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Spots Global Cancer Trial Database for CNS Prophylaxis in Diffuse Large B-cell Lymphoma

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Trial Identification

Brief Title: CNS Prophylaxis in Diffuse Large B-cell Lymphoma

Official Title: 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

Study ID: NCT02777736

Interventions

Methotrexate

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University Hospital Brno-Bohunice, Brno, , Czech Republic

University Hospital Hradec Králové, Hradec Králové, , Czech Republic

University Hospital Ostrava, Ostrava, , Czech Republic

University Hospital Pilsen, Pilsen, , Czech Republic

University Hospital Kralovske Vinohrady, Prague, , Czech Republic

General University Hospital Prague, Prague, , Czech Republic

Contact Details

Name: Heidi Mocikova, M.D., Ph.D.

Affiliation: University Hospital Kralovske Vinohrady, Prague, Czech Republic

Role: PRINCIPAL_INVESTIGATOR

Name: Marek Trněný, prof.M.D.

Affiliation: General University Hospital, Prague

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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