Application of diffusion-weighted whole-body MRI for response monitoring in multiple myeloma after chemotherapy: a systematic review and meta-analysis.


Journal

European radiology
ISSN: 1432-1084
Titre abrégé: Eur Radiol
Pays: Germany
ID NLM: 9114774

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 29 03 2021
accepted: 30 08 2021
revised: 27 07 2021
pubmed: 15 1 2022
medline: 17 3 2022
entrez: 14 1 2022
Statut: ppublish

Résumé

Myeloma Response Assessment and Diagnosis System recently published provides a framework for the standardised interpretation of DW-WBMRI in response assessment of multiple myeloma (MM) based on expert opinion. However, there is a lack of meta-analysis providing higher-level evidence to support the recommendations. In addition, some disagreement exists in the literature regarding the effect of timing and lesion subtypes on apparent diffusion coefficient (ADC) value changes post-treatment. Medline, Cochrane and Embase were searched from inception to 20th July 2021, using terms reflecting multiple myeloma and DW-WBMRI. Using PRISMA reporting guidelines, data were extracted by two investigators. Quality was assessed by the Quality Assessment of Diagnostic Accuracy Studies-2 method. Of the 74 papers screened, 10 studies were included comprising 259 patients (127 males and 102 females) and 1744 reported lesions. Responders showed a significant absolute ADC change of 0.21×10 This meta-analysis supports the use of the DW-WBMRI as an imaging biomarker for response assessment. More evidence is needed to further characterise ADC changes by lesion subtypes over time. • In multiple myeloma patients who received chemotherapy, responders have a significant absolute increase in ADC values that is not seen in non-responders. • A 35% increase in ADC from baseline values is found to classify response post-induction chemotherapy which corroborates with expert opinion from the Myeloma Response Assessment and Diagnosis System. • More evidence is needed to further characterise ADC changes by lesion subtypes over time after induction of therapy.

Identifiants

pubmed: 35028748
doi: 10.1007/s00330-021-08311-z
pii: 10.1007/s00330-021-08311-z
doi:

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2135-2148

Informations de copyright

© 2021. Crown.

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Auteurs

Kaiwen Wang (K)

School of Clinical Medicine, The University of Cambridge, Cambridge, UK.
School of Medicine, The University of Leeds, Leeds, UK.

Elsa Lee (E)

Guy's, King's and St Thomas' School of Medicine, King's College London, London, UK.

Shedrack Kenis (S)

Echolab Radiology and Laboratory Services, Benin, Nigeria.

Simon Hallam (S)

Department of Haemato-oncology, St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.

Athar Haroon (A)

Department of Nuclear Medicine, St Bartholomew's Hospital, Barts Health NHS Trust, London, UK.

Simon Wan (S)

Institute of Nuclear Medicine, UCL and UCL Hospitals, London, UK.

Neil Rabin (N)

Department of Haemato-Oncology, Barts Health NHS Trust, London, UK.

Antonio Rojas-Garcia (A)

Public Health Policy Evaluation Unit, School of Public Health, Imperial College London, London, UK.

Anwar Padhani (A)

Paul Strickland Scanner Centre, Mount Vernon Hospital, Northwood, UK.

Sola Adeleke (S)

School of Cancer & Pharmaceutical Sciences, King's College London, Strand, London, WC2R 2LS, UK. sesola2003@gmail.com.
Department of Oncology, Guy's and St Thomas' Hospital, London, UK. sesola2003@gmail.com.

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