“…A comprehensive review in 2015 summarized contemporary paediatric treatment approaches for de novo HL (Kelly, ). Five‐year DFS in paediatric HL ranged from 79·8% to 97% for low risk HL (Landman‐Parker et al , ; Mauz‐Korholz et al , ; Metzger et al , ; Tebbi et al , ; Wolden et al , ; Keller et al , ) to 77 to 90 % for high risk disease (Schwartz et al , ; Mauz‐Korholz et al , ; Kelly et al , ; Wolden et al , ; Friedman et al , ; Kelly et al , ) in completed trials. With the goal of lowering cumulative doses of anthracyclines to a doxorubicin equivalent dose of ≤250 mg/m 2 and alkylating agents to <7 g/m 2 (cyclophosphamide equivalent dose) (Green et al , ), contemporary paediatric chemotherapy regimens have diverged from the conventional adult approaches of ABVD (adriamycin, bleomycin, vinblastine, dacarbazine) and BEACOPP (bleomycin, etoposide, adriamycin, cyclophosphamide, vincristine, prednisone, procarbazine) by using combination chemotherapy with non‐cross‐resistant agents [adriamycin, bleomycin, vincristine, etoposide, prednisone, cyclophosphamide (ABVE‐PC) or vincristine, etoposide, prednisone, adriamycin/ cyclophosphamide vincristine, prednisone, dacarbazine (OEPA/COPDac)] (Mauz‐Korholz et al , ; Friedman et al , ).…”