Magnetic Resonance Imaging in Detecting Cancer Progression in Patients With Early Stage Prostate Cancer Undergoing Active Surveillance

Roswell Park Comprehensive Cancer Center

Status: Withdrawn

Conditions: Prostate Cancer

Treatments: Procedure: biopsy; Other: imaging biomarker analysis; Other: active surveillance; Procedure: magnetic resonance imaging; Procedure: magnetic resonance spectroscopic imaging; Procedure: dynamic contrast-enhanced magnetic resonance imaging

Study type: Interventional

Funder types: Other

Identifiers

NCT00796874

CDR0000618738

RPCI-I-124107 (Other Identifier)

Details and patient eligibility

About

RATIONALE: Sometimes prostate cancer may not need treatment until it progresses. In this case, active surveillance may be sufficient. Diagnostic procedures, such as magnetic resonance imaging, may be a less invasive method of finding prostate cancer that has progressed.

PURPOSE: This clinical trial is studying how well magnetic resonance imaging works in detecting cancer progression in patients with early-stage prostate cancer who are undergoing active surveillance.

Full description

OBJECTIVES:

Primary

• To determine if MRI parameters (initial volume, number and location of image abnormalities, and MR spectroscopy) can improve the ability to stratify cancer progression risk in patients undergoing active surveillance for early-stage prostate cancer.

Secondary

• Determine if changes in non-invasive MRI, validated by MRI-guided biopsies, can accurately detect progression of prostate cancer.

OUTLINE: Patients undergo prostate MRI scans and MRI-guided biopsies of suspicious lesions at baseline. Patients undergo conventional anatomic imaging followed by research biological imaging tests (e.g., magnetic resonance spectroscopic imaging and/or dynamic contrast-enhanced MRI). MRI are repeated at 6 months, 1 year, and then annually until initiation of definitive therapy or for a total of 5 years.

Tissue biopsy with MRI guidance is done at baseline and annually or as clinically indicated based on change in rectal exam, PSA, or maybe done based on change in MR imaging (i.e., new MR lesion or significant change [> 25% increase] in the size of a MR lesion).

Blood samples are collected at baseline and periodically during study for PSA tests.

Sex: Male

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed prostate cancer

• Low-risk for progression, as evidenced by all of the following:

  • Tumor stage ≤ T2a
  • PSA ≤ 10 ng/mL
  • Gleason score ≤ 7

• Patients informed of treatment options and has already chosen to undergo active surveillance

  • No decision to stop active surveillance

• No node-positive or metastatic disease

PATIENT CHARACTERISTICS:

• Willing to undergo MRI

• Willing to undergo prostate biopsy

• No contraindications to MRI that include, but not limited to, any of the following:

  • Claustrophobia
  • Anxiety
  • Presence of metal or shrapnel in the body
  • Pacemakers
  • Old tattoos with metal-based dye material

• No contraindication to prostate biopsy

• No medical conditions, as deemed by the PI or associates, that would prevent or limit the patient participation on the protocol that include, but not limited to, any of the following:

  • Severe coagulopathy
  • History of severe bleeding
  • Severe coronary artery disease
  • Other comorbid conditions that limit life expectancy to less than 2 years

PRIOR CONCURRENT THERAPY:

• No hormone therapy within the past year
• No prior pelvic radiotherapy
• No prior prostate resection including transurethral resection of prostate
• Concurrent participation in other clinical studies (e.g., vitamin D, selenium) allowed provided active surveillance is continued

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)