A Randomised, Double-blind, Placebo-controlled, Phase III Study to Evaluate the Efficacy and Safety of Afatinib (BIBW 2992) as Adjuvant Therapy After Chemo-radiotherapy in Primary Unresected Patients With Stage III, IVa, or IVb Loco-regionally Advanced Head and Neck Squamous Cell Carcinoma
Overview
- Phase
- Phase 3
- Intervention
- Afatinib
- Conditions
- Head and Neck Neoplasms
- Sponsor
- Boehringer Ingelheim
- Enrollment
- 36
- Locations
- 16
- Primary Endpoint
- Disease Free Survival (DFS)
- Status
- Terminated
- Last Updated
- 7 years ago
Overview
Brief Summary
This randomised, double-blind phase III trial will be performed in patients with head and neck squamous cell carcinoma (HNSCC). The objectives of the trial are to compare the efficacy and safety of afatinib (BIBW 2992) with placebo as adjuvant therapy to patients who have received definitive chemo-radiotherapy.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Arms & Interventions
Afatinib (BIBW2992)
Once daily
Intervention: Afatinib
Placebo
Once daily
Intervention: Placebo
Outcomes
Primary Outcomes
Disease Free Survival (DFS)
Time Frame: up to 4 years
DFS, defined as the number of days from the date of randomisation to the date of tumour recurrence/ Second Primary Tumours (SPT) or death from any cause, whichever occurred first. For patients with known date of tumour recurrence/SPT (or death), the event date was the date of tumour recurrence/SPT or the date of death, whichever came first, i.e. DFS \[day\] = minimum (date of tumour recurrence/SPT, date of death) - date of randomisation +1. For patients known to be alive and without tumour recurrence/SPT by the end of trial or follow-up visit, they were censored at the date of last imaging when the patient was known to be disease-free and alive: DFS (censored) \[days\] = date of last imaging when the patient was known to be diseasefree and alive - date of randomisation + 1. The Kaplan-Meier (KM) method was to be used to estimate the median DFS for each treatment group. 95% confidence interval (CI) was to be constructed using the Greenwood variance estimate.
Secondary Outcomes
- Health Related Quality of Life (HRQOL)(up to 4 years)
- Disease Free Survival (DFS) Rate at 2 Years(up to 2 years)
- Overall Survival (OS)(up to 4 years)