Purpose: Corticosteroids are widely used in the treatment of acute lymphobl
astic leukemia (ALL), To determine the frequency of corticosteroid-associat
ed bony morbidity in children with ALL, we retrospectively evaluated the in
cidence of fractures and osteonecrosis (ON) on two consecutive pediatric AL
L protocols.
Patients and Methods: One hundred seventy-six consecutive children were tre
ated for ALL between 1987 and 1995 at the Dana-Farber Cancer Institute and
Children's Hospital. Prednisone was used as the corticosteroid during postr
emission therapy from 1987 to 1991, and dexamethasone was used from 1991 to
1995; Medical records for all patients were reviewed to assess the occurre
nce of fractures and ON.
Results; With a median follow-up of 7.6 years, the 5-year cumulative incide
nce (CI) +/- SE of any bony morbidity for the 176 patients was 30% +/- 4%,
with a 5-year CI of fractures of 28% +/- 3% and of ON of 7% +/- 2%, With mu
ltivariate analysis, independent predictors of bony morbidity included age
9 to 18 years at diagnosis (P < .01), male sex (P < .01), and treatment wit
h dexamethasane (P = .01). Dexamethasone was associated with a higher risk
of fractures (5-year CI, 36% +/- 5% v 20% +/- 4% with prednisone; P = .04),
but not ON (P = .40). The 5-year event-free survival for the 176 patients
was 79% +/- 3%.
Conclusion: Children treated for ALL had a high incidence of fractures and
ON. Older children, boys, and patients receiving dexamethasone were at incr
eased risk for the development of bony morbidity, Future studies should att
empt to minimize corticosteroid-associated bony morbidity without compromis
ing clinical efficacy. J Clin Oncol 19:3066-3072. (C) 2001 by American Soci
ety of Clinical Oncology.