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Canceled by the investigator. Observational study of tislelizumab combined with zanubrutinib, lenalidomide, obinutuzumab, methotrexate, and temozolomide in the treatment of diffuse large B-cell lymphoma with secondary CNS involvement

Observational study of tislelizumab combined with zanubrutinib, lenalidomide, obinutuzumab, methotrexate, and temozolomide in the treatment of diffuse large B-cell lymphoma with secondary CNS involvement

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200062052
Enrollment
Unknown
Registered
2022-07-21
Start date
2022-07-20
Completion date
Unknown
Last updated
2023-09-04

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 with secondary CNS involvement

Interventions

Observation group:None

Sponsors

The First Affiliated Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with diffuse large B-cell lymphoma confirmed by histopathology; 2. Age 18-80 years old; 3. Previously received rituximab; 4. CNS involvement at presentation (concomitant to systemic disease); 5. At least 1 measurable disease site; 6. The cardiopulmonary function is basically normal; 7. The observed patients have signed the informed consent to participate in the experimental treatment; 8. The observed patient has signed the informed consent to participate in this observational treatment; 9. Volunteer to participate in this study, sign the informed consent before screening and be willing to follow and able to complete all test procedures.

Exclusion criteria

Exclusion criteria: 1. Previous medical history of other malignant tumors; 2. Women of childbearing age with recent birth plans; 3. Uncontrollable active infection; 4. Human immunodeficiency virus (HIV) / AIDS; 5. Difficult to control or serious cardiovascular disease; 6. Possible allergy, allergy, or intolerance to the study drug; 7. Serious diseases that may interfere with the study; 8. Patients received another research drug at the same time; 9. According to the judgment of the researcher, the patient has other conditions that are not suitable for enrollment.

Design outcomes

Primary

MeasureTime frame
Objective response rate;

Secondary

MeasureTime frame
Progression Free Survival;Duration of Response;Overall Survival;Adverse events;Prognostic biomarkers;

Countries

China

Contacts

Public ContactZhiyong Zeng
zengzhiyong049@163.com+86 13799426491

Outcome results

None listed

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