Comparison of Whole-Body MRI, CT, and Bone Scintigraphy for Response Evaluation of Cancer Therapeutics in Metastatic Breast Cancer to Bone.


Journal

Radiology
ISSN: 1527-1315
Titre abrégé: Radiology
Pays: United States
ID NLM: 0401260

Informations de publication

Date de publication:
12 2020
Historique:
pubmed: 21 10 2020
medline: 29 12 2020
entrez: 20 10 2020
Statut: ppublish

Résumé

Background CT and bone scintigraphy have limitations in evaluating systemic anticancer therapy (SACT) response in bone metastases from metastatic breast cancer (MBC). Purpose To evaluate whether whole-body MRI enables identification of progressive disease (PD) earlier than CT and bone scintigraphy in bone-only MBC. Materials and Methods This prospective study evaluated participants with bone-only MBC between May 2016 and January 2019 (ClinicalTrials.gov identifier: NCT03266744). Participants were enrolled at initiation of first or subsequent SACT based on standard CT and bone scintigraphy imaging. Baseline whole-body MRI was performed within 2 weeks of entry; those with extraosseous disease were excluded. CT and whole-body MRI were performed every 12 weeks until definitive PD was evident with one or both modalities. In case of PD, bone scintigraphy was used to assess for bone disease progression. Radiologists independently interpreted images from CT, whole-body MRI, or bone scintigraphy and were blinded to results with the other modalities. Systematic differences in performance between modalities were analyzed by using the McNemar test. Results Forty-five participants (mean age, 60 years ± 13 [standard deviation]; all women) were evaluated. Median time on study was 36 weeks (range, 1-120 weeks). Two participants were excluded because of unequivocal evidence of liver metastases at baseline whole-body MRI, two participants were excluded because they had clinical progression before imaging showed PD, and one participant was lost to follow-up. Of the 33 participants with PD at imaging, 67% (22 participants) had PD evident at whole-body MRI only and 33% (11 participants) had PD at CT and whole-body MRI concurrently; none had PD at CT only (

Identifiants

pubmed: 33078998
doi: 10.1148/radiol.2020192683
doi:

Substances chimiques

Contrast Media 0
Radiopharmaceuticals 0

Banques de données

ClinicalTrials.gov
['NCT03266744']

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

622-629

Auteurs

Michael Kosmin (M)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

Anwar R Padhani (AR)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

Andrew Gogbashian (A)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

David Woolf (D)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

Mei-Lin Ah-See (ML)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

Peter Ostler (P)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

Stephanie Sutherland (S)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

David Miles (D)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

Jillian Noble (J)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

Dow-Mu Koh (DM)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

Andrea Marshall (A)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

Janet Dunn (J)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

Andreas Makris (A)

From the Department of Oncology, University College London NHS Foundation Trust, 250 Euston Road, London NW1 2PG, England (M.K.); Paul Strickland Scanner Centre (A.R.P., A.G.) and Breast Cancer Research Unit (P.O., S.S., D.M., A. Makris), Mount Vernon Cancer Centre, Northwood, Middlesex, England; Department of Clinical Oncology, the Christie NHS Foundation Trust, Manchester, England (D.W.); Astra Zeneca UK Limited, Cambridge, England (M.L.A.); the Royal Marsden Hospital, Sutton, Surrey, England (J.N., D.M.K.); and Warwick Clinical Trials Unit, University of Warwick, Coventry, England (A. Marshall, J.D.).

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Classifications MeSH