The aim of this study is to investigate the efficacy and safety of afatinib alone or in combination with vinorelbine, as treatment in patients with HER2-overexpressing metastatic breast cancer, who have progressive brain lesions after trastuzumab and/or lapatinib based therapy
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
121
Vinorelbine 25 mg/m² on days 1, 8, 15 in a 3-weekly course
Patients will receive, at the investigator's discretion, the most appropriate medical treatment consisting of single agent or combination regimen approved for the treatment of metastatic breast cancer, and according to patient status and local guidelines.
Afatinib monotherapy:once daily, continuous treatment in a 3-weekly course. If well tolerated, the dose may be escalated to 50 mg.
Patient Benefit Rate at 12 Weeks
Percentage of patients with patient benefit at week 12. Patient benefit was defined by the absence of central nervous system (CNS) disease progression according to Response Evaluation Criteria in Solid Tumours (RECIST) version 1.1 in addition to no tumour-related worsening of the neurological signs and symptoms (NSS), no tumour-related increase in corticosteroid dosage and no progression of extra CNS disease according to RECIST 1.1
Time frame: 12 weeks from randomisation
Progression-Free Survival
Progression-Free Survival is defined as the time from the date of randomisation to the date of disease progression or death whichever came first. Disease progression was defined as either disease progression in CNS lesions (including worsening in NSS and use of corticosteroid) or disease progression in extra-CNS lesions according to RECIST 1.1.
Time frame: From first drug administration until 28 days after end of treatment, up to 805 days
Overall Survival
Overall Survival is defined as time from randomisation to the date of death from any cause.
Time frame: From first drug administration until 28 days after end of treatment, up to 805 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Afatinib monotherapy:once daily, continuous treatment in a 3-weekly course. If well tolerated, the dose may be escalated to 50 mg.
1200.67.10106 Boehringer Ingelheim Investigational Site
Bakersfield, California, United States
1200.67.10105 Boehringer Ingelheim Investigational Site
Fullerton, California, United States
1200.67.10001 Boehringer Ingelheim Investigational Site
Los Angeles, California, United States
1200.67.10108 Boehringer Ingelheim Investigational Site
Santa Barbara, California, United States
1200.67.10003 Boehringer Ingelheim Investigational Site
Lake Success, New York, United States
1200.67.10004 Boehringer Ingelheim Investigational Site
Columbus, Ohio, United States
1200.67.11004 Boehringer Ingelheim Investigational Site
Toronto, Ontario, Canada
1200.67.11003 Boehringer Ingelheim Investigational Site
Greenfield Park, Quebec, Canada
1200.67.11002 Boehringer Ingelheim Investigational Site
Montreal, Quebec, Canada
1200.67.35801 Boehringer Ingelheim Investigational Site
Helsinki, Finland
...and 30 more locations