Rectal Neoplasms Clinical Trial
Official title:
Prediction of Response to Neoadjuvant Chemoradiotherapy in Locally Advanced Rectal Cancer.
The purpose of this study is to determine whether 18F-FDG-PET-CT and texture analysis of MRI performed 9 weeks after Neoadjuvant Chemo-radiotherapy in patients with locally advanced rectal cancer has the ability to identify patients with Complete Response.
In recent years, treatment with NCRT has revolutionised management of LARC. In addition to
downstaging the tumour in 62% of cases, half of which decrease by more than 1 T stage;
pathological complete response (pCR), with no viable tumour cells left in resected
specimens, was demonstrated in up to 30% of patients. Only 3% of patients showed progressive
disease. It has recently been shown that those with pathological complete response survive
longer than those with partial response, with figures for 5-year disease free survival
quoted between 83 and 91% for pCR; versus 65% for non pCR. Furthermore, it has been argued
that those tumours which are sensitive to radiotherapy have a favourable biological tumour
profile, with fewer propensities to recur or to metastasise than aggressive
non-radiosensitive tumours. The key is to accurately be able to identify patients who
exhibit complete response to radiotherapy, or to predict those who might show complete
response.
Positron Emission Tomography (18-F-FDG-PET-CT) as a tumour biomarker after radiotherapy has
been shown to be able to predict patients who have responded to chemo radiotherapy, with a
sensitivity of 79% and specificity of 88%. Texture Analysis (TA) assesses the aggressiveness
of the tumour by assessing intra-tumoural heterogeneity. It has already been shown to be
effective in assessing biological characteristics of solid tumours, including the
oesophagus, breast, and liver.
The aim of this study is to utilise these two novel molecular imaging techniques to identify
rectal cancer patients who have responded completely from neoadjuvant chemo-radiotherapy.
Parameters will be calculated as changes in measurable variables from baseline to post
treatment scans.
Pilot data The watch-and-wait approach could potentially reduce treatment-related toxicity
in selected rectal cancer patients who have a clinical complete response (cCR) after
chemoradiation. The "watch & wait" protocol has been adopted from studies performed in
Brazil, United Kingdom, and the Netherlands.
Studies indicate that accurate assessment of response to neoadjuvant therapy is the key to
selecting patients who will benefit from the watch & wait approach. Therefore, determining
the modality with highest accuracy and cost-effectiveness has been the holy grail of
managing locally advanced rectal cancers.
A study performed by our Chief Investigator on the efficiency and accuracy of
18-F-FDG-PET-CT has concluded that PET-CT has a proven role and is cost effective in
monitoring therapy and in detecting recurrence in colorectal cancers; as this technology
combines picomolar sensitivity with high-resolution CT imaging. It has therefore shown to be
more sensitive than plain CT imaging in detecting recurrence and monitoring response to
therapy. In other studies, the reported accuracy for PET-CT in determining responsiveness to
NCRT was around 80%. Baseline PET-CT and subsequent PET-CT parameters, including SUV-based
measurements, have been shown to be highly accurate in determining responses to NCRT.
Texture Analysis is a biomarker technique that measures heterogeneity within solid tumours.
Textural parameters (coefficient of variation [COV], skewness, and kurtosis) applied on
PET-CT images has been shown to be able to predict response to NCRT, and to predict
survival. A pilot study performed at our institution has indeed showed that textural
parameters performed on pelvic MRI were associated with improved overall survival and
disease- free survival.
Study hypothesis
- PET-CT restaging done at 9 weeks rather than 6 weeks will be a more accurate predictor
in assessing response to NCRT.
- Texture analysis of rectal MRI scans is a strong biomarker in assessing tumour response
and identifying patients with Complete Response.
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Diagnostic
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