A clinical study to investigate the maximum tolerated dose of Vandetanib and concurrent WBRT in patients with NSCLC and brain metastases. All patients will receive WBRT, 10 fractions of 3 Gy. Patients will start 7 days prior to start of radiation treatment with Vandetanib. Total treatment time with Vandetanib is 3 weeks (21 days). Patients will have the opportunity to continue Vandetanib until progression at a dose of 300 mg. This multi-centre study will be conducted in a minimum of 9 patients and a maximum of 18 patients at 3 sites.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
5
100 mg as a once daily oral dose, 21 days
200 mg as a once daily oral dose, 21 days
300 mg as a once daily oral dose, 21 days
Research site
Amsterdam, Netherlands
Research site
Groningen, Netherlands
Research site
Maastricht, Netherlands
To investigate the maximum tolerated dose of Vandetanib and concurrent WBRT in patients with NSCLC and brain metastases
Time frame: All evaluable patients (all registered patients who receive at least opne dose of study medication) who have completed week 9 study period
To investigate the time to clinical and radiological progression of brain metastases
Time frame: Until disease progression
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