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A study for the Molecular Subtypes of Bladder Cancer and Organoid Model

A study for the Molecular Subtypes of Bladder Cancer and Organoid Model

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000032765
Enrollment
Unknown
Registered
2020-05-09
Start date
2020-06-01
Completion date
Unknown
Last updated
2020-05-11

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

Conditions

Bladder Cancer

Interventions

Gold Standard:Clinical outcome
model

Sponsors

Department of Department of Urology, Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. From 2008 to 2018, TURBT was performed in our hospital, during which tumor tissues were collected and stored in our biological sample bank; 2. The patients with myometrial infiltrative urothelial carcinoma were evaluated clinically and pathologically; 3. Patients without metastasis found in clinical and imaging examination within 3 months after operation (bone scan, MRI or CT plain scan + enhancement); 4. Patients with clinical stage >=T2a; 5. Patients younger than 80 years old; 6. Patients with preoperative life expectancy >=5 years; 7. Patients who met the following criteria: neutrophils >=1500 / mm^3, platelets >=100000/mm^3, bilirubin 60ml/min); 8. Prior to sample retention, the patient has signed the informed consent for sample retention in biological sample bank of Renji Hospital.

Exclusion criteria

Exclusion criteria: 1. Patients with active infection, history of thromboembolism and uncontrolled cardiovascular complications before operation; 2. Patients with a history of cancer other than basal cell carcinoma of the skin; 3. Any patient with a history of disease that is not consistent with the treatment plan; 4. Patients who have previously received chemotherapy, radiotherapy, endocrine therapy and targeted therapy for other tumors.

Design outcomes

Primary

MeasureTime frame
AUC area, sensitivity and specificity of pathological complete response rate after radical operation;AUC area, sensitivity, and specificity of pathological partial response;DNA profile;RNA profile;IHC;

Secondary

MeasureTime frame
AUC area, sensitivity, and specificity benefiting from the overall survival rate of neoadjuvant chemotherapy;The area, sensitivity and specificity of AUC benefiting from disease-free survival;The area, sensitivity and specificity of AUC benefiting from disease-related mortality;

Countries

China

Contacts

Public ContactRuiyun Zhang

Department of Urology, Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine

zhangruiyun4337@163.com+86 13681687457

Outcome results

None listed

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