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RecruitingNCT06379113

GnRHa + Letrozole in Obese Progestin-insensitive Endometrial Cancer Patients

Gonadotropin-releasing Hormone Agonist (GnRHa) Plus Letrozole in Obese Progestin-insensitive Early-stage Endometrial Cancer Patients With Conservative Treatment

Status
Recruiting
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
29 (estimated)
Sponsor
Xiaojun Chen · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

To investigate the efficacy of GnRHa plus letrozole in obese progestin-insensitive EEC patients.

Detailed description

There were more and more women with early endometrioid endometrial cancer (EEC) and atypical endometrial hyperplasia (EAH) who want to preserve fertility. Approximately 70% to 80% of females who meet the criteria for conservation treatment are able to achieve CR after progestin therapy, with a median time of 6-7 months, but about 20% to 30% of patients get no response or need to take longer time to achieve remission (over one year). With long duration of treatment, there will be more side effects such as weight gain, impaired liver function, endometrial injury, ovarian reserve inhibition etc. which will decrease the efficacy of conservative treatment. Previous researches had shown that GnRHa plus letrozole could be a better second-line treatment for obese progestin-insensitive patients. Till now, no similar studies were found, so we design this study to explore the efficacy of GnRHa plus letrozole in obese progestin-insensitive EEC and EAH patients to provide new evidences for improving conservative treatment efficacy. We defined obese patients as these with BMI ≥ 30kg/m2. This will be a single-centred prospective pilot study. Patients diagnosed as obese progestin-insensitive EEC by dilatation and curettage (D\&C) or hysteroscopy will be enrolled. The primary endpoint is cumulative complete response (CR) rate at 28 weeks of treatment. The secondary endpoints include adverse events, duration of complete response, recurrent rate, pregnancy rate and quality of life of patients.

Conditions

Interventions

TypeNameDescription
DRUGGnRH antagonistGonadotropin-releasing hormone analogue, intramuscular injection of 3.75mg will be given every 4 weeks, and the maximum treatment courses will be 6. If the patient get CR within 6 courses, another 2 courses will be used as consolidation therapy.
DRUGLetrozole 2.5mg2.5mg po qd.

Timeline

Start date
2022-07-13
Primary completion
2026-03-30
Completion
2027-03-30
First posted
2024-04-23
Last updated
2025-08-11

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06379113. Inclusion in this directory is not an endorsement.