Follow‐up of osteonecrosis in paediatric acute lymphoblastic leukaemia patients treated with the NOPHO ALL2008 protocol

dc.contributor.authorRokkanen, Roosa
dc.contributor.authorAarnivala, Henri
dc.contributor.authorHuhtaniska, Sanna
dc.contributor.authorPalmu, Sauli
dc.contributor.authorPokka, Tytti
dc.contributor.authorPöyhönen, Tuuli
dc.contributor.authorSuo‐Palosaari, Maria
dc.contributor.authorUtriainen, Pauliina
dc.contributor.authorJärvelä, Liisa
dc.contributor.authorNiinimäki, Riitta
dc.contributor.organizationfi=lastentautioppi|en=Paediatrics and Adolescent Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.40612039509
dc.converis.publication-id499693400
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/499693400
dc.date.accessioned2026-01-21T12:37:36Z
dc.date.available2026-01-21T12:37:36Z
dc.description.abstract<p>Although osteonecrosis (ON) is a common sequel after childhood acute lymphoblastic leukaemia treatment and may cause debilitating symptoms, its prognosis remains underexplored. We describe the radiological evolution of ON lesions in a Finnish patient cohort treated according to the The Nordic Society of Paediatric Haematology and Oncology (NOPHO) ALL2008 protocol. We aimed to identify the factors influencing the outcome of ON. We collected data from 37 patients diagnosed with ON treated in five tertiary centres. We analysed magnetic resonance imaging scans containing 235 ON lesions (109 affecting joints) and graded them using the Niinimäki classification system. The mean follow-up time from an ON diagnosis was 3.3 years (SD 3.4 range: 0.04–13.5). Among the lesions with follow-up scans, 55% remained stable, 35% resolved, 8% improved to lower grade and 2% progressed. Joint collapse was observed in 18 joint lesions (17%). Factors associated with unfavourable outcomes were female sex, older age at diagnosis and haematopoietic stem cell transplantation (HSCT). The chance for spontaneous resolution of ON was lower in females (adjusted odds ratio [aOR] 10.3, 95% CI 2.0–52.6) and decreased with age (aOR 1.4, 95% CI 1.1–1.7), whereas HSCT was associated with joint collapse already at ON diagnosis (aOR 8.3, 95% CI 2.6–27.0).<br></p>
dc.format.pagerange1912
dc.format.pagerange1919
dc.identifier.eissn1365-2141
dc.identifier.jour-issn0007-1048
dc.identifier.olddbid212755
dc.identifier.oldhandle10024/195773
dc.identifier.urihttps://www.utupub.fi/handle/11111/53367
dc.identifier.urlhttps://doi.org/10.1111/bjh.70085
dc.identifier.urnURN:NBN:fi-fe202601216121
dc.language.isoen
dc.okm.affiliatedauthorJärvelä, Liisa
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherWiley
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumberbjh.70085
dc.relation.doi10.1111/bjh.70085
dc.relation.ispartofjournalBritish Journal of Haematology
dc.relation.issue5
dc.relation.volume207
dc.source.identifierhttps://www.utupub.fi/handle/10024/195773
dc.titleFollow‐up of osteonecrosis in paediatric acute lymphoblastic leukaemia patients treated with the NOPHO ALL2008 protocol
dc.year.issued2025

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