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.
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
80
Blood sample and endometrial sample
Tatiana Cuesta-Guardiola
León, Spain
The proportion of positive H-score of HE4.
HE4 quantified in endometrial tissue is significantly higher in patients with endometrial cancer than in non-EC patients
Time frame: Two years
Concentration of HE4 in tissue correlates linearly with HE4 in serum.
Comparison of tissue H-score with ppmol/L in serum
Time frame: Two years
Difference in preoperative serum CA125 levels in cases and controls.
Measured in terms of U/mL
Time frame: Two years
Difference in preoperative serum HE4 levels in cases and controls.
Measured in terms of ppmol/L
Time frame: Two years
Disease stages
FIGO stages: postsurgical classification drawn up to define the extent of spread of genital cancer
Time frame: Two years
Tissue tumor marker HE4
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.
Time frame: Two years
Relation of the immunohistochemistry intensity in H-score with overall survival
HE4 biomarker measured with H-score in endometrial tissue, explained in outcome 5, in relation to length of time of survival
Time frame: Through study completion, an average of 2 years
Relation of the immunohistochemistry intensity in H-score with disease-free survival
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.
Time frame: Through study completion, an average of 2 years
Analysis of outcomes in relation to age
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.
Time frame: Two years
Analysis of outcomes in relation to menopausal status
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.
Time frame: Two years
Analysis of outcomes in relation to hypertension
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.
Time frame: Two years
Analysis of outcomes in relation to diabetes
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.
Time frame: Two years
Analysis of outcomes in relation to obesity
Obesity is defined as BMI \>27 kg/m2. There is a known high relative risk of EC in patients diagnosed with obesity.
Time frame: Two years
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