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Platinum Priority – Editorial

Referring to the article published on pp. 81–91 of this issue

Magnetic Resonance Imaging and Detection of Metastases

in Prostate Cancer: Learning Lessons from History

Alex P. Hoyle, Noel W. Clarke

*

The Christie and Salford Royal Hospitals, Manchester, UK

In February 2017 the inventor of the magnetic resonance

imaging (MRI) scanner, Sir Peter Mansfield, died at the age

of 83

[1]

. He was awarded the 2003 Nobel Prize for

medicine, and MR scanning has since become ubiquitous

and indispensable in most fields of cancer, but not quite yet

in urological oncology, particularly for advanced and high-

risk prostate cancer staging. Why have we been so slow to

evaluate its utility properly and to put it to work to best

effect in this disease, especially in the critically important

area of detection, localisation, and quantitation of metasta-

ses?

The review by Woo et al

[2]

in this issue of

European

Urology

provides an overview and meta-analysis of the

literature on the utility of MRI in detecting bone metastases,

and compares this in terms of sensitivity and specificity to

the existing urological ‘‘workhorse’’ and traditional 40-yr-

old cornerstone of metastatic prostate cancer staging, the

technetium bone scan

[3]

. It also highlights the weakness of

the uro-oncological literature in this area and draws our

attention to the paucity of high-quality clinical science in

evaluating and using MRI as a staging tool in the advanced

prostate cancer setting.

The relatively low sensitivity (79%) and specificity (82%)

of bone scintigraphy is well known. In addition, modern

practice dictates that scintigraphy cannot stand alone in the

staging process, as supplementary imaging is required to

complete the assessment of soft-tissue disease status and to

confirm the nature of lesions that are scintigraphically

‘‘equivocal’’. Is it time to move to MRI as the primary

imaging modality? Do the data presented here show or help

clinicians to understand how good MRI is as an alternative,

and if it is better, what type of MRI scanner or scan protocol

should be used?

By definition, the review provides level 2a evidence of

accurate MRI-based detection of bone metastases in

prostate cancer. It is a meta-analysis of ten predominantly

prospective studies and it concludes that overall per-patient

MRI sensitivity and specificity is 96% and 98%, respectively.

However, while the study methodology is fundamentally

sound, the individual studies analysed are generally weak,

with significant heterogeneity and inherent bias that limit

the overall interpretation. Heterogeneity between studies is

recognised by the authors in their submission, and

following meta-regression analysis the number of imaging

planes was the only significant explanatory factor. When

two or more planes were used, the sensitivity and

specificity increased to 99%, but data in relation to this

were only available in a small number of the studies. The

meta-analysis also found no statistically significant differ-

ence between diffusion-weighted imaging (DWI) and

standard MRI sequencing between studies. This seems

surprising at first glance, but the data have limited numbers

for comparison and information relating to standardisation

or co-alignment of protocols is fundamentally weak or

missing. It seems clear that while DWI looks better, it needs

further definitive clarification before safe conclusions can

be drawn.

The authors acknowledge the methodological limita-

tions in their study, including the per-patient analysis of

imaging and the predominant use of a best value

comparator (BCV) over histological confirmation as a

reference standard. This lack of per-lesion analysis hinders

E U R O P E A N U R O L O G Y 7 3 ( 2 0 1 8 ) 9 2 – 9 3

available at

www.scienced irect.com

journal homepage:

www.europeanurology.com

DOI of original article:

http://dx.doi.org/10.1016/j.eururo.2017.03.042

.

* Corresponding author. Department of Surgery, Christie Hospital, Wilmslow Road, West Didsbury, Manchester M20 4BX, UK. Tel. +44 161 4463364;

Fax: +44 161 4463365.

E-mail address:

noel.clarke@christie.nhs.uk

(N.W. Clarke).

http://dx.doi.org/10.1016/j.eururo.2017.05.052

0302-2838/

#

2017 Published by Elsevier B.V. on behalf of European Association of Urology.