The Continuation of Erlotinib
- Sponsor
- Samsung Medical Center
- Study ID
- NCT01130779
- Phase
- PHASE2
- Status
- Unknown
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Erlotinib (TARCEVA®) — DRUGErlotinib 150mg/day, everyday
Study Details
Newly developed or progressive brain metastasis during erlotinib treatment is considered progressive disease requiring change of treatment regimens despite no progression in extracranial lesions. Given that there is a dissociation in terms of response to erlotinib between brain and extracranial sites, we intend to conduct this pilot study to determine whether the continuation of erlotinib treatment can prolong the progression free interval of extracranial lesions as long as cranial lesion is controlled separately by conventional treatment modalities such as surgical resection, stereotactic radiosurgery, and whole brain radiotherapy.
Key Dates
- First listed
- May 26, 2010
- Start date
- Aug 31, 2009
- Status verified
- May 2010
- Primary completion
- Aug 31, 2010
Study Design
- Enrollment
- 23 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: tarcevacontinuation of tarceva
Primary Outcome Measure
progression free survival [ Time Frame: 6 months ]
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