Fludeoxyglucose (FDG) F 18 PET Scan, CT Scan, and Ferumoxtran-10 MRI Scan Before Chemotherapy and Radiation Therapy in Finding Lymph Node Metastasis in Patients With Locally Advanced Cervical Cancer or High-Risk Endometrial Cancer

NCT00416455 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 384

Last updated 2019-07-23

Study results available
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Summary

This phase I/II trial is studying how well fludeoxyglucose F 18 PET scan, CT scan, and ferumoxtran-10 MRI scan finds lymph node metastasis before undergoing chemotherapy and radiation therapy in patients with locally advanced cervical cancer or high-risk endometrial cancer. Diagnostic procedures, such as a fludeoxyglucose F 18 positron emission tomography (PET) scan, computed tomography (CT) scan, and ferumoxtran-10 magnetic resonance imaging (MRI) scan, may help find lymph node metastasis in patients with cervical cancer or endometrial cancer.

Conditions

  • Cervical Adenocarcinoma
  • Cervical Adenosquamous Cell Carcinoma
  • Cervical Small Cell Carcinoma
  • Cervical Squamous Cell Carcinoma
  • Endometrial Clear Cell Carcinoma
  • Endometrial Papillary Serous Carcinoma
  • Stage I Endometrial Carcinoma
  • Stage IB Cervical Cancer
  • Stage II Endometrial Carcinoma
  • Stage IIA Cervical Cancer
  • Stage IIB Cervical Cancer
  • Stage III Cervical Cancer
  • Stage III Endometrial Carcinoma
  • Stage IVA Cervical Cancer

Interventions

RADIATION

fludeoxyglucose F 18

Undergo FDG PET/CT

PROCEDURE

positron emission tomography

Undergo FDG PET/CT

PROCEDURE

computed tomography

Undergo FDG PET/CT

DRUG

ferumoxtran-10

Undergo femoxtran-10 MRI

PROCEDURE

magnetic resonance imaging

Undergo femoxtran-10 MRI

PROCEDURE

diagnostic lymphadenectomy

Undergo extraperitoneal, laparoscopic, or trans-peritoneal lymphadenectomy

PROCEDURE

lymph node biopsy

Undergo pelvic and abdominal lymph node biopsy

Sponsors & Collaborators

  • NRG Oncology

    collaborator OTHER
  • National Cancer Institute (NCI)

    lead NIH

Principal Investigators

  • Mostafa Atri · NRG Oncology

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2014-09-30
Completion
2016-07-16

Countries

  • United States
  • Canada
  • Japan
  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00416455 on ClinicalTrials.gov