Identification and Characterization of Endometrial Cancer With Specific Tumor Markers in Serum and Endometrial Tissue

February 9, 2020 updated by: Tatiana Cuesta-Guardiola, Fundación Investigación Sanitaria en León

Prospective Identification and Characterization of Endometrial Cancer With Specific Tumor Markers in Serum and Endometrial Tissue Samples

Endometrial cancer is the most common malignant tumor of the female genital tract in our means. The diagnosis is made by endometrial biopsy sampling with anatomopathological analysis which pinpoints the cell line and the level of cell differentiation. Its treatment is surgical with adjuvant treatment (chemotherapy or radiotherapy) besides, depending on the staging. Thus far, in the first diagnosis it is only request the tumor marker CA125 in serum, but there are studies that identify the HE4 protein in blood as a feasible marker for endometrial cancer. Furthermore, the staging changes the surgical and the adjuvant treatment: in its early stages, surgery is based on hysterectomy and double adnexectomy, however, in later stages it is necessary to add pelvic and paraaortic lymphadenectomy with the associated comorbidity. This makes extremely important that the preoperative diagnosis is accurate. The aim of this study is to identify and characterize the HE4, Ki67, p53 and other potential biomarkers in endometrial tissue in order to diagnose patients with disease only with a biopsy. Moreover, the investigators are searching for connections among these markers and prognostic factors such as grade of cell differentiation, cell line, lymphatic affectation, tumor stage or even features as survival or disease free survival.

Study Overview

Detailed Description

List of abbreviations:

  • HE4: Human Epididymis Protein 4
  • CA125: Carbohydrate Antigen 125
  • Ki67: antigen KI67
  • EC: Endometrial Cancer
  • CT: Computed Tomography
  • NMR: Nuclear Magnetic Resonance
  • FIGO: International Federation of Gynecology and Obstetrics

The purpose of this study is:

  • The proportion of positive H-score of HE4, as quantified in endometrial tissue. It is significantly higher in patients with endometrial cancer than in non-EC patients.
  • Percentage of HE4, CA125 and other markers positives in cases and controls.
  • Concentration of HE4 in tissue, as measured by H-score, correlates linearly with HE4 concentration in serum, as measured in terms of ppmol/l.
  • Differences in serum CA125 levels between cases and controls.
  • Quantification of tissue tumor markers of EC patients, per disease stages.
  • Relation of the immunohistochemistry intensity with survival and disease-free survival times.
  • Analysis of other risk factors adjusting for known variables like age, menopausal status, hypertension, diabetes or obesity.
  • Feasibility of the technique.

Steps in the study:

  1. Patients enter the study when a diagnosis of endometrial cancer is done. As it is ordinary in the clinical practice the diagnosis is made with an endometrial tissue sample taken in the office which is afterwards studied by a pathologist, who makes the final diagnosis.
  2. Patients undergo the regular preoperative study with pelvic ultrasound, CT and/or NMR for the extension study, blood tests and the preanaesthetic consultation. As it is registered in the protocol of Endometrial Cancer Treatment.
  3. Then a matched control is selected from the group of patients that are going to be hysterectomized for other non-malignant reasons (abdominal way, vaginal, or laparoscopic way). Variables considered for matching are: age (variability of five years), pre or postmenopausal status, hypertension, obesity and diabetes.
  4. Every patient then is asked for accept and sign the informed consent. The next step is to prepare the patient for the surgery. In this moment the serum sample is taken. Subsequently the surgery will be performed.
  5. Then the anatomopathological study is conducted over the preoperative tissue sample. HE4 marker in endometrial tissue is defined by H-Score while Ki67 and p53 are defined as usual. Although Ki67 is matched in > or <25% of expression instead of 14% as it is made in breast cancer tissue samples.
  6. After discharge, the patient will be follow-up for two years in order to register the evolution of the disease.

Study Type

Observational

Enrollment (Actual)

80

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Leon, Spain, 24080
        • Tatiana Cuesta-Guardiola

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

Every patient who is treated in Hospital de Leon of endometrial disease between August 2017 and the end of the recruitment

Description

Inclusion Criteria:

  • Female
  • Of legal age (≥ 18 years)
  • Wish to participate in the research study and sign consent forms voluntarily
  • Patients diagnosed of endometrial cancer derived to hysterectomy

Exclusion Criteria:

  • Patients that underwent surgery for other malignant pathologies, whether for ovarian carcinoma, cervical carcinoma or uterine sarcoma.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
CASES
Patients with endometrial cancer
Blood sample and endometrial sample
CONTROLS
Matched controls without neoplasm disease
Blood sample and endometrial sample

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The proportion of positive H-score of HE4.
Time Frame: Two years
HE4 quantified in endometrial tissue is significantly higher in patients with endometrial cancer than in non-EC patients
Two years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Concentration of HE4 in tissue correlates linearly with HE4 in serum.
Time Frame: Two years
Comparison of tissue H-score with ppmol/L in serum
Two years
Difference in preoperative serum CA125 levels in cases and controls.
Time Frame: Two years
Measured in terms of U/mL
Two years
Difference in preoperative serum HE4 levels in cases and controls.
Time Frame: Two years
Measured in terms of ppmol/L
Two years
Disease stages
Time Frame: Two years
FIGO stages: postsurgical classification drawn up to define the extent of spread of genital cancer
Two years
Tissue tumor marker HE4
Time Frame: Two years

H-score determination: Immunohistochemistry results can be evaluated by a semiquantitative approach used to assign an H-score (or "histo" score) to tumor samples. Cytoplasmic staining will be graded for intensity (0-negative, 1-weak, 2-moderate and 3-strong) and the percentage of positive cells was scored as 0 (0%), 1 (1-10%), 2 (11-50%) and 3 (51-100%).

Single scale with scores 0-9 will be obtained by multiplying the intensity and the percentage staining score, and a total score will be calculated by grouping score 0 in total score 0, 1-3 in total score 1, 4-6 in total score 2 and 7-9 in total score 3.

The assumption is that as higher is the score the level of cell differentiation would be minor.

Two years
Relation of the immunohistochemistry intensity in H-score with overall survival
Time Frame: Through study completion, an average of 2 years
HE4 biomarker measured with H-score in endometrial tissue, explained in outcome 5, in relation to length of time of survival
Through study completion, an average of 2 years
Relation of the immunohistochemistry intensity in H-score with disease-free survival
Time Frame: Through study completion, an average of 2 years
HE4 biomarker measured with H-score in endometrial tissue, explained in outcome 5, in relation to length of time after primary treatment that the patient survives without any signs or symptoms of that cancer.
Through study completion, an average of 2 years
Analysis of outcomes in relation to age
Time Frame: Two years
Age of patients is one of the known risk factors for EC, we are going to analysis the results of the study with this variable. As elder the relative risk is higher though there is no accurate cut-off point.
Two years
Analysis of outcomes in relation to menopausal status
Time Frame: Two years
Menopausal status is determined by questionnaire during the preoperative consultant. It is another risk factor for EC, the postmenopausal status has higher relative risk than premenopausal status.
Two years
Analysis of outcomes in relation to hypertension
Time Frame: Two years
Hypertension is diagnosed previously to surgery as Blood Pressure over 140/90 mm Hg in several measures. There is a known high relative risk of EC in patients diagnosed with hypertension.
Two years
Analysis of outcomes in relation to diabetes
Time Frame: Two years
Diabetes is a disease previously diagnosed by high glucose levels in blood. There is a known high relative risk of EC in patients diagnosed with diabetes.
Two years
Analysis of outcomes in relation to obesity
Time Frame: Two years
Obesity is defined as BMI >27 kg/m2. There is a known high relative risk of EC in patients diagnosed with obesity.
Two years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Tatiana Cuesta-Guardiola, Medicine, Hospital de Leon

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2017

Primary Completion (Actual)

August 1, 2018

Study Completion (Actual)

June 1, 2019

Study Registration Dates

First Submitted

February 23, 2018

First Submitted That Met QC Criteria

April 16, 2018

First Posted (Actual)

April 17, 2018

Study Record Updates

Last Update Posted (Actual)

February 11, 2020

Last Update Submitted That Met QC Criteria

February 9, 2020

Last Verified

February 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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