High incidence of treatment failure with vincristine, etoposide, epirubicin, and prednisolone chemotherapy with successful salvage in childhood Hodgkin disease

Abstract

Background and Procedure In an attempt to further reduce the long‐term toxicity of chemotherapy for childhood Hodgkin disease (HD), the Australian and New Zealand Children's Cancer Study Group between 1990 and 1996 enrolled 53 children with biopsy‐proven and imaging‐staged HD into a chemotherapy‐only treatment regimen using 5–6 courses of vincristine, etoposide, epirubicin, and prednisolone (VEEP). Results There were 23 events in these children with 3 progressive disease (PD), 8 partial remissions (PR), and 12 relapses. In the stage I patients, there were 8 events (35%). There was no association between the number of events and the stage of HD. Massive mediastinal disease at diagnosis was present in 16 patients, 11 of whom had an event with 3 PD, 3 PR, and 5 relapses. For all patients with an event at 6–24‐month follow‐up, all but two patients were salvaged with either alkylating agent‐based chemotherapy alone or with irradiation and chemotherapy. The event‐free survival for the whole group with median follow‐up of 33 months was 59%, but only 31% for massive mediastinal disease. Disease‐free survival was 78% and overall survival at 60 months was 92%, with one death due to drug‐induced aplasia and another from acute myeloid leukemia. Conclusions We conclude that VEEP chemotherapy in childhood HD used as the only treatment modality has an unacceptably high treatment failure rate in patients with massive mediastinal disease and 35% incidence of treatment failure in stage I disease. Med. Pediatr. Oncol. 32:255–258, 1999. © 1999 Wiley‐Liss, Inc.