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. 2022 Sep 27;2022(9):CD014638. doi: 10.1002/14651858.CD014638.pub2

Chow 2016.

Methods Method of randomisation not clear.
Participants 94 survivors of paediatric T‐cell ALL (stage nm) or low, intermediate or high risk Hodgkin lymphoma (mean age at time of study 28 years; N = 40 females and N = 54 males) treated with doxorubicin (cumulative dose average 279 mg/m2; peak dose (i.e. maximal dose received in 1 week) nm; infusion duration nm). No prior anthracycline therapy. No prior cardiac radiotherapy. Prior cardiac dysfunction before the long‐term follow‐up: N = 2 in dexrazoxane group clinical cardiomyopathy.
Interventions Dexrazoxane (ratio to doxorubicin 10:1; intravenous bolus before each doxorubicin dose) (N = 51) versus no cardioprotective intervention (N = 43).
Outcomes Heart failure (i.e. clinical cardiomyopathy and different abnormalities on echocardiography): fractional shortening < 28% in 2 dexrazoxane and 1 control participant; no results of other parameters presented.
Notes These are preliminary analyses. Median 16 years since diagnosis. Cumulative anthracycline dose per treatment group nm. Age per treatment group nm. Only a subset of participants (N = 43) had ejection fraction evaluable.