An open-label, non-comparative study conducted to investigate the activity and safety of imatinib mesylate in refractory desmoplastic small round cell tumors expressing PDGF-R. Patients will be treated up to 12 months, or to disease progression. Tumor will be evaluated according to Recist criteria
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
9
Novartis Investigative Site
Ivrea, Italy
Novartis Investigative Site
Milan, Italy
Novartis Investigative Site
Napoli, Italy
Novartis Investigative Site
Padua, Italy
Overall tumor response rates
An imaging technique (CT scan or MRI) determined tumor response according to RECIST criteria.
Time frame: Assessed every 3 months
Explore how Imatinib cooperated with other treatment modatilities
Recorded survival after treatment and other associated treatment modalities.
Time frame: Survival data was collected until death
Safety and tolerability
Time frame: Safety data collected until patients were no longer in study
Conversion rate to surgical resectability
Assessed actual resectability rate after therapy compared to resectability before therapy.
Time frame: After best tumor response.
Mutational analysis of molecular targets of imatinib (at any time during the study)
Time frame: At any time during the study
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Novartis Investigative Site
Ravenna, Italy
Novartis Investigative Site
Rozzano, Italy
Novartis Investigative Site
Torino, Italy
Novartis Investigative Stie
Vatania, Italy