PROspective Trial on EOsinophilia in Non-Small Cell Lung Cancer (NSCLC).

NARecruitingINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

October 27, 2022

Primary Completion Date

May 1, 2025

Study Completion Date

May 1, 2025

Conditions
Non-small Cell Lung Cancer
Interventions
DIAGNOSTIC_TEST

induced sputum

After premedication with 400 μg inhaled salbutamol, sputum will be induced by inhalation of hypertonic (NaCl 3%) or isotonic (NaCl 0.9%) saline combined according to the FEV-1 value (\> or ≤ than 65% predicted). Saline will be combined with additional salbutamol delivered by an ultrasonic nebulizer (Ultra-Neb 2000; Devilbiss, Somerset, PA, USA) with an output set at 0.9 ml/min. Each subject will inhale the aerosol for three consecutive periods of 5 min for a total of 15 min. For safety reasons, FEV-1 will be monitored throughout the induction and will be stopped if FEV-1 would fall by more than 20% from baseline.

DIAGNOSTIC_TEST

lung biopsy

As per standard practice, biopsies will be taken from the primary tumour site or from a metastatic site.

DIAGNOSTIC_TEST

bronchoalveolar lavage

When available, the remaining material from a patient's bronchoalveolar lavage will be collected.

DIAGNOSTIC_TEST

blood draw

As per standard practice, blood will be drawn from patients before and during treatment. Data on white blood cells will be collected.

Trial Locations (1)

4000

RECRUITING

CHU de Liège, Liège

All Listed Sponsors
lead

Centre Hospitalier Universitaire de Liege

OTHER