Prospective Study on Incidence, Risk Factors, and Long-Term Outcome of Osteonecrosis in Pediatric Acute Lymphoblastic Leukemia
AVASCULAR NECROSIS
Male
Adolescent
EMC NIHES-01-66-01
CHILDREN
PREDNISOLONE
Kaplan-Meier Estimate
THERAPY
Dexamethasone
MORBIDITY
03 medical and health sciences
0302 clinical medicine
ONCOL 2: Age-related aspects of cancer
ADOLESCENTS
Antineoplastic Combined Chemotherapy Protocols
Odds Ratio
Prevalence
Humans
Child
Netherlands
COMPLICATIONS
EMC NIHES-03-30-01
Incidence
Age Factors
Osteonecrosis
CHEMOTHERAPY
EMC MM-02-54-03
Precursor Cell Lymphoblastic Leukemia-Lymphoma
CANCER
Magnetic Resonance Imaging
3. Good health
Logistic Models
Child, Preschool
Multivariate Analysis
Female
BONE
Follow-Up Studies
DOI:
10.1200/jco.2011.37.3217
Publication Date:
2011-09-27T06:26:36Z
AUTHORS (12)
ABSTRACT
Purpose We studied cumulative incidence, risk factors, therapeutic strategies, and outcome of symptomatic osteonecrosis in pediatric patients with acute lymphoblastic leukemia (ALL). Patients and Methods Cumulative incidence of osteonecrosis was assessed prospectively in 694 patients treated with the dexamethasone-based Dutch Child Oncology Group–ALL9 protocol. Osteonecrosis was defined by development of symptoms (National Cancer Institute grade 2 to 4) during treatment or within 1 year after treatment discontinuation, confirmed by magnetic resonance imaging. We evaluated risk factors for osteonecrosis using logistic multivariate regression. To describe outcome, we reviewed clinical and radiologic information after antileukemic treatment 1 year or more after osteonecrosis diagnosis. Results Cumulative incidence of osteonecrosis at 3 years was 6.1%. After adjustment for treatment center, logistic multivariate regression identified age (odds ratio [OR], 1.47; P < .01) and female sex (OR, 2.23; P = .04) as independent risk factors. Median age at diagnosis of ALL in patients with osteonecrosis was 13.5 years, compared with 4.7 years in those without. In 21 (55%) of 38 patients with osteonecrosis, chemotherapy was adjusted. Seven patients (18%) underwent surgery: five joint-preserving procedures and two total-hip arthroplasties. Clinical follow-up of 35 patients was evaluated; median follow-up was 4.9 years. In 14 patients (40%), symptoms completely resolved; 14 (40%) had symptoms interfering with function but not with activities of daily living (ADLs; grade 2); seven (20%) had symptoms interfering with ADLs (grade 3). In 24 patients, radiologic follow-up was available; in six (25%), lesions improved/disappeared; in 13 (54%), lesions remained stable; five (21%) had progressive lesions. Conclusion Six percent of pediatric patients with ALL developed symptomatic osteonecrosis during or shortly after treatment. Older age and female sex were risk factors. After a median follow-up of 5 years, 60% of patients had persistent symptoms.
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