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Clinical Trials/NCT01089881
NCT01089881
Unknown
Not Applicable

The Effectiveness of 18F-fluorocholine PET in Detecting, Staging and Following-up Prostate Cancer

National Taiwan University Hospital1 site in 1 country150 target enrollmentJanuary 2008
ConditionsProstate Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
National Taiwan University Hospital
Enrollment
150
Locations
1
Last Updated
16 years ago

Overview

Brief Summary

Choline is one of the components of phosphatidylcholine, an essential element of phospholipids in the cell membrane. Some malignant cells show their ability to actively incorporate choline to produce phosphocholine and phosphatidylcholine to facilitate tumor cell duplication. The efficacy of 18F-fluorocholine (18F-FCH) for localizing primary or metastatic prostate cancer has been recently reported in limited studies. This study will be conducted to delineate the effectiveness of 18F-FCH PET in (1) differentiating benign prostate hypertrophy (BPH) from prostate cancer, (2) staging prostate cancer, (3) following-up patients with prostate cancer after initial curative therapy.

Detailed Description

Background: Prostate cancer is a leading cause of cancer death for male in Taiwan. Although 18F-FDG PET has been shown to be an effective tool in diagnosing many malignancies, previous studies have shown that 18F-FDG is not a suitable PET tracer for detecting prostate cancer. Choline is one of the components of phosphatidylcholine, an essential element of phospholipids in the cell membrane. Some malignant cells show their ability to actively incorporate choline to produce phosphocholine and phosphatidylcholine to facilitate tumor cell duplication. The efficacy of 18F-fluorocholine (18F-FCH) for localizing primary or metastatic prostate cancer has been recently reported in limited studies. Purpose: This study will be conducted to delineate the effectiveness of 18F-FCH PET in (1) differentiating benign prostate hypertrophy (BPH) from prostate cancer, (2) staging prostate cancer, (3) following-up patients with prostate cancer after initial curative therapy. Patients and Methods: This study will include 1. Group 1: 50 patients with BPH 2. Group 2: 50 patients with newly diagnosed prostate cancer and 3. Group 3: 50 patients who have received curative treatment for prostate cancer and are suspicious of recurrence/metastases because of a persistent increase in their serum PSA. 18F-FCH whole-body PET will be performed for each patient Expected Results: To evaluate the effectiveness of 18F-FCH in the diagnosis, staging and follow-up of prostate cancer.

Registry
clinicaltrials.gov
Start Date
January 2008
End Date
December 2010
Last Updated
16 years ago
Study Type
Observational
Sex
Male

Investigators

Eligibility Criteria

Inclusion Criteria

  • Group 1: 50 patients with BPH
  • Age above 35 years old
  • Histologically confirmed BPH
  • Informed consent signed
  • Group 2: 50 patients with newly diagnosed prostate cancer and
  • Age above 35 years old
  • Histologically confirmed prostate cancer
  • Informed consent signed
  • Group 3: 50 patients who have
  • Age above 35 years old

Exclusion Criteria

  • Patients with other known malignancies will be excluded.

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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