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Clinical Trials/NCT03982914
NCT03982914
Unknown
Not Applicable

The Use of a New Biomarker, HE4, in Combination With Simple Ultrasound Rules in the Prediction of Malignancy in a Pelvic Mass Detected on Ultrasound

The University of Hong Kong3 sites in 1 country814 target enrollmentApril 1, 2018
ConditionsPelvic Mass

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pelvic Mass
Sponsor
The University of Hong Kong
Enrollment
814
Locations
3
Primary Endpoint
sensitivity, specificity and predictive powers
Last Updated
4 years ago

Overview

Brief Summary

Our objective is to determine if the combination of simple ultrasound features (IOTA simple rules) and a new biomarker (HE4) together with a common tumour marker (CA 125) can accurately predict ovarian cancer in women found to have a pelvic mass on ultrasound. The investigators hypothesize that the use of two biomarkers (HE4 and CA 125) in a mathematical algorithm (Risk of Malignancy Algorithm, ROMA) can be used to predict malignancy in a pelvic mass which has indeterminate ultrasound features. This is a prospective cohort study involving women undergoing operation for a pelvic mass. 720 women scheduled to have an operation to remove a pelvic mass would be recruited from 3 hospitals (QMH, UCH and PYNEH). Pre-operatively, each woman will have an ultrasound assessment using the IOTA simple rules criteria and have blood taken for tumour markers HE4 and CA 125. In women where IOTA ultrasound rules are inconclusive, 2 strategies for prediction will be compared - calculation of risk by ROMA (Strategy A) vs referral for an expert ultrasound (Strategy B). These pre-operative risk predictions will be correlated with the final pathology found at the operations.

Main outcome measures include the sensitivity, specificity, positive and negative predictive powers for Strategy A compared to Strategy B. Sensitivity and specificity will be compared using the McNemar test. Area Under the ROC Curve (AUC) will be calculated and compared using the Delong method for the 2 strategies.

The investigators expect AUC of both strategies will be similar. This would suggest that ROMA can replace expert ultrasound in the pre-operative prediction of ovarian cancer.

Registry
clinicaltrials.gov
Start Date
April 1, 2018
End Date
August 31, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Women over the age of 18
  • Found to have a pelvic mass on ultrasound, MRI, CT or PET scan
  • Scheduled for operation (laparoscopic or open) for a pelvic mass (including ovarian cystectomy and oophorectomy)
  • Women who would understand the informed consent

Exclusion Criteria

  • Women who refused a transvaginal scan
  • Pregnant women
  • Surgical removal is delayed for more than 120 days from the date of the ultrasound examination
  • Previous history of ovarian, peritoneal or fallopian tube cancer or unknown malignancy
  • History of bilateral oophorectomy

Outcomes

Primary Outcomes

sensitivity, specificity and predictive powers

Time Frame: 3 months after last subject enrolled

The group of women with inconclusive IOTA assessment will undergo further assessment by both tumour markers assessment by ROMA (Strategy A) and expert ultrasound (Strategy B). The prediction of risk of malignancy (high or low) will be correlated with the final histopathology result from the surgery. The sensitivity, specificity and predictive powers for the 2 strategies will be compared.

Secondary Outcomes

  • Accuracy of these 4 different prediction methods in different hospital settings(3 months after last subject enrolled)
  • Best method for predicting malignancy in pelvic mass in HK(3 months after last subject enrolled)
  • Performance of IOTA simple rules followed by ROMA (if IOTA inconclusive) in different histological subtypes(3 months after last subject enrolled)

Study Sites (3)

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