A Phase III Randomised Clinical Trial Comparing Sentinel Node Biopsy With No Retroperitoneal Node Dissection in Apparent Early-Stage Endometrial Cancer
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.
Detailed description
Hypothesis: The primary hypothesis is that SNB will not cause detriment to patients (lymphoedema, morbidity, loss of quality of life) and not increase costs compared to patients without a retroperitoneal node dissection. The secondary hypothesis is that disease-free survival in patients without retroperitoneal node dissection is not inferior to those receiving SNB. Aims: To determine the value of SNB for patients, the healthcare system and to exclude detriment to patients. Objectives: Primary Stage 1: To determine the recovery of participants (defined as incidence of adverse events, lower limb lymphoedema and health-related QOL) and to the healthcare system (cost) of Sentinel Node Biopsy (SNB) for the surgical treatment of endometrial cancer. Primary Stage 2: Compare disease-free survival at 4.5 years for participants randomised to receive hysterectomy, bilateral salpingo-oophorectomy with SNB compared to participants randomised to hysterectomy, bilateral salpingo-oophorectomy without retroperitoneal node dissection. Secondary: * Compare patterns of recurrence and overall survival (OS) between the groups * Determine the cost-effectiveness of SNB * Compare Patient Reported Outcomes (PROMS) between the groups at 12 months from surgery * Compare Health Related Quality of Life (HRQL) and Fear of Recurrence between the groups at 12 months from surgery * Compare perioperative outcomes (duration of surgery, length of hospital stay, intraoperative blood loss, blood transfusion requirements) and the incidence of intra- and postoperative adverse events within 12 months from surgery between the groups * Compare lower limb lymphoedema at 12 months after surgery * Compare the need for postoperative (adjuvant) treatments between groups * Determine the impact of body composition and frailty on survival, quality of life, lymphoedema, peri-, intra- and postoperative outcomes * Compare follow-up strategies (clinical vs symptom checklist) * Translational Research - Trans-ENDO 3 - biobanking strategy - Compare the Molecular profile at 12 months from surgery between the groups
Arms & 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
Outcome measures
Primary
Stage 1: Return to usual activities
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.
Time frame: 12 months from surgery
Stage 2: Disease Free Survival
Compare disease-free survival for participants randomised to receive hysterectomy, bilateral salpingo-oophorectomy with SNB compared to participants randomised to hysterectomy, bilateral salpingo-oophorectomy without retroperitoneal node dissection
Time frame: 4.5 years from surgery
Secondary
Cost Effectiveness using QALYs using EuroQoL-5D (EQ-5D) Questionnaire
Time frame: 12 months from surgery
Cost Effectiveness measuring Intervention costs
Time frame: 12 months from surgery
Cost Effectiveness measuring GP and specialist consultations
Time frame: 12 months from surgery
Cost Effectiveness measuring radiology and imaging requirements
Time frame: 12 months from surgery
Cost Effectiveness measuring prescriptions and over the counter medicine requirements
Time frame: 12 months from surgery
Cost Effectiveness measuring community and health service requirements and days off work and informal care required by family and friends using a combination of the Health Services Questionnaire and clinical files
Time frame: 12 months from surgery
Cost Effectiveness: direct costs using a bottom-up approach by recording the volume of resource use in both groups of the trial, and then applying a unit cost to each component
Time frame: 12 months from surgery
Perioperative Outcomes: Adverse Events
Time frame: 12 months from surgery
Perioperative Outcomes: Length of Surgery
Time frame: At time of surgery
Perioperative Outcomes: Blood Loss during Surgery
Time frame: At time of surgery
Perioperative Outcomes: Blood Transfusion Requirements during Surgery
Time frame: At time of surgery
Perioperative Outcomes: Length of Hospital Stay
Time frame: At time of discharge from hospital following surgery
Health Related Quality of Life and Fear of Recurrence
Time frame: 12 months from surgery
Incidence of Lymphedema
Time frame: 12 months from surgery
Adjuvant Treatment Requirements
Time frame: 12 months from surgery
Value of Molecular Biomarkers
Time frame: 24 months from surgery
Value of Molecular Biomarkers
Time frame: 12 months from surgery
Value of Molecular Biomarkers
Time frame: 12 months from surgery
Value of Molecular Biomarkers
Time frame: 12 months from surgery
Value of Molecular Biomarkers
Time frame: 12 months from surgery
Overall Survival
Time frame: 4.5 years from surgery
Patterns of Recurrence - date and localization of 1st recurrence
Time frame: 4.5 years from surgery
Impact of body composition (sarcopenia) on surgical complications, recovery and overall survival
Time frame: 4.5 years from surgery
Impact of frailty on surgical complications, recovery and overall survival
Time frame: 4.5 years from surgery
Follow-Up Strategies
Time frame: 4.5 years from surgery
Eligibility criteria
Study locations (1)
Houston Methodist Hospital
Houston, Texas, 77030
References
- Obermair A, Nicklin J, Gebski V, Hayes SC, Graves N, Mileshkin L, Lin MY, Beale P, Baxter E, Robledo K, Salomon C, Hanna GB, Janda M. A phase III randomized clinical trial comparing sentinel node biopsy with no retroperitoneal node dissection in apparent early-stage endometrial cancer - ENDO-3: ANZGOG trial 1911/2020. Int J Gynecol Cancer. 2021 Dec;31(12):1595-1601. doi: 10.1136/ijgc-2021-003029. Epub 2021 Nov 2.(PubMed)