InstituteHBDH
Tianjin, Tianjin Municipality, 300020, China
NCT Number: NCT03165851
The investigators adopted the CAMS(Chinese Academy of Medical Sciences)-2009 trial for pediatric acute myeloid leukemia (AML) patients between 2009 to 2015, in which a risk-stratified strategy and dose-dense intensive chemotherapy were introduced. The outcomes of CAMS-2009 trial were retrospectively analyzed, and compared to the CAMS-2005 trial.
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Notify Me6 month–16 year
All sexes
Observational
Tianjin, Tianjin Municipality, 300020, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Dose-dense intensive chemotherapy and high dose of Ara-C in the consolidation therapy.
Time frame: From date of diagnosed until the date of death from any cause, assessed up to 60 months
overall survival
Time frame: From date of diagnosed until the date of first relapse or date of death from any cause, whichever came first, assessed up to 60 months
event-free survival
Time frame: through study completion, an average of 1 year
fewer than 5% blast cells in the bone marrow aspirate and the absence of extramedullary involvement (EMI)
Institute of Hematology & Blood Diseases Hospital, China
Other
Efficacy Analysis of Comparison of CAMS-2005 Trial and CAMS-2009 Trial for Pediatric Acute Myeloid Leukemia
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