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Clinical study of obrutinib, lenalidomide combined with rituximab in the treatment of relapsed/refractory diffuse large B-cell lymphoma in elderly patients based on comprehensive geriatric assessment system

Clinical study of obrutinib, lenalidomide combined with rituximab in the treatment of relapsed/refractory diffuse large B-cell lymphoma in elderly patients based on comprehensive geriatric assessment system

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066211
Enrollment
Unknown
Registered
2022-11-28
Start date
2022-12-01
Completion date
Unknown
Last updated
2023-05-15

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

Diffuse large B-cell lymphoma group:Obrutinib, lenalidomide and rituximab were given

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Cd20-positive diffuse large B-cell lymphoma independently diagnosed by two pathologists; 2. Age >=65, both sexes; 3. Patients who had received at least one previous treatment failure (including immunochemotherapy, chemotherapy, or hematopoietic stem cell transplantation) with no response or a first recurrence after remission; 4. Before starting treatment, comprehensive geriatric assessment (IACA index) was performed, including patients' age, Instrumental Assessment of Activities of daily Living (IADL score), Charlson comorbidibility index (CCI score), and serum albumin level. Patients with IACA score >=1 were defined as ineligible for standard immunochemotherapy, specifically as Instrumental Assessment of Activities of daily Living Scale (IADL) =3, or age >75 years; 5. The estimated survival time is more than 3 months; 6. Patients were informed about this study and signed written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with previous history of hematologic (non-lymphoma) or non-hematologic tumors undergoing chemoradiotherapy 2. There's a serious infection that's not under control 3. Known bleeding tendencies or hemophilia 4. Poor compliance 5. Not suitable considered by the researchers

Design outcomes

Primary

MeasureTime frame
overall response rate;

Secondary

MeasureTime frame
overall survival;Progression free survival;

Countries

China

Contacts

Public ContactLiu Hui

Beijing Hospital

liuhui8140@126.com+86 13520618812

Outcome results

None listed

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