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pieces of information: outcome, measurement device, metric, method of  aggregation, primacy of outcome, whether the outcome was a harm or side effect  of an intervention, study design, sample size, & study type. When coding sample size for studies including non-pediatric-ALL research, all study participants were counted, including adult  patients and pediatric patients with a cancer other than ALL.

 

Analysis:

After coding, outcomes were grouped into eight domains for analysis: 1) Survival; 2) Mortality; 3)  Remission; 4) Relapse; 5) Response to Treatment; 6) Adverse Event; 7) Cognitive  Event; 8) Other.