Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04212910
Other study ID # PET/MRI-ONCOGYN
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 23, 2019
Est. completion date February 28, 2027

Study information

Verified date April 2024
Source IRCCS San Raffaele
Contact Stephanie Steidler, PhD
Phone +39022643
Email steidler.stephanie@hsr.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Endometrial cancer (EC) is the most common gynecological malignancy in high-income countries. Prognosis and treatment are dictated by cancer histological subtype and grade coupled with surgical staging as described by Surgical International Federation of Gynecology and Obstetrics (FIGO) staging system. Surgery is the elective standard treatment and used for staging of EC. The purpose of this study is to collect images from a simultaneous PET/MRI study from which to extrapolate a preoperative, non-invasive, prognostic model.


Description:

Magnetic resonance imaging (MRI) is the most frequently used imaging tool in preoperative staging of endometrial cancer. FDG-PET has demonstrated higher sensitivity than MRI in detecting nodal involvement and metastatic disease and is currently used in adjunction to MRI. Distinct MRI and FDG-PET parameters correlate well with tumor aggressiveness and can and have been used as prognostic factors. The Investigators believe that the combination of data from these two imaging techniques, from which different derived tumor features can be extrapolated, can stratify patients in high-risk and low-risk groups already preoperatively. The aim of combined techniques is to collect large amounts of data leveraging advantages of both modalities (MR's strengths in local staging and PET's strengths in nodal staging) in a single scan from which to extrapolate a preoperative, non-invasive, prognostic model.


Recruitment information / eligibility

Status Recruiting
Enrollment 101
Est. completion date February 28, 2027
Est. primary completion date December 31, 2025
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - histopathological confirmation of a primary endometrial cancer - age > 18 years - no contraindication to surgery (comorbidity, contraindication or lack of consent) - no contraindication to preoperative imaging - visible tumor at imaging - signed inform consent. Exclusion Criteria: - patients unsuitable for surgical intervention (comorbidity, contraindication or lack of consent, poor performance status) - age < 18 years, c) inability to complete the needed imaging examination (ie, severe claustrophobia) - any additional medical condition that may significantly interfere with study compliance - all the contraindication for MRI (ie, pacemaker).

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy IRCCS Ospedale San Raffaele Milano

Sponsors (1)

Lead Sponsor Collaborator
IRCCS San Raffaele

Country where clinical trial is conducted

Italy, 

References & Publications (2)

Kitajima K, Kita M, Suzuki K, Senda M, Nakamoto Y, Sugimura K. Prognostic significance of SUVmax (maximum standardized uptake value) measured by [(1)(8)F]FDG PET/CT in endometrial cancer. Eur J Nucl Med Mol Imaging. 2012 May;39(5):840-5. doi: 10.1007/s00259-011-2057-9. Epub 2012 Feb 17. — View Citation

Nakamura K, Kodama J, Okumura Y, Hongo A, Kanazawa S, Hiramatsu Y. The SUVmax of 18F-FDG PET correlates with histological grade in endometrial cancer. Int J Gynecol Cancer. 2010 Jan;20(1):110-5. doi: 10.1111/IGC.0b013e3181c3a288. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary MRI evaluation Measure tumor volume and correlate to surgical specimen 0-2 years
Primary MRI imaging Changes in ADC normale versus tumor myometrium 0-2 years
Primary MRI imaging evaluation Depth of myometrial invasion 0-2 years
Primary DCE-MRI perfusion parameters Define tumor perfusion in normal versus tumor myometrium 0-2 years
Primary MRI positive lymph node evaluation 0-2 years
Primary PET imaging evaluation PET positive lymph nodes 0-2 years
Primary PET imaging Tumor/positive lymph node/metastases SUV values 0-2 years
Secondary Measure tumor angiogenesis angiogenesis marker, CD1 0-2 years
Secondary Correlate PET and MRI derived functional and morphological parameters with histology Imaging derived parameters correlated with histopathology 0-5 years
See also
  Status Clinical Trial Phase
Recruiting NCT05036681 - A Phase II Study of Futibatinib and Pembrolizumab in Metastatic Microsatellite Stable Endometrial Carcinoma Phase 2
Completed NCT00377520 - A Trial for Patients With Advanced/Recurrent Endometrial Cancer Phase 2
Recruiting NCT06192017 - Development of a Molecular Diagnostic Tool for Endometrial Cancer.
Recruiting NCT05902988 - A Phase I/II Study of VLS-1488 in Subjects With Advanced Cancer Phase 1/Phase 2
Completed NCT03899441 - Multimedia Aid Gynecologic Counseling and Consent N/A
Completed NCT02552121 - Tisotumab Vedotin (HuMax®-TF-ADC) Safety Study in Patients With Solid Tumors Phase 1/Phase 2
Completed NCT02001623 - Tisotumab Vedotin (HuMax®-TF-ADC) Safety Study in Patients With Solid Tumors Phase 1/Phase 2
Completed NCT02997553 - Fluorescence for Sentinel Lymph Node Identification in Cancer Surgery Phase 3
Suspended NCT03095664 - Effect of a Lifestyle Intervention on Nutritional Status and Prognosis of Endometrial Cancer Survivors N/A
Active, not recruiting NCT01466777 - Endometrial Cancer and Robotic-assisted Versus Traditional Laparoscopy N/A
Completed NCT01068483 - Safety of BKM120 Monotherapy in Advanced Solid Tumor Patients Phase 1
Recruiting NCT03896113 - Neoadjuvant Celecoxib in Newly Diagnosed Patients With Endometrial Carcinoma Phase 2
Not yet recruiting NCT03570866 - PET/CT in the Management of Patients With Early Stage Endometrial Cancer
Completed NCT05246462 - The Effect of Logotherapy on Mental Health in Gynecological Cancer Patients N/A
Withdrawn NCT04464967 - Safety and Preliminary Efficacy of SNK01 in Combination With Trastuzumab or Cetuximab in Subjects With Advanced HER2 or EGFR Cancers Phase 1/Phase 2
Recruiting NCT05651282 - Risk Evaluation and Screening to Tailor Prevention and Reduce the Incidence of Endometrial Cancer Phase 4
Completed NCT06187558 - Suspension of the Pelvic and Abdominal Organs During Minimally Invasive Surgery
Completed NCT06312917 - Effect of Physical Activity Intervention on Overweight and Obese Patients With Endometrial Cancer N/A
Active, not recruiting NCT03951415 - Durvalumab and Olaparib in Metastatic or Recurrent Endometrial Cancer Phase 2
Completed NCT02221076 - Probe-based and Needle-based Confocal Laser Endomicroscopy During Gynaecological Procedures. N/A