PET/CT in the Management of Patients With Early Stage Endometrial Cancer

NCT ID: NCT03570866

Last Updated: 2021-09-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-05-01

Study Completion Date

2024-05-01

Brief Summary

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Endometrial cancer (EC) is the most common gynecologic malignancy in the developed countries and is the fifth most common cancer among women worldwide. Typically present well or moderately differentiated, early stage endometrioid histotype with a prognosis usually favorable. Pelvic lymph nodes (LNs) represent the most common site of extra-uterine disease in patients with clinical early stage disease and the role of lymphadenectomy in early stage EC has been one of the major controversies in gynecology oncology. Lymphadenectomy doesn't improve survival or reduce disease recurrence although supported to provide prognostic information and allowing tailoring of adjuvant therapy. Nevertheless, lymphadenectomy is not performed without serious short-term and long-term morbidity. Although surgical staging is the most accurate and standard method to determine LNs involvement, the introduction in clinical practice of a non-invasive modality that allows an accurate staging of EC would be essential. Available evidence report the accuracy of Positron Emission Tomography and Computed Tomography (PET/CT) for the detection of LN metastasis in EC with a sensitivity of 63% and specificity of 94.7%. This prospective comparative analysis between PET/CT, histological findings, and follow up data will be performed to investigate the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and accuracy of integrated PET/CT for nodal staging of EC per patient and per LN chain analyses, in women affected by intermediate (grade 1 and 2 endometrioid lesions with deep myometrial invasion \> 50% or grade 3 endometrioid lesion with \< 50% myometrial invasion) or high risk (grade 3 endometrioid lesion with deep myometrial invasion \> 50% or non-endometrioid histotype) early-stage EC. Furthermore, the preoperative classification of EC in intermediate and high-risk class will allow to investigate its prognostic value.

Detailed Description

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Conditions

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Endometrium Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Early stage endometrial cancer

Women with diagnosis of intermediate and high-risk early stage endometrial cancer.

Positron emission tomography and computed tomography

Intervention Type DIAGNOSTIC_TEST

Preoperative staging of early stage intermediate and high-risk endometrial cancer with positron emission tomography and computed tomography.

Surgical treatment

Intervention Type PROCEDURE

Surgical treatment of early stage intermediate and high-risk endometrial cancer by usual practice: peritoneal cytology, total abdominal hysterectomy, bilateral salpingo-oophorectomy, systematic pelvic and para-aortic lymphadenectomy.

Interventions

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Positron emission tomography and computed tomography

Preoperative staging of early stage intermediate and high-risk endometrial cancer with positron emission tomography and computed tomography.

Intervention Type DIAGNOSTIC_TEST

Surgical treatment

Surgical treatment of early stage intermediate and high-risk endometrial cancer by usual practice: peritoneal cytology, total abdominal hysterectomy, bilateral salpingo-oophorectomy, systematic pelvic and para-aortic lymphadenectomy.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Women with diagnosis of early stage intermediate and high-risk endometrial cancer.

Exclusion Criteria

* Not eligible for standard surgical treatment; Not eligible for preoperative staging with PET/CT
Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Universita di Verona

OTHER

Sponsor Role collaborator

Università degli Studi dell'Insubria

OTHER

Sponsor Role lead

Responsible Party

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Antonio Simone Laganà

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Simone Garzon, M.D.

Role: PRINCIPAL_INVESTIGATOR

Universita di Verona

Antonio Simone Laganà, M.D.

Role: PRINCIPAL_INVESTIGATOR

Università degli Studi dell'Insubria

Massimo Franchi, M.D.

Role: PRINCIPAL_INVESTIGATOR

Universita di Verona

Central Contacts

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Antonio Simone Laganà, M.D.

Role: CONTACT

‭+39 329 6279579‬

Simone Garzon, M.D.

Role: CONTACT

+393470782287

Other Identifiers

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ENCA-1

Identifier Type: -

Identifier Source: org_study_id

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