Diagnostic pathways in multiple myeloma and their relationship to end organ damage: an analysis from the Tackling Early Morbidity and Mortality in Myeloma (TEAMM) trial.


Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
03 2021
Historique:
received: 14 05 2020
accepted: 26 07 2020
pubmed: 17 8 2020
medline: 3 8 2021
entrez: 17 8 2020
Statut: ppublish

Résumé

Multiple myeloma is associated with significant early morbidity and mortality, with considerable end organ damage often present at diagnosis. The Tackling EArly Morbidity and Mortality in Multiple Myeloma (TEAMM) trial was used to evaluate routes to diagnosis in patients with myeloma and the relationship between diagnostic pathways, time to diagnosis and disease severity. A total of 915 participants were included in the study. Fifty-one per cent were diagnosed by direct referral from primary care to haematology; 29% were diagnosed via acute services and 20% were referred via other secondary care specialties. Patients diagnosed via other secondary care specialties had a longer diagnostic interval (median 120 days vs. 59 days) without an increase in features of severe disease, suggesting they had a relatively indolent disease. Marked intrahospital delay suggests possible scope for improvement. A quarter of those diagnosed through acute services reported >30 days from initial hospital consultation to haematology assessment. Participants diagnosed through acute services had poorer performance status (P < 0·0001) and higher burden of end organ damage (P < 0·0001) with no difference in the overall length of diagnostic pathway compared to those diagnosed by direct referral (median 59 days). This suggests that advanced disease in patients presenting through acute services predominantly reflects disease aggression.

Identifiants

pubmed: 32798327
doi: 10.1111/bjh.17044
doi:

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

997-1005

Subventions

Organisme : Department of Health
ID : 08/116/69
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C8640/A23385
Pays : United Kingdom

Informations de copyright

© 2020 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.

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Auteurs

Catherine Atkin (C)

Institute of Inflammation and Ageing, University of Birmingham, Edgbaston, Birmingham, UK.

Gulnaz Iqbal (G)

Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.

Tim Planche (T)

St George's University Hospitals NHS Trust, London, UK.

Guy Pratt (G)

University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Kwee Yong (K)

UCL Cancer Institute, University College London, London, UK.

Jill Wood (J)

Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.

Kerry Raynes (K)

Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.

Eric Low (E)

Eric Low Consulting, London, UK.

Helen Higgins (H)

Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.

Richard D Neal (RD)

Institute of Health Sciences, University of Leeds, Leeds, UK.

Janet Dunn (J)

Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.

Mark T Drayson (MT)

Institute of Immunology and Immunotherapy, University of Birmingham, Edgbaston, Birmingham, UK.

Stella Bowcock (S)

Department of Haematological Medicine, King's College Hospital NHS Trust, London, UK.

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