B. Jereb et al., RADIOTHERAPY IN THE SIOP (INTERNATIONAL-SOCIETY-OF-PEDIATRIC-ONCOLOGY) NEPHROBLASTOMA STUDIES - A REVIEW, Medical and pediatric oncology, 22(4), 1994, pp. 221-227
For decades radiation has generally been accepted as a valuable supple
ment to surgery in the treatment of Wilms' tumor; unfortunately, it ma
y produce undesirable late effects. It turned out, however, that when
treatment is adjusted to known variables, the risk for late sequelae c
an be diminished in some groups of children. SIOP clinical trials have
been based on children with unilateral tumors of standard histology a
nd free of metastasis at diagnosis. The first two clinical trials, SIO
P-1 (started in 1971) and SIOP-2 (started in 1974), established the be
neficial effect (such as less ruptures, lower stage) of preoperative r
adiation and actinomycin D (AMD) in SIOP-2, with all children having r
adiation therapy either preoperatively, postoperatively, or both. In t
he SIOP-5 trial (started in 1977), preoperative radiation therapy and
AMD were compared with preoperative chemotherapy resulting in only 50%
of children having radiation. The result permitted disuse of preopera
tive radiation in the SIOP-6 trial (started in 1980), where only one-t
hird of the patients received postoperative radiation therapy. At pres
ent, in the SIOP-9 trial (started in 1987), fewer than 20% of children
are having radiotherapy. The survival rates meanwhile have been incre
asing steadily from 64% in SIOP-1 to 84% in SIOP-6 for stages I, II, a
nd III combined. (C) 1994 Wiley-Liss, Inc.