THE PROGNOSTIC-SIGNIFICANCE OF NEUROENDOCRINE MARKERS AND CARCINOEMBRYONIC ANTIGEN IN PATIENTS WITH RESECTED STAGE-I AND STAGE-II NONSMALL CELL LUNG-CANCER

Citation
Sl. Graziano et al., THE PROGNOSTIC-SIGNIFICANCE OF NEUROENDOCRINE MARKERS AND CARCINOEMBRYONIC ANTIGEN IN PATIENTS WITH RESECTED STAGE-I AND STAGE-II NONSMALL CELL LUNG-CANCER, Cancer research, 54(11), 1994, pp. 2908-2913
Citations number
49
Categorie Soggetti
Oncology
Journal title
ISSN journal
00085472
Volume
54
Issue
11
Year of publication
1994
Pages
2908 - 2913
Database
ISI
SICI code
0008-5472(1994)54:11<2908:TPONMA>2.0.ZU;2-N
Abstract
Non-small cell lung cancer with neuroendocrine differentiation may rep resent a subset of patients with a more aggressive (like small cell lu ng cancer) or less aggressive (like carcinoid) biological behavior. To investigate their prognostic significance, immunohistochemical stains for 4 neuroendocrine markers (neuron-specific enolase, chromogranin A , Leu-7, and synaptophysin) and carcinoembryonic antigen (CEA) were st udied in 260 patients with surgically resected stage I and II non-smal l cell lung cancer. The following percentages of cases were positive f or each marker: neuron-specific enolase, 70.0%; chromogranin A, 14.2%; Leu-7, 7.7%; synaptophysin, 11.2%; and CEA 68.5%. Sixty-one (23.5%) w ere positive for greater than or equal to 2 neuroendocrine markers. Wh en compared to adenocarcinoma, squamous cell carcinoma displayed lower positivity for CEA and greater than or equal to 2 neuroendocrine mark ers. There was no significant difference in stage, site of relapse (di stant versus local), disease-free, or overall survival for each marker individually or for those with greater than or equal to 2 neuroendocr ine markers. Multivariate analysis showed that higher nodal stage (N-1 versus N-0), tumor stage (T-2 versus T-1), older age, and the presenc e of mucin predicted for poorer overall survival. Neuroendocrine marke rs and CEA were not of prognostic significance in this group of patien ts with resected stage I and II non-small cell lung cancer.