Testing Zanidatamab and Tislelizumab Before Surgery for Bladder Cancer

Trial details

Who runs it

Fujian Medical University Union Hospital

Trial code

NCT07296705

Record updated

22 December 2025

Original description

This is a multicenter, open-label, prospective, single-arm, phase II study designed to evaluate the efficacy and safety of neoadjuvant zanidatamab combined with tislelizumab and chemotherapy, followed by selective bladder preservation, in patients with HER2-positive muscle-invasive bladder cancer (MIBC) staged cT2-4aN0-1M0.Read full original descriptionShow less

Selective Bladder Preservation After Neoadjuvant Zanidatamab Combined With Tislelizumab and Chemotherapy in Patients With HER2-Positive Muscle-Invasive Bladder Cancer: A Multicenter Study

This is a multicenter, open-label, prospective, single-arm, phase II study designed to evaluate the efficacy and safety of neoadjuvant zanidatamab combined with tislelizumab and chemotherapy, followed by selective bladder preservation, in patients with HER2-positive muscle-invasive bladder cancer (MIBC) staged cT2-4aN0-1M0.

Inclusion: Willing to participate, able to provide written informed consent, and able to understand and comply with study requirements and the assessment schedule; Age 18 to 85 years on the date of informed consent; Residual disease after TURBT; histologically confirmed urothelial carcinoma of the bladder staged cT2-T4aN0-1M0 per AJCC 8th edition by histology and imaging. For mixed histology, urothelial carcinoma must be predominant (≥50%); Availability of TURBT tumor tissue and corresponding pathology report; either fresh surgical tissue or unstained slides may be submitted; HER2-positive: IHC 2+ or 3+; No prior anti-HER2-directed therapy (including but not limited to HER2 antibodies, HER2-targeting ADCs, or HER2-targeted TKIs) and no prior PD-(L)1 therapy; ECOG performance status 0-2; Adequate organ function based on screening labs obtained ≤14 days before enrollment:; For the following counts, no growth-factor support within 14 days prior to sample collection: i. Absolute neutrophil count ≥ 1.5 × 10\^9/L ii. Platelets ≥ 100 × 10\^9/L iii. Hemoglobin ≥ 90 g/L b. INR or aPTT ≤ 1.5 × upper limit of normal (ULN) c. Total bilirubin ≤ 1.5 × ULN (≤ 3 × ULN for Gilbert syndrome or isolated indirect hyperbilirubinemia) d. AST, ALT, and alkaline phosphatase ≤ 2.5 × ULN; Women of childbearing potential must have a negative urine or serum pregnancy test within ≤7 days before enrollment and agree to use highly effective contraception during the study and for ≥120 days after the last dose of zanidatamab, tislelizumab, or chemotherapy (whichever occurs later); Non-sterilized men must agree to use highly effective contraception during the study and for ≥120 days after the last dose of zanidatamab, tislelizumab, or chemotherapy (whichever occurs later).

Exclusion: Major surgery or significant trauma within 28 days prior to enrollment (placement of a vascular access device and TURBT are not considered major surgery); Prior radiotherapy to the bladder for bladder cancer; Concurrent participation in another clinical study, unless observational (non-interventional) or in the follow-up phase of an interventional study; Uncontrolled infection requiring systemic therapy; Diagnosis of another malignancy within the past 5 years; Active autoimmune disease requiring systemic treatment that, in the investigator's judgment, would affect study therapy; History of acute myocardial infarction or ischemic stroke within 6 months; Human immunodeficiency virus (HIV) infection (i.e., positive antibodies to HIV-1/2), active syphilis infection, or active tuberculosis infection; Active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection; History of interstitial lung disease, non-infectious pneumonitis, or uncontrolled pulmonary disease, including pulmonary fibrosis or acute lung disease; Known hypersensitivity to any study drug; Any other condition deemed by the investigator to render the patient ineligible; Any of the following cardiovascular criteria:; Cardiac chest pain within ≤28 days before first study dose, defined as moderate pain that limits activities of daily living; Symptomatic pulmonary embolism within ≤28 days before first study dose; Any acute myocardial infarction within ≤6 months before first study dose; Any history of heart failure of New York Heart Association (NYHA) Class III or IV within ≤6 months before first study dose; Any ventricular arrhythmia of severity ≥ Grade 2 within ≤6 months before first study dose; Any cerebrovascular accident within ≤6 months before first study dose; Corrected QT interval (QTc by Fridericia): ≥470 msec for women or ≥450 msec for men; Note: If the initial ECG shows QTc >450 msec (men) or >470 msec (women), a follow-up ECG should be performed to confirm; Left ventricular ejection fraction (LVEF) ≤50% by multigated acquisition (MUGA) scan or echocardiography (ECHO). The same modality used at baseline must be used for follow-up assessments; Pregnant or breastfeeding women.

ClinicalTrials.gov NCT07296705