Clinical Trials /

Study of the Efficacy, Safety and Quality of Life After TOOKAD® Soluble (VTP) for Intermediate Risk Prostate Cancer.

NCT03315754

Description:

Single center, single-arm, open-label, 60-month follow-up phase IIb clinical trial. Men with localized prostate cancer will receive TOOKAD® Soluble VTP under general anesthesia. To evaluate the absence of biopsy detectable Gleason grade 4 or 5 prostate cancer tumors anywhere in the prostate gland on 12-month, post-treatment biopsy following TOOKAD® Soluble-VTP in men with prostate cancer Gleason score 7(3+4).

Related Conditions:
  • Prostate Carcinoma
Recruiting Status:

Active, not recruiting

Phase:

Phase 2

Trial Eligibility

Document

Title

  • Brief Title: Study of the Efficacy, Safety and Quality of Life After TOOKAD® Soluble (VTP) for Intermediate Risk Prostate Cancer.
  • Official Title: Study of the Efficacy, Safety and Quality of Life After TOOKAD® Soluble Vascular Targeted Photodynamic Therapy (VTP) for Minimally Invasive Treatment of Localized Intermediate Risk Prostate Cancer.

Clinical Trial IDs

  • ORG STUDY ID: CLIN1601 PCM204
  • NCT ID: NCT03315754

Conditions

  • Localized Prostate Cancer

Interventions

DrugSynonymsArms
TOOKAD Soluble 4 mg/kgWST11TOOKAD Soluble 4 mg/kg

Purpose

Single center, single-arm, open-label, 60-month follow-up phase IIb clinical trial. Men with localized prostate cancer will receive TOOKAD® Soluble VTP under general anesthesia. To evaluate the absence of biopsy detectable Gleason grade 4 or 5 prostate cancer tumors anywhere in the prostate gland on 12-month, post-treatment biopsy following TOOKAD® Soluble-VTP in men with prostate cancer Gleason score 7(3+4).

Detailed Description

      This is a single center, single-arm, open-label, 60-month follow-up phase IIb clinical trial.
      The primary objective of the study is to evaluate the absence of biopsy detectable Gleason
      grade 4 or 5 prostate cancer tumors anywhere in the prostate gland on 12-month,
      post-treatment biopsy following TOOKAD® Soluble-VTP. Men with Gleason score 7 (3+4) prostate
      cancer on one half of the prostate will receive TOOKAD® Soluble VTP under general anesthesia.
      Treatment will consist in hemiablation procedure designed to destroy the lobe of the prostate
      gland that contains the Gleason score 7 (3+4) cancer. Afterwards, patients will be followed
      for 5 years (60 months) with clinical evaluation, questionnaires on QOL, erectile and urinary
      functions, and PSA testing. In addition, treatment outcomes will be assessed based on
      prostate biopsy results at 3, 12, 24, 36, 48 and 60 months after the TOOKAD® Soluble
      treatment. All patients will undergo biopsy at 3 and 12 months. If the Month 3 biopsy is
      positive for any cancer, patients will be allowed a single re-treatment by TOOKAD® Soluble
      VTP to one or both lobes.
    

Trial Arms

NameTypeDescriptionInterventions
TOOKAD Soluble 4 mg/kgExperimentalTOOKAD® Soluble VTP treatment consist of the combination of a single, 10-minute IV infusion of TOOKAD® Soluble at the dose of 4 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.
  • TOOKAD Soluble 4 mg/kg

Eligibility Criteria

        Inclusion Criteria:

          1. Men over 18 years of age.

          2. Patients who have had a multiparametric MRI of the prostate performed and have
             undergone transrectal systematic biopsy plus biopsy of any volumes considered
             suspicious per the MRI (PIRADS version 2 score of 4 or 5) within 6 months before
             signing consent.

          3. Histologic diagnosis of prostate cancer identifying Gleason score of 3+4 on one half
             of the prostate gland in no more than 2 sextants of the prostate gland and not present
             in more than 50% of any one core taken systematically. The involvement criterion does
             not apply to cores taken from MRI suspicious volumes.

          4. Patients with concomitant Gleason score 3+3 prostate cancer in less than 50% of any
             core at any site will be considered eligible.

          5. Prostate cancer stage up to cT2a - N0/Nx - M0/Mx.

          6. Prostate volume ≥25 mL and ≤70 mL.

          7. Serum PSA ≤10 ng/mL.

          8. Men who are sexually active with women of childbearing potential must use
             contraceptive method with a failure rate of less than 1% per year. Contraception
             should be continued for a period of 90 days after the VTP procedure. The individual
             methods of contraception may be determined in consultation

          9. Signed Informed Consent Form.

        Exclusion Criteria:

          1. Unwillingness to accept the treatment;

          2. Any prior or current treatment for prostate cancer, including surgery, radiation
             therapy (external or brachytherapy) or chemotherapy;

          3. Any surgical intervention for benign prostatic hypertrophy;

          4. Any condition or history of illness or surgery that might pose an additional risk to
             men undergoing the VTP procedure;

          5. Life expectancy less than 10 years;

          6. Participation in another clinical study involving an investigational product within 1
             month before study entry;

          7. Inability to understand the informed consent document, to give consent voluntarily or
             to complete the study tasks, especially inability to understand and fulfill the
             health-related QOL questionnaire;

          8. Subjects in custody and or residing in a nursing home or rehabilitation facility;

          9. Biopsy proven locally advanced or metastatic prostate cancer.

         10. Any condition or history of illness or surgery that in the opinion of the investigator
             might affect the conduct and results of the study or pose additional risks to the
             subject (e.g., cardiac or respiratory disease precluding general anesthesia;
             anticoagulant treatment which cannot be temporarily withdrawn for the procedure).

         11. Medical conditions that preclude the use of general anesthesia;

         12. Any condition or history of active rectal inflammatory bowel disease or other factors
             which might increase the risk of fistula formation;

         13. Hormonal manipulation (excluding 5-alpha-reductase inhibitors) that alters androgen
             production within the previous 6 months;

         14. History of urethral stricture disease;

         15. History of acute urinary retention within 6 months of study entry;

         16. Condition requiring medication with potential photosensitizing effects (tetracyclines,
             quinolones, sulphonamides, phenothiazines, sulfonylurea hypoglycaemic agents, thiazide
             diuretics, griseofulvin, and amiodarone) if these treatments could not be stopped at
             least 10 days before and for 3 days after the VTP procedure or replaced by treatments
             without photosensitizing properties;

         17. Anticoagulant drugs (e.g., warfarin) that could not be withdrawn during the 10 days
             prior to the VTP procedure or antiplatelet drugs (e.g. aspirin) that could not be
             withdrawn during the 10 days prior to the VTP procedure and 3 days after VTP;

         18. Renal and hepatic disorders with values of >1.5 times the upper limit of normal (ULN)
             or blood disorders (upon clinician judgment);

         19. A history of sun hypersensitivity or photosensitive dermatitis.
      
Maximum Eligible Age:N/A
Minimum Eligible Age:18 Years
Eligible Gender:Male
Healthy Volunteers:No

Primary Outcome Measures

Measure:absence of Gleason grade 4 or 5
Time Frame:12 months
Safety Issue:
Description:Binary response to treatment defined as absence of Gleason grade 4 or 5 on biopsy

Secondary Outcome Measures

Measure:absence of Gleason grade 4 or 5
Time Frame:months 24, 36, 48 and 60
Safety Issue:
Description:Binary response to treatment defined as the absence of any Gleason grade 4 or 5 biopsy on or before months 24, 36, 48 and 60. If a subject is retreated following a positive biopsy at 3 months and subsequent biopsy shows absence of gleason grade 4 or 5, the subject will be considered to have responded;
Measure:absence of any prostate cancer on biopsy
Time Frame:months 3, 12, 24, 36 and 60
Safety Issue:
Description:Binary response to treatment defined as the absence of any prostate cancer on biopsy on or before months 3, 12, 24, 36 and 60. If a subject is retreated following a positive biopsy at 3 months and subsequent biopsy shows absence of any cancer, the subject will be considered to have responded;
Measure:absence of any Gleason 4 or 5 in the treated lobe
Time Frame:months 12, 24, 36, 48 and 60
Safety Issue:
Description:Binary response to treatment defined as the absence of any Gleason grade 4 or 5 biopsy on or before months 12, 24, 36, 48 and 60 in the treated lobe. If a subject is retreated following a positive biopsy at 3 months and subsequent biopsy shows absence of gleason grade 4 or 5, the subject will be considered to have responded;
Measure:absence of any prostate cancer on biopsy in the treated lobe
Time Frame:months 3, 12, 24, 36, 48 and 60
Safety Issue:
Description:Binary response to treatment defined as the absence of any prostate cancer on biopsy on or before months 3, 12, 24, 36, 48 and 60 in the treated lobe. If a subject is retreated following a positive biopsy at 3 months and subsequent biopsy shows absence of any cancer, the subject will be considered to have responded
Measure:Changes in biopsy parameters (Gleason score)
Time Frame:months 3, 12, 24, 36, 48 and 60
Safety Issue:
Description:Changes in biopsy parameters (Gleason score) between the baseline biopsy and Month 3, Month12, Month 24, Month 36, Month48 and Month 60 biopsies
Measure:Changes in biopsy parameters (number of positive score)
Time Frame:months 3, 12, 24, 36, 48 and 60
Safety Issue:
Description:Changes in biopsy parameters (number of positive score) between the baseline biopsy and Month 3, Month12, Month 24, Month 36, Month48 and Month 60 biopsies
Measure:Changes in biopsy parameters (cancer core length)
Time Frame:months 3, 12, 24, 36, 48 and 60
Safety Issue:
Description:Changes in biopsy parameters (cancer core length) between the baseline biopsy and Month 3, Month12, Month 24, Month 36, Month48 and Month 60 biopsies
Measure:IPSS questionnaire
Time Frame:months 1, 3, 6, 12, 24, 36, 48 and 60
Safety Issue:
Description:Changes in patients' reported outcome measures (PROMs) for urinary symptoms using IPSS (changes in IPSS scores from baseline to 1, 3, 6, 12, 24, 36, 48 and 60 months after treatment)
Measure:IIEF15 questionnaire
Time Frame:months 1, 3, 6, 12, 24, 36, 48 and 60
Safety Issue:
Description:Changes in patients' reported outcome measures (PROMs) for erectile function using IIEF 15 (changes in IIEF 15 scores from baseline to 1, 3, 6, 12, 24, 36, 48 and 60 months after treatment)
Measure:Severe prostate cancer-related events
Time Frame:Up to 60 months
Safety Issue:
Description:Severe prostate cancer-related events: cancer extension to T3, metastasis or prostate cancer-related death
Measure:secondary prostate cancer treatment
Time Frame:Up to 60 months
Safety Issue:
Description:Use of secondary prostate cancer treatment following VTP will include surgical removal of the prostate gland, radiation treatment to the prostate gland, use of hormone or chemotherapies
Measure:Adverse events
Time Frame:Up to 60 months
Safety Issue:
Description:Collection Adverse events
Measure:PSA
Time Frame:Months 1, 3, 6, 12, 24, 36, 48, 60
Safety Issue:
Description:Serum PSA measurements in ng/mL.

Details

Phase:Phase 2
Primary Purpose:Interventional
Overall Status:Recruiting
Lead Sponsor:Steba Biotech S.A.

Last Updated

January 24, 2019