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Research on the Consolidation Treatment of CD5+DLBCL with ASCT

DA-EPOCH-R combined with ASCT in patients with newly diagnosed CD5-positive diffuse large B-cell lymphoma: a prospective, multicenter, single-arm study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108603
Enrollment
Unknown
Registered
2025-09-02
Start date
2025-09-15
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CD5-positive diffuse large B-cell lymphoma

Interventions

Intervention group:Patients received induction therapy with the DA-EPOCH-R regimen (riximab 375 mg/m^2, d0
Etoposide 50mg/m^2/d
vinpodisin 0.8mg/m^2/d
Epirubicin 15mg/m^2/d, continuous intravenous infusion for 96h
cyclophosphamide 750mg/m^2, d5
Prednisone 60mg/m^2/d, d1-5
1 course of treatment every 3 weeks, and the dose adjustment refers to previous studies). Patients with PR or above in the mid-term evaluation of 4 courses of treatment entered the preparation stage f
Foot leaf acetoside 200mg/m^2, d6-3
cytarabine 20mg/m^2, d6-3
Inphalon 70mg/m^2, d3~2).

Sponsors

The FIrst Affiliated Hospital, College of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosed by histopathology as CD5 positive diffuse large B-cell lymphoma; 2.Previously untreated; 3.ECOG score <= 2 points; 4.No serious complications, such as liver failure, kidney failure, or heart failure; 5.Voluntarily sign a written informed consent form before experimental screening; 6.18 <= Age <= 65 years old, gender not limited.

Exclusion criteria

Exclusion criteria: 1.Lymphoma involving the central nervous system; 2.Active infectious diseases such as HIV, tuberculosis; 3.Patients with severe organ dysfunction; 4.History of other active tumors; 5.Researchers believe that there are other situations that are not suitable for participating in this experiment.

Design outcomes

Primary

MeasureTime frame
2-year disease-free survival;

Secondary

MeasureTime frame
2y-OS;

Countries

China

Contacts

Public ContactWenjuan Yu

The FIrst Affiliated Hospital, College of Medicine, Zhejiang University

drwjyu@163.com+86 571 87235983

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026