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Clinical Trials/NCT01522118
NCT01522118
Completed
Phase 1

Focal Therapy With Magnetic Resonance Guided Focused Ultrasound Treatment of Locally Non-Advanced Prostate Cancer: Phase 1 Study

University of Roma La Sapienza1 site in 1 country12 target enrollmentJanuary 2011
ConditionsProstate Cancer

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
University of Roma La Sapienza
Enrollment
12
Locations
1
Primary Endpoint
Safety
Status
Completed
Last Updated
13 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
June 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Sponsor
University of Roma La Sapienza
Responsible Party
Principal Investigator
Principal Investigator

Alessandro Napoli

Assistant Professor

University of Roma La Sapienza

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

Outcomes

Primary Outcomes

Safety

Time Frame: One year

Measure of expected or UN-expected adverse events

Secondary Outcomes

  • Efficacy(18 months)

Study Sites (1)

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