Skip to content

A New Pathway With BronchOscopic or Oesophageal Ultrasound for Lung Cancer Diagnosis and STaging (BOOST)

A Randomized Controlled Trial of Endobronchial or Endoscopic Ultrasound as a First Test in the Diagnosis and Staging of Lung Cancer

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00652769
Acronym
BOOST
Enrollment
168
Registered
2008-04-04
Start date
2008-03-31
Completion date
2012-07-31
Last updated
2017-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchogenic Carcinoma

Keywords

Lung, Cancer, Staging, Endobronchial, Ultrasound, Endoscopic

Brief summary

In the UK, staging of lung cancer is time consuming (taking on average more than 3 weeks), costly and inaccurate in up to 20% of cases. The investigators wish to determine whether using the newer techniques of endobronchial ultrasound (EBUS) and endoscopic ultrasound (EUS) improves lung cancer staging. The investigators' hypothesis is that EUS (endoscopic ultrasound) or EBUS (endobronchial ultrasound guided transbronchial needle aspirate) as a first test after CT scan in the diagnosis and staging of lung cancer will result in a reduction in the time from first outpatient appointment to treatment decision, a reduction in the total number of scans and investigative operations, fewer outpatient attendances and a reduction in healthcare costs.

Interventions

PROCEDUREEndobronchial or Endoscopic Ultrasound

Patients with anterior mediastinal or subcarinal disease will undergo EBUS. Patients with posterior, subcarinal or AP window disease will undergo EUS. Patients with no mediastinal disease on CT scan will undergo EBUS.

PROCEDUREBronchoscopy, CT-guided biopsy, PET scan, Mediastinoscopy

Investigations will be determined by the multi-disciplinary team responsible for the patient

Sponsors

North Middlesex University Hospital
CollaboratorOTHER
Barnet and Chase Farm Hospitals NHS Trust
CollaboratorOTHER
The Whittington Hospital NHS Trust
CollaboratorOTHER_GOV
University College London Hospitals
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Consecutive patients suspected of lung cancer on CT scan * Written informed consent * Able to tolerate bronchoscopy and thoracic surgery

Exclusion criteria

* Evidence of severe or uncontrolled systemic disease that makes it undesirable for the patient to participate in the trial * Any disorder making reliable informed consent impossible * Patients with extra-thoracic disease, supraclavicular lymphadenopathy or pleural effusion

Design outcomes

Primary

MeasureTime frame
Time from first outpatient appointment to decision to treat1 - 3 months

Secondary

MeasureTime frame
The healthcare costs for diagnosing and staging lung cancerEnd of study
The number of tests and outpatient visits a patient requires to be diagnosed and staged with lung cancer1 - 3 months
The proportion of lung cancer patients that are diagnosed and staged with a single test after CT scan1 - 3 months
The time from first outpatient appointment to treatment1 - 3 months
The number of futile thoracotomies1 - 3 years

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026