IRE + MRgRT for Prostate Cancer
(RTIRE Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new treatment approach for men with intermediate-risk prostate cancer. It combines two methods: Irreversible Electroporation (IRE), which uses electrical pulses to target cancer cells, and Magnetic Resonance guided Radiotherapy (MRgRT), which uses MRI scans for precise radiation treatment. Researchers aim to determine if this combined therapy is safe and effective. Men diagnosed with intermediate-risk prostate cancer who can undergo both IRE and MRI-guided radiotherapy may be suitable for this study. As an unphased trial, this study allows participants to contribute to groundbreaking research that could lead to innovative prostate cancer treatments.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
What prior data suggests that this combined treatment is safe for prostate cancer patients?
Research has shown that Irreversible Electroporation (IRE) is generally safe for men with localized prostate cancer, leading to positive outcomes for urinary and sexual health. For patients with low to intermediate risk prostate cancer, IRE is considered very safe.
Magnetic Resonance guided Radiotherapy (MRgRT) is also part of this treatment. Evidence suggests that combining IRE with MRgRT can be done safely. Although detailed information on side effects might not be available, past patients have tolerated these procedures well.
Overall, the combination of IRE and MRgRT appears well-tolerated with low risks, indicating that the treatment is safe for those considering joining a trial.12345Why are researchers excited about this trial?
Researchers are excited about the combination of Irreversible Electroporation (IRE) and Magnetic Resonance guided Radiotherapy (MRgRT) for prostate cancer because it offers a novel approach compared to traditional treatments like surgery, hormone therapy, and conventional radiotherapy. IRE uses electrical pulses to create tiny holes in cancer cells, leading to their destruction without harming surrounding healthy tissue. MRgRT leverages real-time MRI imaging to precisely target and deliver radiation, enhancing accuracy and sparing nearby organs. This combination could potentially improve treatment outcomes and minimize side effects, offering a more tailored and less invasive option for patients.
What evidence suggests that this trial's treatments could be effective for prostate cancer?
This trial will evaluate the combination of two treatments, irreversible electroporation (IRE) and magnetic resonance-guided radiotherapy (MRgRT), for treating prostate cancer. Research has shown that IRE led to a 73% drop in prostate-specific markers, indicating a strong effect on cancer cells. Another study found that IRE helped maintain good urinary and sexual function, which is important for quality of life. Additionally, targeted scans found no cancer in patients 12 months after receiving this combined treatment. These findings suggest that IRE and MRgRT could be effective for patients with intermediate-risk prostate cancer.12346
Who Is on the Research Team?
Timothy McClure, MD
Principal Investigator
Weill Medical College of Cornell University
Are You a Good Fit for This Trial?
Men over 18 with intermediate risk prostate cancer, specifically grade group 2 or 3 as seen in MRI. They must be able to undergo IRE and MRgRT treatments, have a prostate gland size under 80 cc, an ECOG performance status of 0-1 (fully active or restricted in physically strenuous activity), and agree to follow-up biopsies. Excluded are those with metastatic cancer, prior pelvic radiotherapy or focal therapy, inflammatory bowel disease, TURP history, general anesthesia risks, or urethral strictures.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Irreversible Electroporation (IRE) Treatment
Participants undergo the NanoKnife procedure under general anesthesia, targeting the prostate for ablation.
Radiotherapy (MRgRT)
Participants receive radiotherapy to the prostate and seminal vesicles with a total dose of 32.5 Gy in 5 fractions.
Follow-up
Participants are monitored for safety and effectiveness after treatment, including assessments at 6 weeks post-MRgRT and 12 weeks post-IRE.
Long-term Follow-up
Participants are assessed for changes in prostate multiparametric MRI and quality of life measures every 3 months up to 60 months.
What Are the Treatments Tested in This Trial?
Interventions
- IRreversible Electroporation and Magnetic Resonance guided Radiotherapy
IRreversible Electroporation and Magnetic Resonance guided Radiotherapy is already approved in European Union, United States for the following indications:
- Prostate cancer
- Prostate cancer
- Soft tissue ablation
Find a Clinic Near You
Who Is Running the Clinical Trial?
Weill Medical College of Cornell University
Lead Sponsor