Systematic endoscopic staging of mediastinum to determine impact on radiotherapy for locally advanced lung cancer (SEISMIC): protocol for a prospective single arm multicentre interventional study.


Journal

BMC pulmonary medicine
ISSN: 1471-2466
Titre abrégé: BMC Pulm Med
Pays: England
ID NLM: 100968563

Informations de publication

Date de publication:
24 Sep 2022
Historique:
received: 13 06 2022
accepted: 14 09 2022
entrez: 24 9 2022
pubmed: 25 9 2022
medline: 28 9 2022
Statut: epublish

Résumé

Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) is established as the preferred method of mediastinal lymph node (LN) staging in non-small cell lung cancer (NSCLC). Selective (targeted) LN sampling is most commonly performed however studies in early stage NSCLC and locally advanced NSCLC confirm systematic EBUS-TBNA evaluation improves accuracy of mediastinal staging. This study aims to establish the rate of detection of positron emission tomography (PET)-occult LN metastases following systematic LN staging by EBUS-TBNA, and to determine the utility of systematic mediastinal staging for accurate delineation of radiation treatment fields in patients with locally advanced NSCLC. Consecutive patients undergoing EBUS-TBNA for diagnosis/staging of locally advanced NSCLC will be enrolled in this international multi-centre single arm study. Systematic mediastinal LN evaluation will be performed, with all LN exceeding 6 mm to be sampled by TBNA. Where feasible, endoscopic ultrasound staging (EUS-B) may also be performed. Results of minimally invasive staging will be compared to FDG-PET. The primary end-point is proportion of patients in whom systematic LN staging identified PET-occult NSCLC metastases. Secondary outcome measures include (i) rate of nodal upstaging, (ii) false positive rate of PET for mediastinal LN assessment, (iii) analysis of clinicoradiologic risk factors for presence of PET-occult LN metastases, (iv) impact of systematic LN staging in patients with discrepant findings on PET and EBUS-TBNA on target coverage and dose to organs at risk (OAR) in patients undergoing radiotherapy. With specificity of PET of 90%, guidelines recommend tissue confirmation of positive mediastinal LN to ensure potentially early stage patients are not erroneously denied potentially curative resection. However, while confirmation of pathologic LN is routinely sought, the exact extent of mediastinal LN involvement in NSCLC in patient with Stage III NSCLC is rarely established. Studies examining systematic LN staging in early stage NSCLC report a significant discordance between PET and EBUS-TBNA. In patients with locally advanced disease this has significant implications for radiation field planning, with risk of geographic miss in the event of PET-occult mediastinal LN metastases. The SEISMIC study will examine both diagnostic outcomes following systematic LN staging with EBUS-TBNA, and impact on radiation treatment planning. ACTRN12617000333314, ANZCTR, Registered on 3 March 2017.

Sections du résumé

BACKGROUND BACKGROUND
Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) is established as the preferred method of mediastinal lymph node (LN) staging in non-small cell lung cancer (NSCLC). Selective (targeted) LN sampling is most commonly performed however studies in early stage NSCLC and locally advanced NSCLC confirm systematic EBUS-TBNA evaluation improves accuracy of mediastinal staging. This study aims to establish the rate of detection of positron emission tomography (PET)-occult LN metastases following systematic LN staging by EBUS-TBNA, and to determine the utility of systematic mediastinal staging for accurate delineation of radiation treatment fields in patients with locally advanced NSCLC.
METHODS METHODS
Consecutive patients undergoing EBUS-TBNA for diagnosis/staging of locally advanced NSCLC will be enrolled in this international multi-centre single arm study. Systematic mediastinal LN evaluation will be performed, with all LN exceeding 6 mm to be sampled by TBNA. Where feasible, endoscopic ultrasound staging (EUS-B) may also be performed. Results of minimally invasive staging will be compared to FDG-PET. The primary end-point is proportion of patients in whom systematic LN staging identified PET-occult NSCLC metastases. Secondary outcome measures include (i) rate of nodal upstaging, (ii) false positive rate of PET for mediastinal LN assessment, (iii) analysis of clinicoradiologic risk factors for presence of PET-occult LN metastases, (iv) impact of systematic LN staging in patients with discrepant findings on PET and EBUS-TBNA on target coverage and dose to organs at risk (OAR) in patients undergoing radiotherapy.
DISCUSSION CONCLUSIONS
With specificity of PET of 90%, guidelines recommend tissue confirmation of positive mediastinal LN to ensure potentially early stage patients are not erroneously denied potentially curative resection. However, while confirmation of pathologic LN is routinely sought, the exact extent of mediastinal LN involvement in NSCLC in patient with Stage III NSCLC is rarely established. Studies examining systematic LN staging in early stage NSCLC report a significant discordance between PET and EBUS-TBNA. In patients with locally advanced disease this has significant implications for radiation field planning, with risk of geographic miss in the event of PET-occult mediastinal LN metastases. The SEISMIC study will examine both diagnostic outcomes following systematic LN staging with EBUS-TBNA, and impact on radiation treatment planning.
TRIAL REGISTRATION BACKGROUND
ACTRN12617000333314, ANZCTR, Registered on 3 March 2017.

Identifiants

pubmed: 36153502
doi: 10.1186/s12890-022-02159-9
pii: 10.1186/s12890-022-02159-9
pmc: PMC9509615
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

364

Informations de copyright

© 2022. The Author(s).

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Auteurs

Daniel P Steinfort (DP)

Department of Respiratory and Sleep Medicine, Royal Melbourne Hospital, 300 Grattan Street, VIC, Melbourne, 3050, Australia. Daniel.Steinfort@mh.org.au.

Shankar Siva (S)

Department of Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.

Kanishka Rangamuwa (K)

Department of Respiratory and Sleep Medicine, Royal Melbourne Hospital, 300 Grattan Street, VIC, Melbourne, 3050, Australia.

Percy Lee (P)

Department of Radiation Oncology, MD Anderson Cancer Center, The University of Texas, Houston, USA.

David Fielding (D)

Department of Thoracic Medicine, Royal Brisbane and Women's Hospital, Brisbane, Australia.

Phan Nguyen (P)

Department of Thoracic Medicine, Royal Adelaide Hospital, Adelaide, Australia.

Barton R Jennings (BR)

Department of Lung and Sleep, Monash Health, Melbourne, Australia.

Shaun Yo (S)

Department of Lung and Sleep, Monash Health, Melbourne, Australia.

Nick Hardcastle (N)

Department of Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.

Gargi Kothari (G)

Department of Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.

Laurence Crombag (L)

Department of Pulmonology (VUmc), University of Amsterdam, Amsterdam, The Netherlands.

Jouke Annema (J)

Department of Pulmonology (AMC), University of Amsterdam, Amsterdam, The Netherlands.

Kazuhiro Yasufuku (K)

Division of Thoracic Surgery, Toronto General Hospital, Toronto, Canada.

David E Ost (DE)

Department of Pulmonary Medicine, MD Anderson Cancer Center, The University of Texas, Houston, USA.

Louis B Irving (LB)

Department of Respiratory and Sleep Medicine, Royal Melbourne Hospital, 300 Grattan Street, VIC, Melbourne, 3050, Australia.

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Classifications MeSH