Diffuse Large B-cell Lymphoma
Conditions
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
i.v. or intrathecal CNS prophylaxis
Sponsors
Study design
Eligibility
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
| Measure | Time frame |
|---|---|
| Cumulative incidence of CNS relapse in patients treated either with methotrexate i.v. or methotrexate i.t. or without CNS prophylaxis | 1 year |
Secondary
| Measure | Time frame |
|---|---|
| Overall survival | 2 years |
| Progression-free survival | 2 years |
| Complete remission rate | 1 year |
| Overall response rate | 1 year |
Countries
Czechia