CD155 in Bladder Cancer
Predictive Value of CD155 for Survival and Effectiveness of Chemotherapy in Patients With Muscle Invasive Bladder Cancer
1 other identifier
observational
151
1 country
1
Brief Summary
This research is designed to investigate the prognostic and predictive value of CD155 in muscle invasive bladder cancer.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2018
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2018
CompletedFirst Submitted
Initial submission to the registry
December 27, 2018
CompletedFirst Posted
Study publicly available on registry
December 28, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2025
CompletedApril 16, 2025
April 1, 2025
5 years
December 27, 2018
April 13, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Recurrence free survival
Time to recurrence or metastasis
2018.1.1-2023.12.31
Secondary Outcomes (3)
Overall survival
2018.1.1-2028.1.1
Benefit from neoadjuvant chemotherapy
2018.1.1-2028.1.1
Benefit from adjuvant chemotherapy
2018.1.1-2028.1.1
Study Arms (1)
FUSCC cystectomy cohort
patients underwent cystectomy in Fudan University Shanghai Cancer Center
Interventions
adjuvant chemotherapy using Gemcitabine plus Cisplatin
Eligibility Criteria
patients with non-metastatic muscle invasive bladder cancer underwent cystectomy in Fudan University Shanghai Cancer Center is included
You may qualify if:
- patients with non-metastatic muscle invasive bladder cancer
- pathology confirmed urothelial carcinoma
- underwent cystectomy and pelvic lymph node dissection
You may not qualify if:
- not enough tissue for immunohistochemistry
- patients with a second neoplasm
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Fudan Universitylead
Study Sites (1)
Fudan University Shanghai Cancer Center
Shanghai, Shanghai Municipality, 200032, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Department of Urology
Study Record Dates
First Submitted
December 27, 2018
First Posted
December 28, 2018
Study Start
January 1, 2018
Primary Completion
January 1, 2023
Study Completion
January 1, 2025
Last Updated
April 16, 2025
Record last verified: 2025-04