Clinical trial · Interventional
Neoadjuvant Afatinib in Early Stage Non Small Cell Lung Cancer.
Resectable EGFR Mutant NSCLC With (or Without) Afatinib as Neoadjuvant Treatment; REMNANT an Exploratory Study of the EORTC Lung Cancer Group
NCT02470065CI-TRIAL-00020628REMNANTsuspendedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Study never started
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Non Small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Afatinib | Drug | Afatinib | ALIAS |
| Immediate surgery | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Neo adjuvant afatinib
- description
- 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).
- interventionNames
- Drug: Afatinib
- Procedure: Immediate surgery
- type
- ACTIVE_COMPARATOR
- label
- Immediate surgery
- description
- immediate surgery with curative intent (anatomical resection and systematic lymph node dissection).
- interventionNames
- Procedure: Immediate surgery
Primary outcomes (1)
- measure
- Decrease in cT-stage
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 90 Years
Show eligibility criteria text
Inclusion Criteria: Histological or cytological diagnosis of NSCLC; * Patients considered operable and with resectable tumor with curative intent (anatomical resection and systematic lymph node dissection) based on evaluation by a thoracic multi-disciplinary team composed of at least a thoracic surgeon, oncologist and radiologist; * Stage I-III (T1a-3, N0-1, M0 according to UICC version 7) NSCLC by local staging criteria potentially treatable by radical (curative) surgery. Patients with T1 tumor at baseline will be limited to 20%; * Radiologically measurable disease according to RECIST criteria 1.1; assessed by chest and upper abdomen CT scan within 2 weeks (+1 week) prior to registration); brain CT scan or MRI according to local practice; * No prior treatment for NSCLC is allowed; * Adequate tissue in terms of quality and quantity for EGFR local testing. Exclusion Criteria: * no adequate bone marrow function within 2 weeks prior to randomization * no adequate liver function. Patients with Gilbert's syndrome total bilirubin must be below 4 times institutional upper limit of normal; within 2 weeks prior to randomization * no adequate renal function within 2 weeks prior to randomization * known positivity to human immunodeficiency virus (HIV), hepatitis B or hepatitis C; * known history of allergic reactions attributed to compounds of similar chemical or biological composition; * history of a hematologic or primary solid tumor malignancy, unless no evidence of that disease for 5 years, except pT1-2 prostatic cancer Gleason score \< 6, superficial bladder cancer, non melanoma skin cancer or carcinoma in situ of the cervix;
References
Publications (0)
Data not yet available
No reference posted for this study.