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Right arrow Lung - cancer

Eur J Cardiothorac Surg 2001;19:555-561
© 2001 Elsevier Science NL

Prognostic factors in patients with resected pathologic (p-) T1-2N1M0 non-small cell lung cancer (NSCLC)

Fumihiro Tanaka, Kazuhiro Yanagihara, Yosuke Otake, Tomoko Yamada, Tsuyoshi Shoji, Ryo Miyahara, Kenji Inui, Hiromi Wada

Department of Thoracic Surgery, Faculty of Medicine, Kyoto University, Shogoin-kawahara-cho 54, Sakyo-ku, Kyoto 606-8507, Japan

Received 9 October 2000; received in revised form 12 February 2001; accepted 8 March 2001.

Corresponding author. Tel.: +81-75-751-3835; fax: +81-75-751-4647
e-mail: wadah{at}kuhp.kyoto-u.ac.jp

Objectives: To clarify prognostic factors in resected pathologic (p-) T1-2N1M0 non-small cell lung cancer (NSCLC). Methods: A total of 95 consecutive patients who underwent complete tumor resection and mediastinal dissection for pT1-2N1M0 NSCLC between 1976 and 1997 were retrospectively reviewed. p53 status and proliferative activity were evaluated immunohistochemically. Results: The extent of N1 stations and p53 status proved to be significant prognostic factors. The 5-year survival rate for tumor without hilar node (#10) involvement was 66%, significantly higher than that for tumor with #10 involvement (39%, P<0.01). The 5-year survival rate for tumor with aberrant p53 expression was 37%, significantly lower than that for tumor without aberrant p53 expression (74%, P<0.01). There proved to be no significant difference in the prognosis between pT1 disease and pT2 disease; the 5-year survival rates for pT1 and pT2 diseases were 62 and 56%, respectively. Age, gender, performance status, grade of tumor differentiation, histological type, or proliferative activity were not significant factors. Multivariate analysis of prognostic factors using Cox's proportional hazard model confirmed these results. Conclusions: Involvement of the hilar node and aberrant p53 expression were significant factors to predict a worse prognosis in resected T1-2N1M0 NSCLC.

Key Words: Lung cancer • Stage II • N1 • Prognosis • Nodal station • p53




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