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dc.contributor.authorDonners, R
dc.contributor.authorFigueiredo, I
dc.contributor.authorTunariu, N
dc.contributor.authorBlackledge, M
dc.contributor.authorKoh, D-M
dc.contributor.authorde la Maza, MDLDF
dc.contributor.authorChandran, K
dc.contributor.authorde Bono, JS
dc.contributor.authorFotiadis, N
dc.date.accessioned2022-04-26T15:11:24Z
dc.date.available2022-04-26T15:11:24Z
dc.date.issued2022-01-29
dc.identifier.citationEuropean radiology, 2022en
dc.identifier.issn0938-7994
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5097
dc.identifier.eissn1432-1084en_US
dc.identifier.eissn1432-1084
dc.identifier.doi10.1007/s00330-022-08536-6en_US
dc.identifier.doi10.1007/s00330-022-08536-6
dc.description.abstract<h4>Objectives</h4>To evaluate whether multiparametric bone MRI (mpBMRI) utilising a combination of DWI signal, ADC and relative fat-fraction (rFF) can identify bone metastases, which provide high diagnostic biopsy yield and next-generation genomic sequencing (NGS) feasibility.<h4>Methods</h4>A total of 150 CT-guided bone biopsies performed by interventional radiologists (3/2013 to 2/2021) at our centre were reviewed. In 43 patients, contemporaneous DWI and rFF images, calculated from 2-point T1w Dixon MRI, were available. For each biopsied lesion, a region of interest (ROI) was delineated on ADC and rFF images and the following MRI parameters were recorded: visual classification of DWI signal intensity (SI), mean, median, 10th and 90th centile ADC and rFF values. Non-parametric tests were used to compare values between tumour positive/negative biopsies and feasible/non-feasible NGS, with p-values < 0.05 deemed significant.<h4>Results</h4>The mpBMRI combination high DWI signal, mean ADC < 1100 µm<sup>2</sup>/s and mean rFF < 20% identified tumour-positive biopsies with 82% sensitivity, 80% specificity, a positive predictive value (PPV) of 93% (p = 0.001) and NGS feasibility with 91% sensitivity, 78% specificity and 91% PPV (p < 0.001). The single MRI parameters DWI signal, ADC and rFF failed to distinguish between tumour-positive and tumour-negative biopsies (each p > 0.082). In NGS feasible biopsies, mean and 90th centile rFF were significantly smaller (each p < 0.041). Single ADC parameters did not show significant difference regarding NGS feasibility (each p > 0.292).<h4>Conclusions</h4>MpBMRI utilising the combination of DWI signal, ADC and rFF can identify active bone metastases, which provide biopsy tissue with high diagnostic yield and NGS feasibility.<h4>Key points</h4>• Multiparametric bone MRI with diffusion-weighted and relative fat-fraction images helps to identify active bone metastases suitable for CT-guided biopsy. • Target lesions for CT-guided bone biopsies in cancer patients can be chosen with greater confidence. • CT-guided bone biopsy success rates, especially yielding sufficient viable tissue for advanced molecular tissue analyses, can be improved.en_US
dc.formatPrint-Electronicen_US
dc.languageengen_US
dc.language.isoengen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.titleMultiparametric bone MRI can improve CT-guided bone biopsy target selection in cancer patients and increase diagnostic yield and feasibility of next-generation tumour sequencing.en
dc.typeJournal Article
dcterms.dateAccepted2021-12-20
rioxxterms.versionVoRen
rioxxterms.versionofrecord10.1007/s00330-022-08536-6en
rioxxterms.licenseref.startdate2022-01-29
dc.relation.isPartOfEuropean radiologyen_US
pubs.notesNot knownen_US
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Prostate Cancer Targeted Therapy Group
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublisheden_US
pubs.embargo.termsNot knownen_US
icr.researchteamProstate Cancer Targeted Therapy Group
dc.contributor.icrauthorDe Bono, Johannen_US
dc.contributor.icrauthorKoh, Dow-Muen_US


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Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by/4.0/