Megestrol Acetate or Levonorgestrel-Releasing Intrauterine System in Treating Patients With Atypical Endometrial Hyperplasia or Endometrial Cancer

Phase 2

Withdrawn

• Conditions: Endometrial Adenocarcinoma; Stage IA Endometrial Carcinoma; Recurrent Endometrial Carcinoma; Stage IIIA Endometrial Carcinoma; Stage IIIC Endometrial Carcinoma; Stage IVA Endometrial Carcinoma; Stage IVB Endometrial Carcinoma; Atypical Endometrial Hyperplasia; Stage IB Endometrial Carcinoma; Stage II Endometrial Carcinoma
• Interventions: Device: levonorgestrel-releasing intrauterine system; Drug: megestrol acetate; Other: laboratory biomarker analysis; Other: questionnaire administration

• Registration Number: NCT01943058
• Lead Sponsor: University of Southern California

Brief Summary

This randomized phase II trial studies how well megestrol acetate or levonorgestrel-releasing intrauterine system works in treating patients with atypical endometrial hyperplasia or endometrial cancer. Progesterone can cause the growth of endometrial cancer cells. Hormone therapy using megestrol acetate or levonorgestrel-releasing intrauterine system may fight endometrial cancer by lowering the amount of progesterone the body makes. It is not yet known whether megestrol acetate is more effective than levonorgestrel-releasing intrauterine system in treating atypical endometrial hyperplasia or endometrial cancer.

Detailed Description

PRIMARY OBJECTIVES:

I. To determine if the levonorgestrel-releasing intrauterine system (IUS) results in histologic regression of the endometrial lesion (complex atypical hyperplasia \[CAH\] and grade 1 endometrial cancer \[EC\]) comparable to that achieved with oral megestrol (megestrol acetate).

SECONDARY OBJECTIVES:

I. To compare both the side effect profiles, such as weight gain and mood changes as well as compliance with assigned treatment between the 2 treatment arms.

TERTIARY OBJECTIVES:

I. To describe fertility-related outcomes, ovulation, menstrual pattern and fertility abnormalities determined during usual workup (e.g., semen analysis), pregnancy and delivery within 18-months of treatment.

II. To characterize the incidence of endocrine comorbidities (e.g., hypothyroidism, polycystic ovarian syndrome, and diabetes).

III. To characterize the association of levels of endoplasmic reticular (ER) stress and protein kinase B (Akt)-activation in endometrial samples with clinicopathologic-response to Progestin (therapeutic progesterone) therapy.

OUTLINE:

Patients are randomized to 1 of 2 treatment arms.

ARM A: Patients receive megestrol acetate orally (PO) twice daily (BID) for up to 18 months in the absence of disease progression or unacceptable toxicity.

ARM B: Patients receive levonorgestrel-releasing IUS with continuous release for up to 18 months in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up at 3 and 6 months.

Study Timeline

• Study First Submitted: 2013-09-11
• Study First Submitted QC: 2013-09-11
• Study First Posted: 2013-09-16
• Study Start: 2014-03
• Status Verified: 2014-09
• Last Update Submitted: 2014-09-09
• Last Update Posted: 2014-09-10
• Primary Completion: 2016-10
• Study Completion: 2017-10

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

• A histologic diagnosis of complex atypical hyperplasia or grade 1 endometrioid adenocarcinoma of the endometrium diagnoses within 3 months of study enrollment who strongly desire to maintain fertility

• A diagnosis of endometrioid adenocarcinoma will undergo a magnetic resonance imaging (MRI) scan of the pelvis to rule out deep (> 50%) myometrial invasion and extrauterine metastases

• A negative urine or serum pregnancy test at the time of enrollment

• Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for 90 days following completion of therapy; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately; a female of child-bearing potential is any woman (regardless of sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria:

  • Has not undergone a hysterectomy or bilateral oophorectomy; or
  • Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months)

• Willing and able to consent for treatment with office endometrial biopsies every 3 months

• Ability to understand and the willingness to sign a written informed consent

Exclusion Criteria

• A diagnosis of grade 1 endometrioid adenocarcinoma of the endometrium who does not wish to maintain fertility
• MRI evidence of deep myometrial and/or extrauterine spread
• Congenital or other structural uterine or tubal abnormality
• An acute pelvic inflammatory disease or medical conditions, such as, but not limited to acquired immunodeficiency syndrome (AIDS) and chronic immunosuppression, that may be associated with an increased susceptibility to infections
• Current diagnosis of breast cancer or any other cancer
• Currently pregnant or breastfeeding
• Thromboembolic disease, deep vein thrombosis, hypercoagulable state

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Arm B (levonorgestrel-releasing IUS)	laboratory biomarker analysis	Patients receive levonorgestrel-releasing IUS with continuous release for up to 18 months in the absence of disease progression or unacceptable toxicity.
Arm B (levonorgestrel-releasing IUS)	questionnaire administration	Patients receive levonorgestrel-releasing IUS with continuous release for up to 18 months in the absence of disease progression or unacceptable toxicity.
Arm A (megestrol acetate)	questionnaire administration	Patients receive megestrol acetate PO BID for up to 18 months in the absence of disease progression or unacceptable toxicity.
Arm B (levonorgestrel-releasing IUS)	levonorgestrel-releasing intrauterine system	Patients receive levonorgestrel-releasing IUS with continuous release for up to 18 months in the absence of disease progression or unacceptable toxicity.
Arm A (megestrol acetate)	megestrol acetate	Patients receive megestrol acetate PO BID for up to 18 months in the absence of disease progression or unacceptable toxicity.
Arm A (megestrol acetate)	laboratory biomarker analysis	Patients receive megestrol acetate PO BID for up to 18 months in the absence of disease progression or unacceptable toxicity.

Primary Outcome Measures

Name	Time	Method
Histologic regression from endometrioid adenocarcinoma or complex atypical hyperplasia to benign endometrium	Up to 6 months after completion of study treatment	Histologic regression will be dichotomized as a binary outcome variable, yes if patients have a confirmed histologic regression at the time of the scheduled biopsy, and no if the histologic regression is not observed regardless of compliance, lost-to-follow-up, or other issues. A contingency table and a bar plot will be used to show the histologic regression rate between the 2 arms. Two-group test of equivalence in proportions will be used to detect whether the histologic regression rate in Arm B is not significantly lower than that in Arm A.

Secondary Outcome Measures

Name	Time	Method
Change in weight	Baseline to up to 6 months after completion of study treatment	Weight gain will be recorded longitudinally at each 3-month clinic visit and body mass index (BMI) will be calculated and analyzed over time. Can be evaluated using chi squared tests, logistic regression, or repeated measures analysis of variance (ANOVA) whenever appropriate.
Change in mood ascertained using the self-reported Beck Depression Inventory-Primary Care (BDI-PC)	Baseline to up to 6 months after completion of study treatment	Can be evaluated using chi squared tests, logistic regression, or repeated measures ANOVA whenever appropriate.
Compliance	Up to 6 months after completion of study treatment	Can be evaluated using chi squared tests, logistic regression, or repeated measures ANOVA whenever appropriate.