About this trial
This study is trying to explore the mechanism of R-CHOP regimen or tucidinostat plus R-CHOP (CR-CHOP) regimen in the treatment of BCL2/MYC protein double expressor lymphoma.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Each potential subject must satisfy all of the following criteria to be enrolled in the study.
Disqualifiers
Any potential subject who meets any of the following criteria will be excluded from participating in the study.
Trial population
Patients with accessible tissue samples were selected from a phase III study of tucidinostat in combination with R-CHOP in patients with newly diagnosed double expressor DLBCL (NCT04231448).
Trial design
Cohort
Retrospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Event Free Survival (EFS)
Defined as the duration from the date of randomization to the date of disease progression, relapse from CR , initiation of subsequent systemic antilymphoma therapy for residual disease, or death, whichever occurs first.
Secondary outcomes
Progression-Free Survival (PFS)
Defined as the duration from the date of randomization to the date of progression, relapse from CR, or death, whichever occurred first.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: