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Clinical Trials/NCT01655745
NCT01655745CompletedNot Applicable

LCCC 1209: Pilot Study of [18F] Fluorodeoxyglucose Positron Emission Tomography-Magnetic Resonance Imaging (FDG-PET-MRI) for Staging of Muscle-Invasive Bladder Cancer

UNC Lineberger Comprehensive Cancer Center1 site in 1 country22 target enrollmentStarted: July 24, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
22
Locations
1
Primary Endpoint
Sensitivity and specificity of the FDG-PET-MRI for staging of muscle-invasive bladder cancer

Study Overview

Brief Summary

This prospective pilot study will enroll 30 patients with cT2/T3-N0-M0 urothelial carcinoma of the bladder for whom radical cystectomy with pelvic lymph node dissection is planned. This pilot study is designed to provide preliminary information on the accuracy of [18F] Fluorodeoxyglucose Positron Emission Tomography MRI (FDG-PET-MRI) in the staging of muscle-invasive bladder cancer.

Detailed Description

This prospective pilot study will enroll 30 patients with cT2/T3-N0-M0 urothelial carcinoma of the bladder for whom radical cystectomy with pelvic lymph node dissection is planned. This pilot study is designed to provide preliminary information on the accuracy of [18F] Fluorodeoxyglucose Positron Emission Tomography MRI (FDG-PET-MRI) in the staging of muscle-invasive bladder cancer. All patients will undergo baseline FDG-PET-MRI and routine (standard of care) contrast enhanced abdominal/pelvic multi-detector computed tomography (MDCT). The imaging results will ultimately be compared to final pathology as the gold standard. If the accuracy of FDG-PET-MRI is improved as compared to standard MDCT, the investigators plan to conduct a larger follow-up study to confirm the results of this pilot study. In addition, this pilot study will set the stage for the evaluation of novel PET tracers in the imaging of bladder cancer.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •≥ 18 years of age (no upper age limit)
  • •Informed consent obtained and signed
  • •cT2/T3-N0-M0 urothelial carcinoma of the bladder
  • •Planned radical cystectomy with pelvic lymph node dissection
  • •No known local regional or distant metastatic disease
  • •Women of childbearing potential must have a negative serum or urine pregnancy test performed within 7 days prior to FDG-PET-MRI

Exclusion Criteria

  • •History of severe reaction to contrast-enhanced CT scan
  • •Poorly controlled diabetes mellitus
  • •Inability to tolerate PET and/or MRI
  • •Presence of pacemaker or intracranial aneurysm clip
  • •Serum creatinine >1.8 mg/dL OR GFR < 30mL/min
  • •Pregnant or lactating female
  • •Inability to lie flat for >1 hour
  • •Body Mass Index (BMI) >35
  • •History of a prior malignancy within past 5 years are excluded unless they have been disease free for 3 or more years or unless they have a completely resected non-melanoma skin cancer.
  • •Substance abuse, medical, psychological, or social conditions that may interfere with the patient's participation in the study

Arms & Interventions

FDG PET/MR, No Chemotherapy Arm

Experimental

Patients that are NOT receiving chemotherapy but are only completing surgical intervention.

Intervention: FDG PET/MR (Procedure)

FDG PET/MR, Chemotherapy Arm

Experimental

Patients that are receiving chemotherapy prior to completing surgical intervention. These patients will receive a FDG PET/MR prior to chemotherapy and after completion of chemotherapy (at the time of pre-op, before surgical intervention).

Intervention: FDG PET/MR (Procedure)

Outcomes

Primary Outcomes

Sensitivity and specificity of the FDG-PET-MRI for staging of muscle-invasive bladder cancer

Time Frame: 3 years

The sensitivity and specificity of the FDG-PET-MRI for staging of muscle-invasive bladder will be evaluated by using the pathology from the radical cystectomy and lymph node dissection specimen or biopsy as the reference standard. The sensitivity and specificity of FDG-PET-MRI will be compared to conventional CT performed in all patients in this pilot study and FDG-PET-CT.

Secondary Outcomes

  • Association of FDG-PET-MRI with RFS, DSS and OS in patients with muscle-invasive bladder cancer(3 years)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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