About this trial
Evaluation of the Safety and Efficacy of CR-CHOP Treatment in Newly Diagnosed Double-Expressor DLBCL with Other Molecular Subtypes
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
≥18 years of age;
Diffuse large B-cell lymphoma diagnosed by pathological diagnosis according to WHO 2016 classification criteria;
Molecular subtyping, determined through high-throughput sequencing of pathological tissue or peripheral blood, is categorized as the "Other" subtype;
Immunohistochemistry revealed overexpression of MYC and BCL2: MYC ≥ 40%, BCL2 ≥ 50%;
Disqualifiers
Patients who meet any of the following criteria will be excluded from the study:
Currently enrolled in another clinical trial;
Received prior lymphoma treatment with alternative regimens before enrollment;
Presence of concurrent malignant tumors;
Trial design
Single group
Treatments tested in this trial
Chidamide plus R-CHOP
DrugChidamide Plus R-CHOP (Rituximab、Cyclophosphamide、Doxorubicin、Vincristine and Prednisone)
Treatment groups
Trial outcomes
Primary outcomes
PFS
from date of inclusion to date of progression, relapse, or death from any cause
Secondary outcomes
CR rate
complete remission rate
OS
Overall Survival: from the date of inclusion to date of death, irrespective of cause
ORR
The Overall Response Rate
Sponsors and contacts
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