Skip to content

CNS Prophylaxis in Diffuse Large B-cell Lymphoma

Study Evaluating Relapses in Central Nervous System in Patients With Diffuse Large B-Cell Lymphoma Treated With Chemotherapy With or Without CNS Prophylaxis. Multicentric, Prospective, Randomized Phase III Study

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02777736
Acronym
CLSG-CNS-001
Enrollment
500
Registered
2016-05-19
Start date
2015-07-31
Completion date
2019-12-31
Last updated
2016-06-06

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

Keywords

Lymphoma, B cell, Central nervous system relapse, Methotrexate, Intrathecal chemotherapy

Brief summary

Comparison of cumulative incidence of CNS relapses in patients with diffuse large B-cell lymphoma with intermediate or high risk of CNS relapse treated with CNS prophylaxis: either with 2 doses of intravenous methotrexate 3g/m2 i.v.(arm A) or 6 doses of intrathecal methotrexate 12mg (arm B) and in patients with low risk of CNS relapse without CNS prophylaxis (arm C).

Detailed description

Patients with diffuse large B-cell lymphoma are evaluated for risk factors of CNS relapse during initial staging (age \> 60years, lactate dehydrogenase (LDH) \> reference range, clinical stage III/IV, performance status according to Eastern Cooperative Oncology Group (ECOG) \>1, kidney and/or adrenal gland involvement, involvement \> 1 extranodal organ) including evaluation of cerebrospinal fluid. All patients with systemic DLBCL without CNS involvement are treated with systemic chemotherapy: either 6 cycles of R CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednison) +2xR (rituximab) or 6 cycles of DA EPOCH R (dose adjusted etoposide, prednison, vincristin, cyclophosphamide, doxorubicin) +2xR (rituximab). Patients with ≥ 2 risk factors for CNS relapse or with occult meningeal involvement will be randomized in 1:1 ratio either into arm A with 2 cycles of prophylactic methotrexate 3g/m2 i.v., or into arm B with prophylactic 6x intrathecal methotrexate 12mg (1x intrathecal methotrexate in each cycle of systemic chemotherapy). Patients with 0-1 risk factor will be allocated into arm C without CNS prophylaxis. Patients will be observed for CNS relapse during the follow-up of 1year after the end of the first-line treatment.

Interventions

DRUGMethotrexate

i.v. or intrathecal CNS prophylaxis

Sponsors

Czech Lymphoma Study Group
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 72 Years
Healthy volunteers
No

Inclusion criteria

* histologically confirmed DLBCL * age 18-72 years * signed informed consent with the study * first-line treatment 6 cycles of R CHOP +2x R or 6 cycles of DA EPOCH R+ 2xR

Exclusion criteria

* DLBCL and concomitant initial CNS involvement * PMBL (primary mediastinal B-cell lymphoma) * treatment with another chemotherapy than R CHOP or DA EPOCH R * HIV positive, or active hepatitis B or C * other concomitant serious disease (based on the decision of the physician-investigator) * non-compliance of a patient * any contraindication for application of anthracycline based chemotherapy or high dose methotrexate * pregnancy or breast-feeding

Design outcomes

Primary

MeasureTime frame
Cumulative incidence of CNS relapse in patients treated either with methotrexate i.v. or methotrexate i.t. or without CNS prophylaxis1 year

Secondary

MeasureTime frame
Overall survival2 years
Progression-free survival2 years
Complete remission rate1 year
Overall response rate1 year

Countries

Czechia

Contacts

Primary ContactHeidi Mocikova, M.D., Ph.D.
heidi.mocikova@fnkv.cz+420267163554

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 2, 2026