Phase 1 Study of MRI Targeted Focal Laser Thermal Therapy of Biopsy Confirmed Prostate Cancer

University Health Network, Toronto1 site in 1 country12 target enrollmentMarch 2007

ConditionsProstate Cancer

Overview

Phase: Phase 1
Intervention: Not specified
Conditions: Prostate Cancer
Sponsor: University Health Network, Toronto
Enrollment: 12
Locations: 1
Primary Endpoint: validated self assessment tools of urinary, rectal, erectile function.
Status: Completed
Last Updated: 13 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

The objective of this study is to establish the safety of MRI targeted laser thermal treatment for men with biopsy confirmed early stage low grade single sector prostate cancer.

Detailed Description

This is a single center, single arm, open-label Phase I study to establish the safety of interstitial laser thermal therapy (ILTT) in patients with a single site of low grade (Gleason \<7) prostate cancer who have not yet received treatment for their cancer. No control group will be utilized and all patients will receive laser thermal therapy. The patient will undergo multimode MRI to determine if a single site of prostate cancer can be localized by this technique and to localize the tumor in 3 dimensions within the prostate. A multicore (12 + cores) mapping transrectal ultrasound guided biopsy of the prostate would then confirm that no other sites of cancer exist. Each patient will complete quality of life and performance questionnaires. ILLT will be performed under general anesthetic in a procedure similar to brachytherapy, using transrectal ultrasound to guide insertion of the laser and monitoring probes into the sector containing the cancer as visualized by the MR scan. Following the procedure, patients will be assessed for clinical signs of urinary, rectal, and erectile complications and will complete validated self-assessment tools on these functions. MRI at 7 days and MRI and biopsy at 6 months will be used to assess the extent of tissue effect and presence of cancer due to ILTT. Patients will remain on standard Watchful Waiting surveillance for any further sign of disease progression. ILLT will not restrict any future treatment of prostate cancer. To minimize the treatment risk, participants in the trial will be staged according to location of the disease in the prostate. The first 3 participants recruited to the trial will have targeted loci well separated from the urethra, erectile nerves and the rectum, and so treatment in this region poses minimal risk of injury to these vital structures. Lesions sizes measured in this initial stage will be used in planning fiber placement in the three remaining stages, in which fiber placement is closer to critical structures such as the urethra (Stage 2), erectile nerves (Stage 3) and rectum (Stage 4).

Registry

clinicaltrials.gov

Start Date

March 2007

End Date

October 2008

Last Updated

13 years ago

Study Type

Interventional

Study Design

Single Group

Sex

Male

Investigators

Sponsor

University Health Network, Toronto

Eligibility Criteria

Inclusion Criteria

•Men \> 18 years of age;
•Histologically-proven prostate carcinoma;
•Prostate cancer clinical stage T1c
•Only one sector of the prostate demonstrating prostate cancer with no more than 1 core positive
•Gleason score \<7 ;
•Each core must range between of 10 to 50% adenocarcinoma.
•Prostate MRI must confirm area suspicious for cancer in the sector of the positive biopsy;
•A minimum of six (6) weeks between the prostate biopsy and the Inclusion Visit;
•Prostate specific antigen (PSA) level £ 10 ng/mL
•PORPUS, IPSS, and IIEF complete prior to procedure

Exclusion Criteria

•Patients with any of the following exclusion criteria will be excluded from study participation:
•Patients who are unwilling or unable to give informed consent;
•Patients with foci location in the Apex of the prostate or isolated transition zone cancers
•Patients who have received androgen suppression therapy
•Patients who have received or are receiving chemotherapy for prostate carcinoma;
•Patients previously treated with surgery to the prostate (traditional, endoscopic or minimally invasive including HIFU, TUNA, RITA, microwave, TURP ,cryotherapy or any curative treatment
•Patients whose has undergone radiation therapy for prostate cancer
•Any condition, or history of illness or surgery that, in the opinion of the Investigator , might confound the results of the study or pose additional risks to the patient (e.g. significant cardiovascular conditions or allergies);
•Patients with a history of non compliance with medical therapy and/or medical recommendations;
•Patients who are unwilling or unable to complete the patient self-assessment questionnaires;