Repeatability and response to therapy of dynamic contrast-enhanced magnetic resonance imaging biomarkers in rheumatoid arthritis in a large multicentre trial setting
Creators
- 1. Personalised Healthcare and Biomarkers, AstraZeneca, Macclesfield (United Kingdom)
- 2. University of Manchester, Stopford Building, Manchester Academic Health Sciences Centre, Manchester (United Kingdom)
- 3. AstraZeneca, Global Medicines Development, Macclesfield (United Kingdom)
- 4. AstraZeneca, Global Medicines Development, Moelndal (Sweden)
- 5. AstraZeneca, Global Medicines Development, Cambridge (United Kingdom)
- 6. Spire Sciences Inc, Boca Raton, FL (United States)
- 7. Imorphics, Manchester (United Kingdom)
- 8. Bioxydyn, Manchester (United Kingdom)
- 9. Private Practice and Division of Rheumatology KHI Neuwittelsbach, Muenchen (Germany)
- 10. University of Oxford, Kennedy Institute, Oxford (United Kingdom)
Description
To determine the repeatability and response to therapy of dynamic contrast-enhanced (DCE) MRI biomarkers of synovitis in the hand and wrist of rheumatoid arthritis (RA) patients, and in particular the performance of the transfer constant Ktrans, in a multicentre trial setting. DCE-MRI and RA MRI scoring (RAMRIS) were performed with meticulous standardisation at baseline and 6 and 24 weeks in a substudy of fostamatinib monotherapy in reducing synovitis compared with placebo or adalimumab. Analysis employed statistical shape modelling to avoid biased regions-of-interest, kinetic modelling and heuristic analyses. Repeatability was also evaluated. At early study termination, DCE-MRI data had been acquired from 58 patients in 19 imaging centres. Ktrans intra-subject coefficient of variation (N = 14) was 30%. Ktrans change demonstrated inferiority of fostamatinib (N = 11) relative to adalimumab (N = 10) after 6 weeks (treatment ratio = 1.92, p = 0.003), and failed to distinguish fostamatinib from placebo (N = 10, p = 0.79). RAMRIS showed superiority of fostamatinib relative to placebo at 6 weeks (p = 0.023), and did not distinguish fostamatinib from adalimumab at either 6 (p = 0.175) or 24 (p = 0.230) weeks. This demonstrated repeatability of Ktrans and its ability to distinguish treatment groups show that DCE-MRI biomarkers are suitable for use in multicentre RA trials. (orig.)
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00330-017-4736-9Additional details
Identifiers
Publishing Information
- Journal Title
- European Radiology
- Journal Volume
- 27
- Journal Issue
- 9
- Journal Page Range
- p. 3662-3668
- ISSN
- 0938-7994
- CODEN
- EURAE3
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 48084140
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- BIOLOGICAL MARKERS; BLOOD FLOW; BONE JOINTS; CLINICAL TRIALS; COMPARATIVE EVALUATIONS; CONTRAST MEDIA; DRUGS; DYNAMICS; HANDS; IMAGE PROCESSING; INFLAMMATION; NMR IMAGING; RELAXATION TIME; RHEUMATIC DISEASES; SPIN ECHO; WEIGHTING FUNCTIONS
- Descriptors DEC
- ARMS; BODY; DIAGNOSTIC TECHNIQUES; DISEASES; EVALUATION; FUNCTIONS; LIMBS; MECHANICS; ORGANS; PATHOLOGICAL CHANGES; PROCESSING; SKELETON; SYMPTOMS; TESTING