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Osteonecrosis in patients with acute lymphoblastic leukaemia: a national questionnaire study
  1. Nadia Laila Amin1,2,
  2. Richard Feltbower1,
  3. Sally Kinsey1,2,
  4. Ajay Vora3,
  5. Beki James1
  1. 1 Paediatric haematology, Leeds Children’s Hospital, Leeds, UK
  2. 2 University of Leeds, Leeds, UK
  3. 3 Paediatric haematology, Great Ormond Street Hospital, London, UK
  1. Correspondence to Dr Nadia Laila Amin; nadia{at}cantab.net

Abstract

Objectives To establish prevalence, management and long-term outcomes of osteonecrosis (ON) in young people diagnosed with acute lymphoblastic leukaemia (ALL) between 2003 and 2011.

Design, setting, participants This study assessed ON in 3113 patients aged 1–24 years who participated in the UK national leukaemia study UKALL 2003. UKALL 2003 recruited patients in 40 UK hospitals between 2003 and 2011 and included patients between ages 1 and 25 diagnosed with ALL.

Results 170 patients were diagnosed with ON, giving a prevalence of 5.5%. The multivariable analysis showed that the risk of ON was highest for children aged between 10 and 20 years (ages 10–15 years, OR 23.7, 95% CI 14.8 to 38.0; ages 16–20 years, OR 22.5, 95% CI 12.7 to 39.8, compared with age <10 years). Among ethnic groups, Asian patients had the highest risk of ON (OR 1.92, 95% CI 1.1 to 3.6, compared with White patients). Eighty-five per cent of patients with ON had multifocal ON. Thirty-eight per cent of patients with ON required surgery and 19% of patients with ON required a hip replacement. Fifteen per cent of patients who had surgery still describe significant disability or use of a wheelchair.

Conclusions ON has considerable morbidity for patients being treated for ALL, with a high burden of surgery. Age and ethnicity were found to be the most significant risk factors for development of ON, with Asian patients and patients aged 10–20 years at diagnosis of ALL at greatest risk. These results will help risk stratify patients at diagnosis of ALL, and help tailor future prospective studies in this area.

  • bone disease
  • haematology
  • musculoskeletal

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

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Footnotes

  • Contributors NLA designed the data collection tools, developed the methodology, acquired, analysed and interpreted the data, and wrote and revised the manuscript. She is the guarantor. BJ designed the data collection tools, developed the methodology, and wrote and revised the manuscript. RF analysed and interpreted the data, and wrote and revised the manuscript.SK developed the data collection tools, and wrote and revised the manuscript. AV wrote and revised the manuscript. Study supervision was by BJ, SK and RF.

  • Competing interests None declared.

  • Ethics approval Scottish Multi-Centre Research Ethics Committee.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement The relevant anonymised patient-level data are available on reasonable request from the authors.

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