Sarasota Memorial Research Institute Participates in Groundbreaking Prostate Cancer Imaging Study
The study seeks to determine if Copper Cu 64 PSMA I&T Injection can safely and effectively be used to accurately stage prostate cancer by taking precise pictures of tumors in the body. Accurate staging is critical in guiding treatment decisions and improving patient outcomes. The safety and effectiveness of copper Cu 64 PSMA I&T have not been established by the United States Food and Drug Administration.
Participants in the study will undergo a series of evaluations. The process includes a screening visit to review medical history and obtain consent, followed by an imaging day where the injection will be administered, and PET/CT scans will be conducted to capture detailed images of the prostate cancer tumors. Participants will also receive follow-up care to monitor for any side effects and ensure their well-being. If surgery is part of their medical care, information from the procedure may be used in the research study.
"In terms of cancer specific survival, the higher the risk of prostate cancer at the time of diagnosis, the greater the benefit to have a robotic prostatectomy with an extended pelvic lymph node dissection as the first treatment for prostate cancer," said
Inclusion Criteria:
- Male patients aged 18 or older, with histologically confirmed prostate adenocarcinoma.
- Scheduled for prostatectomy with pelvic lymph node dissection.
- Classified as having unfavorable intermediate-risk, high-risk, or very high-risk prostate cancer according to the NCCN Guidelines Version 1.2023 or earlier.
- Able to understand and sign a written informed consent form.
Exclusion Criteria:
- Patients who have received androgen deprivation therapy, neoadjuvant chemotherapy, radiation therapy, local ablation, or any investigational treatment for prostate cancer before the prostatectomy.
- Participation in another interventional clinical trial within the last 30 days or receipt of an investigational product within five biological half-lives before study administration.
- Any medical condition or situation that, in the investigator's opinion, could compromise study data or interfere with study requirements, including inability to undergo a PET scan.
- Planned administration of x-ray contrast within 24 hours, or another PET radiotracer within 10 half-lives, before the PET scan. If barium contrast is used, it must be cleared before the PET scan.
- Administration of high-energy (greater than 300 KeV) gamma-emitting radioisotopes within five half-lives before Copper Cu 64 PSMA I&T administration.
- Known hypersensitivity to the active substance or any excipient of the investigational product.
- Patients who have had a PSMA PET scan as part of standard care within 90 days before enrollment.
Sarasota Memorial Research Institute remains committed to advancing medical research and improving patient care through innovative clinical trials. The Curium 64 Solar Stage Research Study represents a promising opportunity to explore new diagnostic tools that could significantly impact the future of prostate cancer treatment.
For more information about the trial and enrollment criteria, call Sarasota Memorial's Research Institute at (941) 917-2225 or visit the FDA clinical trial webpage at: https://clinicaltrials.gov/study/NCT06235151
About the Sarasota Memorial Research Institute
Sarasota Memorial Research Institute (SMRI) provides advanced research and a highly qualified staff to advance the latest treatment options for patients in the Suncoast community. Located on Sarasota Memorial Health Care System's
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SOURCE Sarasota Memorial Health Care System
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