Arash Latifoltojar1, Margaret Hall-Craggs1, Alan Bainbridge2, Neil Rabin2, Ali Rismani2, Rakesh Popat1, Kwee Yong3, and Shonit Punwani4
1University College London, London, United Kingdom, 2University College London Hospital, United Kingdom, 3University College London, 4University College London, United Kingdom
Synopsis
Whole body MRI (WB-MRI) is increasingly being used to assess plasma cell disorders (PCDs). The adoption of WB-MRI provides a niche to further incorporate novel imaging technique into assessment of PCDs, streamlining decision making progress in a cost-effective way.
Clinical Question:
To adopt whole-body
MRI for initial assessment of plasma cell disorders (PCDs) including multiple
myeloma (MM)Impact:
Currently, the initial assessment of PCDs consists of a wide
range of biochemical and imaging investigations [1]. For imaging
investigations, a combination of skeletal survey, CT scan, PET-CT and
whole-spine MRI (WS-MRI) is usually adopted [1-3]. In the past decade,
whole-body MRI (WB-MRI) is increasingly being used for baseline assessment of
PCDs due to its superior diagnostic ability compared to multi-modality imaging
[4-7].
There is still no accepted uniform imaging protocol for WB-MRI in
PCDs despite the adoption of technique by various institutions and guidelines
[8] for use in early detection [9] and potential prognostication [9,10]. The
lack of an agreed protocol limits the generalizability and wider adoption of
this technique.
The potential advantage of WB-MRI is not limited to diagnosis.
The limited resources and financial strains in modern medicine era necessitate
the adoption of ‘cost-effective’ diagnostic procedures. Table 1 provides an
estimate of the cost of current imaging techniques available for the assessment
of MM in the UK. In addition, the
adoption of WB-MRI for MM evaluation might reduce the use of additional imaging
modalities (such as skeletal survey, PET etc), and this in turn may save money
and speed up clinical decision-making. For instance, because WS-MRI is commonly
required for assessment of the axial skeleton for fracture and neural
compression, a combined single-session MRI approach (WB-MRI + WS-MRI) could
well be preformed in a reasonable time using modern MRI scanners. Such approach
has been previously tested for local and metastatic staging of prostate cancer [11].Approach:
Standard approaches for PCD assessment are based on ‘global
measure’ of disease and its response following chemo/radiotherapy. The
conventional imaging techniques (skeletal survey, CT) are not sensitive for
detection of bone disease, especially at early stages of disease [12].
Despite its enhanced diagnostic ability; PET-CT imparts a
substantial radiation exposure to patients [13,14]. Furthermore, PET-CT is not
readily available in all institutions (health equality) and compared to WB-MRI,
it is more expensive. Whole-spine MRI is now an integrated imaging technique
for detection of disease and assessing the risk of insufficiency fracture
[2,3,12], however, performed alone, it can miss up to 50% of bone lesions
because of its limited coverage [12]. To increase patient comfort, decrease the
cost, and increase effectiveness, we have designed, modified and updated a
WB-MRI protocol on a 3.0T MRI scanner that can be run in under 30 minutes using
novel MRI sequences. The current protocol can accommodate WS-MRI protocol in
combination with WB-MRI.
We believe by incorporating WB-MRI, we can provide a radiation
free, fast and cost-effective technique with an improved diagnostic performance
that can benefit patients by streamlining the imaging process, reducing
management decision time and improving overall patients’ experience.Gains and Losses
The main challenges for WB-MR imaging are the big data sets
(specifically in case of multi-parametric WB-MRI protocols) requiring improved
infrastructure for data handling/viewing. Furthermore, considering its novelty,
the lack of experience in WB-MR imaging amongst general radiologists might
necessitate further educational and training programs. Finally, the capacity to
implement WB-MRI exams on allocated ‘clinical’ time-slots on available
scanner(s) might prove difficult. Conversely, the parallel developments and
innovations in analyzing and viewing software packages, together with an
increase in accessibility of MRI scanners might alleviate some of the current
relative limitations.
Acknowledgements
No acknowledgement found.References
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