Fertility Sparing Management of EndomeTrial Cancer and Hyperplasia

Endometrial Cancer Clinical Trial

— FETCH  

Official title:

Fertility Preservation Using Endomyometrial Resection for Atypical Hyperplasia and Low Grade, Stage 1A, Endometrial Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04362046
• Other study ID #: H17-00780
• Status: Recruiting
• Phase: N/A
• Start date: November 15, 2020
• Est. completion date: July 2028

Study information

• Verified date: October 2021
• Source: Vancouver Coastal Health Research Institute
• Contact: Neeraj Mehra, MD
• Phone: 604-875-5508
• Email: neeraj.mehra[@]ubc.ca
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study protocol evaluates the use of hysteroscopic endomyometrial resection in women diagnosed with atypical endometrial hyperplasia or grade I endometrial cancer who have not responded to anti-hormone therapy. Patients in this study wish to preserve fertility.

Description:

Endometrial cancer (EC) is the most common gynecological cancer among Canadian women. This cancer often arises from a precursor lesion called atypical endometrial hyperplasia (AH). Hysterectomy is the most effective treatment for EC and AH. It is well recognized that EC may be diagnosed in younger women of child-bearing age. The diagnosis of EC or AH in these younger women is devastating as a hysterectomy is frequently required. Though some of these women respond to high-dose progestin treatment, the failure rate is high (60%), necessitating surgery. Recent case series show that some women with AH and early EC can be treated by resecting the precursor lesion of the early cancerous area in the uterus by hysteroscopy without the need for hysterectomy. The fertility-sparing approach is outlined in this research protocol.This is a multidisciplinary research project with input from gynaecologic oncology, general gynaecology, reproductive endocrinology and infertility, and pathology. Our hypothesis is that hysteroscopic resection (HR) is a safe and effective treatment for AH or EC in women who want to preserve their fertility and have not been successfully treated using progestin therapy. Patients will be closely monitored to ensure that this is a safe and effective treatment option.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: July 2028
• Est. primary completion date: July 2028
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 19 Years to 39 Years

Eligibility

All candidates for this protocol must have an adequate trial of anti-hormone therapy prior to hysteroscopic resection. In cases of EC, the minimum trial is 6 months of high-dose progestin. In cases of AH, being that this is a benign condition (pre-malignant), patients may not require a full 6 months of anti-hormone therapy. All patients must have a pre-HR hysteroscopic evaluation to confirm that they are suitable candidates for this study. Patients being considered for the experimental intervention (hysteroscopic resection) will be reviewed and discussed by the study committee in order to ensure that the following criterion are met in order to proceed with the surgical resection:

Inclusion criteria:

• Age less than 40 years

• Pathologist confirmed biopsy evidence of one of the following:

1. Grade I endometrial endometrioid adrenocarcinoma (EC) with less than 1/3 of the endometrial surface involved.

2. Atypical endometrial hyperplasia (AH)

• MRI demonstrating less than 1/3 myometrial invasion if the patient has EC

• Absence of significant surgical co-morbidities e.g. pulmonary hypertension, significant cardiac valvular disease, or contraindication to surgery.

• Desire to preserve fertility

• Reasonable chance to conceive based on consultation with an infertility specialist

• Adequate dose and duration of progesterone therapy prior to enrolment:

• Adequate dose:

1. Medroxyprogesterone acetate (Provera; 200mg/day)

2. Megestrol acetate (Megace; 160mg/day)

• Adequate duration: 6 months

• Failure of progestin therapy defined as:

1. Unsuccessful eradication of hyperplasia or cancer in the uterus

2. Intolerance to the side effects

• Signed informed consent

Exclusion criteria:

• Age 40 years and over

• Grade 2 or 3 endometrioid endometrial adenocarcinoma or non-endometrioid pathology

• Greater than 1/3 involvement of the endometrial surface in patients with Grade I EC

• Women who are not able to provide informed consent

• Women without pathologic confirmation of low-grade endometrioid carcinoma or AH

• Myometrial invasion on MRI greater than 1/3 total myometrial thickness.

• MRI evidence of ovarian or adnexal involvement

• The diagnosis of another cancer or medical condition that would interfere with the assessment of the hysteroscopic surgery success rates.

• Significant underlying fertility impairment that would significantly interfere with the success rate of HR

Related Conditions & MeSH terms

• Endometrial Cancer
• Endometrial Hyperplasia
• Endometrial Neoplasms
• Gynecologic Cancer
• Hyperplasia

Intervention

Procedure:
• Hysteroscopic uterine resection
Hysteroscopic Resection will be evaluated as a fertility-sparing treatment for patients with early Endometrial Cancer or Endometrial Hyperplasia (atypical or persisting typical) who fail progestin therapy. Failure of progesterone therapy is defined as: (a) Unsuccessful eradication of hyperplasia or cancer in the uterus or (b) Intolerance to the side effects of th hormone therapy. HR is a common gynecologic procedure that is offered to women for treatment of several benign gynecologic conditions. The conduct, risks, and complications of it are well-understood. In relation to this protocol, it is the indication for HR that constitutes the experimental intervention including the assessment of it's outcome. Patients deemed appropriate for hysteroscopic endomyometrial resection will be counselled on the nature of the procedure along with its risks and complications.

Locations

Country	Name	City	State
Canada	Vancouver General Hospital	Vancouver	British Columbia

Sponsors (2)

Lead Sponsor	Collaborator
Vancouver Coastal Health Research Institute	University of British Columbia

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Conception rate of women attempting pregnancy	live births / women attempting pregnancy	3 years post-resection
Primary	Overall conception rate	live births / all women participating in study, including those who failed hysteroscopic resection and have a hysterectomy	3 years post-resection
Primary	Local disease control rate (short-term failure of hysteroscopic resection)	Patients with persisting atypical hyperplasia or Grade I endometrial cancer / patients treated with hysteroscopic resection	3 months post-resection
Primary	Distant disease control rate (long-term failure of hysteroscopic resection)	patients developing distant recurrence / patients treated with hysteroscopic resection	3 years post-resection
Secondary	Complications/side-effects	The investigators will tabulate complications/side-effects of the procedure such as the rate of uterine perforation, uterine adhesion, procedure infection, and others.	3 years post-resection