Prognostic value of tumor markers ProGRP, NSE and CYFRA 21-1 in patients with small cell lung cancer and chemotherapy-induced remission

Author:

Muley Thomas12ORCID,Herth Felix J.13,Heussel Claus Peter145,Kriegsmann Mark56,Thomas Michael17,Meister Michael12,Schneider Marc A.12,Wehnl Birgit8,Mang Anika8,Holdenrieder Stefan9

Affiliation:

1. Translational Lung Research Centre Heidelberg, Member of the German Centre for Lung Research, Heidelberg, Germany

2. Translational Research Unit, Thoraxklinik, Heidelberg University Hospital, Heidelberg, Germany

3. Department of Pneumology and Respiratory Medicine, Thoraxklinik, University Hospital, Heidelberg, Germany

4. Diagnostic and Interventional Radiology, University Hospital, Heidelberg, Germany

5. Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany

6. Pathology Wiesbaden, Wiesbaden, Germany

7. Department of Oncology, Thoraxklinik, University Hospital, Heidelberg, Germany

8. Roche Diagnostics GmbH, Penzberg, Germany

9. Munich Biomarker Research Center, Institute of Laboratory Medicine, German Heart Centre, Technical University of Munich, Munich, Germany

Abstract

BACKGROUND: Despite successful response to first line therapy, patients with small-cell lung cancer (SCLC) often suffer from early relapses and disease progression. OBJECTIVE: To investigate the relevance of serum tumor markers for estimation of prognosis at several time points during the course of disease. METHODS: In a prospective, single-center study, serial assessments of progastrin-releasing peptide (ProGRP), neuron-specific enolase (NSE), cytokeratin-19 fragments (CYFRA 21-1) and carcino-embryogenic antigen (CEA) were performed during and after chemotherapy in 232 SCLC patients, and correlated with therapy response and overall survival (OS). RESULTS: ProGRP, NSE and CYFRA 21-1 levels decreased quickly after the first chemotherapy cycle and correlated well with the radiological response. Either as single markers or in combination they provided valuable prognostic information regarding OS at all timepoints investigated: prior to first-line therapy, after two treatment cycles in patients with successful response to first-line therapy, and prior to the start of second-line therapy. Furthermore, they were useful for continuous monitoring during and after therapy and often indicated progressive disease several months ahead of radiological changes. CONCLUSIONS: The results indicate the great potential of ProGRP, NSE and CYFRA 21-1 for estimating prognosis and monitoring of SCLC patients throughout the course of the disease.

Publisher

IOS Press

Subject

General Medicine

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