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EUS-B-FNA vs EUS-FNA for Left Adrenal Gland Analysis in Lung Cancer Patients

EUS-B-FNA vs EUS-FNA for Left Adrenal Gland Analysis in Lung Cancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02538380
Enrollment
40
Registered
2015-09-02
Start date
2015-03-31
Completion date
Unknown
Last updated
2015-09-02

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

Conditions

Suspected Left Adrenal Gland Metastasis in Lung Cancer

Keywords

Lung cancer, Adrenal gland metastasis

Brief summary

The purpose of this study is to compare EUS-B-FNA (using the EBUS scope)with EUS-FNA for left adrenal gland analysis in lung cancer patients.

Detailed description

Rationale: The adrenal glands are a predilection site for distant metastases (M1b) in patients with lung cancer. However, even in a patient with a confirmed lung cancer an enlarged adrenal lesion is still more likely to be benign than to be malignant(4). Therefore tissue sampling of the left adrenal gland (LAG) is obligatory to either confirm or rule out metastases. Sampling is regularly performed by a transgastric endoscopic approach using a conventional GI-EUS scope. The aim of this study is investigate the success rate of endoscopic ultrasound guided fine-needle aspiration using the EBUS scope (EUS-BFNA) for left adrenal gland analysis in patients with lung cancer and an on imaging suspected left adrenal gland. Hypothesis: EUS-B guided transgastric FNA of suspected left adrenal glands (LAG) reduces the need for conventional EUS- FNA by half. Study design: A prospective cohort design Setting: international, multicenter Study population: Patients with (suspected) lung cancer, an indication for mediastinal nodal staging and a for malignancy suspected LAG on imaging. Intervention: All patients will undergo a mediastinal nodal staging procedure with the EBUS scope (EBUS + EUSB) (routine clinical care) followed by an evaluation of the LAG including LAG sampling (experimental). Subsequently, all patients undergo a conventional EUS procedure with sampling of the LAG (current standard of care) Main study endpoint: The proportion of patients with a successful EUS-B-FNA procedure for LAG analysis. Successful is defined as: LAG is visible, sampling is possible and adequate material for cytopathological evaluation is obtained. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Distant metastases of lung cancer like LAG metastases have significant impact on both the prognosis and treatment. In the majority of patients with an indication for LAG sampling by endosonography, there is also an indication for mediastinal nodal tissue sampling. In case both the mediastinal lymph nodes and the LAG can be evaluated with the same scope, patients can be evaluated for nodal and distant metastasis with just a single instead of two separate scopes. This will be beneficial for patients (reduced investigation time) and is additionally cost -effective. So far EUS-B of LAG has been shown to be safe and feasible.

Interventions

PROCEDUREEUS-B-FNA followed by EUS-FNA for LAG analysis

Sponsors

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

* (Suspected) Lung Cancer * For malignancy suspected LAG on imaging (enlarged based on CT and/or FDG avid based on FDG-PET); * Indication for endosonographic mediastinal staging by EBUS; * Indication for LAG sampling;

Exclusion criteria

* Contraindication for EUS; * Pregnancy;

Design outcomes

Primary

MeasureTime frameDescription
The proportion of patients with a successful EUS-B-FNA procedure for LAG analysis.within 3 weeks after inclusionSuccessful is defined as: LAG is visible, sampling is possible and adequate material for cytopathological evaluation is obtained.

Countries

Netherlands

Contacts

Primary ContactLaurence MM Crombag, MD
l.m.crombag@amc.nl+31205664356
Backup ContactJouke T Annema, MD PhD
j.t.annema@amc.nl+31205663173

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026