Osimertinib Resistance Analysis in Patients With EGFR Mutation Positive Non-small-cell Lung Carcinoma That Have Progressed on Osimertinib Treatment'

Who is this study for? Patients with EGFR mutation positive NSCLC
What treatments are being studied? Biopsy+Blood
Status: Recruiting
Location: See all (6) locations...
Intervention Type: Diagnostic test
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Initially, patients with EGFR mutation positive NSCLC respond well to osimertinib, a third generation EGFR tyrosine kinase inhibitor (TKI), but eventually progress. Upon progression multiple resistance mechanisms have been described and new therapeutic strategies are being developed to target these resistance mechanisms. Thorough and complete osimertinib resistance analysis enables optimal treatment decision making and might identify new targets for molecular treatment, thereby potentially improving patient outcome.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Histologically confirmed metastatic NSCLC, characterized by a sensitizing EGFR mutation.

• 2\. Progressive disease, as assessed by the treating physician during osimertinib monotherapy.

• 3\. Eligible for subsequent treatment. 4. Willing to undergo a histological biopsy and withdrawal of a blood sample for ctDNA analysis.

• 5\. Technically possible to take a histological biopsy.

Locations
Other Locations
Netherlands
The Netherlands Cancer Institute-Antoni van Leeuwenhoek
RECRUITING
Amsterdam
Vrije Universiteit Medisch Centrum
NOT_YET_RECRUITING
Amsterdam
Universitair Medisch Centrum Groningen
NOT_YET_RECRUITING
Groningen
Academisch Ziekenhuis Maastricht
NOT_YET_RECRUITING
Maastricht
Radboud Universitair Medisch Centrum
NOT_YET_RECRUITING
Nijmegen
Erasmus MC, Universitair Medisch Centrum Rotterdam
NOT_YET_RECRUITING
Rotterdam
Contact Information
Primary
J de Langen, MD, PhD
j.d.langen@nki.nl
0031205129111
Backup
M Jebbink
m.jebbeink@nki.nl
0031205129111
Time Frame
Start Date: 2019-08-22
Estimated Completion Date: 2024-08-22
Participants
Target number of participants: 200
Treatments
Other: Biopsy and blood
A histological core biopsy of a tumor lesion and a blood sample for ctDNA analysis will be collected
Sponsors
Leads: The Netherlands Cancer Institute
Collaborators: AstraZeneca

This content was sourced from clinicaltrials.gov