between 2 carcinomas from the same patient was 90.8%, 81.6%, and 86.5%, respectively, with a kappa value below 0.3, indicating slight to fair agreement. Conclusion: We found a considerable intertumoral heterogeneity of target protein overexpression in SMGCs. Our findings support a multicentric origin for SMGC and emphasize the need to perform immunohistochemistry for all synchronous lesions.
| Original language | English |
|---|---|
| Pages (from-to) | 27-35 |
| Number of pages | 9 |
| Journal | Analytical and Quantitative Cytology and Histology |
| Volume | 35 |
| Issue number | 1 |
| State | Published - Feb 2013 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Carcinoma
- EGFR genes
- Gastric cancer
- Genes
- HER2
- MET
- Stomach cancer
- Synchronous multiple primary neoplasms
- Targeted molecular therapy
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