Evaluation of the Efficacy of Addition of Progesterone to Standard Chemotherapy in Adrenocortical Carcinoma (ACC)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

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

Treatment groups

80 Participants
are divided into 2 treatment groups