Intra-operative Optical Imaging Utilizing Anti-PSMA (Prostate Specific Membrane Antigen) Fluorescent Antibody During Robotic Assisted Laparoscopic Prostatectomy
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Adenocarcinoma of the Prostate
- Sponsor
- City of Hope Medical Center
- Enrollment
- 7
- Locations
- 1
- Primary Endpoint
- Imaging ability of anti-PMSA monoclonal antibody MDX1201-A488
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
This pilot clinical trial studies the best dose of anti-prostate specific membrane antigen (PSMA) monoclonal antibody MDX1201-A488 (MDX1201-A488) given before surgery to aid in visualization of the prostate. Attaching a fluorescence, a substance that emits radiation that is visible, to the anti-PMSA antibody and injecting it into the body may help identify the tumor when specialized microscopes are used.
Detailed Description
PRIMARY OBJECTIVES: I. Determine the preferred imaging dose (if any), based on image quality and correlation with pathological findings, of intravenously administered MDX1201-A488 in a dose-escalating study (doses of 5 and 15 mg) in patients with moderate to high-risk prostate cancer prior to undergoing robotic assisted laparoscopic prostatectomy (RALP), subject to predetermined safety stopping rules. SECONDARY OBJECTIVES: I. Correlate intra-operative optical imaging (IOOI) findings with pre-operative magnetic resonance imaging (MRI) findings and clinical staging. OUTLINE: This is a dose-escalation study. Patients receive anti-PSMA monoclonal antibody MDX1201-A488 intravenously (IV) over 30 minutes on day 1 and undergo IOOI during RALP on day 5. After completion of study treatment, patients are followed up at 4-7 weeks, 3 months, 6 months, 9 months, and 1 year.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Histologically confirmed adenocarcinoma of the prostate; patients with small cell, neuroendocrine, and transitional cell carcinomas are not eligible
- •Patients being considered for RALP and pelvic lymphadenectomy with life expectancy greater than 10 years as determined by treating physician
- •Patients with moderate to high-risk disease as defined by D' Amico risk stratification and having at least one of the following:
- •Prostate-specific antigen (PSA) level \> 10 ng/ml
- •Gleason score \>= 7
- •Clinical stage \>= T2c
- •Any performance status on the Eastern Cooperative Oncology Group (ECOG)
- •Men must agree to use adequate contraception (hormonal or barrier method of birth control or abstinence) prior to study entry and for six months following duration of study participation
- •Bone scan without evidence of skeletal metastases
- •Skeletal x-ray film or MRI confirmation of absent skeletal metastases if bone scan findings are equivocal
Exclusion Criteria
- •Patients should not have any uncontrolled illness including ongoing or active infection
- •Prior treatment of prostate cancer including brachytherapy, radiation therapy, cryosurgery, high-intensity focused ultrasound (HIFU), or vaccine therapy
- •Prior pelvic surgery or radiation
- •Urinary incontinence requiring condom catheter use or \>= 1 pad/day
- •Prior anti-incontinence surgery
- •Use of neoadjuvant hormonal manipulation
- •History of active co-existing non-prostatic malignancies except basal cell skin cancer or squamous cell skin cancer
- •Subjects, who in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study
Outcomes
Primary Outcomes
Imaging ability of anti-PMSA monoclonal antibody MDX1201-A488
Time Frame: Up to 1 year
The main fluorescence metric will be the minimum fluorescence observed in 10 sampled high power fields from a single representative cancerous section taken per patient. Other metrics will be the mean fluorescence observed in the 10 sampled high power fields, and the median fluorescence observed. The minimum fluorescence is chosen based on the concept that the primary focus is on observing the fluorescence, and areas of peak fluorescence greatly influence the mean, and also have some influence on the median, yet may be of limited relevance.