RecruitingPhase 3NCT04073706

Sentinel Node Biopsy in Endometrial Cancer

A Phase III Randomised Clinical Trial Comparing Sentinel Node Biopsy With No Retroperitoneal Node Dissection in Apparent Early-Stage Endometrial Cancer


Sponsor

Queensland Centre for Gynaecological Cancer

Enrollment

760 participants

Start Date

Jan 18, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

Endometrial cancer (EC) is the most common gynaecological cancer. Current treatment of EC typically includes removal of the uterus and to determine the extent of the disease (removal of fallopian tubes, ovaries \& if required a lymph node dissection (surgical staging)). While lymph node dissection may be valuable to guide the need for adjuvant treatment (chemo or radiotherapy) after surgery, it has been a topic of controversy for the last 30 years. In some patients it causes morbidity, specifically lymphoedema. This recently has been replaced with sentinel node biopsy (SNB). It requires an injection of a dye into the cervix with specific equipment \& surgical dissection of the lymph node in which the dye first becomes visible. Despite this promising proposition \& similar to a lymph node dissection, the value to patients, cost effectiveness \& potential harms (e.g. lymphedema) of SNB compared to no-node dissection in EC has never been established. Aim: determine the value of SNB for patients, the healthcare system and exclude detriment to patients using a randomised approach 1:1. Stage 1 - 444 patients. Stage 2 additional 316 patients. Primary Outcome Stage 1: Proportion of participants returning to usual daily activities at 12 months from surgery using the EQ-5D which will determine when women in both groups can return to their usual activities. Primary Outcome Stage 2: Treatment non-inferiority as evaluated by disease-free survival status at 4.5 years post-surgery, as measured by the time interval between the date of randomisation and date of first recurrence. Confirmation of recurrent disease will be ascertained through clinical assessment, radiological work-up and/or histological results.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a technique called sentinel node biopsy in women with uterine (endometrial) cancer. Instead of removing all the lymph nodes in the pelvis during surgery (which can cause side effects), a sentinel node biopsy removes only the first one or two nodes that cancer is most likely to drain into first — reducing unnecessary surgery while still checking for cancer spread. **You may be eligible if...** - You are female and over 18 years old - You have been diagnosed with early-stage (Stage I) endometrial cancer or uterine carcinosarcoma confirmed by biopsy - All imaging shows the cancer is confined to the uterus - You are well enough for laparoscopic or robotic surgery - Tumor invasion into the uterine wall is no more than 50% on MRI **You may NOT be eligible if...** - There is evidence cancer has spread outside the uterus - You are not a suitable candidate for minimally invasive surgery - Your ECOG performance status is 2 or higher Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURETH BSO with SNB Note: If participants (≤45yo), Grade 1 endometrial adenocarcinoma with myometrial invasion <50%, wish to retain their ovaries a BSO may be omitted

Removal of uterus, tubes and ovaries with a sentinel node biopsy. A tracer dye (ICG) +/- Methylene Blue Dye is injected into the surroundings of the primary tumour, it is transported via local lymphatic channels towards the draining lymphatic basin, and the first node that the tracer reaches is called the "sentinel node". These one or two nodes are thought to be first involved with cancer spread.

PROCEDURETH BSO without retroperitoneal node dissection Note: If participants (≤45yo), Grade 1 endometrial adenocarcinoma with myometrial invasion <50%, wish to retain their ovaries a BSO may be omitted

Removal of uterus, tubes and ovaries without retroperitoneal node dissection


Locations(19)

Houston Methodist Hospital

Houston, Texas, United States

Hospital Britanico

Buenos Aires, Ciudad Autónoma de Buenos Aires (caba), Argentina

Chris O'Brien Lifehouse

Camperdown, New South Wales, Australia

Liverpool Hospital

Liverpool, New South Wales, Australia

The Wesley Hospital

Auchenflower, Queensland, Australia

Buderim Private Hospital

Buderim, Queensland, Australia

North West Private Hospital

Everton Park, Queensland, Australia

Royal Brisbane and Women's Hospital

Herston, Queensland, Australia

Mater Hospital

South Brisbane, Queensland, Australia

Gold Coast University Hospital

Southport, Queensland, Australia

St Andrews War Memorial Hospital

Spring Hill, Queensland, Australia

Mercy Hospital for Women

Heidelberg, Victoria, Australia

Royal Women's Hospital

Parkville, Victoria, Australia

Hospital de Base

São José do Rio Preto, São Paulo, Brazil

Fundacao Antonio Prudente, AC Camargo Cancer Center

São Paulo, São Paulo, Brazil

Hospital Israelita Albert Einstein

São Paulo, São Paulo, Brazil

Centro de tratamiento e investigación sobre Cáncer Luis Carlos Sarmiento Angulo

Bogotá, Bogotá, Distrito Capital, Colombia

Azienda Sanitaria Universitaria Friuli Centrale (ASUFC)

Udine, Via Pozzuolo, Italy

National University Hospital and National University Cancer Institute

Singapore, NUH Zone B, Singapore

View Full Details on ClinicalTrials.gov

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NCT04073706


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