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Multi-Omics-Based Phase Ⅱ Trial of Trastuzumab Rezetecan Plus Camrelizumab for Perioperative Therapy in HER2-Positive Muscle-Invasive Urothelial Carcinoma

2026年6月8日 更新者:Sheng Tai

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

For patients with HER2-expressing muscle-invasive bladder cancer (MIBC), current neoadjuvant therapies dominated by platinum-based chemotherapy remain unsatisfactory with respect to improved clinical efficacy, pathological complete response (pCR) rates, and the achievement rate of tumor downstaging for bladder preservation; in addition, a subset of patients have limited tolerance or eligibility to chemotherapy. Therefore, this study aims to evaluate the neoadjuvant regimen of Ruikang Trastuzumab combined with Camrelizumab, to determine whether this regimen can, with acceptable safety profiles: elevate pCR rate and the proportion of patients downstaged to ≤T1 disease, enable bladder preservation based on TURBT for eligible patients, and explore predictive biomarkers to identify the population most likely to derive clinical benefits.

研究概览

研究类型

介入性

注册 (估计的)

44

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Aged ≥18 years old with no restriction on gender.
  2. Voluntarily participate in this trial, sign written informed consent form and have good treatment compliance.
  3. Histopathologically confirmed bladder urothelial carcinoma (carcinoma with squamous/glandular differentiation is acceptable only when urothelial component dominates the lesion).
  4. 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.
  5. HER2-positive tumor defined as IHC 1+, 2+ or 3+ tested on archival tumor specimen before enrollment via designated or central laboratory.
  6. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.
  7. Candidates eligible for radical surgery: planned to receive radical cystectomy (RC), and investigators confirm feasibility of subsequent TURBT consistent with study protocol.
  8. 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).
  9. Fertile subjects agree to use effective contraception throughout study period and for defined duration after last study drug administration.

Exclusion Criteria:

  1. Patients with distant metastasis (M1), unresectable disease ineligible for radical surgery, or concomitant active malignancy requiring systematic anti-tumor therapy as assessed by investigator.
  2. 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.
  3. Previous pelvic radiotherapy, or unrecovered major surgery/severe trauma within predefined time window before enrollment.
  4. 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).
  5. 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.
  6. 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.
  7. Known severe hypersensitivity to trastuzumab, camrelizumab or any excipients of investigational drugs; pregnant or breastfeeding females, or those planning pregnancy throughout study period.
  8. Severe psychiatric/cognitive disorder or substance abuse preventing regular follow-up and efficacy assessment.
  9. Any other conditions inappropriate for trial enrollment such as severe comorbidities or extremely short expected survival, as determined by the investigator.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的: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.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Pathological Complete Response Rate (pCR rate)
大体时间: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

次要结果测量

结果测量
措施说明
大体时间
Event-Free Survival (EFS)
大体时间: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)
大体时间: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
大体时间: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
大体时间: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

其他结果措施

结果测量
措施说明
大体时间
Multi-omics spatial biomarkers predicting neoadjuvant treatment response
大体时间: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.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

调查人员

  • 首席研究员:Sheng Tai、The First Affiliated Hospital of Anhui Medical University
  • 首席研究员:Hanjiang Xu、The First Affiliated Hospital of Anhui Medical University

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月5日

初级完成 (估计的)

2028年6月5日

研究完成 (估计的)

2028年12月31日

研究注册日期

首次提交

2026年6月3日

首先提交符合 QC 标准的

2026年6月8日

首次发布 (实际的)

2026年6月10日

研究记录更新

最后更新发布 (实际的)

2026年6月10日

上次提交的符合 QC 标准的更新

2026年6月8日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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