MedPath

Basal Tumours in Bladder Cancer, Response to chemoTherapy

Completed
Conditions
Bladder Cancer
Chemotherapy Effect
Registration Number
NCT04089748
Lead Sponsor
University Hospital, Rouen
Brief Summary

Determine the sensitivity/resistance to chemotherapy of the various subgroups of muscle-invasive bladder cancers, including the basal subgroup (about 25% of these tumours) according to 4 different classifications based on molecular or immunohistochemical classifiers.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
293
Inclusion Criteria

Not provided

Exclusion Criteria

-Patients enrolled in VESPER study:Tumors from patient having withdrawn his/her informed consent form for the participation to the collection and/or VESPER project.

OR

-Patients from St Louis not enrolled in VESPER study:Tumors from patient having expressed opposition against research program after 1 month for the participation to the collection.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Identifying mechanisms of resistance in basal subgroups.through study completion, an average of 3 years
Identifying molecular subgroups of bladder cancer patients within VESPER and Saint-Louis cohort, who could benefit from neoadjuvant chemotherapy, taking into account the existence of different classification systems.through study completion, an average of 3 years
Determining which classification(s) has(ve) the best ability to identifying subgroups of tumours sensitive or resistant to neoadjuvant chemotherapy.through study completion, an average of 3 years
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

DRCI

🇫🇷

Rouen, France

DRCI
🇫🇷Rouen, France

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