Medroxyprogesterone Acetate Plus Atorvastatin in Young Women With Early Endometrial Carcinoma and Atypical Endometrial Hyperplasia

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age17-45
SponsorPeking University People's Hospital

About this trial

To explore the treatment efficacy of medroxyprogesterone acetate plus atorvastatin in patients with atypical endometrial hyperplasia (AEH) and early endometrial carcinoma (EEC) for conservative treatment.

Eligibility criteria

Qualifiers

Have a confirmed pathological diagnosis based upon hysteroscopy: histologically prove AEH or well-differentiated EEC G1 without myometrial invasion: 1. Untreated patients; 2. Patients with persistent lesions after one course (12 weeks) of progesterone therapy; 3. Patients who did not achieve complete remission after 2 courses (24 weeks) of progesterone therapy;

No signs of suspicious extrauterine involvement on enhanced magnetic resonance imaging (MRI) or enhanced computed tomography (CT) or ultrasound

Have a desire for remaining reproductive function or uterus

Good compliance with adjunctive treatment and follow-up

Disqualifiers

Hypersensitivity or contradiction for using MPA or atorvastatin

Pregnancy or potential pregnancy

Confirmed diagnosis of any cancer in reproductive system

Already diagnosed with hyperlipidemia and using lipid-lowering drugs

Trial design

Treatments tested in this trial

  • Medroxyprogesterone acetate + Atorvastatin

Treatment groups

82 Participants
are divided into 2 treatment groups