Studies in the 1970s and 1980s suggested that the outcome of childhood acute lymphoblastic leukemia could be improved by intensification of conventional continuation chemotherapy with pulses of vincristine sulfate and steroids. We aimed to investigate the efficacy and toxic effects of vincristine-dexamethasone pulses as an addition to the continuation-therapy phase in a large cohort of children with intermediate-risk disease who were treated with the BFM treatment strategy
The study enrols children from 8 participating organizations. All children are treated with similar protocols based on the BFM treatment strategy, which include induction, consolidation, reinduction and continuation-therapy phases. At the beginning of the continuation-therapy phase, those patients in complete remission are randomly assigned to either a treatment or a control group. Control patients are given conventional mercaptopurine and methotrexate chemotherapy only. Patients in the treatment arm are also given pulses of vincristine (1.5 mg/sqm weekly for 2 weeks) and dexamethasone (6 mg/sqm daily for 7 days) every 10 weeks for six cycles.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
2,600
Department of Pediatric Hematology-Oncology, Italian Hospital
Buenos Aires, Argentina
Children's Cancer Research Institute, St Anna Kinderspital
Vienna, Austria
Department of Pediatric Hemato-Oncology, Gent University Hospital
Ghent, Belgium
Department of Pediatrics Hematology and Oncology, Hospital Roberto del Rio
disease free survival
survival
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Santiago, Chile
Department of Pediatric Hematology and Oncology, University Hospital Motol
Prague, Czechia
Medizinische Hochschule Hannover
Hanover, Germany
Department of Pediatrics, Semmelweis University
Budapest, Hungary
Pediatric Clinic - University of Milano-Bicocca
Monza, Italy