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An observational study to evaluate the sensitivity and efficacy of drug therapy for bladder cancer based on organoid model technique

An observational study to evaluate the sensitivity and efficacy of drug therapy for bladder cancer based on organoid model technique

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300072354
Enrollment
Unknown
Registered
2023-06-12
Start date
2023-06-12
Completion date
Unknown
Last updated
2023-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bladder cancer

Interventions

Case series:None

Sponsors

Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients who are pathologically diagnosed as bladder cancer and need further drug treatment; 2. Patients with a pathological and/or radiographic diagnosis of myoinvasive bladder cancer (MIBC) and subsequent need for neoadjuvant chemotherapy, immunotherapy, targeted therapy, etc.; 3. Non-muscular invasive bladder cancer (NMIBC) was diagnosed pathologically and the preoperative tumor size was =3cm, high-grade, T1 tumor patients; 4. Age =18 years old, gender unlimited; 5. The ECOG PS status score is 0-1; 6. Able to comply with research and follow-up procedures; 7. The patient has the ability to understand and voluntarily sign the informed consent;

Exclusion criteria

Exclusion criteria: 1. Previous or co-existing other malignant tumors, whose natural history or treatment may interfere; 2. There is a serious or uncontrolled systemic disease; 3. Female patients planning pregnancy or breastfeeding; 4. Severe infections during the 2 weeks prior to study participation, including but not limited to hospitalization due to complications of infection, bacteremia, or severe pneumonia;

Design outcomes

Primary

MeasureTime frame
IC50 of drugs acting on organoids;Overall response rate;

Secondary

MeasureTime frame
Overall survival;Progression free survival;

Countries

China

Contacts

Public ContactTianxin Lin

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

lintx@mail.sysu.edu.cn+86 137 2400 8338

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026