[Pre-treatment and treatment-induced neuron-specific enolase in patients with small-cell lung cancer: an open prospective study]
- PMID: 20537457
- DOI: 10.1016/j.arbres.2010.04.005
[Pre-treatment and treatment-induced neuron-specific enolase in patients with small-cell lung cancer: an open prospective study]
Abstract
Background: Neuron-specific enolase (NSE) is the most sensitive tumor marker for small-cell lung carcinoma (SCLC) at the time of diagnosis. The main purpose of this study was to review the usefulness of serum NSE level as a prognostic factor in patients with SCLC and to determine the correlation between the NSE level and the stage of disease and response to chemotherapy.
Methods: In this prospective study, patients with SCLC were evaluated for response to chemotherapy, survival without disease progression, and overall survival. The end point was designated at patient death due to SCLC. NSE assays were performed before and after completion of chemotherapy.
Results: Sixty-five patients were included in study. NSE levels were significantly higher in patients who died of SCLC. The pre-treatment NSE levels in patients who responded to treatment were significantly lower. The post-treatment NSE levels were not significantly correlated with response to chemotherapy, progression-free survival, overall survival, and prognosis of patients. Change in the NSE level between the pre- and post-treatment periods was not significantly correlated with response to treatment, progression-free survival, and overall survival.
Conclusions: NSE levels might not be related with the stage of the disease. However, a low pre-treatment NSE level might be used in predicting good response to chemotherapy in patients with SCLC. The post-treatment serum NSE levels and the rate of change between pre- and post-treatment serum levels of NSE were not related with response to chemotherapy, progression-free survival, and overall survival.
Copyright 2009 SEPAR. Published by Elsevier Espana. All rights reserved.
Similar articles
-
Significance of neuron-specific enolase levels before and during therapy for small cell lung cancer.Clin Cancer Res. 2000 Feb;6(2):597-601. Clin Cancer Res. 2000. PMID: 10690544 Clinical Trial.
-
Comparison of changes in the NSE levels with clinical assessment in the therapy monitoring of patients with SCLC.Anticancer Res. 2002 Mar-Apr;22(2B):1083-9. Anticancer Res. 2002. PMID: 12168905
-
ProGRP and NSE in therapy monitoring in patients with small cell lung cancer.Anticancer Res. 2008 Sep-Oct;28(5B):3027-33. Anticancer Res. 2008. PMID: 19031951
-
[Neuron specific enolase (NSE)].Nihon Rinsho. 1999 Dec;57 Suppl:540-2. Nihon Rinsho. 1999. PMID: 10778185 Review. Japanese. No abstract available.
-
Updates in small cell lung cancer treatment.Clin J Oncol Nurs. 2003 Sep-Oct;7(5):563-8. doi: 10.1188/03.CJON.563-568. Clin J Oncol Nurs. 2003. PMID: 14603554 Review.
Cited by
-
A systemic inflammation-based prognostic scores (mGPS) predicts overall survival of patients with small-cell lung cancer.Tumour Biol. 2015 Jan;36(1):337-43. doi: 10.1007/s13277-014-2623-4. Epub 2014 Sep 26. Tumour Biol. 2015. PMID: 25256672
-
[meta-analysis of serum tumor markers in lung cancer].Zhongguo Fei Ai Za Zhi. 2010 Dec;13(12):1136-40. doi: 10.3779/j.issn.1009-3419.2010.12.11. Zhongguo Fei Ai Za Zhi. 2010. PMID: 21159250 Free PMC article. Chinese.
-
Decreased levels of serum cytokeratin 19 fragment CYFRA 21-1 predict objective response to chemotherapy in patients with non-small cell lung cancer.Exp Ther Med. 2013 Aug;6(2):355-360. doi: 10.3892/etm.2013.1171. Epub 2013 Jun 20. Exp Ther Med. 2013. PMID: 24137188 Free PMC article.
-
The value of folate receptor-positive circulating tumor cells in the diagnosis of lung cancer and its correlation with clinical characteristics.Clin Respir J. 2023 May;17(5):374-383. doi: 10.1111/crj.13601. Epub 2023 Mar 28. Clin Respir J. 2023. PMID: 36977421 Free PMC article.
-
A Highly Efficient Gene Expression Programming (GEP) Model for Auxiliary Diagnosis of Small Cell Lung Cancer.PLoS One. 2015 May 21;10(5):e0125517. doi: 10.1371/journal.pone.0125517. eCollection 2015. PLoS One. 2015. PMID: 25996920 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical