Clinical trial · Interventional
Afatinib Treatment for Patients With EGFR Mutation Positive NSCLC Who Are Age 70 or Older
A Single Arm Phase IV Study of Afatinib in Elderly Patients With Stage IV or Recurrent Non-Small Cell Lung Cancer Whose Tumors Have Epidermal Growth Factor Receptor (EGFR) Exon 19 Deletions or Exon 21(L858R) Substitution Mutations
NCT02514174CI-TRIAL-00044312completedPhase 4Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Continuous treatment until progression or occurence of intolerable Adverse Event (AE) or end of trial. The end of trial is one year after the last patient has entered the study.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Carcinoma, Non-Small-Cell Lung | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
| ErbB Receptors | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Afatinib | Drug | Afatinib | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Afatinib
- description
- afatinib starting at 30 mg daily dose
- interventionNames
- Drug: Afatinib
Primary outcomes (1)
- measure
- Percentage of Participants Reporting an Adverse Event (AE) Leading to Dose Reduction of Afatinib
- timeFrame
- On-treatment period + 28 days (residual effect period), up to 1057 + 28 days
- description
- On-treatment period = First administration of afatinib until progression or intolerable adverse events or other reasons necessitating withdrawal (participant's withdrawal of consent for study treatment, participant diagnosed with interstitial lung disease, participant no longer able to receive study treatments, participant had a significant deviation from the protocol or eligibility criteria).
Secondary outcomes (5)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 70 Years
Show eligibility criteria text
Inclusion criteria: * Pathologically or cytologically confirmed NSCLC Stage IV Cancer (includes cytologically proven pleural effusion or pericardial effusion) or recurrent disease. Staging is based on American Joint Committee on Cancer (AJCC) Staging for NSCLC 7th edition (R12-4710) * Evidence of common EGFR mutation (Del 19 and/or L858R) * Age \>= 70 years * Eastern Cooperative Oncology Group (ECOG) performance status 0-1 (R01-0787) * Further inclusion criteria apply. Exclusion criteria: * Prior participation in an afatinib clinical study, even if not assigned to afatinib treatment * Prior systemic therapy for metastatic or recurrent NSCLC. * Concurrent investigational therapy or investigational therapy within 4 weeks of start of afatinib therapy * Radiotherapy within 4 weeks prior to start of study treatment, except as follows: * Palliative radiation to target organs other than chest may be allowed up to 2 weeks prior to study treatment, or * Single dose palliative treatment for symptomatic metastasis outside above allowance to be discussed with sponsor prior to enrolling. * Major surgery within 4 weeks before starting study treatment or scheduled for surgery during the projected course of the study * Systemic chemotherapy, biological therapy, immunotherapy or investigational agents within 5 half-life of the drug or within four weeks prior to the start of afatinib treatment (if the half-life of the drug is unknown). * Men, capable of fathering a child, who are unwilling to use adequate contraception prior to study entry, for the duration of study participation, and for at least 28 days after treatment has ended. * Further exclusion criteria apply.
References
Publications (0)
Data not yet available
No reference posted for this study.