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   <subfield code="a">Evaluation of HER2 Protein Expression in Gastric Carcinomas: Comparative Analysis of 1414 Cases of Whole-Tissue Sections and 595 Cases of Tissue Microarrays</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Kab Kim, Young Koh, Heung-Moon Chang, Tae Kim, Jeong Yook, Byung Kim, Se Jang, Young Park]</subfield>
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   <subfield code="a">Background: Recent advances in molecular targeted therapy have identified HER2 as an important target for anti-cancer therapy in gastric cancer (GC). Although the clinical relevance and prognostic significance of HER2 in breast cancer has been well acknowledged, it remains controversial in GC. Methods: HER2 expression was investigated in two independent series of GC by immunohistochemical staining. One series corresponded to 1,414 cases of whole-tissue sections and the other corresponded to 595 cases of tissue microarrays (TMAs). Results were compared and correlated with clinicopathologic parameters. Results: HER2-positivity was detected in 12.3% of whole-tissue sections and 17% of TMAs. Among samples scored 3+, 90.1% stained ≥50% of the tumor area, but only 40.9% in score 2+ cases stained ≥50% of the tumor area. In whole-tissue sections, HER2-positivity was correlated with age (P=0.002), histological type (differentiated or intestinal, P&lt;0.001), lymphovascular invasion (P=0.005), and lymph node metastasis (P=0.009). In TMAs, HER2-positivity was correlated only with age (P=0.003) and histological type (P&lt;0.001). Multivariate analyses of the differentiated GC subgroup revealed that HER2-positivity was an independent poor prognostic factor (P=0.042). The cases with HER2-positive in ≥50% of the tumor area showed worse prognosis than those of &lt;50% (P=0.021). Conclusions: Despite discrepancies in the results from whole-tissue sections and TMAs, HER2 overexpression was positively correlated with aggressive biological behavior and was an independent poor prognostic factor for recurrence in differentiated GCs. Therefore, HER2-positive GCs should be considered for adjuvant trastuzumab therapy.</subfield>
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   <subfield code="a">Kim</subfield>
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   <subfield code="u">Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea</subfield>
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   <subfield code="a">Koh</subfield>
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   <subfield code="a">Yook</subfield>
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   <subfield code="t">Annals of Surgical Oncology</subfield>
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   <subfield code="g">18/10(2011-10-01), 2833-2840</subfield>
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