This study will evaluate the efficacy, safety, tolerability of imatinib in the neoadjuvant treatment (pre-operatory) of patients with GIST. It will also evaluate the potential of imatinib to convert a tumor from inoperable to operable.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Novartis Investigative Site
Belo Horizonte, Minas Gerais, Brazil
Novartis Investigative Site
Rio de Janeiro, Rio de Janeiro, Brazil
Novartis Investigative Site
Florianópolis, Santa Catarina, Brazil
Objective response using the RECIST criteria
Time frame: 16 weeks
Progression free survival
Time frame: 16 weeks
Time and duration of response
Time frame: 16 weeks
Time to treatment failure
Time frame: 16 weeks
Overall survival
Time frame: 16 weeks
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Novartis Investigative Site
São Paulo, São Paulo, Brazil
Novartis Investigative Site
São Paulo, São Paulo, Brazil
Novartis Investigative Site
São Paulo, São Paulo, Brazil
Novartis Investivative site
Belo Horizonte, Brazil
Novartis Investivative site
Florianópolis, Brazil
Novartis Investivative site
Porto Alegre, Brazil
Novartis Investivative site
Rio de Janeiro, Brazil
...and 1 more locations