Dutasteride in Patients With Low Grade Non-muscle Invasive Bladder Cancer

Official title

A Phase II Prospective Single-arm Study of Dutasteride in Patients With Low Grade Non-muscle Invasive Bladder Cancer

Overview

Low grade non-muscle-invasive bladder cancer (NMIBC) often recurs after treatment, requiring repeated surgeries, especially in older patients. These recurrences can cause complications, reduce quality of life, and increase healthcare costs. Currently, there is no well-tolerated preventive treatment routinely used for patients with low-risk disease. This study will evaluate whether dutasteride, an oral medication that blocks androgen activity, can reduce the risk of bladder cancer recurrence. Dutasteride is generally well tolerated and easy to take. The study will also assess its safety in women. The goal of this study is to determine whether dutasteride can provide a simple and effective way to prevent recurrences of low grade non-muscle invasive bladder cancer.

Detailed description

The study will therefore include two separate cohorts of men (n=70) and women (n=25).

After the screening phase, eligible male and female patients who provide informed consent will receive dutasteride at a dose of 0.5 mg once daily for the duration of the study. All participants will follow the same treatment regimen.

Treatment will be continued until tumor recurrence or for up to two years in the absence of recurrence. Prior data suggests a long-term mecanism of action of dutasteride in preventing tumor recurrences. Therefore, in the event of tumor recurrence, patients will be offered the option to continue dutasteride treatment for a total duration of up to two years. The decision to continue or discontinue treatment, as well as the reasons for this decision, will be documented.

Regarding analyses, the male cohort is designed to provide the first prospective data on efficacy; data will be compared to a historical control cohort, while also collecting adherence and safety data specific to men with low grade NMIBC.

The parallel female cohort is primarily intended to assess feasibility of recruitment and safety. In the published literature and our own institutional data, women represent approximately 25% of patients with low grade NMIBC. Recruitment of female patients is therefore more challenging, compounded in part by the limited safety data available and the absence of demonstrated urinary benefits. Consequently, this cohort aims to determine whether inclusion of women in a subsequent phase 3 study will be feasible and safe.

Interventions

• Drug Dutasteride (0.5mg)
  Dutasteride 0.5 mg orally once daily. Treatment begins after enrollment and continues for 2 years or until tumor recurrence. Patients may opt to continue treatment after recurrence for a total of 2 years.

Primary outcome measures

• Incidence of NMIBC recurrences in patients treated with dutasteride [Time frame: From enrolment until first recurrence or 4 years of extended follow-up, whichever occurs first]

Secondary outcome measures (8)

• Time to surgery [Time frame: From enrolment until surgery for suspected recurrence of bladder cancer or 4 years of extended follow-up, whichever occurs first]
• Incidence of tumour progression [Time frame: From enrolment until first progression or 4 years of extended follow-up, whichever occurs first]
• Number of tumour recurrences: [Time frame: From enrolment until first recurrence or 4 years of extended follow-up, whichever occurs first]
• Number of tumours at recurrence [Time frame: From enrolment until first recurrence or 4 years of extended follow-up, whichever occurs first]
• Concordance of cystoscopic recurrence with pathologic recurrence [Time frame: From enrolment until 4 years of extended follow-up, whichever occurs first]
• Quality of life assessed by the European Organisation for Research and Treatment of Cancer(EORTC) Quality of Life Questionnaire (QLQ) non-muscle invasive bladder cancer questionnaire(NMIBC) module 24 [Time frame: From enrolment to 24 months (end of treatment)]
• Urinary symptoms assessed by Bladder Utility Symptom Score (BUSS) [Time frame: From enrollment until 2 years (end of treatment)]
• Urinary symptoms assessed by the Internation Prostate Symptom Score (IPSS) questionnaire [Time frame: From enrollment until 2 years (end of treatment)]

Eligibility criteria

Inclusion criteria

• Patients aged 18 or greater;
• Patients with histologically confirmed low grade non-muscle invasive urothelial carcinoma. Patients with any mix of low- and high-grade urothelial carcinoma remain eligible given the frequent histological heterogeneity and the presence of a low grade component;
• Patients have not been recommended for a course of intravesical BCG or chemotherapy induction treatment by their urologist;
• Male patients with partners of child-bearing potential must agree to 2 acceptable forms of birth control and be continued for at least 6 months after study drug is discontinued.

Exclusion criteria

• Patients who are scheduled to receive BCG therapy or have received BCG therapy within the last 5 years will be ineligible for enrollment.
• Patients who are scheduled to receive intravesical chemotherapy or have received an induction course of intravesical chemotherapy within the last 5 years will be ineligible for enrollment. Patients who received a single, post-operative (<24h) intravesical chemotherapy (e.g. gemcitabine, epirubicin or mitomycin C) dose are eligible.
• Patients with clinical hypogonadism, those on androgen replacement therapy, or those with prostate cancer or other diseases treated with various forms of hormonal therapy will be ineligible for study enrollment.
• Patients receiving 5-alpha-reductase inhibitors within the last 2 years are ineligible for enrollment.
• Patients with a history of allergy or severe adverse reaction to finasteride or dutasteride are ineligible for enrollment.
• Patients with a history of liver disease whose hepatic enzymes, alkaline phosphatase or bilirubin are greater than twice the upper limit of normal will be ineligible. Nonetheless, patients with Gilbert's disease may be accepted in the study.
• Patients with multiple hospital admissions for heart failure within the previous 12 months or who have unstable cardiovascular status will be ineligible for enrolment.
• Female patients with child-bearing potential are ineligible for enrollment, which is defined as any female under 50 years of age. Exceptions to this age limit may be permitted on a case-by-case basis by the Principal Investigator, based on documented confirmation that there is no child-bearing potential (such as a female without a uterus).
• Patients receiving chronic treatment with potent CYP3A4 inhibitors, including but not limited to ritonavir, ketoconazole, verapamil, diltiazem, cimetidine, troleandomycine, or ciprofloxacin, are ineligible for participation in the study. Occasional use of CYP3A4 inhibitors such as ciprofloxacin for an infection is not prohibited.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

Canada · 1 center

• CHU de Québec - Université Laval — Québec

Identifiers

NCT: NCT07420517 · MP-20-2026-8412

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗