The purpose of this study is to evaluate activity and toxicity of the combination of carboplatin and liposomal doxorubicin as first-line chemotherapy of patients with advanced or recurrent endometrial carcinoma.
Treatment is planned with carboplatin AUC 5 given IV on day 1 and liposomal doxorubicin 40 mg/m2 given IV on day 1, with treatment repeated every 28 days. Delays in treatment administration and dose reductions have been planned according to toxicity.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
42
Ospedale Fatebenefratelli, U.O. di Oncologia
Benevento, BN, Italy
Ospedale Pierantoni, Divisione di Oncologia Medica
Forlì, FO, Italy
Ospedale S. Giovanni Calibita Fatebenefratelli
Roma, Roma, Italy
Istituto Nazionale dei Tumori , Divisione di Oncologia Medica B
Naples, Italy
Objective response rate (complete and partial responses)
Toxicity
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