Springer Nature [academic journals on nature.com], British Journal of Cancer, 7(109), p. 1782-1785, 2013
DOI: 10.1038/bjc.2013.527
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Background:Interactions between prognostic and pharmacodynamic (PD) biomarkers have received little attention.Methods:Prognostic and PD utilities were assessed with linear mixed-effects models using published data on repeated measurements of circulating caspase-cleaved (ctCK18) and total (tCK18) cytokeratin 18, in 57 patients with metastatic colorectal cancer undergoing chemotherapy.Results:The model for tCK18 (but not cCK18) separated the prognostic/PD interaction from the pure prognostic effect, illustrating the principle of dual prognostic and PD characteristics for a given biomarker.Conclusion:These models provide the framework for the analysis and interpretation of longitudinal data to detect prognostic/PD biomarker interactions.British Journal of Cancer advance online publication, 3 September 2013; doi:10.1038/bjc.2013.527 www.bjcancer.com. ; Bouranis, L Sperrin, M Greystoke, A Dive, C Renehan, A G Br J Cancer. 2013 Sep 3. doi: 10.1038/bjc.2013.527.