Endoscopic Suture Gastroplasty (ESG) for Treatment of Obese Patients With Endometrial Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age21-75
SponsorCentro di Riferimento Oncologico - Aviano

About this trial

Obesity increases the risk of endometrial cancer, with higher Body Mass Index (BMI) leading to a significant increase in both cancer risk and recurrence. Because of the excellent cancer-specific outcomes and preponderance of obesity-related complications, women with endometrial cancer are more likely to die of cardiovascular disease and other obesity-related illnesses than endometrial cancer itself. This makes an endometrial cancer diagnosis a critical moment to emphasizes the importance of actively managing the underlying issue of obesity in the endometrial cancer survivorship period.

Bariatric surgery has shown long-term benefits, including weight loss and reduction of obesity-related comorbidities, and has been linked to a decrease in endometrial cancer incidence. However, bariatric surgery has limitations, such as irreversibility and potential complications. Recent interest in less invasive methods, like bariatric endoscopy, shows promising results in achieving weight loss and improving metabolic profiles. Endoscopic procedures, such as Endomina Endoscopic suture gastroplasty (E-ESG), have shown effectiveness in weight loss and could offer a safer, more accessible alternative to surgery, in particular if associated to a lifestyle modifications program. Efficacy and safety of Bariatric endoscopy has been stressed within the recently published "Guideline of the Italian Society of Surgery of Obesity and Metabolic Diseases on Bariatric Endoscopy in the treatment of obesity and associated complications" that suggest the use of bariatric endoscopy in patients with class I obesity and in patients with class II obesity regardless of the presence of comorbidities, for the treatment of obesity.

This study aims to assess the feasibility and safety of the E-ESG procedure in treating obesity in women after curative treatment for endometrial cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Women with endometrial cancer scheduled for hysterectomy with a curative intent

Age 21-75

BMI ≥ 30

Willingness to undergo E-ESG and lifestyle modifications program

Disqualifiers

History of foregut or gastrointestinal (GI) surgery (except uncomplicated cholecystectomy or appendectomy)

Prior gastrointestinal surgery with sequelae, i.e., obstruction, and/or adhesive peritonitis or known abdominal adhesions

Prior open or laparoscopic bariatric surgery

Prior surgery of any kind on the esophagus, stomach, or any type of hiatal hernia surgery

Trial population

Women with endometrial cancer scheduled for hysterectomy with a curative intent, with BMI ≥ 30 and Willingness to undergo E-ESG and lifestyle modifications program

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Evaluation of the feasibility of E-ESG procedure in obese patients with endometrial cancer.

Absolute and relative frequency of patients with technical success of E-ESG procedure, reported with relative 95% Confidence Interval

Time frame
up to 4 years

Secondary outcomes

1

Evaluation of patients who refused E-ESG procedure

Evaluation of the number and percentage of women with endometrial cancer and obese who refused E-ESG procedure

Time frame
up to 4 years
2

Evaluation of patients who refused E-ESG procedure

Description with absolute and relative frequencies of baseline characteristics of women with endometrial cancer and obese who refused E-ESG procedure

Time frame
up to 4 years
3

Evaluation of E-ESG safety in obese endometrial cancer patients.

Absolute and relative frequencies of adverse events

Time frame
up to 4 years
4

To evaluate efficacy of E-ESG effects on obesity-associated comorbidities.

Evaluation of % Excess weight loss (EWL) with the formula (Weight loss)/ (Excess weight at T0) x 100 and %TBWL(total body weight loss) with the formula (weight loss) / (weight at T0) x 100 in enrolled patients at 1 year

Time frame
up to 4 years

Other outcomes

Sponsors and contacts

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