Prognostic value of baseline carcinoembryonic antigen and cytokeratin 19 fragment levels in advanced non-small cell lung cancer

BACKGROUND: Serum carcinoembryonic antigen (CEA) and cytokeratin 19 fragment (CYFRA 21-1) levels are prognostic predictors in non-small cell lung cancer (NSCLC). However, even in patients with the same stage of cancer, the serum levels of those markers often vary. OBJECTIVE: We investigated the asso...

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Veröffentlicht in:Cancer biomarkers : section A of Disease markers 2018-01, Vol.22 (1), p.55-62
Hauptverfasser: Baek, Ae Rin, Seo, Hyun Jung, Lee, June Hyuk, Park, Sung Woo, Jang, An Soo, Paik, Sang Hyun, Koh, Eun Suk, Shin, Hwa Kyun, Kim, Do Jin
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Sprache:eng
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Zusammenfassung:BACKGROUND: Serum carcinoembryonic antigen (CEA) and cytokeratin 19 fragment (CYFRA 21-1) levels are prognostic predictors in non-small cell lung cancer (NSCLC). However, even in patients with the same stage of cancer, the serum levels of those markers often vary. OBJECTIVE: We investigated the association between the initial biomarker levels and prognosis. METHODS: We retrospectively reviewed 445 patients with advanced NSCLC and their baseline serum CEA and CYFRA 21-1 levels. Patients were divided into four groups according to the initial levels of those markers: the NN, HN, NH, and HH group. Kaplan-Meier survival analysis with Log-rank test and Cox proportional hazards regression analysis were performed. RESULTS: The 5-year overall survival (OS) rate in the HN group was the highest (32.2%). Multivariate analyses indicated that the HN group (HR 0.520, 95% CI 0.309–0.878, P = 0.014), female sex (HR 0.685, 95% CI 0.498–0.944, P = 0.021), serum CRP level (HR 1.057, 95% CI 1.034–1.080, P < 0.001), chemotherapy (HR 0.324, 95% CI 0.228–0.460, P < 0.001), and chemotherapy/radiotherapy (HR 0.266, 95% CI 0.171–0.414, P < 0.001) were independent prognostic factors for overall survival. CONCLUSIONS: In advanced NSCLC, patients with baseline high serum CEA but low CYFRA 21-1 level have a significant longer overall survival regardless of clinical stage.
ISSN:1574-0153
1875-8592
DOI:10.3233/CBM-170885