Carbon Monoxide Poisoning |
Carbon Monoxide |
Clinical Trial: Positron Emission Tomography Using Carbon-11 Acetate in Finding Metastasis and Predicting Recurrence in Patients with Newly Diagnosed Prostate Cancer Who Are At Risk for Recurrence After Treatment
This study is currently recruiting patients.
Purpose
RATIONALE: Diagnostic procedures, such as positron emission tomography using carbon-11 acetate, may help find metastasis from prostate cancer and may help predict whether prostate cancer will come back after treatment.
PURPOSE: This clinical trial is studying how well positron emission tomography using carbon-11 acetate works in finding metastasis and predicting recurrence in patients with prostate cancer who are at risk for recurrence after treatment.
| Condition | Intervention |
|---|---|
| stage I prostate cancer stage II prostate cancer stage III prostate cancer stage IV prostate cancer | Drug: carbon-11 acetate Procedure: diagnostic test Procedure: tomography, emission computed |
MedlinePlus related topics: Prostate Cancer
Study Type: Interventional
Study Design: Diagnostic
Official Title: Diagnostic Study of Positron Emission Tomography Using Carbon-11 Acetate in Detecting Metastasis and Predicting Recurrence in Patients with Newly Diagnosed Prostate Cancer At Medium Or High Risk for Recurrence After Initial Curative Therapy
OBJECTIVES:
- Determine the role of positron emission tomography using carbon-11 acetate (AC-PET) in changing initial management of patients with newly diagnosed prostate cancer at medium or high risk for recurrence after initial curative therapy.
- Compare the value of AC-PET in predicting recurrence of prostate cancer with that of conventional approaches (e.g., pre-operative clinical staging, prostate-specific antigen, and Gleason score) in these patients.
- Compare the efficacy of AC-PET in detecting lymph node metastasis with that of biopsy in these patients.
OUTLINE: Patients undergo positron emission tomography using carbon-11 acetate.
Patients are followed periodically.
PROJECTED ACCRUAL: A total of 285 patients will be accrued for this study.
Eligibility
DISEASE CHARACTERISTICS:
- Newly diagnosed prostate cancer
- Has completed conventional staging examinations, including biopsy with Gleason score, CT scan of the abdomen and pelvis, and whole-body bone scintigraphy AND conventional staging examinations negative
- Candidate for curative radical prostatectomy OR curative radiotherapy OR staging lymphadenectomy prior to surgery
- Deemed to be at medium or high risk for recurrence after initial curative treatment, as defined by 1 of the following criteria:
- Gleason score 7 AND prostate-specific antigen (PSA) 10-20 ng/mL
- Gleason score ≥ 8 AND PSA < 10 ng/mL
- Gleason score ≥ 8 AND PSA > 10 ng/mL
- Any Gleason score AND PSA > 20 ng/mL
PATIENT CHARACTERISTICS: Age
- 18 to 90
Performance status
- Not specified
Life expectancy
- Not specified
Hematopoietic
- Not specified
Hepatic
- Not specified
Renal
- Not specified
PRIOR CONCURRENT THERAPY: Biologic therapy
- No prior or concurrent biologic therapy
Chemotherapy
- No prior or concurrent chemotherapy
Endocrine therapy
- Initiation of hormonal therapy allowed
Radiotherapy
- No prior or concurrent radiotherapy
Surgery
Location and Contact Information
Missouri
Siteman Cancer Center at Barnes-Jewish Hospital, Saint Louis, Missouri, 63110, United States; Recruiting
Tom R. Miller, MD, PhD, Study Chair, Barnes-Jewish Hospital
More Information
Clinical trial summary from the National Cancer Institute''''s PDQ® database
Record last reviewed: July 2005
Last Updated: July 25, 2005
Record first received: July 20, 2005
ClinicalTrials.gov Identifier: NCT00121212
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-07-26

Not Signed In -


