The aim of this study is to determine preliminary efficacy of capecitabine and interferon-alpha in second-line after interleukin-2 based regimens in patients with MRCC
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
49
Patients who meet inclusion/exclusion criteria will receive combination of study drugs.
N.N. Blokhin Russian Cancer Research Center
Moscow, Russia
Evaluate progression-free survival with capecitabine and interferon treatment in metastatic renal cell carcinoma (MRCC) patients (pts) with IL-2 failure in first-line
Time frame: one year
Evaluate the safety and tolerability of the capecitabine and interferon combination
Time frame: one year
Evaluate response rate and overall survival with the capecitabine and interferon combination in MRCC pts with progression on IL-2 based regimens
Time frame: one year
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