Loading clinical trials...
Loading clinical trials...
Prediction of Recurrence Among Low Risk Endometrial Cancer Population
This study investigates whether molecular testing can help to predict the risk of endometrial cancer coming back (recurrence) after treatment in patients diagnosed with low risk endometrial cancer and scheduled to have surgery to remove the uterus and/or cervix (hysterectomy). Having sentinel lymph node mapping performed may help researchers to see if the cancer has spread in patients with low risk endometrial cancer.
PRIMARY OBJECTIVE: I. Validate the use of a molecular panel of estrogen-induced genes to predict recurrence in low risk endometrial cancer. SECONDARY OBJECTIVES: I. Calculate the positive predictive value (PPV)/negative predictive value (NPV)/sensitivity (Sens)/specificity (Spec) of lymph node mapping to predict pelvic lymph node involvement. II. Correlate CA125 and HE4 levels with recurrence and to explore the use of other serum biomarkers to predict recurrence. III. Describe patterns of recurrence in a low risk patient population. IV. Determine if molecular panel can predict lymph node involvement in low risk endometrial cancer patients who undergo pelvic and para-aortic lymphadenectomy. V. Compare performance of molecular panel to the Mayo low risk criteria for prediction of lymph node involvement. VI. Compare performance of molecular panel to the high intermediate risk criteria from Gynecologic Oncology Group, trial 99 (GOG 99) for prediction of recurrence. VII. Determine the feasibility of lymph node mapping in this patient population. VIII. Determine the morbidity and mortality of lymph node dissection and mapping. OUTLINE: Patients undergo hysterectomy and sentinel lymph node mapping. Patients may also undergo bilateral salpingo-oophorectomy at the direction of the treating physician. If peritoneal disease or other contraindications to lymphatic mapping are detected at the time of surgery, mapping and sentinel node biopsy are performed at the surgeon's discretion. At the time of hysterectomy, patients undergo collection of tissue for molecular testing. Before and after surgery, patients also undergo collection of blood samples for tumor marker analysis.
Age
All ages
Sex
FEMALE
Healthy Volunteers
No
M D Anderson Cancer Center
Houston, Texas, United States
Start Date
November 8, 2012
Primary Completion Date
December 31, 2026
Completion Date
December 31, 2026
Last Updated
March 9, 2026
518
ACTUAL participants
Bilateral Salpingectomy with Oophorectomy
PROCEDURE
Biospecimen Collection
PROCEDURE
Hysterectomy
PROCEDURE
Laboratory Biomarker Analysis
OTHER
Lymph Node Mapping
PROCEDURE
Sentinel Lymph Node Biopsy
PROCEDURE
Lead Sponsor
M.D. Anderson Cancer Center
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and Conditions