Non Small Cell Lung Cancer Clinical Trial
Official title:
Resectable EGFR Mutant NSCLC With (or Without) Afatinib as Neoadjuvant Treatment; REMNANT an Exploratory Study of the EORTC Lung Cancer Group
This is a multicenter, randomized, 1:1, non-comparative phase II trial. Patients with early stage NSCLC will be randomized between ARM A: neoadjuvant afatinib followed by surgery and ARM B: immediate surgery with curative intent.
This is a multicenter, prospective, open-label, randomized, non-comparative, two-arm phase
II trial aiming to evaluate afatinib treatment in pre-operative setting in patients with
EGFR mutated NSCLC.
After signing of the informed consent, patients will be registered and screened for
eligibility and upon confirmation of all eligibility criteria, patients will be randomized
1:1 to:
- Arm A: once daily afatinib at a dose of 40 mg for 8 weeks followed by surgery with
curative intent (anatomical resection and systematic lymph node dissection).
- Arm B: immediate surgery with curative intent (anatomical resection and systematic
lymph node dissection).
Response evaluation in the pre-operative arm will be performed through CT scans at baseline,
4 and 8 weeks.
The first 5 patients enrolled in arm A will be part of a safety run-in to check that
afatinib treatment doesn't delay surgery.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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