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The Use of Nanoparticles to Guide the Surgical Treatment of Prostate Cancer

Memorial Sloan Kettering Cancer Center (MSK) logo

Memorial Sloan Kettering Cancer Center (MSK)

Status and phase

Enrolling
Phase 1

Conditions

Prostate Cancer

Treatments

Other: Blood and urine sampling
Procedure: laparoscopic radical prostatectomy and bilateral pelvic LN dissection or a salvage lymph node dissection
Diagnostic Test: PET/MRI
Drug: (64Cu)-labeled PSMA-targeting particle tracer, or 64Cu-NOTA-PSMAi-PEG-Cy5.5-C' dots

Study type

Interventional

Funder types

Other
Industry
NIH

Identifiers

Details and patient eligibility

About

The purpose of this study is to see whether using the 64Cu-NOTA-PSMA-PEG-Cy5.5-C' dot tracer is a safe way to identify tumor cells before and during surgery for prostate cancer. The researchers want to find out whether PET/MRI scans done after the injection of this investigational tracer are more accurate than the usual imaging scans used to locate deposits of prostate tumor cells. The researchers will study how the tracer travels through your body and where it is distributed. This study is the first time that this tracer will be used in people who are undergoing surgery for prostate cancer.

Enrollment

10 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Primary RP + PLND

  • Age ≥18 years

  • Patients meeting one of the following criteria:

    • Tumor clinical stage T3a or higher
    • Gleason score 8-10, or
    • PSA level > 20 ng/mL
  • Patients deemed fit for surgery on the basis of preoperative evaluation at the physician's discretion

  • Patient is scheduled for standard of care laparoscopic radical prostatectomy (with or without robotic assistance) Salvage PLND

  • Age ≥18 years

  • Patients with presence of suspicious lymph node on CT or MRI (of a pelvic node => 10mm in short axis or a node with abnormal morphology such as roundness irregularity or loss of fatty hilum, or PSMA-avid on PSMA PET imaging

  • Patients deemed fit for surgery on the basis of preoperative evaluation at the physician's discretion

  • Patient is scheduled for standard of care salvage pelvic lymph node dissection (with or without robotic assistance)

Exclusion criteria

  • Contraindications to standard-of-care MR imaging (e.g., metal implants, claustrophobia)

  • Prior androgen-deprivation therapy for prostate cancer (N/A for Salvage PLND)

  • Prior pelvic radiotherapy (N/A for Salvage PLND )

  • Medical illness unrelated to the tumor that, in the opinion of the attending physician and principal investigator, will preclude administration of the tracer

    °This includes patients with uncontrolled infection, chronic renal insufficiency (EGFR < 60 mL/min/1.73m2), myocardial infarction within the past 6 months, unstable angina, cardiac arrhythmias other than chronic atrial fibrillation and chronic active or persistent hepatitis, or New York Heart Association Classification III or IV heart disease

  • Weight greater than the 400-lb weight limit of the PET scanner

  • Unmanageable claustrophobia

  • Inability to lie in the scanner for 30 min

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Prostate cancer patients
Experimental group
Description:
Patients will receive an intravenous (IV) injection of approximately 5 mCi (+/- 10%) of PSMAtargeting C' dot tracer up to 48 hours before surgery. Patients will then undergo serial preoperative PET/MR imaging to help characterize the safety, biodistribution/pharmacokinetics, and dosimetry of this agent. To assess total radioactivity in whole blood/plasma and urine samples, as well as radioactive metabolites, blood and urine samples will be collected at approximately 30 min post-injection as well as before each imaging session
Treatment:
Diagnostic Test: PET/MRI
Other: Blood and urine sampling
Drug: (64Cu)-labeled PSMA-targeting particle tracer, or 64Cu-NOTA-PSMAi-PEG-Cy5.5-C' dots
Procedure: laparoscopic radical prostatectomy and bilateral pelvic LN dissection or a salvage lymph node dissection

Trial contacts and locations

1

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Central trial contact

Karim Touijer, MD, MPH; Alberto Vargas, MD

Data sourced from clinicaltrials.gov

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