BJR
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH

Published online before print August 18, 2009
British Journal of Radiology 2009, doi:10.1259/bjr/76979647
This Article
Right arrow Full Text (Rapid PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Google Scholar
Right arrow Articles by NOTERDAEME, O
Right arrow Articles by BRADY, M
PubMed
Right arrow PubMed Citation
Right arrow Articles by NOTERDAEME, O
Right arrow Articles by BRADY, M
© 2009 The British Institute of Radiology

SHORT COMMUNICATION

Initial assessment of a model relating intratumoral genetic heterogeneity to radiological morphology

O NOTERDAEME 1, M KELLY 1, P FRIEND 1, Z SOONOWALLA 1, G STEERS 1, M BRADY 1

1 Department of Engineering Science, University of Oxford, South Parks Road, Oxford OX1 3PJ, 2Nuffield Department of Surgery, John Radcliffe Hospital, Headington Oxford OX3 9DU and 3Cancer Research UK, Tumour Pathology Group, Nuffield Department of Clinical Laboratory Sciences, University of Oxford, John Radcliffe Hospital, Headington, Oxford OX3 9DU, UK


   Abstract

Tumour heterogeneity has major implications for tumour development and response to therapy. Tumour heterogeneity results from mutations in the genes responsible for mismatch repair or maintenance of chromosomal stability. Cells with different genetic properties may grow at different rates and exhibit different resistance to therapeutic interventions. To date, there exists no approach to non-invasively assess tumour heterogeneity. Here we present a biologically inspired model of tumour growth, which relates intratumoral genetic heterogeneity to gross morphology visible on radiological images. The model represents the development of a tumour as a set of expanding spheres, each sphere representing a distinct clonal centre, with the sprouting of new spheres corresponding to new clonal centres. Each clonal centre may possess different characteristics relating to genetic composition, growth rate and response to treatment. We present a clinical example for which the model accurately tracks tumour growth, and shows the correspondence to genetic variation (as determined by array comparative genomic hybridisation). One clinical implication of our work is that the assessment of heterogeneous tumours using Response Evaluation Criteria In Solid Tumours (RECIST) or volume measurements may not accurately reflect tumour growth, stability or the response to treatment. We believe that this is the first model linking the macro-scale appearance of tumours to their genetic composition. We anticipate that our model will provide a more informative way to assess the response of heterogeneous tumours to treatment, which is of increasing importance with the development of novel targeted anti-cancer treatments.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
BJR DMFR IMAGING  ALL BIR JOURNALS 
Copyright © 2009 by the British Institute of Radiology.