Up to 60% of endometrial cancer cases are attributed to obesity, in part because obesity promotes development of atypical endometrial hyperplasia (AEH), and up to 40% of women with AEH go on to develop endometrial cancer. The increasing prevalence of obesity in premenopausal women has resulted in increasing rates of AEH in this age group. Hysterectomy with removal of the fallopian tubes and ovaries is 100% effective in preventing endometrial cancer, but this approach results in infertility. Fertility-sparing treatments exist, such as treatment with oral or intrauterine progestin, but these treatments do not work uniformly and do not combat the underlying cause of endometrial cancer, which is obesity and metabolic syndrome. Additionally, up to 41% of women on progestin eventually experience relapse of AEH or endometrial cancer. Third, many patients have insulin resistance that may worsen with progestin therapy. Thus, to improve treatment of AEH and grade 1 endometrial cancer, prevent and reverse endometrial cancer, and allow women to preserve their fertility, the investigators must integrate an effective weight loss strategy to be given with progestin treatment. It is the hypothesis that premenopausal women with AEH desire uterine preservation will be more likely to have atypia-free uterine preservation at one year if they receive progestin in combination with a behavioral weight loss intervention versus progestin plus enhanced usual care.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
96
Weekly telephone calls during the first month, biweekly during the next 5 months, and then monthly for the last 7 months (12 months total). Each telephone session will be 30 minutes long.
Released via the levonorgestrel-releasing IUD.
1-3 page handouts
Standard of care
Washington University School of Medicine
St Louis, Missouri, United States
RECRUITINGUniversity of New Mexico
Albuquerque, New Mexico, United States
RECRUITINGUniversity of Oklahoma
Oklahoma City, Oklahoma, United States
RECRUITINGNumber of participants with atypical endometrial hyperplasia (AEH)-free biopsy
Time frame: At 1 year
Time to resolution of atypical endometrial hyperplasia (AEH)
Defined as the period of time in months/days from the first biopsy to show AEH or grade 1 endometrial cancer to the first biopsy that shows no evidence of hyperplasia or malignancy
Time frame: Through completion of follow-up (estimated to be 2 years)
Time to resolution of endometrial cancer
Time frame: Through completion of follow-up (estimated to be 2 years)
Atypia-free survival
-Defined as the time interval from the date of positive treatment response (as determined by biopsy) to the date of atypical endometrial hyperplasia (AEH) recurrence. AEH-free or the patients with lost to follow-up will be censored at the last follow-up.
Time frame: Through completion of follow-up (estimated to be 2 years)
Endometrial cancer progression-free survival (EC-PFS)
EC-PFS is defined as the time interval from the date of positive treatment response (as determined by biopsy) to the date of recurrence of EC. Endometrial cancer-free patients or the patients with lost to follow-up will be censored at the last follow-up.
Time frame: Through completion of follow-up (estimated to be 2 years)
Change in weight
Time frame: Through completion of follow-up (estimated to be 2 years)
Change in Cancer Worry Impact Events Scale (CWIES)
The CWIES is a 15-item self-report measure evaluating stress reactions and traumatic experiences, specifically inquiring about cancer worry-specific distress. Range of values for each individual item will be a Likert Scale from 0-5. 0=not at all and 5=often. The higher the score, the more cancer-worry specific distress the participant has.
Time frame: At enrollment, 6 months, 12 months, end of intervention, and 24 months (estimated to be 2 years)
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