Multi-parameter Magnetic Resonance Imaging Guides Precise Treatment of Urothelial Carcinoma

• Status: Recruiting
• Trial end date: 2026-06-01
• Target enrollment: 0
• Participant gender: All

Summary

Purpose：To evaluate whether immediate multiparametric MRI evaluate the sensitivity of modified neoadjuvant chemotherapy early in patient with muscle invasive bladder cancer（MIBC）.

Rationale：Multiparametric MRI may help detect the early changes of bladder cancer receiving neoadjuvant chemotherapy.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: The First Affiliated Hospital with Nanjing Medical University

Criteria

Inclusion Criteria:

• Pathologically confirmed primary or recurrent bladder cancer.

• Planned to undergo transurethral resection of bladder tumor (TURBT) or modified GC regimen neoadjuvant chemotherapy plus radical total cystectomy.

• 18 years old and older.

• Willing to give valid written informed consent.

• No contraindications to the MRI(magnetic resonance imaging) and MRI contrast agent.

Exclusion Criteria:

• Abnormal liver function (1.5 times higher than normal).

• Glomerular filtration rate < 60ml /min·kg.

• Heart failure.

• Acute myocardial infarction.

• Severe heart and lung disease.

• Hypotension and hypoxia.

• Brain metastases, or other known central nervous system metastases.

• A history of severe central nervous system diseases, including unexplained loss of consciousness or transient ischemic attack.

• Known congenital or acquired immunodeficiency, active hepatitis, active tuberculosis and other active infections, etc.

• Pregnant or lactating women.

• Patients participating in other drug trials.

• Patients with poor general condition (eg malnutrition, dehydration). Behavioral status score (ZPS quintile) ≥ 2.

• Patients with previous autoimmune diseases or existing autoimmune diseases. (including controlled or uncontrolled drugs).

• Patients undergoing organ transplantation (transplantation of liver, kidney, heart, lung and other organs) or those who require long-term administration of immunosuppressive agents due to personal conditions.

• Those who are intolerant or allergic to cytotoxic chemotherapeutic drugs.

• Bone marrow transplantation, severe leukopenia.

• Patients with severe infection or trauma.

• Any condition based on the investigation's clinical judgment that the patient is not suitable for completing this study (such as not meeting the patient's most beneficial treatment, patient compliance, etc.)