Kim Sivesgaard1, Maria Louise Jöhnk2, Lars Peter Skovgaard Larsen1, Michael Sørensen3, Stine Kramer3, Flemming Hansen2, and Erik Morre Pedersen1
1Department of Radiology, Aarhus University Hospital, Aarhus, Denmark, 2Department of Oncology, Aarhus University Hospital, Aarhus, Denmark, 3PET-centre, Aarhus University Hospital, Aarhus, Denmark
Synopsis
A whole
body (WB) MRI protocol added to a dedicated liver MRI in one scan session,
could alleviate the need for a PET/CT for staging patients prior to local
treatment of colorectal liver metastases. With the aim of developing a disease
optimised WB protocol, 30 patients with extra-hepatic metastases from
colorectal cancer were prospectively recruited and scanned on a 1.5 T scanner
and using a PET/CT scan within an average of 1.33 days as reference.
Preliminary results show that combining a traditional whole body MRI protocol
with DWIBS produces superior results compared to the traditional protocol
alone.Background
Liver MRI
is increasingly used for staging of patients prior to local treatment of
colorectal liver metastases(1). PET/CT is still necessary to
exclude extra hepatic disease(2). A whole body MRI protocol, which can
be added to a dedicated liver MRI, could alleviate the need for the PET/CT and
offer a single modality one-stop-shop approach to staging patients before treatment
of colorectal liver metastases. Prior to a direct comparison of whole body MRI
and PET/CT, the appropriate MRI protocol should be decided from a variety of
available whole body MRI sequences. It is recognised that a whole body MRI
protocol should be tailored to the specific malignancy(3), hence a prospective study in
colorectal cancer patients was decided.
Purpose
The overall
purpose of the study was to define a proper whole body MRI protocol for
detection of extra-hepatic colorectal cancer metastases with PET/CT as the
reference standard. In this preliminary analysis we assess the effect of adding
DWIBS to a standard whole body MRI protocol.
Method
30 patients
with extra-hepatic metastases from colorectal cancer were prospectively recruited
and informed consent was obtained. All patients were scanned on a 1.5 T scanner
(Philips 1.5 T Ingenia, Philips Medical Systems, Best, The Netherlands) using
the dS Flex Coverage posterior coil, dS HeadNeck Coil and two Flex Coverage
anterior coils. The patients were scanned from shoulders to upper thighs using
transverse and coronal T2W single shot respiratory triggered TSE, breath hold coronal
STIR, post-contrast 3D GRE mDixon and free-breathing DWIBS (B=0, 50, 900). The
MRI contrast used was gadoxetic acid (Primovist, Bayer Pharma, Berlin, Germany)
when the participant had an estimated glomerular filtration rate (eGFR) > 60
ml/min/1.73 m2 body surface area and gadoteric acid (Dotarem,
Guerbet, Roissy CdG Cedex, France) when eGFR was between 30 and 60.
All
patients were scanned on an integrated PET/CT system, (Siemens Biograph
Truepoint 64-slice, Siemens Healthcare, Erlangen, Germany) according to the standard clinical protocol, as
reference.
In this
preliminary analysis two MRI sets were constructed for each patient: One
traditional set with all sequences excluding DWIBS and one set with all
sequences including DWIBS.
Case report
forms were completed during the blinded reporting of all 60 MRI sets. On the
case report forms lesions were categorized into 13 anatomic regions and a maximum
of three lesions were reported for each region. For each lesion location, size (mm)
and confidence of malignancy (1 – 5) was recorded.
Similar
case report forms were completed during the reporting of the PET/CTs, which
were reported with knowledge of all prior imaging and medical records.
Per lesion
sensitivity and false positive rate was calculated and per region sensitivity
and specificity was calculated. Findings were compared using McNemars Chi2-test.
Results
175 lesions
were detected in 90/390 anatomic regions by PET/CT in the 30 patients.
Mean interval between PET/CT and whole body MRI was 1.33 days (range 0-19 days).
The results
of the preliminary analysis are displayed in table 1.
Discussion
The preliminary
results show that an MRI protocol incorporating DWIBS is superior compared to a
standard whole body MRI protocol for detecting extra-hepatic colorectal cancer
metastases. This illustrates the huge benefit of using diffusion weighted imaging
to localize areas of impeded water diffusion to detect malign lesions(4).
The cost of
a higher sensitivity is as expected an increase in the false positive rate and
correspondingly a decrease in specificity (although not statistically
significant). This could be attributed to lymph nodes, which present as high
signal lesions on diffusion weighted sequences regardless of their nature.
Further statistical analysis will reveal if this explains a large proportion of
the higher false positive rate in the sets containing DWIBS.
The choice
of PET/CT as the reference standard entails the possibility that false positive
PET/CT findings are recorded as false negative findings on MRI, resulting in a
lower sensitivity. Equivalently, lesions appearing as false negative on PET/CT
e.g. due to size under the detectability limit of PET/CT, would result in an
increased false positive rate / reduced specificity of the most sensitive MRI
sets. Nevertheless, we chose to consider PET/CT as the reference standard in
accordance with the purpose of defining an MRI protocol. Therefore, this study cannot
be considered a comparison between whole body MRI and PET/CT.
A further subgroup
analysis is planned to decide if it is possible to use DWIBS in combination
with fewer sequences (w/wo iv. contrast) to allow for a decreased examination
time and maintain acceptable sensitivity and specificity.
Conclusion
Preliminary
results reveal the superiority of using DWIBS in detecting extra-hepatic
colorectal cancer metastases.
Acknowledgements
No acknowledgement found.References
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