IRE + MRgRT for Prostate Cancer

(RTIRE Trial)

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Overseen ByHolly Kuczynski
Age: 18+
Sex: Male
Trial Phase: Academic
Sponsor: Weill Medical College of Cornell University
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Approved in 2 JurisdictionsThis treatment is already approved in other countries

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.12345

Why 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?

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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

I am a man aged 18 or older.
My gland is smaller than 80 cc.
I am fit for IRE treatment.
See 8 more

Exclusion Criteria

I have had a prostate surgery known as TURP.
I have had radiation therapy to my pelvic area before.
I have had targeted treatment for a specific area of my body.
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Irreversible Electroporation (IRE) Treatment

Participants undergo the NanoKnife procedure under general anesthesia, targeting the prostate for ablation.

1 day
1 visit (in-person)

Radiotherapy (MRgRT)

Participants receive radiotherapy to the prostate and seminal vesicles with a total dose of 32.5 Gy in 5 fractions.

1-2 weeks
5 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment, including assessments at 6 weeks post-MRgRT and 12 weeks post-IRE.

12 weeks
Multiple visits (in-person and virtual)

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.

60 months

What Are the Treatments Tested in This Trial?

Interventions

  • IRreversible Electroporation and Magnetic Resonance guided Radiotherapy
Trial Overview The trial is testing the combination of Irreversible Electroporation (IRE) and Magnetic Resonance guided Radiotherapy (MRgRT) on men with intermediate risk prostate cancer. The goal is to see if this combined treatment can be done safely with low side effects while being effective for patients who meet specific criteria.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: Irreversible Electroporation and RadiotherapyExperimental Treatment1 Intervention

IRreversible Electroporation and Magnetic Resonance guided Radiotherapy is already approved in European Union, United States for the following indications:

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Approved in European Union as IRE for:
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Approved in United States as IRE for:

Find a Clinic Near You

Who Is Running the Clinical Trial?

Weill Medical College of Cornell University

Lead Sponsor

Trials
1,103
Recruited
1,157,000+

Published Research Related to This Trial

In a study of 30 men with localized prostate cancer, focal irreversible electroporation (IRE) demonstrated low urogenital toxicity, with stable erectile function and continence rates at 12 months post-treatment.
The treatment resulted in a significant reduction in prostate-specific antigen (PSA) levels, indicating promising oncologic outcomes, with a 17.9% rate of in-field treatment failure observed at 6 months.
Image-guided Irreversible Electroporation of Localized Prostate Cancer: Functional and Oncologic Outcomes.Collettini, F., Enders, J., Stephan, C., et al.[2020]
In a study of 13 male patients with low-risk prostate cancer, irreversible electroporation (IRE) was performed, showing that the ablation area appeared either homogeneously or heterogeneously hypo attenuating on MRI, indicating different responses to the treatment.
Most patients exhibited a peripheral contrast enhancement after IRE, suggesting reactive hyperemia, which may indicate ongoing vascularization in the treated area, highlighting the need for careful imaging follow-up post-ablation.
Effect of irreversible electroporation of prostate cancer on microcirculation: Imaging findings in contrast-enhanced T1-weighted 3D MRI.Beyer, LP., Pregler, B., Verloh, N., et al.[2018]
Irreversible electroporation (IRE) effectively ablated both healthy canine and cancerous human prostates in preliminary trials, demonstrating its potential as a safe treatment for prostate cancer while minimizing damage to surrounding tissues.
The study identified that the electric field strength required to achieve tissue necrosis in the prostate is significantly higher than previously reported, providing critical data to optimize IRE treatment protocols for better outcomes.
In vivo characterization and numerical simulation of prostate properties for non-thermal irreversible electroporation ablation.Neal, RE., Millar, JL., Kavnoudias, H., et al.[2022]

Citations

Radiation therapy and IRreversible electroporation for ...RTIRE is a phase II clinical trial testing combination of radiation therapy and irreversible electroporation for intermediate risk prostate cancer.
IRE + MRgRT for Prostate Cancer (RTIRE Trial)In a study of 10 patients with localized prostate cancer treated with irreversible electroporation (IRE), there was a significant 73% reduction in prostate- ...
A multi-center international study to evaluate the safety ...For men with localized prostate cancer, IRE could achieve good urinary and sexual function outcomes and a reasonable oncological result. The ...
Irreversible Electroporation for Prostate Tissue Ablation in ...The data from this study demonstrated that the NanoKnife System can be used successfully and safely for prostate tissue ablation in patients ...
mp04-01 radiation therapy and irreversible electroporation ...80% of patients enrolled within eight months, meeting the feasibility endpoint. At 12 months, no cancer was detected by targeted with systematic ...
Irreversible Electroporation (IRE) for Prostate Cancer (PCa) ...In conclusion, in males with localized low–intermediate-risk prostate cancer, IRE had an excellent safety profile and might have positive ...
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