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Nuclear survivin in pN2 nonsmall cell lung cancer: prognostic and clinical implications

Depts of ¹ Thoracic Surgery, and ³ Diagnostic Pathology, Graduate School of Medicine, Chiba University, Chiba, Japan, ² Dept of Pulmonology, Faculty of Medicine, Assiut University, Assiut, Egypt.

CORRESPONDENCE: K. Yasufuku, Dept of Thoracic Surgery, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-Ku, Chiba 260-8670, Japan. Fax: 81 432262172. E-mail: kyasufuku{at}faculty.chiba-u.jp

Keywords: Nonsmall cell lung cancer, nuclear, pathological N2, prognosis, survivin

Received: May 3, 2008
Accepted August 1, 2008

Patients with N2 nonsmall cell lung cancer (N2-NSCLC) represent heterogeneous groups. Survivin is a member of the inhibitor of apoptosis family. If N2-NSCLC patients could be stratified, based on survivin expression and/or its relation to cell cycle proteins, into homogeneous subgroups, certain therapies could be selected for those patients.

Survivin expression in 78 surgically resected primary pathological N2-NSCLC tumours was evaluated using immunohistochemistry. Relationships of survivin expression to overall survival, clinical features and expression of six cell cycle-related proteins (pRb, cyclin D1, p16^INK4A, p53, p21^Waf1 and Ki-67) were analysed.

Nuclear survivin and the number of mediastinal lymph node (LN) stations were independent prognostic factors. The patient group with combined negative survivin/single mediastinal LN station were the most favourable prognostic group, and was related to the clinical nodal factor. Indeed, patients with negative survivin/low Ki-67 labelling indices had the best survival, especially in nonsquamous histopathology.

The current authors conclude that nuclear survivin is strongly related to lymph node metastasis and proliferative potentials in pathological N2 nonsmall cell lung cancer patients. Pre-operative N2 nonsmall cell lung cancer patients with combined negative nuclear survivin and a single mediastinal lymph node station, or low proliferative indices, particularly in clinical N0-1 disease and nonsquamous histopathology, respectively, are expected to have a favourable post-operative prognosis and may be candidates for primary resection.