- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03498924
Identification and Characterization of Endometrial Cancer With Specific Tumor Markers in Serum and Endometrial Tissue
Prospective Identification and Characterization of Endometrial Cancer With Specific Tumor Markers in Serum and Endometrial Tissue Samples
Study Overview
Status
Conditions
Intervention / Treatment
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:
- 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.
- 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.
- 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.
- 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.
- 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.
- After discharge, the patient will be follow-up for two years in order to register the evolution of the disease.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Leon, Spain, 24080
- Tatiana Cuesta-Guardiola
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
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
Investigators
- Principal Investigator: Tatiana Cuesta-Guardiola, Medicine, Hospital de Leon
Publications and helpful links
General Publications
- Creasman WT, Morrow CP, Bundy BN, Homesley HD, Graham JE, Heller PB. Surgical pathologic spread patterns of endometrial cancer. A Gynecologic Oncology Group Study. Cancer. 1987 Oct 15;60(8 Suppl):2035-41. doi: 10.1002/1097-0142(19901015)60:8+3.0.co;2-8.
- Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. CA Cancer J Clin. 2018 Jan;68(1):7-30. doi: 10.3322/caac.21442. Epub 2018 Jan 4.
- Li X, Gao Y, Tan M, Zhuang H, Gao J, Hu Z, Wang H, Zhu L, Liu J, Lin B. Expression of HE4 in Endometrial Cancer and Its Clinical Significance. Biomed Res Int. 2015;2015:437468. doi: 10.1155/2015/437468. Epub 2015 Oct 11. Erratum In: Biomed Res Int. 2018 Sep 12;2018:6795629.
- Bignotti E, Ragnoli M, Zanotti L, Calza S, Falchetti M, Lonardi S, Bergamelli S, Bandiera E, Tassi RA, Romani C, Todeschini P, Odicino FE, Facchetti F, Pecorelli S, Ravaggi A. Diagnostic and prognostic impact of serum HE4 detection in endometrial carcinoma patients. Br J Cancer. 2011 Apr 26;104(9):1418-25. doi: 10.1038/bjc.2011.109. Epub 2011 Apr 5.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY17104
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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