EV + Toripalimab vs GC as Neoadjuvant Therapy in Locally Advanced/High-Risk MIBC
A Phase II, Two-arm, Open-label, Multicenter, Randomized Controlled Clinical Study Evaluating the Safety and Efficacy of Enfortumab Vedotin Combined With Toripalimab Versus Gemcitabine Combined With Cisplatin in the Neoadjuvant Treatment of Patients With Locally Advanced/High-risk Muscle-invasive Bladder Cancer
Przegląd badań
Status
Status
Warunki
Warunki
Interwencja / Leczenie
Interwencja / Leczenie
Typ studiów
Typ studiów
Zapisy (Szacowany)
Zapisy
Faza
Faza
- Faza 2
Kontakty i lokalizacje
Lokalizacje studiów
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Beijing Municipality
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Beijing, Beijing Municipality, Chiny, 100191
- Rekrutacyjny
- Peking University Third Hospital
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Kontakt:
- Clinical Trial Office
- Numer telefonu: +86 10 8226 5573
- E-mail: bysy@bjmu.edu.cn
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Kryteria uczestnictwa
Kryteria kwalifikacji
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Opis
Inclusion Criteria:
- Voluntarily agree to participate in the study and sign the informed consent form (ICF).
- Age ≥ 18 and ≤ 80 years at the time of signing the ICF.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Histologically confirmed muscle-invasive urothelial carcinoma of the bladder, with variant histology components comprising < 50%.
- Radiographically confirmed non-metastatic urothelial carcinoma (M0). Clinical stage must be locally advanced or possess high-risk features, including at least one of the following: clinical stage cT3-T4aNxM0, or definitive high-risk cT2 (e.g., accompanied by tumor-related hydronephrosis, lymphovascular invasion).
- Participants must be evaluated as fit for and scheduled to undergo radical surgery, and clinically fit to tolerate cisplatin-based chemotherapy.
- Able to provide tumor tissue samples (at least 5 unstained slides, or paraffin scrolls/blocks).
- Expected life expectancy of at least 12 weeks.
- Adequate organ function, defined by the following laboratory values (obtained without blood transfusion within 14 days or growth factor support within 7 days prior to testing): Absolute neutrophil count (ANC) ≥ 1.5 × 10^9/L; Platelet count (PLT) ≥ 100 × 10^9/L; Hemoglobin (Hb) ≥ 90 g/L; Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3 × Upper Limit of Normal (ULN); Total bilirubin (TBIL) ≤ 1.5 × ULN; International Normalized Ratio (INR) ≤ 1.5 × ULN; Creatinine clearance ≥ 60 mL/min (calculated using the Cockcroft-Gault formula); Left ventricular ejection fraction (LVEF) ≥ 50%; QTcF interval ≤ 480 ms.
- Female participants of childbearing potential must have a negative serum pregnancy test within 7 days prior to the first dose of study treatment and must be willing to use highly effective contraception during the study and for 180 days after the last dose.
- Male participants with female partners of childbearing potential must be surgically sterile or willing to use highly effective contraception during the study and for 180 days after the last dose.
- Able to understand and comply with study visits, treatment plans, laboratory tests, and other study procedures.
Exclusion Criteria:
- Prior systemic anti-tumor therapy for urothelial carcinoma, including radiotherapy, chemotherapy, targeted therapy, or biological therapy (except for intravesical instillation therapy).
- Prior treatment with PD-1/PD-L1 inhibitors or antibody-drug conjugates (ADCs).
- Active malignancies other than urothelial carcinoma within 3 years prior to the first dose, except for curatively treated malignancies (e.g., basal or squamous cell skin cancer, localized low-risk prostate cancer, papillary thyroid cancer, carcinoma in situ of the cervix, ductal carcinoma in situ of the breast).
- Active autoimmune disease requiring systemic treatment (e.g., use of disease-modifying agents, corticosteroids, or immunosuppressants) within 2 years prior to the first dose; or received high-dose steroids (>10 mg/day prednisone equivalent) or other immunosuppressive medications within 14 days prior to the first dose. (Physiological replacement therapies are permitted).
- Severe thromboembolic events or severe cardiovascular/cerebrovascular diseases within 1 year prior to the first dose, including but not limited to myocardial infarction, unstable angina, pulmonary embolism, cerebral hemorrhage, cerebral infarction, and deep vein thrombosis.
- Major surgical procedure within 28 days prior to the first dose; or cystoscopy/ureteroscopy biopsy or intravesical therapy within 7 days prior to the first dose.
- Peripheral neuropathy ≥ Grade 2.
- Severe dry eye syndrome, active keratitis, corneal ulcers, or conditions assessed by the investigator as increasing the risk of corneal disease and unsuitable for participation.
- Active infections, including: Positive HBsAg with HBV-DNA copy number ≥ 500 IU/mL; Positive HCV antibody with positive HCV-RNA; Positive HIV antibody; Active tuberculosis infection; Other active infections requiring systemic therapy within 7 days prior to the first dose.
- Other severe or uncontrolled diseases, including but not limited to: Severe respiratory diseases (e.g., moderate-to-severe interstitial or obstructive pulmonary disease, severe asthma); New York Heart Association (NYHA) Class III or IV heart failure; HbA1c ≥ 8% (except for participants whose fasting blood glucose is stably controlled at ≤ 10 mmol/L with medication); Poorly controlled hypertension (systolic BP ≥ 160 mmHg and/or diastolic BP ≥ 100 mmHg); Large pleural effusion or ascites requiring symptomatic treatment within 14 days prior to the first dose.
- Receipt of live vaccines within 28 days prior to the first dose or plans to receive live vaccines during the study.
- Prior allogeneic hematopoietic stem cell transplantation or solid organ transplantation.
- Use of strong CYP3A4 inhibitors or inducers within 14 days prior to the first dose.
- Known severe hypersensitivity or intolerance to the study drugs or any of their excipients.
- Substance abuse or psychiatric disorders that may interfere with study compliance.
- Any other condition that, in the opinion of the investigator, makes the participant unsuitable for the study.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Liczba ramion
Broń i interwencje
Grupa uczestników / ArmGrupa uczestników / Arm |
Interwencja / LeczenieInterwencja / Leczenie |
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Eksperymentalny: Experimental: Enfortumab Vedotin + Toripalimab
Participants in this arm will receive neoadjuvant therapy consisting of Enfortumab Vedotin and Toripalimab.
Enfortumab Vedotin (1.25 mg/kg) will be administered intravenously on Days 1 and 8 of each 21-day cycle.
Toripalimab (240 mg) will be administered intravenously on Day 1 of each 21-day cycle.
The treatment will be administered for a total of 3 cycles, followed by radical cystectomy and pelvic lymph node dissection.
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Enfortumab Vedotin is administered intravenously at a dose of 1.25 mg/kg on Day 1 and Day 8 of each 21-day cycle for a total of 3 cycles
Toripalimab is administered intravenously at a dose of 240 mg on Day 1 of each 21-day cycle for a total of 3 cycles.
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Aktywny komparator: Active Comparator: Gemcitabine + Cisplatin
Participants in this arm will receive standard neoadjuvant chemotherapy consisting of Gemcitabine and Cisplatin.
Gemcitabine (1000 mg/m^2) will be administered intravenously on Days 1 and 8 of each 21-day cycle.
Cisplatin (70 mg/m^2) will be administered intravenously on Day 1 of each 21-day cycle.
The treatment will be administered for a total of 3 cycles, followed by radical cystectomy and pelvic lymph node dissection.
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Gemcitabine is administered intravenously at a dose of 1000 mg/m² on Day 1 and Day 8 of each 21-day cycle for a total of 3 cycles.
Cisplatin is administered intravenously at a dose of 70 mg/m² on Day 1 of each 21-day cycle for a total of 3 cycles.
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Co mierzy badanie?
Podstawowe miary wyniku
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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1-Year Event-Free Survival (EFS) Rate
Ramy czasowe: Up to 1 year post-surgery
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The percentage of participants who remain free of an event at 1 year.
An event is defined as the first occurrence of any of the following: 1) radiographically confirmed disease progression during neoadjuvant therapy (per RECIST v1.1); 2) unresectable tumor or extensive pelvic metastasis identified during surgical exploration; 3) any type of local recurrence or distant metastasis (confirmed radiologically or pathologically) after radical surgery; 4) death from any cause.
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Up to 1 year post-surgery
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Miary wyników drugorzędnych
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
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Pathological Complete Response (pCR) Rate
Ramy czasowe: At the time of radical surgery (Expected to be within 4-6 weeks after the last cycle of neoadjuvant therapy)
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The percentage of participants achieving a pathological complete response, defined as the absence of residual tumor in the bladder and lymph nodes (ypT0N0) upon postoperative pathological evaluation.
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At the time of radical surgery (Expected to be within 4-6 weeks after the last cycle of neoadjuvant therapy)
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Pathological Downstaging Rate (pDR)
Ramy czasowe: At the time of radical surgery (Expected to be within 4-6 weeks after the last cycle of neoadjuvant therapy)
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The percentage of participants achieving pathological downstaging, defined as pathological stage ≤ ypT1N0 upon postoperative pathological evaluation.
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At the time of radical surgery (Expected to be within 4-6 weeks after the last cycle of neoadjuvant therapy)
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Disease-Free Survival (DFS)
Ramy czasowe: From the date of radical surgery up to study completion (Assessed every 12 weeks for the first 48 weeks, then every 24 weeks, estimated up to 3 years)
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The time from the date of radical surgery to the first documented local recurrence or distant metastasis (identified radiologically or pathologically), or death from any cause, whichever occurs first.
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From the date of radical surgery up to study completion (Assessed every 12 weeks for the first 48 weeks, then every 24 weeks, estimated up to 3 years)
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Overall Survival (OS)
Ramy czasowe: From the date of randomization up to study completion (Assessed every 12 weeks, estimated up to 3 years)
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The time from the date of randomization to death from any cause.
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From the date of randomization up to study completion (Assessed every 12 weeks, estimated up to 3 years)
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Incidence and Severity of Adverse Events (AEs) and Serious Adverse Events (SAEs)
Ramy czasowe: From the first dose of study drug up to 28 days after the last dose (or before starting new anti-tumor therapy, whichever is earlier)
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Safety will be evaluated by the incidence, severity, and causality of AEs and SAEs.
The severity of adverse events will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 5.0.
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From the first dose of study drug up to 28 days after the last dose (or before starting new anti-tumor therapy, whichever is earlier)
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Biomarker Expression: Nectin-4 and PD-L1
Ramy czasowe: Baseline (Screening) and at the time of radical surgery
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To evaluate the expression levels of Nectin-4 and PD-L1 in tumor tissue samples (obtained at baseline and post-surgery) and to analyze the relationship between these biomarker expressions and clinical efficacy.
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Baseline (Screening) and at the time of radical surgery
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Inne miary wyników
Inne miary wyników
Miara wyniku |
Opis środka |
Ramy czasowe |
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Patient-Reported Outcomes (PROs)
Ramy czasowe: From baseline up to study completion (Estimated up to 36 months)
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Patient-reported general cancer quality of life is assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30).
The EORTC QLQ-C30 is a validated 30-item questionnaire incorporating a Global Health Status/Quality of Life scale, 5 functional scales (physical, role, emotional, cognitive, and social), and multiple symptom scales.
All scale scores are linearly transformed to range from 0 to 100.
For the Global Health Status and functional scales, higher scores indicate better quality of life or higher functioning.
For symptom scales and items, higher scores indicate greater symptom burden.
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From baseline up to study completion (Estimated up to 36 months)
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Współpracownicy i badacze
Sponsor
Sponsor
Współpracownicy
Współpracownicy
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Rozpoczęcie studiów
Zakończenie podstawowe (Szacowany)
Zakończenie podstawowe
Ukończenie studiów (Szacowany)
Ukończenie studiów
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Pierwszy wysłany
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia wysłana aktualizacja
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
- Nowotwory
- Nowotwory według typu histologicznego
- Nowotwory gruczołowe i nabłonkowe
- Rak
- Rak, komórka przejściowa
- Związki heterocykliczne, 1-ring
- Związki heterocykliczne
- Lecznictwo
- Chemikalia nieorganiczne
- Związki chloru
- Związki azotu
- Deoksycytydyna
- Cytydyna
- Nukleozydy pirymidynowe
- Pirymidyn
- Związki platynowe
- Gemcytabina
- Cisplatyna
- Toripalimab
- Terapia lecznicza
- enfortumab vedotyna
Inne numery identyfikacyjne badania
Inne numery identyfikacyjne badania
- LM2025412
- IRB00006761 (Inny identyfikator: Peking University Third Hospital Medical Science Research Ethics Committee)
- M20250227 (Inny identyfikator: Peking University Third Hospital Medical Science Research Ethics Committee)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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