Multi-Omics-Based Phase Ⅱ Trial of Trastuzumab Rezetecan Plus Camrelizumab for Perioperative Therapy in HER2-Positive Muscle-Invasive Urothelial Carcinoma
Phase Ⅱ Clinical Study on Predicting Perioperative Efficacy of Trastuzumab Rezetecan Combined With Camrelizumab in HER2-Positive Muscle-Invasive Urothelial Carcinoma Based on Multi-Omics
Studieoversikt
Status
Status
Forhold
Forhold
Intervensjon / Behandling
Intervensjon / Behandling
Studietype
Studietype
Registrering (Antatt)
Registrering
Fase
Fase
- Fase 2
Kontakter og plasseringer
Studiekontakt
Studiekontakt
- Navn: Sheng Tai, MD
- Telefonnummer: +86-551-62922234
- E-post: taisheng@ahmu.edu.cn
Deltakelseskriterier
Kvalifikasjonskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Aged ≥18 years old with no restriction on gender.
- Voluntarily participate in this trial, sign written informed consent form and have good treatment compliance.
- Histopathologically confirmed bladder urothelial carcinoma (carcinoma with squamous/glandular differentiation is acceptable only when urothelial component dominates the lesion).
- Clinically or radiologically diagnosed muscle-invasive bladder cancer (MIBC): cT2-T4a, N0-1, M0 per AJCC/UICC staging system; all imaging assessments shall be completed within 28 days prior to enrollment.
- HER2-positive tumor defined as IHC 1+, 2+ or 3+ tested on archival tumor specimen before enrollment via designated or central laboratory.
- Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.
- Candidates eligible for radical surgery: planned to receive radical cystectomy (RC), and investigators confirm feasibility of subsequent TURBT consistent with study protocol.
Satisfactory major organ function to tolerate perioperative treatment:
- Hematology: ANC ≥1.5×10⁹/L, PLT ≥100×10⁹/L, Hb ≥90 g/L;
- Liver function: ALT/AST ≤2.5×ULN, total bilirubin ≤1.5×ULN;
- Renal function: creatinine clearance ≥50 mL/min calculated by Cockcroft-Gault or MDRD formula;
- Cardiac function: LVEF ≥50% detected by echocardiography without symptomatic heart failure (due to trastuzumab-related cardiac risk).
- Fertile subjects agree to use effective contraception throughout study period and for defined duration after last study drug administration.
Exclusion Criteria:
- Patients with distant metastasis (M1), unresectable disease ineligible for radical surgery, or concomitant active malignancy requiring systematic anti-tumor therapy as assessed by investigator.
- Prior systemic anti-tumor therapy for current bladder cancer, including neoadjuvant/adjuvant/metastatic chemotherapy, immunotherapy or anti-HER2 agents; previous exposure to PD-1/PD-L1 inhibitors, anti-HER2 monoclonal antibodies or ADCs that may interfere with efficacy or safety evaluation per investigator's judgment.
- Previous pelvic radiotherapy, or unrecovered major surgery/severe trauma within predefined time window before enrollment.
- Active autoimmune disease or patients requiring long-term systemic immunosuppressive therapy (daily prednisone>10 mg or equivalent dose; topical/inhaled/short-course steroid use is permitted).
- Uncontrolled active or severe bacterial infection, active tuberculosis; viral infection: HBsAg positive with elevated HBV DNA without standardized antiviral treatment, positive HCV RNA without disease control, or confirmed HIV infection per local institutional standard; clinically significant cardiovascular disorders including congestive heart failure, recent myocardial infarction, unstable angina, uncontrolled arrhythmia, baseline LVEF<50%, or subjects inappropriate for trastuzumab administration judged by investigator.
- Previous or ongoing interstitial lung disease/non-infectious pneumonitis, or obvious interstitial pulmonary changes on imaging with high risk of immune-related pneumonitis assessed by investigator.
- Known severe hypersensitivity to trastuzumab, camrelizumab or any excipients of investigational drugs; pregnant or breastfeeding females, or those planning pregnancy throughout study period.
- Severe psychiatric/cognitive disorder or substance abuse preventing regular follow-up and efficacy assessment.
- Any other conditions inappropriate for trial enrollment such as severe comorbidities or extremely short expected survival, as determined by the investigator.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Antall våpen
Våpen og intervensjoner
Deltakergruppe / ArmDeltakergruppe / Arm |
Intervensjon / BehandlingIntervensjon / Behandling |
|---|---|
|
Eksperimentell: Perioperative Therapy with Trastuzumab Rezetecan Combined with Camrelizumab
|
Eligible screened participants will receive assigned treatment after satisfying all inclusion/exclusion criteria. Neoadjuvant Phase: Patients receive Trastuzumab Rezetecan (4.8 mg/kg, intravenous infusion) plus Camrelizumab (200 mg, intravenous infusion); each treatment cycle lasts 21 days, for a total of 2-3 cycles. Following a 2-4 week rest interval, clinical reassessment is performed prior to radical cystectomy (RC). Postoperative Adjuvant Phase: After surgery, Trastuzumab Rezetecan (4.8 mg/kg, IV infusion, once every 3 weeks for 6 cycles) and Camrelizumab (200 mg, IV infusion once every 3 weeks) are administered, with camrelizumab maintained for up to 1 year. |
Hva måler studien?
Primære resultatmål
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Pathological Complete Response Rate (pCR rate)
Tidsramme: Up to approximately 1 year
|
Proportion of patients achieving pathological complete response (pCR, no residual invasive urothelial carcinoma in bladder and regional lymph nodes) in surgical specimen after perioperative neoadjuvant therapy.
|
Up to approximately 1 year
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Event-Free Survival (EFS)
Tidsramme: From treatment start until disease progression/death, follow-up up to 12 months.
|
Time from study treatment initiation to first occurrence of local recurrence, distant metastasis, disease progression or all-cause death.
|
From treatment start until disease progression/death, follow-up up to 12 months.
|
|
Overall Survival (OS)
Tidsramme: From treatment start until death, follow-up up to 12 months.
|
Time from study treatment initiation to all-cause death of any reason.
|
From treatment start until death, follow-up up to 12 months.
|
|
Safety and Tolerability
Tidsramme: From first study drug administration to 30 days after last study medication.
|
Incidence, severity and causality of adverse events (AEs) graded per CTCAE v6.0 throughout perioperative treatment period.
|
From first study drug administration to 30 days after last study medication.
|
|
Proportion of patients downstaged to T1 stage
Tidsramme: Up to approximately 1 year
|
Percentage of enrolled patients whose postoperative pathological tumor stage is downstaged to T1 after perioperative therapy.
|
Up to approximately 1 year
|
Andre resultatmål
Andre resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Multi-omics spatial biomarkers predicting neoadjuvant treatment response
Tidsramme: Baseline tumor specimen collection before neoadjuvant therapy and matched postoperative pathological outcome.
|
Correlation between pre-treatment tumor multi-omics profiles (WES whole exome sequencing, 10x Xenium spatial transcriptome, PhenoCycler-Fusion spatial single-cell proteomics) and pathological treatment response; explore predictive factors for perioperative regimen efficacy in HER2-positive MIBC.
|
Baseline tumor specimen collection before neoadjuvant therapy and matched postoperative pathological outcome.
|
Samarbeidspartnere og etterforskere
Sponsor
Sponsor
Etterforskere
Etterforskere
- Hovedetterforsker: Sheng Tai, The First Affiliated Hospital of Anhui Medical University
- Hovedetterforsker: Hanjiang Xu, The First Affiliated Hospital of Anhui Medical University
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Studiestart
Primær fullføring (Antatt)
Primær fullføring
Studiet fullført (Antatt)
Studiet fullført
Datoer for studieregistrering
Først innsendt
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Først lagt ut
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Sist oppdatering lagt ut
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Urogenitale sykdommer
- Urogenitale neoplasmer
- Neoplasmer etter nettsted
- Neoplasmer
- Mannlige urogenitale sykdommer
- Urologiske sykdommer
- Kvinnelige urogenitale sykdommer
- Kvinnelige urogenitale sykdommer og graviditetskomplikasjoner
- Urologiske neoplasmer
- Urinblæresykdommer
- Neoplasmer i urinblæren
- Camrelizumab
Andre studie-ID-numre
Andre studie-ID-numre
- KY2026-04-47 (1)
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