Ireland
--:--IST
Latest
Clinical Trials in South Korea / NCT06373055
Recruiting Observational

Prediction of Therapeutic Response to Neoadjuvant Chemotherapy in Muscle Invasive Bladder Cancer Patients Using Spatial Transcriptomics

NCT06373055 · tracked via the Priya Life Science South Korea tracker
Phase
Observational
Started
2024-05-01
Last updated
2024-04-18

Condition(s) studied

Muscle-invasive Bladder Cancer

Investigational drug(s) / intervention(s)

neoadjuvant chemotherapy followed by radical cystectomy

neoadjuvant chemotherapy followed by radical cystectomy: combination of dose-dense methotrexate, vinblastine, doxorubicin, and cisplatin (ddMVAC) or combination of gemcitabine and cisplatin (GC) followed by radical cystectomy

Study summary

Although neoadjuvant chemotherapy in muscle-invasive bladder cancer has significantly improved oncological outcomes, approximately 50% of patients do not respond to neoadjuvant chemotherapy, which has adverse effects on patients by causing treatment toxicity and surgical delays. Therefore, treatment tailored specifically to the individual patient based on the genetic and/or molecular profile of the patient is urgently needed. Among patients scheduled for neoadjuvant chemotherapy, the investigators should differentiate between patients who will be highly effective with neoadjuvant chemotherapy and those who will not, and preferentially select other treatments including radical cystectomy in the patients with high probability of failure to neoadjuvant chemotherapy. However, there is no standard which patients would benefit from neoadjuvant chemotherapy. This study plans to predict treatment response to neoadjuvant chemotherapy in patients with muscle-invasive bladder cancer by analyzing genetic and molecular profiles of tumor tissues obtained through transurethral bladder tumor resection.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion criteria: * Suspicious of bladder cancer scheduled to have transurethral resection of bladder tumor * Consent to the provision of their biospecimen. * Willing to cooperate with this study and comply with the restrictions. * Voluntarily signed the consent form for participation in the study. * Age ≥18. Exclusion criteria: * Do not agree with this study. * Vulnerable participants

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Urology and Urological Science Institute, Yonsei University College of Medicine Seoul, Republic of Korea Seoul South Korea Recruiting

More Yonsei University trials in South Korea

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06373055 on ClinicalTrials.gov ↗ ← All trials in South Korea