LITT or FLA: Phase II Laser Focal Therapy of Prostate Cancer

Sponsor
Desert Medical Imaging (Industry)
Overall Status
Active, not recruiting
CT.gov ID
NCT02243033
Collaborator
(none)
1,000
1
246
4.1

Study Details

Study Description

Brief Summary

Target recruitment: 1000 subjects. The purpose of this research study is to continue to investigate the safety and effectiveness of using MR (magnetic resonance) guided laser focal therapy for prostate cancer and to evaluate oncologic control over 20 years. We hypothesize that laser focal therapy can be used to achieve oncologic control in carefully selected patients.

MR uses large magnets to produce pictures of areas/organs inside the body. The laser uses light to heat a target area to try to destroy cancerous cells.

The laser system that will be used is called the Visualase® Thermal Therapy System. This system has been used for the treatment of brain, bone (spine), thyroid, and liver cancers. However; this study is the first time this system has been studied for use in the treatment of prostate cancer with a trans-rectal approach.

MR-guided biopsies and laser applicator placement will be performed using the Invivo DynaTRIM trans-rectal biopsy guidance system. This system is cleared (approved) by the U.S. Food and Drug Administration (FDA) for such uses.

Condition or Disease Intervention/Treatment Phase
  • Device: MR-guided laser focal therapy

Detailed Description

Laser-induced interstitial thermal therapy (LITT) is a novel form of controlled, targeted thermal ablation that may offer measurable advantages over other ablative therapies for focal prostate therapy. Because LITT is magnetic resonance (MR) compatible, it enables an imaging advantage over other surgical or ablation techniques that utilize transrectal ultrasound to target and monitor treatment. MR imaging provides excellent soft-tissue contrast and three-dimensional (3D) anatomical imaging in any arbitrary plane, which can help to improve treatment planning and targeting. Additionally, MR-based temperature monitoring allows real-time feedback during MRI-guided thermal therapy as both deposition of light energy and MR signal acquisition can be performed simultaneously without degradation in the MR signal. Also, being in the MR diagnostic environment allows use of post- treatment imaging to verify tissue damage. Because MR images clearly depict the prostate anatomy and the surrounding critical structures, MR imaging has been incorporated into planning for external- beam radiotherapy, brachytherapy, and other treatments of the prostate. In addition to these basic features, Multiparametric prostate MRI (mpMRI) may be used to identify regions of disease in the prostate and better target therapy.

In this study, the investigators propose to evaluate the efficacy of a novel, FDA-approved thermal therapy and feedback system (Visualase® Thermal Therapy System) for the treatment of biopsy confirmed and MR-imageable prostate lesions. This system has been used in humans for the treatment of brain, bone (spine), thyroid, and liver cancers. Early feasibility studies for prostate cancer used a transperineal approach; however it is now being evaluated for the primary treatment of prostate cancer using a transrectal approach. This system allows delivery of laser energy while the patient is simultaneously being imaged by an MRI unit. The system's real-time MR thermal imaging (MRTI) provides information on the thermal dose delivered to the target, resulting in a more precise and controlled delivery which has previously not been possible with other ablative therapies. The investigators hypothesize the system can be integrated into a practical and feasible outpatient treatment paradigm for focal treatment of localized prostate cancer and allow patients to avoid the complications associated with radical whole-gland therapy.

Study Design

Study Type:
Observational
Anticipated Enrollment :
1000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Phase II Study to Evaluate Outpatient Magnetic Resonance Image-guided Laser Focal Therapy for Prostate Cancer, a 20-year Survival Study
Study Start Date :
May 1, 2016
Anticipated Primary Completion Date :
May 1, 2036
Anticipated Study Completion Date :
Nov 1, 2036

Arms and Interventions

Arm Intervention/Treatment
Visualase

MR-guided laser focal therapy

Device: MR-guided laser focal therapy
Placement of laser applicator under MRI guidance and real-time MR thermal imaging of tissue necrosis.
Other Names:
  • Visualase
  • Tranberg
  • Outcome Measures

    Primary Outcome Measures

    1. Safety and adverse events [1 yr. post treatment]

      Number of subjects reporting serious adverse events.

    Secondary Outcome Measures

    1. Efficacy of treatment [1 yr. post treatment]

      MR-guided biopsy results of treated area and PSA.

    Other Outcome Measures

    1. Time to biochemical recurrence [Up to 20 years]

      PSA measurement

    2. Time to metastasis [Up to 20 years]

      Imaging utilizing PET/CT or other modality

    3. Cause of death [Up to 20 years]

      Death certificate or report from partner/spouse/primary care physician

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    45 Years to 90 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    Treatment Naïve patients:
    • Male, 45 years of age or older.

    • Diagnosis of prostate adenocarcinoma.

    • Clinical stage T1c or T2a.

    • Gleason score of 7 (3+4 or 4+3) or less.

    • Three or fewer biopsy cores with prostate cancer.

    • PSA density not exceeding 0.375.

    • One, two, or three tumor suspicious regions identified on multiparametric MRI.

    • Negative radiographic indication of extra-capsular extent.

    • Karnofsky performance status of at least 70.

    • Estimated survival of 5 years or greater, as determined by treating physician.

    • Tolerance for anesthesia/sedation.

    • Ability to give informed consent.

    • At least 6 weeks since any previous prostate biopsy.

    • MR-guided biopsy confirmation of one or more MRI-visible prostate lesion(s) with Gleason score of 7 (3+4 or 4+3) or less.

    Salvage candidates will be accepted upon physician referral.

    Exclusion Criteria:
    • Presence of any condition (e.g., metal implant, shrapnel) not compatible with MRI.

    • Severe lower urinary tract symptoms as measured by an International Prostate Symptom Score (IPSS) of 20 or greater

    • History of other primary non-skin malignancy within previous three years.

    • Diabetes

    • Smoker

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Desert Medical Imaging Indian Wells California United States 92210

    Sponsors and Collaborators

    • Desert Medical Imaging

    Investigators

    • Principal Investigator: John F. Feller, MD, Desert Medical Imaging
    • Study Director: Bernadette M. Greenwood, MSc, Desert Medical Imaging

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Desert Medical Imaging
    ClinicalTrials.gov Identifier:
    NCT02243033
    Other Study ID Numbers:
    • DMI-Laser-001
    • WIRB Pr. No.: 20140945
    First Posted:
    Sep 17, 2014
    Last Update Posted:
    Mar 25, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Keywords provided by Desert Medical Imaging
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 25, 2022