Back to Search Start Over

Prognostic Significance of Reversion-Inducing Cysteine-Rich Protein With Kazal Motifs Expression in Resected Pathologic Stage IIIA N2 Non–Small-Cell Lung Cancer

Authors :
Kazuhiro Yanagihara
Hiromi Wada
Seiki Hasegawa
Fumihiro Tanaka
Yosuke Otake
Yoko Morioka
Shinya Ishikawa
Harumi Ito
Chiaki Takahashi
Makoto Noda
Ryo Miyahara
Kazumasa Takenaka
Source :
Annals of Surgical Oncology. 12:817-824
Publication Year :
2005
Publisher :
Springer Science and Business Media LLC, 2005.

Abstract

Reversion-inducing cysteine-rich protein with Kazal motifs (RECK) is a novel membrane-anchored matrix metalloproteinase inhibitor, and experimental studies have shown that RECK can suppress tumor progression through angiogenesis inhibition. We have already revealed that enhanced RECK expression is significantly correlated with a favorable prognosis in non-small-cell lung cancer (NSCLC). In this study, further analyses focused on pN2 disease were conducted to assess the clinical significance of RECK expression.A total of 118 patients with completely resected pathologic stage IIIA N2 NSCLC were retrospectively examined. RECK expression in the primary tumor, along with involved N2 nodes, was examined immunohistochemically.RECK expression in the primary tumor was strong in 53 patients (44.9%) and was weak in the other 65 patients. The 5-year survival rate of patients with RECK-strong tumor (42.9%) was significantly higher than that of patients with RECK-weak tumor (23.1%; P = .017). Reduced RECK expression significantly correlated with a poor prognosis for patients with a single N2 node involved (P = .019), but not for patients with multiple N2 nodes involved (P = .440). A multivariate analysis confirmed that reduced RECK expression was an independent and significant factor to predict a poor prognosis (P = .031). RECK expression in involved N2 nodes was significantly higher than in primary tumors (P.001).RECK status was a novel prognostic factor in pathologic stage IIIA N2 NSCLC.

Details

ISSN :
15344681 and 10689265
Volume :
12
Database :
OpenAIRE
Journal :
Annals of Surgical Oncology
Accession number :
edsair.doi.dedup.....0051ebb12995ba7e693babb9a02dbaa0