About this trial
This is a prospective randomized, double blind, placebo controlled phase II study planned in patients with advanced ACC. The study will be conducted at ASST Spedali Civili Hospital and University of Brescia in Brescia.
Eligibility criteria
Qualifiers
Histologically confirmed diagnosis of ACC
Locally advanced or metastatic disease not amenable to radical surgery resection
ECOG performance status 0-2
Effective contraception
Disqualifiers
History of recent or active prior malignancy, except for cured non-melanoma skin cancer, cured in situ cervical carcinoma, breast ductal carcinoma in situ, or other treated malignancies where there has been no evidence of disease for at least 2 years
Renal insufficiency (estimated glomerular filtration rate [GFR]<50 mL/min/1.73 m2) or significant liver insufficiency (serum bilirubin>2 times the upper normal range and/or serum alanine aminotransferase [ALT] or aspartate aminotransferase [AST]>3 times the upper normal range). GFRs will be calculated according to the validated formula (MDRD)
Pregnancy or breast feeding
Congestive heart failure (ejection fraction<45%)
Trial design
Treatments tested in this trial
- Etoposide, doxorubicin, cisplatin and Mitotane plus Megestrol Acetate 160 MG
- Etoposide, doxorubicin, cisplatin and Mitotane plus Placebo