Evaluation of the Efficacy of Anti-HER2 Antibody-Drug Conjugates (ADC) in Locally Advanced or Metastatic Bladder Cancer Based on Organoid Technology.

NCT07379268 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 224

Last updated 2026-01-30

No results posted yet for this study

Summary

This study, through a clinical controlled trial, compares the one-year, two-year, and three-year overall survival rates of patients in the treatment group guided by organoid drug sensitivity intervention with those of patients whose medication was based on HER-2 protein expression levels (IHC method). Univariate Kaplan-Meier survival analysis was used to compare differences in overall survival between the two groups. The study aims to evaluate the application value of tumor organoid drug sensitivity testing in guiding anti-HER2-ADC drug treatment for bladder cancer.

Conditions

Interventions

OTHER

Organoid culture

Organoid culture of tumor tissue obtained during patient surgery

Sponsors & Collaborators

  • The Second Hospital of Shandong University

    collaborator OTHER
  • Qianfoshan Hospital

    collaborator OTHER
  • Shandong Provincial Hospital

    collaborator OTHER_GOV
  • Shandong Province Third hospital

    collaborator OTHER
  • Taian City Central Hospital

    collaborator OTHER
  • Weifang People's Hospital

    collaborator OTHER
  • Binzhou Medical University

    collaborator OTHER
  • The Affiliated Hospital of Qingdao University

    collaborator OTHER
  • Jining First People's Hospital

    collaborator OTHER
  • Liaocheng People's Hospital

    collaborator OTHER
  • Linyi People's Hospital

    collaborator OTHER
  • Yantai Yuhuangding Hospital

    collaborator OTHER
  • Zibo Central Hospital

    collaborator OTHER_GOV
  • Dezhou Hospital Qilu Hospital of Shandong University

    collaborator OTHER
  • Zaozhuang Municipal Hospital

    collaborator OTHER
  • Qilu Hospital of Shandong University (Qingdao)

    collaborator OTHER
  • Qilu Hospital of Shandong University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-01
Primary Completion
2028-12-31
Completion
2028-12-31

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07379268 on ClinicalTrials.gov