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Megestrol Acetate Plus Rosuvastatin in Young Women With Early Endometrial Carcinoma

Primary Purpose

Endometrial Carcinoma Stage I

Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Megestrol Acetate
Rosuvastatin
Sponsored by
Fudan University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Endometrial Carcinoma Stage I focused on measuring megestrol acetate, rosuvastatin, endometrial carcinoma stage I limited to endometrium, conservative treatment

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Have a confirmed pathological diagnosis based upon hysteroscopy: histologically prove well-differentiated EEC G1 without myometrial invasion
  • 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
  • Abnormal blood lipid. At least meet one of the following five items:

    1. Total cholesterol (TC) ≥ 5.2mmol/L (200mg/dL)
    2. Low-density lipoprotein cholesterol (LDL-C) ≥ 3.4mmol/L (130mg/dL)
    3. Fasting triglycerides (TG) ≥ 1.7mmol/L (150mg/dL)
    4. High-density lipoprotein cholesterol (HDL-C) #1.03mmol/L (40mg/dL)
    5. Apo-lipoprotein-A (Apo-A) ≥ 1.0g/L

Exclusion Criteria:

  • Acute liver disease or liver tumor (benign or malignant) or renal dysfunction
  • Pregnancy or potential pregnancy
  • Under treatment of high-dose progestin therapy more than 1 months in recent 6 months
  • Confirmed diagnosis of any cancer in reproductive system
  • Acute severe disease such as stroke or heart infarction or a history of thrombosis disease
  • Hypersensitivity or contradiction for using MA or atorvastatin
  • Already diagnosed with hyperlipidemia and using lipid-lowering drugs
  • With other factors of reproductive dysfunction;
  • Strong request for uterine removal or other conservative treatment
  • Smoker (>15 cigarettes a day)
  • Drinker (>20 grams a day)

Sites / Locations

  • Obstetrics and Gynecology Hospital, Fudan UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

MA + Rosuvastatin

Arm Description

Patients will receive MA 160 mg and rosuvastatin 10 mg by mouth daily for at least 6 months. Then every 3 months, hysteroscopy will be used to evaluate the endometrial condition, and findings will be recorded. Due to personal reasons, patients may not accept hysteroscopic evaluation every three months, then the longest duration will be 8 months.

Outcomes

Primary Outcome Measures

Pathological response rate
From date of initial therapy until the date of CR or date of hysterectomy, whichever come first, assessed up to 16 weeks.

Secondary Outcome Measures

Pathological response rate
From date of initial therapy until the date of CR or date of hysterectomy, whichever come first, assessed up to 32 weeks.
Pathological response duration
Pathological response duration
Pathological response rate classified by different blood lipid level
Pathological response rate classified by different blood lipid level
Toxicity evaluation
Toxicity evaluation according to CTCAE 5.0 version.
Relapse rate
Pregnancy rate

Full Information

First Posted
June 21, 2020
Last Updated
February 16, 2023
Sponsor
Fudan University
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1. Study Identification

Unique Protocol Identification Number
NCT04491643
Brief Title
Megestrol Acetate Plus Rosuvastatin in Young Women With Early Endometrial Carcinoma
Official Title
Megestrol Acetate Plus Rosuvastatin in Young Women With Early Endometrial Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2020 (Actual)
Primary Completion Date
August 31, 2023 (Anticipated)
Study Completion Date
August 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fudan University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
To explore the treatment efficacy of megestrol acetate plus rosuvastatin in patients with early endometrial carcinoma (EEC) seeking for conservative treatment.
Detailed Description
After diagnosed of EEC by hysteroscopy, patients meet the study criteria will be enrolled. Age, height, weight, waist circumstances, blood pressure, basic history of infertility and blood pressure will be collected. Blood tests, including fasting blood glucose (FBG), fasting insulin (FINS), OGTT 2h blood glucose and insulin, blood lipids, SHBG, sex hormone levels, anti-müllerian hormone(AMH), creatine kinase(CK) and renal/liver function tests will be performed before treatment to evacuate their basic conditions. Each subject will receive body fat testing by Inbody 520. Patients will receive MA (megestrol acetate) 160 mg by mouth daily plus rosuvastatin 10mg by mouth daily for at least 6 months. Then hysteroscopy will be used to evaluate the endometrial condition every 3 months, and intra-operative findings will be recorded. Complete response (CR) is defined as the reversion of endometrial atypical hyperplasia to proliferative or secretory endometrium; partial response (PR) is defined as regression to hyperplasia with or without atypic; stable disease (SD) is defined as the persistence of the disease; and progressive disease (PD) is defined as the appearance of higher pathological progression, or myometrial invasion, or extra-uterine metastasis. Continuous therapies will be needed in PR or NR. Patients with PD will be recommended for hysterectomy. Due to personal reasons, patients may not accept hysteroscopic evaluation every three months, then the longest duration will be 8 months. For patients remained SD after 6 to 8 months of treatment but refused hysterectomy, a multiple disciplinary discussion would be held for individual case, and alternative treatment would be given. Two months of maintenance treatment will be recommended for patients with CR, and participants will be followed up for 2 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometrial Carcinoma Stage I
Keywords
megestrol acetate, rosuvastatin, endometrial carcinoma stage I limited to endometrium, conservative treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Simon two-stage optimal design
Masking
None (Open Label)
Allocation
N/A
Enrollment
48 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MA + Rosuvastatin
Arm Type
Experimental
Arm Description
Patients will receive MA 160 mg and rosuvastatin 10 mg by mouth daily for at least 6 months. Then every 3 months, hysteroscopy will be used to evaluate the endometrial condition, and findings will be recorded. Due to personal reasons, patients may not accept hysteroscopic evaluation every three months, then the longest duration will be 8 months.
Intervention Type
Drug
Intervention Name(s)
Megestrol Acetate
Intervention Description
At a dosage of 160 mg/day
Intervention Type
Drug
Intervention Name(s)
Rosuvastatin
Intervention Description
At a dosage of 10 mg/day
Primary Outcome Measure Information:
Title
Pathological response rate
Description
From date of initial therapy until the date of CR or date of hysterectomy, whichever come first, assessed up to 16 weeks.
Time Frame
12 to 16 weeks
Secondary Outcome Measure Information:
Title
Pathological response rate
Description
From date of initial therapy until the date of CR or date of hysterectomy, whichever come first, assessed up to 32 weeks.
Time Frame
28 to 32 weeks
Title
Pathological response duration
Description
Pathological response duration
Time Frame
up to 2 years
Title
Pathological response rate classified by different blood lipid level
Description
Pathological response rate classified by different blood lipid level
Time Frame
up to 32 weeks
Title
Toxicity evaluation
Description
Toxicity evaluation according to CTCAE 5.0 version.
Time Frame
up to 32 weeks
Title
Relapse rate
Time Frame
Up to 2 years after the end of treatment
Title
Pregnancy rate
Time Frame
Up to 2 years after the end of treatment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Have a confirmed pathological diagnosis based upon hysteroscopy: histologically prove well-differentiated EEC G1 without myometrial invasion 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 Abnormal blood lipid. At least meet one of the following five items: Total cholesterol (TC) ≥ 5.2mmol/L (200mg/dL) Low-density lipoprotein cholesterol (LDL-C) ≥ 3.4mmol/L (130mg/dL) Fasting triglycerides (TG) ≥ 1.7mmol/L (150mg/dL) High-density lipoprotein cholesterol (HDL-C) #1.03mmol/L (40mg/dL) Apo-lipoprotein-A (Apo-A) ≥ 1.0g/L Exclusion Criteria: Acute liver disease or liver tumor (benign or malignant) or renal dysfunction Pregnancy or potential pregnancy Under treatment of high-dose progestin therapy more than 1 months in recent 6 months Confirmed diagnosis of any cancer in reproductive system Acute severe disease such as stroke or heart infarction or a history of thrombosis disease Hypersensitivity or contradiction for using MA or atorvastatin Already diagnosed with hyperlipidemia and using lipid-lowering drugs With other factors of reproductive dysfunction; Strong request for uterine removal or other conservative treatment Smoker (>15 cigarettes a day) Drinker (>20 grams a day)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaojun Chen, PhD
Phone
862163455050
Email
cxjlhjj@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Bingyi Yang, MD
Phone
862163455050
Email
xiaomihaoku@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiaojun Chen, PhD
Organizational Affiliation
Obstetrics and Gynecology Hospital, Fudan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Obstetrics and Gynecology Hospital, Fudan University
City
Shanghai
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaojun Chen
Email
cxjlhjj@163.com

12. IPD Sharing Statement

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Megestrol Acetate Plus Rosuvastatin in Young Women With Early Endometrial Carcinoma

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