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Treatment for CD20-positive central nervus system lymphoma with autologous serum and rituximab into the ventricle

Treatment for CD20-positive central nervus system lymphoma with autologous serum and rituximab into the ventricle - CNS lymphoma treatment with auto-serum and rituximab into the ventricle

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000000968
Enrollment
5
Registered
2008-01-15
Start date
2007-01-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

CD20-positive primary central nervus system lymphoma, or relapsed CD20-positive non-Hodgkin lymphoma in CNS alone

Interventions

Day 1: Intraventricle injection of 10 mg (1 ml) of rituximab and 8 ml of autologous serum via Ommaya reservoir. Day 3: Intraventricle injection of 40 mg (4 ml) of rituximab and 8 ml of autologous ser

Sponsors

Division of Hematology, University of Tsukuba
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: With written informed concent, relapsed or primary refractory CD20-positive primary CNS lymphoma, or relapsed non-Hodgkin lymphoma in CNS alone, which was treated with chemotherapy of multiple drugs including high dose methotrexate or high dose AraC, or with autologous hematopoietic cell transplantation (AHCT). The patient must be considered but are not candidate for radiation or other therapies because these therapies are considered to be ineffective or bring serious side effects, or the patient did not consent to these therapies. If the patient has not been treated with AHCT, the modality must be considered but is concluded as not feasible because of the patient's age, comobidities or rejection.

Exclusion criteria

Exclusion criteria: Poor general status (ECOG Performance status 3 or 4). Inablity in understanding of the therapy even due to the primary disease. Lesions outside of central nervas system which are uncontroled or less than three months from shrinking.

Design outcomes

Primary

MeasureTime frame
Response

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026