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Clinical Trials/NCT01768156
NCT01768156
Completed
Not Applicable

Determination of the Prognostic and Predictive Value of the New Marker HE4 in Metastatic Ovarian Cancer Monitoring

Institut du Cancer de Montpellier - Val d'Aurelle2 sites in 1 country101 target enrollmentSeptember 24, 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Metastatic Ovarian Cancer
Sponsor
Institut du Cancer de Montpellier - Val d'Aurelle
Enrollment
101
Locations
2
Primary Endpoint
To evaluate the predictive and prognostic value of HE4 marker
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

HE4 is a new marker that could improve the detection of ovarian cancer. The HE4 assay may have an advantage over the CA-125 assay in that it is less frequently positive in patients with non malignant disease. Since the evaluation of HE4 for detection and diagnosis of ovarian cancer is well known, the behaviour of the marker during chemotherapy and follow-up period after treatment in metastatic ovarian cancer should be studied. It could be used in patient with non CA-125 secretary tumors. Prognosis and predictive value of HE4 should be compared with information provided by CA-125. The kinetics of HE4 values after treatment should be also analysed to determine the role that HE4 could play in the detection of recurrences during the follow-up of metastatic patients.

Registry
clinicaltrials.gov
Start Date
September 24, 2010
End Date
November 15, 2016
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
Institut du Cancer de Montpellier - Val d'Aurelle
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Histologically proved epithelial ovarian cancer (serous, mucinous, clear cell, endometrioid, undifferentiated type)
  • Recurrence of anytime necessitating a new line of chemotherapy
  • Patient having received adjuvant chemotherapy
  • Informed consent signed prior any study specific procedures

Exclusion Criteria

  • More than 3 lines of chemotherapy
  • Pregnancy or breastfeeding
  • History of other cancers within the past 5 years (except curatively treated non-melanoma skin cancer and in situ cervical cancer)
  • Psychological, social, geographical disorders or any other condition that would preclude study compliance (treatment modalities and study follow-up).

Outcomes

Primary Outcomes

To evaluate the predictive and prognostic value of HE4 marker

Time Frame: 18 months

Secondary Outcomes

  • Determine the rate of patients without elevation of CA-125 presenting an elevation of HE4 that could be used for monitoring the disease.(18 months)

Study Sites (2)

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