Skip to content

A prospective, multicenter clinical study of PET/CT and IPI adapted treatment for newly diagnosed diffuse large B-cell lymphoma patients

A prospective, multicenter clinical study of individualized regimen based on interim PET/CT and IPI risk stratification in the treatment of newly diagnosed diffuse large B-cell lymphoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057914
Enrollment
Unknown
Registered
2022-03-22
Start date
2022-04-01
Completion date
Unknown
Last updated
2023-11-21

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

Conditions

Diffuse large B-cell lymphoma

Interventions

Group 1 :6*R-CHOP
Group 2:6*R-CHOP + 2*R
Group 3:6*R-CHOP + 2*R, 6*Obutinib
Group 4:8*R-CHOP, 6*Obutinib

Sponsors

The First Affiliated Hospital of Medical College, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Understand and voluntarily sign the informed consent form; 2. The age ranged from 18 to 75 years (excluding the boundary value); 3. Pathological biopsy confirmed diffuse large B-cell lymphoma (tumor cells expressed CD20); 4. The patient has lesions that can be evaluated.

Exclusion criteria

Exclusion criteria: 1. Primary mediastinal large B-cell lymphoma, testicular lymphoma, or primary central large B-cell lymphoma; 2. Lymphoma with central involvement; 3. The patient has any serious medical condition that would cause the patient to develop an unbearable risk for participating in the study or require continued immunosuppressive therapy, such as unstable heart disease, stroke, rheumatoid arthritis, lupus, etc.; 4. Pregnant or lactating women; 5. History of malignancies other than lymphoma, unless the patient has been disease-free for more than 3 years; 6. The patient has an infectious or contagious disease (including HIV) that requires treatment; 7. The patient had previously received anti-lymphoma therapy.

Design outcomes

Primary

MeasureTime frame
Complete response rate, CRR;Event-free survival time;

Secondary

MeasureTime frame
Overall survival time, OS;safety;

Countries

China

Contacts

Public ContactHe Jingsong

The First Affiliated Hospital of Medical College, Zhejiang University

hejingsong@zju.edu.cn+86 13600547247

Outcome results

None listed

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