What Is the Accuracy of Clinical Staging for Stage III-Single-station N2 NSCLC? A Multi-Centre UK Study.

Clinical staging Endobronchial ultrasound Multimodality treatment strategies NSCLC Pulmonology

Journal

JTO clinical and research reports
ISSN: 2666-3643
Titre abrégé: JTO Clin Res Rep
Pays: United States
ID NLM: 101769967

Informations de publication

Date de publication:
Aug 2024
Historique:
received: 21 01 2024
revised: 19 05 2024
accepted: 25 05 2024
medline: 20 8 2024
pubmed: 20 8 2024
entrez: 20 8 2024
Statut: epublish

Résumé

Single-station N2 (ssN2) versus multi-station N2 has been used as a selection criterion for treatment recommendations between surgical versus non-surgical multimodality treatment in stage III-N2 NSCLC. We hypothesized that clinical staging would be susceptible to upstaging on pathologic staging and, therefore, challenge this practice. A retrospective study of prospectively collected routine clinical data for patients with stage III-N2 NSCLC that had completed computed tomography (CT), positron emission tomography (PET), and staging endobronchial ultrasound (EBUS) and had been confirmed clinical stage III-ssN2 at multidisciplinary team discussion and went on to complete surgical resection as the first treatment to provide pathologic staging. The study was completed in two cohorts (A) across a single cancer alliance in England (Greater Manchester) January 1, 2015 to December 31, 2018 and (B) across five United Kingdom centers to validate the findings in part A January 1, 2016 to December 31, 2020. A total of 115 patients met the inclusion criteria across cohort A (56 patients) and cohort B (59 patients) across 15 United Kingdom hospitals. The proportion of cases in which clinical stage III-ssN2 was upstaged to pathologic stage III-multi-station N2 was 34% (19 of 56) in cohort A, 32% in cohort B (19 of 59), and 33% across the combined study cohort (38 of 115). Most patients had a single radiologically abnormal lymph node on CT and PET (88%, 105 of 115). In the majority, the reasons for missed N2 disease on staging EBUS were due to inaccessible (stations 5, 6, 8, 9) N2 nodes at EBUS (34%, 13 of 38) and accessible lymph nodes not sampled during staging EBUS as not meeting sampling threshold (40%, 15 of 38) rather than false-negative sampling during EBUS (26%, 10 of 38). During multidisciplinary team discussions, clinicians must be aware that one-third of patients with stage III-ssN2 on the basis of CT, PET, and staging EBUS do not truly have ssN2 and this questions the use of this criterion to define treatment recommendations.

Identifiants

pubmed: 39161961
doi: 10.1016/j.jtocrr.2024.100694
pii: S2666-3643(24)00064-X
pmc: PMC11332836
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100694

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

Auteurs

Christopher Craig (C)

Lung Cancer & Thoracic Surgery Directorate, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, United Kingdom.

Janet Johnston (J)

Lung Cancer & Thoracic Surgery Directorate, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, United Kingdom.

Patrick Goodley (P)

Lung Cancer & Thoracic Surgery Directorate, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, United Kingdom.

Paul Bishop (P)

Department of Thoracic Histopathology, Clinical Support Services, Manchester University NHS Foundation Trust, Manchester, United Kingdom.

Haider Al-Najjar (H)

Manchester Royal Infirmary, Manchester University NHS Foundation Trust, Manchester, United Kingdom.

Louise Brown (L)

North Manchester General Hospital, Manchester, United Kingdom.

Joanna Gallagher (J)

Macclesfield Hospital, East Cheshire NHS Trust, Macclesfield, United Kingdom.

Ramachandran Sundar (R)

Royal Albert Edward Infirmary, Wrightington, Wigan & Leigh NHS Foundation Trust, Wigan, United Kingdom.

Sara Upperton (S)

Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.

Matthew Callister (M)

Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.

David Meek (D)

Royal Papworth Hospital NHS Foundation Trust, Cambridge, United Kingdom.

Laura Succony (L)

Royal Papworth Hospital NHS Foundation Trust, Cambridge, United Kingdom.

Wadood Parvez (W)

University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

Muhammad Tufail (M)

University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

Geeshath Jayasekera (G)

Glasgow Royal Infirmary, NHS Greater Glasgow and Clyde, Glasgow, United Kingdom.

John Maclay (J)

Glasgow Royal Infirmary, NHS Greater Glasgow and Clyde, Glasgow, United Kingdom.

Alana Livesey (A)

University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.

Ian Woolhouse (I)

University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.

Natalie Smith (N)

North Bristol NHS Trust, Bristol, United Kingdom.

Anna Bibby (A)

North Bristol NHS Trust, Bristol, United Kingdom.

Matthew Evison (M)

Lung Cancer & Thoracic Surgery Directorate, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
Manchester Academic Health Science Centre (MAHSC), Faculty of Biology, Medicine & Health, University of Manchester, Manchester, United Kingdom.

Classifications MeSH