Efficacy and Safety of Pembrolizumab (MK-3475) in Combination With Bacillus Calmette-Guerin (BCG) in High-Risk Non-Muscle Invasive Bladder Cancer (HR NMIBC) (MK-3475-676/KEYNOTE-676)
- Conditions
- on-muscle Invasive Bladder Cancer
- Registration Number
- JPRN-jRCT2031200390
- Lead Sponsor
- Koh Yasuhiro
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 96
1. Have locally and blinded independent central review (BICR)-confirmed histological diagnosis of high risk (HR) non-muscle invasive (T1, high grade Ta and/or CIS) Urothelial Carcinoma (UC) of the bladder
2. Has undergone cystoscopy/ transurethral resection of bladder tumor (TURBT) to remove all resectable disease
3. Has provided tissue for biomarker analysis
4. Has Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2
5. Has adequate organ function
6. During the treatment period and for >=7 days after the last dose of BCG, male participants are EITHER abstinent from heterosexual intercourse as their preferred and usual lifestyle and agree to remain abstinent, OR, must agree to use contraception unless confirmed to be azoospermic
7. Female participants who are not pregnant, not breastfeeding, and either not a woman of child bearing potential (WOCBP); or are a WOCBP who agrees to use a contraception method that is highly effective or remains abstinent from heterosexual intercourse during the treatment period and for >=7 days after the last dose of BCG or 120 days after the last dose of pembrolizumab, whichever comes last
BCG Post-induction Cohort (Cohort A) Only
8. Has been treated with one adequate course of BCG induction therapy for the treatment of HR NMIBC
9. Following adequate BCG induction therapy, must have persistent or recurrent HR NMIBC
1. Has a history of or concurrent locally advanced (i.e., T2, T3, T4) or metastatic UC
2. Has concurrent extra-vesical (ie, urethra, ureter, renal pelvis) non-muscle invasive urothelial carcinoma or a history of extra-vesical non-muscle invasive UC
3. Has received prior therapy with anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor
4. Has received prior systemic anti-cancer therapy including investigational agents within 4 weeks of start of study treatment
5. Is currently participating in or has participated in a study of an investigational agent or has used an investigational device within 4 weeks of start of study treatment
6. Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy or any other form of immunosuppressive therapy within 7 days of start of study treatment
7. Has a known additional malignancy that is progressing or requires active treatment within the past 3 years
8. Has an active autoimmune disease that has required systemic treatment in past 2 years
9. Has a history of (non-infectious) pneumonitis that required steroids or has current pneumonitis
10. Has one or more of the following contraindications to BCG: prior BCG sepsis or systemic infection, total bladder incontinence, or an adverse experience to a previous BCG instillation that resulted in treatment discontinuation and precludes retreating with BCG
11. Has an active infection requiring systemic therapy
12. Has a known history of human immunodeficiency virus (HIV) infection
13. Has a known history of Hepatitis B or known active Hepatitis C virus infection
14. Has current active tuberculosis
15. Has had an allogenic-tissue/solid organ transplant
16. Has any contraindication(s) to IV contrast or is otherwise unable to have computed tomography urography (CTU) imaging with IV contrast performed
BCG Post-induction Cohort (Cohort A) Only
17. Has persistent T1 disease following an induction course of BCG
BCG Naive Cohort (Cohort B) Only
18. Has received any prior treatment with BCG for their NMIBC within the past 2 years prior to study entry
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cohort A: Complete response rate (CRR) in participants with CIS<br>Cohort B: Event Free Survival (EFS)
- Secondary Outcome Measures
Name Time Method EFS, Recurrence-free survival (RFS), Overall survival (OS), Disease-specific survival (DSS), Time to cystectomy, Duration of Response (DOR), Safety and tolerability, Changes from baseline and Time to true deterioration (TTD) in Health-related quality of life (HRQoL), CRR in participants with CIS (Cohort B only)