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MR-guided Focused Ultrasound Treatment of Prostate Cancer: Focal Therapy for Locally Non-Advanced Disease

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Phase 1
Locations
Italy
Study Type
Interventional
Intervention
ExAblate 2100; InSightec
Sponsored by
University of Roma La Sapienza
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Prostate Cancer focused on measuring Prostate Cancer, High Intensity Focused Ultrasound, Magnetic Resonance guided Focused Ultrasound, Non-invasive therapy, Focal Disease

Eligibility Criteria

40 Years - 85 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient of age between 40 to 85
  • Patient with organ-confined Pca (cT1c and cT2a, N0, M0), diagnosed with TRUS biopsy (min:12 cores)
  • Patient with PSA ≤ 10 ng/mL
  • Gleason score 6 (3+3) or max 7 (3+4)
  • Up to two (2) MR identifiable lesions
  • No definite evidence of extracapsular extension

Exclusion Criteria:

  • Patient under medications that can affect PSA for the last 3 months prior to MRgFUS treatment (Androgen Deprivation Treatment; alpha reductase inhibitors)
  • Any rectal pathology, anomaly or previous treatment
  • Identified calcification of 2 mm or more in largest diameter neighboring the rectal wall
  • Bladder cancer
  • Seminal vesicle/lymph node
  • Prostate with multiple cystic lesions

Sites / Locations

  • Department of Radiological Sciences, Sapienza University of Rome

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

HIFU

Arm Description

(high intensity focused ultrasound)

Outcomes

Primary Outcome Measures

Safety
Measure of expected or UN-expected adverse events

Secondary Outcome Measures

Efficacy
Measure of ablated area in terms of necrosis vs residual tumor

Full Information

First Posted
January 23, 2012
Last Updated
February 25, 2013
Sponsor
University of Roma La Sapienza
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1. Study Identification

Unique Protocol Identification Number
NCT01522118
Brief Title
MR-guided Focused Ultrasound Treatment of Prostate Cancer: Focal Therapy for Locally Non-Advanced Disease
Official Title
Focal Therapy With Magnetic Resonance Guided Focused Ultrasound Treatment of Locally Non-Advanced Prostate Cancer: Phase 1 Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2013
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
February 2012 (Actual)
Study Completion Date
June 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Roma La Sapienza

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Since prostate specific antigen (PSA) was introduced as a clinical screening tool for prostate cancer, more men are diagnosed with small foci of cancers instead of the advanced disease. The present choice of treatment for men with localized prostate cancer lies between active surveillance and radical therapy. Thus, the option of treating only the cancer within the prostate gland and sparing the non-cancerous tissue is quite appealing, yet very controversial. At present there are no consistent scientific data on focal therapy and its major effectiveness. Focal therapy for prostate cancer is defined as therapy that selectively ablates known disease while preserving existing functions, with the overall aim of minimizing lifetime morbidity without compromising life expectancy. The aim of the investigators study is to test if Magnetic Resonance guided Focused Ultrasound ablation can determine non-invasive necrosis of focal, locally non-advanced prostate cancer. The study i designed as Phase 1, treatment & resection protocol. With this project the investigators further aim to evaluate the safety and identify side effects of Magnetic Resonance guided Focused Ultrasound in treating focal prostate cancer. This design will also expand knowledge of the effect of Magnetic Resonance guided Focused Ultrasound onto peri-prostatic environment and to determine if surgery can safely be adopted after this non-invasive treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate Cancer, High Intensity Focused Ultrasound, Magnetic Resonance guided Focused Ultrasound, Non-invasive therapy, Focal Disease

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HIFU
Arm Type
Experimental
Arm Description
(high intensity focused ultrasound)
Intervention Type
Device
Intervention Name(s)
ExAblate 2100; InSightec
Intervention Description
Patients with biopsy proven locally non-advanced T2 prostate cancer identified at 3T MR examination including dynamic contrast enhanced (DCE-with time to peak and mean transit time evaluation) and candidate to radical prostatectomy will undergo Magnetic Resonance guided Focused Ultrasound (MRgFUS) ablation. The procedure is carried out either under general anesthesia or spinal block. MR images allow correct identification of the target as well as vital structure to avoid during energy delivery. Treatment safety and efficacy is monitored in real time using MR thermometry. Adjustments of energy direction and intensity can be made according to the real time monitoring. Pre- and post-ablative MR examinations will serve to analyze differences of DCE features of the neoplastic tissue; therapy-induced alterations will also be compared to histopathology findings from whole section prostate specimens
Primary Outcome Measure Information:
Title
Safety
Description
Measure of expected or UN-expected adverse events
Time Frame
One year
Secondary Outcome Measure Information:
Title
Efficacy
Description
Measure of ablated area in terms of necrosis vs residual tumor
Time Frame
18 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient of age between 40 to 85 Patient with organ-confined Pca (cT1c and cT2a, N0, M0), diagnosed with TRUS biopsy (min:12 cores) Patient with PSA ≤ 10 ng/mL Gleason score 6 (3+3) or max 7 (3+4) Up to two (2) MR identifiable lesions No definite evidence of extracapsular extension Exclusion Criteria: Patient under medications that can affect PSA for the last 3 months prior to MRgFUS treatment (Androgen Deprivation Treatment; alpha reductase inhibitors) Any rectal pathology, anomaly or previous treatment Identified calcification of 2 mm or more in largest diameter neighboring the rectal wall Bladder cancer Seminal vesicle/lymph node Prostate with multiple cystic lesions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
alessandro napoli, MD, PhD
Organizational Affiliation
Department of Radiological Sciences, Sapienza University of Rome
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Radiological Sciences, Sapienza University of Rome
City
Rome
ZIP/Postal Code
00100
Country
Italy

12. IPD Sharing Statement

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MR-guided Focused Ultrasound Treatment of Prostate Cancer: Focal Therapy for Locally Non-Advanced Disease

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