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Clinical Trials/NCT03971175
NCT03971175
Unknown
Not Applicable

A Prospective, Randomized, Single Blinded Multicentre Trial to Evaluate Molecular Genetic Characterisation of Primary Diagnosed or Relapsed Non Small Cell Lung Cancer by Single or Combination of Diagnostic Procedures

University Hospital Tuebingen1 site in 1 country540 target enrollmentDecember 19, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Carcinoma, Non-Small-Cell Lung
Sponsor
University Hospital Tuebingen
Enrollment
540
Locations
1
Primary Endpoint
Differences in the detection of total mutational burden between both techniques.
Last Updated
3 years ago

Overview

Brief Summary

Study design Prospective multicentre explorative randomized single blinded study to evaluate accuracy of molecular genetic characterisation of NSCLC. Patients with suspected lung cancer are randomized in a 1:1-setting for bronchoscopic tumor tissue either by forceps or by cryobiopsy. Apart from the bronchoscopic techniques liquid biopsy of peripheral blood and if feasible transbronchial needle aspiration with or without endobronchial ultrasound guidance are performed for in all patients.

Objectives

Primary Objective:

assessment of differences in detection of molecular genetic alterations in NSCLC between bronchoscopic forceps biopsy and bronchoscopic cryobiopsy

Secondary Objective:

assessment of differences in detection of molecular genetic alterations in NSCLC between

  • liquid biopsy, solid tumor tissue by bronchoscopic techniques, cytologic material by TBNA
  • combination of methods (tissue biopsy, TBNA and liquid biopsy) and single techniques
  • naïve and processed tumor tissue specimen (eg. microdissection)

To assess differences in side effects e.g. periinterventional bleeding

Explorative Objective:

To explore tumor mutational burden with regard to

  • solid tumor tissue by bronchoscopic forceps biopsy by bronchoscopic cryobiopsy
  • cytologic material by (EBUS-guided) TBNA
  • liquid biopsy

Target subject population Patients with suspected lung cancer or proven NSCLC and visible tumor suspicious lesion(s) requiring tissue diagnosis form the study population of this trial.

Registry
clinicaltrials.gov
Start Date
December 19, 2018
End Date
June 30, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Provision of informed consent to the study and the study specific procedures prior to any study intervention
  • Male or female patients aged ≥18 years
  • Patients with primary diagnosis of suspected lung cancer OR Patients with known NSCLC and suspected relapse after therapy
  • Bronchoscopically visible tumor

Exclusion Criteria

  • Preexisting malignancy other than NSCLC
  • Contraindication for bronchoscopy according to the international guidelines, daily clinical practice and the local regulations with
  • Patients with existing or at risk of pulmonary and cardiovascular decompensation
  • Patients at increased risk of bleeding with antiplatelet agents except of aspirin (clopidogrel, ticlopidine, ...) , anticoagulant therapy (prolonged PTT), thrombocytopenia (\< 50.000/ul) or coagulopathy (prolonged in vitro bleeding time).
  • Intolerance to sedation
  • Unstable or immobile cervical spine
  • Limited motion of the temporomandibular joint
  • Previous enrolment in the present study

Outcomes

Primary Outcomes

Differences in the detection of total mutational burden between both techniques.

Time Frame: recruiting period approximately 24 months

assessment of differences in detection of molecular genetic alterations in NSCLC between bronchoscopic forceps biopsy and bronchoscopic cryobiopsy

Detection of at least one molecular and/ or genetic alteration.

Time Frame: recruiting period approximately 24 months

assessment of differences in detection of molecular genetic alterations in NSCLC between bronchoscopic forceps biopsy and bronchoscopic cryobiopsy

Secondary Outcomes

  • Combinations of molecular and/ or genetic alterations(recruiting period approximately 24 months)
  • Detection of any molecular and/ or genetic alterations(recruiting period approximately 24 months)
  • Differences in the quantity of total mutational burden between the different techniques(recruiting period approximately 24 months)

Study Sites (1)

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