Drug intelligence / Profile preview

standard consolidation therapy-Federal Research Institute of Pediatric Hematology, Oncology and Immunology-acute lymphoblastic leukemia

Development stage
Unknown
Lead developer
Federal Research Institute of Pediatric Hematology
Modality
Recombinant Proteins and Enzymes, Small Molecules
Administration
Oral, Intravenous, Intramuscular, Intrathecal
01

Overview

Standard consolidation therapy-Federal Research Institute of Pediatric Hematology, Oncology and Immunology-acute lymphoblastic leukemia refers to a specific multi-agent chemotherapy regimen used as the control or standard-of-care arm in the ALL-MB 2015 (Moscow-Berlin 2015) clinical trial. Developed by the Federal Research Institute of Pediatric Hematology, Oncology and Immunology (Dmitry Rogachev National Medical Research Center), this protocol is designed for children, adolescents, and young adults with acute lymphoblastic leukemia (ALL). The consolidation phase is structured into three 6-week cycles (S1, S2, and S3) and utilizes a combination of 6-mercaptopurine, methotrexate, L-asparaginase, vincristine, dexamethasone, and daunorubicin. It also incorporates central nervous system prophylaxis through triple intrathecal therapy consisting of methotrexate, cytarabine, and prednisone. The regimen aims to eliminate minimal residual disease following induction therapy to prevent relapse and improve long-term event-free survival.

Other names
Standard consolidation therapy (ALL-MB 2015)
02

Targets

HPRT1 (Hypoxanthine-guanine phosphoribosyltransferase)TOP2A (DNA topoisomerase II)GR (Glucocorticoid receptor)DHFR (Dihydrofolate reductase)DNATUBB (Tubulin (alpha and beta subunits))

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