Volume 155, Issue 5 pp. 549-560
State of the art review

Management of osteonecrosis in children and young adults with acute lymphoblastic leukaemia

Ajay Vora

Ajay Vora

Department of Paediatric Haematology, The Children’s Hospital Sheffield, Sheffield, UK

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First published: 21 September 2011
Citations: 44
Professor Ajay Vora, Department of Paediatric Haematology, The Children’s Hospital Sheffield, Western Bank Sheffield, S10 2TH, UK
E-mail:[email protected]

Summary

Osteonecrosis is a disabling complication in children and young adults with acute lymphoblastic leukaemia. It can affect any or multiple joints but the hip and knee are most frequently involved and a cause of long-term disability. The problem is almost exclusively that of older children and young adults of whom over 70% have asymptomatic changes on screening magnetic resonance imaging and 15–20% have resulting symptoms. Dexamethasone is associated with a higher risk than prednisolone in US but not European or UK trials and alternate week scheduling of dexamethasone in the intensification course is associated with a lower risk than a continuous 3-week schedule in US trials. Genetic factors and obesity contribute to the risk, as do metabolic abnormalities caused by drugs, such as asparaginase, which increase tissue exposure to steroids. Management is primarily supportive but a minority of patients require surgical intervention including replacement of the affected joint. A variety of surgical techniques and, latterly, bisphophonates, have been tried to prevent progression but their efficacy remains uncertain. Whether patients should continue to receive steroids after diagnosis of osteonecrosis is uncertain but most trial investigators recommend stopping them after completion of the intensification phase of treatment.

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