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Nucleosomes and CYFRA 21-1 indicate tumor response after one cycle of chemotherapy in recurrent non-small cell lung cancer

Authors :
Holdenrieder, Stefan
von Pawel, Joachim
Dankelmann, Elke
Duell, Thomas
Faderl, Bernhard
Markus, Andreas
Siakavara, Maria
Wagner, Horst
Feldmann, Knut
Hoffmann, Harald
Raith, Hannelore
Nagel, Dorothea
Stieber, Petra
Source :
Lung Cancer (01695002). Jan2009, Vol. 63 Issue 1, p128-135. 8p.
Publication Year :
2009

Abstract

Summary: The increasing panel of systemic therapies enables the individual management of cancer patients, even in advanced stages. However, diagnostic tools indicating early the efficacy of therapy are still needed. In prospectively collected sera of 161 patients with recurrent non-small cell lung cancer (NSCLC) receiving second-line chemotherapy, the courses of nucleosomes, cytokeratin-19 fragments (CYFRA 21-1), carcinoembryonic antigen (CEA), neuron-specific enolase (NSE), and progastrin-releasing peptide (ProGRP) were investigated and correlated with therapy response. At high specificity for detection of progressive disease, most sensitive biomarkers were identified and included in a combination model. High levels and insufficient decreases of nucleosomes and CYFRA 21-1 during the first cycle of therapy indicated poor outcome. Combination of nucleosome concentrations at day 8 and CYFRA 21-1 before start of the second cycle enabled the early detection of progressive disease with a sensitivity of 34.4% at 95% specificity (AUC 0.79) prior to imaging techniques. When cutoffs were fixed at the 90th percentile of responding patients, the combination model achieved sensitivities of 19% at 100% specificity and of 52% at 88% specificity. Thus, nucleosomes and CYFRA 21-1 showed to be valuable for the individual management of patients with recurrent NSCLC. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
01695002
Volume :
63
Issue :
1
Database :
Academic Search Index
Journal :
Lung Cancer (01695002)
Publication Type :
Academic Journal
Accession number :
35768120
Full Text :
https://doi.org/10.1016/j.lungcan.2008.05.001