Clinical trial · Interventional
R2 and Combination Chemotherapy Versus R and Combination Chemotherapy in Newly Diagnosed Highly Aggressive B-NHL
Lenalidomide, Rituximab and Combination Chemotherapy Versus Rituximab and Combination Chemotherapy in Treating Patients With Newly Diagnosed Highly Aggressive Non-Hodgkin B-cell Lymphoma
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
In this study,lenalidomide was added in the first-line treatment in the newly diagnosed highly invasively non-Hodgkin B-cell lymphoma. The R2-CHOP/R2-EPOCH etc was applied compared with the classical R-CHOP/R-EPOCH etc. The investigators tried to explore a more effective and safe treatment regimen for patients with high-risk B-cell lymphoma to improve the patient's poor prognosis.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lymphoma, B-Cell | B-Cell Malignant Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| R2-combination chemotherapy | Drug | — | UNRESOLVED |
| R-combination chemotherapy | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- R2-combination chemotherapy
- description
- R2-CHOP/CHOPE/DA-EPOCH/HD MTX R2-CHOP : lenalidomide 25mg/d po D1-10; Rituximab:375mg/m2,ivgtt,D0 Cyclophosphamide 750mg / m2 d1, doxorubicin 70mg / m2 or Doxorubicin liposome 30-40 mg / m2 d2, vincristine 1.4mg / m2 or vindesine 3mg / m2 d2, prednisone 100mg d1-5 R2-DA-EPOCH: lenalidomide 25mg/d po D1-10; Rituximab:375mg/m2,ivgtt,D0 Epirubicin 15mg/m2 ,d1-4; Etoposide 50mg/m2 ,d1-4; Vincristine 0.4mg/ m2 ,d1-4; Cyclophosphamide 750mg/ m2 , d5; Prednisone 60mg/m2/d, d1-5; R2-HD MTX: lenalidomide 25mg/d po D1-10; Rituximab:375mg/m2,ivgtt,D0; MTX 3.5g/m2,d1
- interventionNames
- Drug: R2-combination chemotherapy
- type
- ACTIVE_COMPARATOR
- label
- R-combination chemotherapy
- description
- R-CHOP/CHOPE/DA-EPOCH/HD MTX R-CHOP : Rituximab:375mg/m2,ivgtt,D0 Cyclophosphamide 750mg / m2 d1, doxorubicin 70mg / m2 or Doxorubicin liposome 30-40 mg / m2 d2, vincristine 1.4mg / m2 or vindesine 3mg / m2 d2, prednisone 100mg d1-5 R-DA-EPOCH: Rituximab:375mg/m2,ivgtt,D0 Epirubicin 15mg/m2 ,d1-4; Etoposide 50mg/m2 ,d1-4; Vincristine 0.4mg/ m2 ,d1-4; Cyclophosphamide 750mg/ m2 , d5; Prednisone 60mg/m2/d, d1-5; R-HD MTX: Rituximab:375mg/m2,ivgtt,D0; MTX 3.5g/m2,d1
- interventionNames
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. Newly diagnosed highly aggressively B-Cell Non-Hodgkin's lymphoma (NHL) confirmed by histopathology 2. The patient has at least ≥1 measurable tumor lesion with a diameter \>1.5 cm; 3. The patient has not undergone systemic chemotherapy or immunotherapy before; 4. ECOG score ≤ 2 points; 5. Liver and kidney function meets the following conditions: creatinine clearance rate ≥ 30ml / min, total bilirubin, AST and ALT ≤ 2.5 × ULN; 6. No history of malignant tumors within 5 years, except for cured carcinomas in situ such as basal cell carcinoma of the skin, cervical cancer, breast cancer, prostate cancer, etc.; 7. agree to take contraceptive measures during the trial period and within 3 months after the end of the trial; 8. Patients volunteered to participate in the study and signed informed consent. Exclusion Criteria: 1. Serious cardiovascular and other important organs and blood, endocrine system lesions, and other history of malignant tumors; 2. Severe mental illness; 3. Pregnant or lactating women and men or women who intend to conceive in the near future; 4. The expected survival time is less than 6 months; 5. HBV, HCV or HIV infection or seropositive; 6. there are active infections; 7. Allergies or allergies to rituximab; 8. Compliance or poor follow-up; 9. Other circumstances that the investigator believes are not suitable for inclusion.
References
Publications (0)
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