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PET/CT: will it change the way that we use CT in cancer imaging?
Abstract
Accurate staging of cancer is of fundamental importance to
treatment selection and planning. Current staging paradigms
focus, first, on a detailed delineation of the primary tumour in
order to determine its suitability for resection, and,
thereafter, on assessment of the presence of metastatic spread
that would alter the surgical approach, or mandate non-surgical
therapies. This approach has, at its core, the assumption that
the best, and sometimes the only, way to cure a patient of
cancer is by surgical resection. Unfortunately, all non-invasive
techniques in current use have imperfect ability to identify
those primary tumours that are able to be completely excised,
and even worse ability to define the extent of metastatic
spread. Nevertheless, because of relatively low cost and
widespread availability, computed tomography (CT) scanning is
the preferred methodology for tumour, nodal and systemic
metastasis (TNM) staging. This is often supplemented by other
tests that have improved performance in particular staging
domains. For example, magnetic resonance imaging (MRI),
mammography, or endoscopic ultrasound may be used as
complementary tests for T-staging; surgical nodal sampling for
N-staging; and bone scanning, MRI or ultrasound for M-staging.
Accordingly, many patients undergo a battery of investigations
but, even then, are found to have been incorrectly staged based
on subsequent outcomes. Even for those staged surgically,
pathology can only identify metastases within the resection
specimens and has no capability for detecting remote disease. As
a result of this, many patients undergo futile operations for
disease that could never have been cured by surgery. In the case
of restaging, the situation is even worse. The sequelae of prior
treatment can be difficult to differentiate from residual cancer
and the likelihood of successful salvage therapy is even less
than at presentation. More deleteriously, patients may be
subjected to additional morbid treatments when cure has already
been achieved. Thus, in post-treatment follow-up, the presence
and extent of disease is equally critical to treatment selection
and patient outcome as it is in primary staging. One of the
major strengths of positron emission tomography (PET)/CT as a
cancer staging modality is its ability to identify systemic
metastases. At any phase of cancer evaluation, demonstration of
systemic metastasis has profound therapeutic and prognostic
implications. Only in the absence of systemic metastasis does
nodal status become important, and only when unresectable nodal
metastasis has been excluded does T-stage become important.
There are now accumulating data that PET/CT could be used as the
first, rather than the last test to assess M- and N-stage for
evaluating cancers with an intermediate to high pre-test
likelihood of metastatic disease based on poor long-term
survival. In this scenario, there is great opportunity for
subsequently selecting and tailoring the performance of
anatomically based imaging modalities to define the structural
relations of abnormalities identified by PET, when this
information would be of relevance to management planning.
Primary staging of oesophageal cancer and restaging of
colorectal cancer are illustrative examples of a new paradigm
for cancer imaging.
Author
Rodney J Hicks, Robert E Ware and Eddie W F Lau
Contact Details
Corresponding address: Professor Rod Hicks, MBBS (Hons), MD, FRACP,
The Centre for Molecular Imaging,
The Peter MacCallum Cancer Centre,
12 Cathedral Place,
East Melbourne VIC 2002,
Australia
Reference
ICIS Cancer Imaging Volume 6 Special Issue A
DOI: 10.1102/1470-7330.2006.9012
Date Posted
31 October 2006
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