Results of the Meso-ORIGINS feasibility study regarding collection of matched benign-mesothelioma tissue pairs by longitudinal surveillance.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
08 08 2023
Historique:
medline: 10 8 2023
pubmed: 9 8 2023
entrez: 8 8 2023
Statut: epublish

Résumé

To assess key elements of the design for Meso-ORIGINS (Mesothelioma Observational study of RIsk prediction and Generation of paired benign-meso tissue samples, Including a Nested MRI Substudy), an ambitious, UK-wide, prospective study that will collect ≥63 matched benign-mesothelioma tissue pairs through longitudinal surveillance and repeat biopsy of patients with asbestos-associated pleural inflammation (AAPI). A multicentre, mixed-methods feasibility study, comprising a prospective observational element, evaluating recruitment feasibility, technical feasibility of repeat local anaesthetic thoracoscopy (LAT) and patient acceptability, and a retrospective cohort study focused on AAPI-mesothelioma evolution rate, informing sample size. 4 UK pleural disease centres (February 2019-January 2020). Patients with AAPI (history or typical imaging plus appropriate pleural histology) were eligible for both elements. In August 2019, eligibility for the prospective element was broadened, including addition of radiological AAPI for technical feasibility and patient acceptability endpoints only. Retrospective cases required ≥2 years follow-up. A prospective recruitment target was set a priori at 27 histological AAPI cases (or 14 in any 6 months). Technical feasibility and patient acceptability were determined at 6-month follow-up by thoracic ultrasound surrogates and questionnaires, respectively. Retrospective malignant pleural mesothelioma evolution rate was defined by proportion (95% CI). Baseline predictors of evolution were identified using logistic regression. 296 patients with AAPI (39 prospective, 257 retrospective) were recruited/selected. 21/39 prospective recruits were histologically diagnosed (target n=27). Repeat LAT was technically feasible and acceptable in 13/28 (46%) and 24/36 (67%) cases with complete follow-up data. Mesothelioma evolution was confirmed histologically in 36/257 retrospective cases (14% (95% CI 10.3% to 18.8%)) and associated with malignant CT features (OR 4.78 (95% CI 2.36 to 9.86)) and age (OR 1.06 (95% CI 1.02 to 1.12)). Our initial eligibility criteria were too narrow. Meso-ORIGINS will recruit a broader cohort, including prevalent cases, any biopsy type and patients with malignant CT features. A range of rebiopsy techniques will be allowed, accounting for technical and patient factors. The sample size has been reduced to 500. ISRCTN12840870.

Identifiants

pubmed: 37553196
pii: bmjopen-2022-067780
doi: 10.1136/bmjopen-2022-067780
pmc: PMC10414089
doi:

Substances chimiques

Asbestos 1332-21-4

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e067780

Subventions

Organisme : Cancer Research UK
ID : 29372
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Katie Ferguson (K)

Glasgow Pleural Disease Unit, Queen Elizabeth University Hospital Campus, Glasgow, UK.
School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Matthew Neilson (M)

The Beatson Institute for Cancer Research, Glasgow, UK.

Rachel Mercer (R)

Oxford Centre for Respiratory Medicine, Churchill Hospital, Oxford, UK.

Jenny King (J)

Department of Respiratory Medicine, University Hospital of South Manchester, Manchester, UK.

Kelly Marshall (K)

Department of Respiratory Medicine, University Hospital of South Manchester, Manchester, UK.

Hugh Welch (H)

Academic Respiratory Unit, University of Bristol, Bristol, UK.

Selina Tsim (S)

Glasgow Pleural Disease Unit, Queen Elizabeth University Hospital Campus, Glasgow, UK.

Nick A Maskell (NA)

University of Bristol Academic Respiratory Unit, Westbury on Trym, UK.

Najib M Rahman (NM)

Oxford Centre for Respiratory Medicine, Churchill Hospital, Oxford, UK.

Matthew Evison (M)

Department of Respiratory Medicine, University Hospital of South Manchester, Manchester, UK.

Kevin G Blyth (KG)

Glasgow Pleural Disease Unit, Queen Elizabeth University Hospital Campus, Glasgow, UK Kevin.Blyth@glasgow.ac.uk.
School of Cancer Sciences, University of Glasgow, Glasgow, UK.

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