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Ann Thorac Surg 1998;66:1159-1163
© 1998 The Society of Thoracic Surgeons
a Division of Thoracic Surgery, Department of Surgery, Cancer Center, Section of Thoracic Oncology, Chest Department, and Department of Pathology, Veterans General Hospital-Taipei, Taipei, Taiwan, Republic of China
b National Yang Ming University, Taipei, Taiwan, Republic of China
Accepted for publication May 5, 1998.
Address reprint requests to Dr Wang, Division of Thoracic Surgery, Department of Surgery, Veterans General Hospital-Taipei, No. 201, Sec 2, Shih-Pai Rd, Taipei, Taiwan, ROC
e-mail: (gcliu{at}www.vghtpe.gov.tw)
Abstract
Background. Even with early diagnosis and adequate resection, the 5-year survival rate for stage I lung cancer patients is around 60% to 70%. Overexpression of HER-2/neu protein is associated with poor prognosis in lung cancers. In this study, we evaluated the expression of HER-2/neu in cancer cells of lung and assessed their clinicopathologic and prognostic significance.
Methods. From 1986 to 1995, clinical data on 42 consecutive patients who underwent complete surgical resection for stage I lung adenocarcinoma were collected. Expression of HER-2/neu in paraffin-embedded tumor samples was determined by immunohistochemistry and scored with a semiquantitative method.
Results. Twenty-one of 42 patients were positive for HER-2/neu overexpression in tumor. Compared with patients with low HER-2/neu expression, patients with HER-2/neu overexpression had a significantly higher incidence of early tumor recurrence (p = 0.014). Survival was also significantly better in patients without HER-2/neu overexpression than in those with HER-2/neu overexpression (p = 0.0047). By univariate analysis, HER-2/neu overexpression and poor cell differentiation are two important factors correlated with poor prognosis.
Conclusions. Expression of HER-2/neu oncoprotein in stage I lung adenocarcinoma can predict the tumors aggressiveness. Early tumor recurrence was frequently detected in patients with HER-2/neu overexpression. We recommend an individualized therapeutic strategy based on the level of HER-2/neu oncoprotein in the tumor cells.
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