Low Risk Prostate Cancer
Conditions
Brief summary
Multiple center, single-arm, open-label, 12-month follow-up phase IV pragmatic clinical trial in men with unilateral prostate cancer meeting eligibility criteria for the drug (as per the European Economic Area (EEA) Marketing Authorisation) to assess the occurrence and dynamics of the time with toxicities (urinary incontinence Grade 2 and over and/or erectile dysfunction Grade 2 and over) in patients 12 months following TOOKAD® VTP.
Detailed description
This is a multiple center, single-arm, open-label, 12-month follow-up phase IV pragmatic clinical trial. Men with unilateral prostate cancer meeting eligibility criteria for the drug (as per the EEA Marketing Authorisation) will receive TOOKAD® VTP under general anesthesia. The primary objective is to assess the occurrence and dynamics of the time with toxicities (urinary incontinence Grade 2 and over and/or erectile dysfunction Grade 2 and over) in patients 12 months following TOOKAD® VTP. Prior to the TOOKAD® VTP, patients will undergo routine ultrasound examination in the operating room for morphometric description of the prostate and to facilitate accurate treatment guidance for the treatment with TOOKAD® VTP. Treatment will then be applied to the prostate gland as a hemi-ablation procedure designed to destroy the lobe of the prostate gland that contains the cancer. Afterwards, patients will be followed for 12 months with clinical evaluation, data collection on erectile and urinary functions at 1, 2, 3 6 and 12 months, using the Expanded Prostate Cancer Index Composite (EPIC), International Index of Erectile Function (IIEF) and International Prostate Score Symptom (IPSS) questionnaires on Quality Of Life (QOL) and Prostate Specific Antigen (PSA) testing at 3, 6 and 12 months. The clinical follow-up of patients will follow local standard of care processes, based on recommendations in the European Summary of Product Characteristics (SmPC). This study is a phase IV pragmatic trial using optimal dose of TOOKAD® and optimal light-energy level conditions that were determined during development and approved by the European Commission.
Interventions
DRUGTOOKAD VTP
TOOKAD® VTP consists of the combination of a single, 10-minute IV infusion of TOOKAD® at the dose of 3.66 mg/kg, followed by the illumination of the zone to be treated with a 753-nm laser light delivered through transperineal interstitial optical fibers at a power of 150 mW/cm and light energy of 200 J/cm applied over 22 minutes and 15 seconds.
Sponsors
International Drug Development Institute
PrimeVigilance Ltd., UK
Steba Biotech S.A.
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Multiple center, single-arm, open-label, 12-month follow-up phase IV pragmatic clinical trial.
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Men over 18 years of age with a life expectancy ≥ 10 years -.Unilateral adenocarcinoma of the prostate accurately located and confirmed as unilateral using high resolution biopsy strategies based on current best practice, such as multi- parametric MRI based strategies or template-based biopsy procedures. * Clinical stage T1c or T2a, * Gleason Score ≤ 6, based on high-resolution biopsy strategies * 3 positive cancer cores with a maximum cancer core length of 5 mm in any one core or 1 -2 positive cancer cores with ≥ 50 % cancer involvement in any one core or a PSA density ≥ 0.15 ng/mL/cm3. * PSA ≤ 10 ng/mL * If the patient is sexually active with women who are capable of getting pregnant, he and/or his partner should use an effective form of birth control to prevent getting pregnant during a period of 90 days after the VTP procedure. * Signed Informed Consent Form
Exclusion criteria
GENERAL
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Cumulated time with toxicity (duration) | 12 months | Time to onset, average duration and average time to resolution (either Erectile Dysfunction (ED) and/or Urinary Incontinence(UI)) during the 12 months following VTP of ED with severity grade 2 or over and/or UI of severity grade 2 or over, as assessed using the EPIC instrument |
| Cumulated time with toxicity (prevalence) | 12 months | Prevalence at different points in time (either ED and/or UI) during the 12 months following VTP of ED with severity grade 2 or over and/or UI of severity grade 2 or over, as assessed using the EPIC instrument. |
| Cumulated time with toxicity (area under the curve) | 12 months | Area under the curve with the presence of ED with severity grade 2 or over and/or UI of severity grade 2 or over, as assessed using the EPIC instrument |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Time with urinary incontinence (duration) | 12 months | Time to onset, duration, time to resolution of urinary Incontinence grade 2 or above, as assessed using the EPIC instrument, |
| Time with urinary incontinence (prevalence) | 12 months | Prevalence at different points in time of urinary Incontinence grade 2 or above, as assessed using the EPIC instrument. |
| Time with urinary incontinence (Area under the curve) | 12 months | Area under the curve with the presence of urinary Incontinence grade 2 or above, as assessed using the EPIC instrument. |
| Correspondence between results of EPIC and IIEF instruments | 12 months | Average variation on urinary symptoms (UI) using the EPIC and IPSS instruments, erectile functions (ED) using the EPIC and IIEF instruments, and bowel function using the EPIC instrument, prior to treatment beginning and then at 1, 2, 3, 6 and 12 months after completing treatment: absolute scores and changes as compared to baseline (absolute difference of means and proportion change) |
| Time with erectile dysfunction (prevalence) | 12 months | Prevalence at different points in time of erectile dysfunction grade 2 or above, as assessed using the EPIC instrument |
| Rate of Adverse Events | 12 months | Rate of adverse events (AE) of TOOKAD® VTP treatment : all AE, important AE identified in Risk Management Plan (RMP) and suspected AE listed in RMP. |
| Time to resolution of Adverse events | 12 months | Time to resolution of adverse events for each adverse event reported |
| Additional prostate cancer treatments | 12 months | Rate of additional treatment as decided by local practice, such as radical therapy (surgical removal of the prostate gland, radiation treatment to the prostate gland) or other intervention therapy to the ipsilateral and/or contralateral lobe, use of hormone or chemotherapies. |
| Extension of prostate cancer | 12 months | Rate of reported extension of prostate cancer based on locally decided investigations (such as clinical examination, biopsy, Magnetic resonance Imaging (MRI), other). |
| PSA density | 12 months | Average changes from baseline in PSA density at month 12 |
| Time with erectile dysfunction (duration) | 12 months | Time to onset, duration, time to resolution of erectile dysfunction grade 2 or above, as assessed using the EPIC instrument |
| Time with erectile dysfunction (Area under the curve) | 12 months | Area under the curve with the presence of erectile dysfunction grade 2 or above, as assessed using the EPIC instrument |
Countries
France
Outcome results
None listed