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Multi-level evidence that circulating CK18 is a biomarker of tumour burden in colorectal cancer
BACKGROUND: Circulating total cytokeratin 18 (tCK18) and/or caspase cleaved cytokeratin 18 (cCK18) (measured by M65 and M30 enzyme-linked immunosorbent assays (ELISAs), respectively) are used as pharmacodynamic (PD) biomarkers of epithelial cell death in clinical trials. Having validated these ELISA...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493762/ https://www.ncbi.nlm.nih.gov/pubmed/22996610 http://dx.doi.org/10.1038/bjc.2012.416 |
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author | Greystoke, A Dean, E Saunders, M P Cummings, J Hughes, A Ranson, M Dive, C Renehan, A G |
author_facet | Greystoke, A Dean, E Saunders, M P Cummings, J Hughes, A Ranson, M Dive, C Renehan, A G |
author_sort | Greystoke, A |
collection | PubMed |
description | BACKGROUND: Circulating total cytokeratin 18 (tCK18) and/or caspase cleaved cytokeratin 18 (cCK18) (measured by M65 and M30 enzyme-linked immunosorbent assays (ELISAs), respectively) are used as pharmacodynamic (PD) biomarkers of epithelial cell death in clinical trials. Having validated these ELISAs, we assessed their utility in colorectal cancer (CRC). METHODS: We applied the assays in several settings: 53 controls; 97 patients undergoing surgery and 74 patients with metastatic CRC undergoing chemotherapy (55 first line; 56 patients with repeated sampling through chemotherapy). Prognostic significance was evaluated using Kaplan–Meier life tables and Cox models; PD utility was assessed by analysis of repeated measures. RESULTS: Median cCK18 and tCK18 levels were elevated in patients with cancer (both P=0.0001), and among cancer patients, there were increasing trends from early to advanced stages (both P(trends)=0.0001). Increasing tCK18 predicted for reduced survival after surgery with curative intent (adjusted hazard ratio (HR) for doubling in concentration 1.77, 95% CI: 1.04, 3.01) and after first-line chemotherapy in metastatic disease (adjusted HR per doubling in concentration=1.78, 95% CI: 1.37, 2.30). In patients with progressive disease during chemotherapy, repeated sampling revealed profiles with high baselines and progressive upwardly increases after cycle 1. CONCLUSION: This study provides evidence for cytokeratin 18 (CK18) as a prognostic and PD biomarker in patients with CRC and supports continued deployment of circulating CK18 in biomarker-enhanced trials. |
format | Online Article Text |
id | pubmed-3493762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-34937622013-10-23 Multi-level evidence that circulating CK18 is a biomarker of tumour burden in colorectal cancer Greystoke, A Dean, E Saunders, M P Cummings, J Hughes, A Ranson, M Dive, C Renehan, A G Br J Cancer Molecular Diagnostics BACKGROUND: Circulating total cytokeratin 18 (tCK18) and/or caspase cleaved cytokeratin 18 (cCK18) (measured by M65 and M30 enzyme-linked immunosorbent assays (ELISAs), respectively) are used as pharmacodynamic (PD) biomarkers of epithelial cell death in clinical trials. Having validated these ELISAs, we assessed their utility in colorectal cancer (CRC). METHODS: We applied the assays in several settings: 53 controls; 97 patients undergoing surgery and 74 patients with metastatic CRC undergoing chemotherapy (55 first line; 56 patients with repeated sampling through chemotherapy). Prognostic significance was evaluated using Kaplan–Meier life tables and Cox models; PD utility was assessed by analysis of repeated measures. RESULTS: Median cCK18 and tCK18 levels were elevated in patients with cancer (both P=0.0001), and among cancer patients, there were increasing trends from early to advanced stages (both P(trends)=0.0001). Increasing tCK18 predicted for reduced survival after surgery with curative intent (adjusted hazard ratio (HR) for doubling in concentration 1.77, 95% CI: 1.04, 3.01) and after first-line chemotherapy in metastatic disease (adjusted HR per doubling in concentration=1.78, 95% CI: 1.37, 2.30). In patients with progressive disease during chemotherapy, repeated sampling revealed profiles with high baselines and progressive upwardly increases after cycle 1. CONCLUSION: This study provides evidence for cytokeratin 18 (CK18) as a prognostic and PD biomarker in patients with CRC and supports continued deployment of circulating CK18 in biomarker-enhanced trials. Nature Publishing Group 2012-10-23 2012-09-20 /pmc/articles/PMC3493762/ /pubmed/22996610 http://dx.doi.org/10.1038/bjc.2012.416 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by-nc-sa/3.0/From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Molecular Diagnostics Greystoke, A Dean, E Saunders, M P Cummings, J Hughes, A Ranson, M Dive, C Renehan, A G Multi-level evidence that circulating CK18 is a biomarker of tumour burden in colorectal cancer |
title | Multi-level evidence that circulating CK18 is a biomarker of tumour burden in colorectal cancer |
title_full | Multi-level evidence that circulating CK18 is a biomarker of tumour burden in colorectal cancer |
title_fullStr | Multi-level evidence that circulating CK18 is a biomarker of tumour burden in colorectal cancer |
title_full_unstemmed | Multi-level evidence that circulating CK18 is a biomarker of tumour burden in colorectal cancer |
title_short | Multi-level evidence that circulating CK18 is a biomarker of tumour burden in colorectal cancer |
title_sort | multi-level evidence that circulating ck18 is a biomarker of tumour burden in colorectal cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493762/ https://www.ncbi.nlm.nih.gov/pubmed/22996610 http://dx.doi.org/10.1038/bjc.2012.416 |
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