A Phase II Trial of Bicalutamide in Patients Receiving Intravesical BCG for Non-muscle Invasive Bladder Cancer
Non-Muscle Invasive Bladder CancerThis is a phase II randomized controlled clinical trial comparing standard induction BCG versus bicalutamide and standard induction BCG among patients with non-muscle invasive bladder cancer.
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Conditions de participation
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Sexe:
MALE -
Âges admissibles:
18 and up
Critères de participation
Inclusion Criteria:
1. Males, age 18 or greater.
2. Patients with histologically confirmed non-muscle invasive urothelial carcinoma.
3. Patients have been recommended for a course of intravesical BCG induction treatment by their urologist
4. Patients who received gemcitabine, epirubicin or mitomycin C instillations immediately post-operatively will be eligible for enrollment.
5. Patients with partners of child-bearing potential must agree to 2 acceptable forms of birth control and be continued for at least 3 months after study drug is discontinued.
Exclusion Criteria:
1. Patients who have received induction BCG therapy within the last 5 years will be ineligible for enrolment.
2. Patients with a history of myocardial infarction or hospital admission for heart failure within the previous 12 months or who have unstable cardiovascular status will be ineligible for enrolment.
3. Patients who have uncontrolled hypertension (for our purposes, defined as those having a systolic blood pressure \> 160 documented on 2 occasions despite appropriate medical therapy) will similarly be ineligible.
4. 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.
5. Patients with clinical hypogonadism, those on androgen replacement therapy, or those with prostate cancer or other diseases treated with systemic hormonal therapy will be ineligible for study enrolment. Patients receiving 5ARIs will not be excluded.
6. Patients who have cancer treatment ongoing or planned in the near future which can be anticipated to decrease their 2-year survival or BCa treatment plan will be ineligible.
7. Patients taking an investigational drug within 2 weeks of enrolment into this study will be ineligible.
8. Patients receiving or planning to receive coumadin therapy will be ineligible.
Lieu de l'étude
Centre intégré universitaire de santé et services sociaux du Saguenay-Lac-Saint-Jean
Centre intégré universitaire de santé et services sociaux du Saguenay-Lac-Saint-JeanChicoutimi, Quebec
Canada
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University Health Network, Princess Margaret Cancer Centre
University Health Network, Princess Margaret Cancer CentreToronto, Ontario
Canada
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CIUSSS de l'Estrie - CHUS
CIUSSS de l'Estrie - CHUSSherbrooke, Quebec
Canada
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Centre Hospitalier de l'Université De Montréal_CHUM
Centre Hospitalier de l'Université De Montréal_CHUMMontréal, Quebec
Canada
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Jean-Baptiste Lattouf, MD
London Health Sciences Centre
London Health Sciences CentreLondon, Ontario
Canada
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McGill University Health Centre_CUSM
McGill University Health Centre_CUSMMontréal, Quebec
Canada
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Centre intégré de santé et services sociaux de Chaudière Appalaches
Centre intégré de santé et services sociaux de Chaudière AppalachesLévis, Quebec
Canada
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CHU de Québec-Université Laval
CHU de Québec-Université LavalQuébec, Quebec
Canada
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- Étude parrainée par
- CHU de Quebec-Universite Laval
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT05327647