Cm. Kullendorff et An. Bekassy, SALVAGE TREATMENT OF RELAPSING WILMS-TUMOR BY AUTOLOGOUS BONE-MARROW TRANSPLANTATION, European journal of pediatric surgery, 7(3), 1997, pp. 177-179
Despite the remarkable success in treatment of Wilms' tumour there is
still a small group who will suffer from relapse. The optimal therapy
for relapsing Wilms tumour has not been determined. We have treated fo
ur children with high-dose chemotherapy (HDC) followed by stem-cell su
pport known as autologous bone marrow transplantation (ABMT). The pati
ents were two girls and two boys aged 1-9 years. The histology was fav
ourable in 3 cases and unfavourable, clear cell sarcoma, in 1. The rel
apses were pulmonary in 2 cases and skeletal in 2 cases. There was no
detectable disease prior to ABMT. After ABMT 2 children got further re
lapses and died. On the other hand a children had no further relapse a
nd are alive and well 1.5-2.5 years later. Treatment with HDC and ABMT
is complicated and expensive but may be of benefit and should be adde
d to the treatment options in children with otherwise poor prognosis o
f Wilms' tumour.