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   <subfield code="a">10.1245/s10434-011-1768-2</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1245/s10434-011-1768-2</subfield>
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   <subfield code="a">Borrmann's Macroscopic Criteria and p-Smad2 Expression Are Useful Predictive Prognostic Markers for Cytology-Positive Gastric Cancer Patients Without Overt Peritoneal Metastasis</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Satoru Noda, Masakazu Yashiro, Takahiro Toyokawa, Jyunya Morimoto, Osamu Shinto, Kazuya Muguruma, Tetsuji Sawada, Kosei Hirakawa]</subfield>
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   <subfield code="a">Background: All patients with peritoneal-free cancer cells (CY1) do not always develop a peritoneal recurrence (P1). The goal of this study was to identify characteristic features of peritoneal-free cancer cells that could develop into peritoneal recurrence. Methods: Of 1,474 patients, 91 were identified with CY1P0, and the remaining 1,383 with CY0P0. Immunohistochemical staining with anti-phosphorylated Smad 2 (p-Smad2) was performed on paraffin-embedded specimens from the 91 CY1P0 patients. Results: CY1 was significantly correlated with Borrmann's type-4 cancer, clinical T stage, and lymph node metastasis. CY1P0 patients with Borrmann's type-4 cancer more frequently develop peritoneal recurrence than do those with other types of tumors. The 5-year survival rate of patients with Borrmann's type-4 tumors was significantly (p=0.023) low (6.3%) compared with that of patients with other types of tumors (27.7%). The prognosis for p-Smad2-positive patients was significantly poorer than that of p-Smad2-negative patients. In CY1 and/or P1 patients with Borrmann's type-4 tumors, no significant difference in prognosis was identified between those who had surgery and those who did not. Conclusions: Activated Smad signaling might be associated with a high potential for peritoneal recurrence in CY1P0 patients. Borrmann's macroscopic criteria and p-Smad2 expression are useful markers for surgeons selecting advanced gastric cancer patients with CY1P0 for gastrectomy.</subfield>
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   <subfield code="a">Society of Surgical Oncology, 2011</subfield>
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   <subfield code="u">Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka, Japan</subfield>
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   <subfield code="a">Yashiro</subfield>
   <subfield code="D">Masakazu</subfield>
   <subfield code="u">Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka, Japan</subfield>
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   <subfield code="a">Toyokawa</subfield>
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   <subfield code="u">Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka, Japan</subfield>
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   <subfield code="u">Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka, Japan</subfield>
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   <subfield code="a">Shinto</subfield>
   <subfield code="D">Osamu</subfield>
   <subfield code="u">Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka, Japan</subfield>
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   <subfield code="a">Muguruma</subfield>
   <subfield code="D">Kazuya</subfield>
   <subfield code="u">Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka, Japan</subfield>
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   <subfield code="a">Sawada</subfield>
   <subfield code="D">Tetsuji</subfield>
   <subfield code="u">Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka, Japan</subfield>
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   <subfield code="u">Department of Surgical Oncology, Osaka City University Graduate School of Medicine, Osaka, Japan</subfield>
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   <subfield code="t">Annals of Surgical Oncology</subfield>
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   <subfield code="g">18/13(2011-12-01), 3718-3725</subfield>
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