Na. Heerema et al., Prognostic impact of trisomies of chromosomes 10, 17, and 5 among childrenwith acute lymphoblastic leukemia and high hyperdiploidy (> 50 chromosomes), J CL ONCOL, 18(9), 2000, pp. 1876-1887
Purpose: Children with acute lymphoblastic leukemia (ALL) and high hyperdip
loidy (> 50 chromosomes) have improved outcome compared with other ALL pati
ents. We sought to identify cytogenetic features that would predict differe
nces in outcome within this low-risk subset of ALL patients.
Materials and Methods: High-hyperdiploid ALL patients (N = 480) were enroll
ed between 1988 and 1995 on Children's Cancer Group (CCG) trials. Karyotype
s were determined by conventional banding. Treatment outcome was analyzed b
y life-table methods.
Results: Patients with 54 to 58 chromosomes had better outcome than patient
s with 51 to 53 or 59 to 68 chromosomes (P = .0002). Patients with a trisom
y of chromosome 10 (P < .0001), chromosome 17 (P = .0002), or chromosome 18
(P = .004) had significantly improved outcome compared with their counterp
arts who lacked the given trisomy. Patients with a trisomy of chromosome 5
had worse outcome than patients lacking this trisomy (P = .02). Patients wi
th trisomies of both chromosomes 10 and 17 had better outcome than those wi
th ct trisomy of chromosome 10 (P = .09), a trisomy of chromosome 17 (P = .
01), or neither trisomy (P < .0001). Multivariate analysis indicated that t
risomy of chromosome 10 (P = .001) was the most significant prognostic fact
or for high-hyperdiploid patients, yet trisomy of chromosome 17 (P =.02) or
chromosome 5 (P = .01) and modal chromosome number (P = .02) also had sign
ificant multivariate effects.
Conclusion: Trisomy of chromosomes 10 and 17 as well as modal chromosome nu
mber 54 to 58 identify subgroups of patients with high-hyperdiploid ALL who
have a better outcome than high-hyperdiploid patients who lack these cytog
enetic features. Trisomy of chromosome 5 confers poorer outcome among high-
hyperdiploid patients. (C) 2000 by American Society of Clinical Oncology.