An international strategy to determine the role of high dose therapy in recurrent Wilms%26apos; tumour

作者:Ha Tam C; Spreafico Filippo; Graf Norbert; Dallorso Sandro; Dome Jeffrey S; Malogolowkin Marcio; Furtwaengler Rhoikos; Hale Juliet P; Moroz Veronica; Machin David; Pritchard Jones Kathy*
来源:European Journal of Cancer, 2013, 49(1): 194-210.
DOI:10.1016/j.ejca.2012.07.010

摘要

Purpose: To review event-free (EFS) and overall survival (OS) from publications describing outcome for children with relapsed Wilms%26apos; tumour. Comparisons are made between those receiving myeloablative high dose chemotherapy with autologous stem-cell rescue (HDT) and those not (NoHDT). %26lt;br%26gt;Materials and methods: Relevant information was extracted from individual patient or summary data and 3-year EFS and OS rates established. These rates were combined in a weighted manner to derive hazard ratios (HRs). %26lt;br%26gt;Results: Nineteen publications were identified (5 HDT, 6 NoHDT, 8 both). Pooling all studies suggested an advantage to HDT with a hazard ratio (HR) for EFS of 0.87 (95% confidence interval (CI) 0.67-1.12) and 0.94 (0.71-1.24) for OS. A stratified analysis confined to studies that provided individual patient data on both HDT and NoHDT gave HRs of 0.83 (0.56-1.24) and 0.92 (0.59-1.41). Further, analyses of risk groups, defined by treatment and/or histology prior to first relapse, suggested a HR for EFS of 0.90 (95% CI 0.62-1.31) for those of high and 0.50 (CI 0.31-0.82) for the very high risk patients. %26lt;br%26gt;Conclusion: The evidence suggests, although there are many caveats since the information summarised here is not from randomised trials, a great deal of uncertainty concerning the role of HDT in patients following relapse after treatment for their Wilms%26apos; tumour. For each risk group we propose a randomised trial comparing a standard with a more intensive therapy with specific choice of regimen tailored to the risk group (and co-operative groups) concerned. A synthesis of updated evidence from studies in this overview together with any emerging studies and future trial information will form the basis for future evidence-based clinical decision-making.

  • 出版日期2013-1