Current challenges in clinical target volume definition: Tumour margins and microscopic extensions

Authors

  • Leyla Moghaddasi Department of Medical Physics, Royal Adelaide Hospital, South Australia, Australia; School of Chemistry and Physics, University of Adelaide, South Australia, Australia
  • Eva Bezak Department of Medical Physics, Royal Adelaide Hospital, South Australia, Australia; School of Chemistry and Physics, University of Adelaide, South Australia, Australia
  • Loredana G. Marcu Department of Medical Physics, Royal Adelaide Hospital, South Australia, Australia;School of Chemistry and Physics, University of Adelaide, South Australia, Australia; Faculty of Science, University of Oradea, Romania

DOI:

https://doi.org/10.3109/0284186X.2012.720381

Abstract

Determination of optimal clinical target volume (CTV) margins around gross tumour volume (GTV) for modern radiotherapy techniques, requiring more precise target definitions, is controversial and complex. Tumour localisation has been greatly improved using molecular imaging integrated with conventional imaging techniques. However, the exact incidence and extent of microscopic disease, to be encompassed by CTV, cannot be visualised by any techniques developed to date and remain uncertain. As a result, the CTV is generally determined by clinicians based on their experience and patients’ histopathological data. In this article we review histopathological studies addressing the extent of subclinical disease and its possible correlation with tumour characteristics in various tumour sites. The data have been tabulated to facilitate a comparison between proposed margins by different investigations and with current margins generally accepted for each tumour site. It is concluded that there is a need for further studies to reach a consensus on the optimal CTV pertaining to each tumour site.

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Published

2012-11-01

How to Cite

Moghaddasi, L., Bezak, E., & Marcu, L. G. (2012). Current challenges in clinical target volume definition: Tumour margins and microscopic extensions. Acta Oncologica, 51(8), 984–995. https://doi.org/10.3109/0284186X.2012.720381