Bony morbidity in children treated for acute lymphoblastic leukemia

被引:179
作者
Strauss, AJ
Su, JT
Dalton, WMK
Gelber, RD
Sallan, SE
Silverman, LB
机构
[1] Dana Farber Canc Inst, Qual Control Ctr, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Dept Biostat Sci, Boston, MA 02115 USA
[4] Massachusetts Gen Hosp, Dept Pediat, Boston, MA 02114 USA
[5] Childrens Hosp, Div Hematol Oncol, Boston, MA 02115 USA
[6] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
关键词
D O I
10.1200/JCO.2001.19.12.3066
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Corticosteroids are widely used in the treatment of acute lymphoblastic leukemia (ALL), To determine the frequency of corticosteroid-associated bony morbidity in children with ALL, we retrospectively evaluated the incidence of fractures and osteonecrosis (ON) on two consecutive pediatric ALL protocols. Patients and Methods: One hundred seventy-six consecutive children were treated for ALL between 1987 and 1995 at the Dana-Farber Cancer Institute and Children's Hospital. Prednisone was used as the corticosteroid during postremission therapy from 1987 to 1991, and dexamethasone was used from 1991 to 1995; Medical records for all patients were reviewed to assess the occurrence of fractures and ON. Results; With a median follow-up of 7.6 years, the 5-year cumulative incidence (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 multivariate analysis, independent predictors of bony morbidity included age 9 to 18 years at diagnosis (P < .01), male sex (P < .01), and treatment with 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 increased risk for the development of bony morbidity, Future studies should attempt to minimize corticosteroid-associated bony morbidity without compromising clinical efficacy. J Clin Oncol 19:3066-3072. (C) 2001 by American Society of Clinical Oncology.
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收藏
页码:3066 / 3072
页数:7
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