Overview
Weight-loss Drug for Fertility-Sparing Treatment of Atypical Hyperplasia and Grade 1 Cancer of the Endometrium
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2031-09-01
2031-09-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The incidence of endometrial cancer is increasing at an alarming rate. This trend parallels the rising rate of obesity, the most significant risk factor for endometrial cancer. Young women with obesity and endometrial cancer or atypical hyperplasia who want to maintain their fertility are treated with progestin therapy, such as progestin intra-uterine device (pIUD), which is associated with a mediocre response rate and high recurrence rate, and does not address the underlying cause, obesity. Therefore, the investigators want to assess whether the addition of a weight-loss drug to pIUD will improve their oncologic, reproductive and metabolic outcomes.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University Health Network, TorontoTreatments:
Progestins
Tirzepatide
Criteria
Inclusion Criteria:1. People aged ≥ 18 and ≤ 41 years of age
2. BMI ≥ 27
3. Diagnosis of grade 1 or 2 endometrioid EC or AH made by either endometrial biopsy or
dilation and curettage
4. Clinical FIGO 2009 stage 1A disease - no evidence of metastatic disease beyond the
uterus and no evidence of myometrial invasion by imaging performed (MRI, CT)
5. ECOG status <2
6. Desire for fertility preservation
7. Have signed an approved informed consent form
Exclusion Criteria:
1. Evidence of myometrial invasion or extra-uterine disease on imaging
2. High grade or p53 mutated (p53mut) EC
3. Estrogen receptor (ER) EC
4. Mismatch repair deficient (MMRd) EC
5. History of other malignancies, except if:
a. Curatively treated with no evidence of disease for >5 years
6. Previous surgical treatment of obesity
7. Current use of weight loss medication (no use in last 6 months)
8. Medical co-morbidity with end-organ dysfunction
9. Unable to understand and participate in the informed consent process
10. Currently pregnant or breastfeeding (negative serum bhCG at screening)
11. Contraindications to progestin intra-uterine device (pIUD)
12. History of chronic pancreatitis or acute pancreatitis within 180 days prior to
screening
13. Contraindications to tirzepatide
1. Personal or first-degree history of multiple endocrine neoplasia type 2 or
medullary thyroid carcinoma
2. Anaphylactic reaction