Symptomatic osteonecrosis in children treated for Hodgkin lymphoma: A population-based study in Sweden, Finland, and Denmark

IF 2.4 3区 医学 Q2 HEMATOLOGY Pediatric Blood & Cancer Pub Date : 2024-08-14 DOI:10.1002/pbc.31250
Mia Giertz, Henri Aarnivala, Sascha Wilk Michelsen, Caroline Björklund, Annika Englund, Marika Grönroos, Lisa Lyngsie Hjalgrim, Pasi Huttunen, Tuukka Niinimäki, Eva Penno, Tuuli Pöyhönen, Päivi Raittinen, Susanna Ranta, Johan E. Svahn, Lisa Törnudd, Riitta Niinimäki, Arja Harila
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Abstract

Background

Osteonecrosis (ON) is a potentially disabling skeletal complication of cancer treatment. Although symptomatic osteonecrosis (sON) is well-known in acute lymphoblastic leukemia (ALL), with an incidence around 6%, studies on sON in pediatric Hodgkin lymphoma (HL) are scarce. The aim of this study was to examine the incidence, risk factors, and outcome of sON in children treated for HL.

Procedure

A total of 490 children under 18, diagnosed with HL between 2005 and 2019 in Sweden, Finland, and Denmark were eligible for the study. Data on patient characteristics, HL treatment, and development of sON were collected from patients’ medical records. Magnetic resonance imaging scans were used to establish ON diagnosis and grade ON according to the Niinimäki grading system.

Results

Cumulative 2-year incidence of sON among the 489 included patients was 5.5% (n = 30). The risk for developing sON was higher for those with older age (odds ratio [OR] 1.25, 95% confidence interval [CI]: 1.05–1.49, < .010), female sex (OR 4.45, CI 1.87–10.58, < .001), high total cumulative glucocorticoid (GC) doses (OR 1.76, 95% CI: 1.21-2.56, = 0.003), and advanced HL (OR 2.19, 95% CI: 1.03-4.65, = .042). Four (13.3%) patients underwent major surgical procedures and 13 (43.3%) had persistent symptoms due to ON at follow-up.

Conclusions

This study shows that sON is as common in pediatric HL as in pediatric ALL, with risk factors such as older age, female sex, high cumulative GC doses, and advanced HL. Future HL protocol development should aim to reduce the burden of ON by modifying GC treatment.

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霍奇金淋巴瘤患儿的症状性骨坏死:一项基于瑞典、芬兰和丹麦人口的研究。
背景:骨坏死(ON)是癌症治疗的一种潜在致残性骨骼并发症。尽管症状性骨坏死(sON)在急性淋巴细胞白血病(ALL)中的发病率约为6%,但有关小儿霍奇金淋巴瘤(HL)中症状性骨坏死的研究却很少。本研究旨在探讨接受 HL 治疗的儿童中 sON 的发生率、风险因素和结果:2005年至2019年期间,瑞典、芬兰和丹麦共有490名18岁以下儿童被诊断为HL,符合研究条件。从患者病历中收集了有关患者特征、HL治疗和sON发展的数据。磁共振成像扫描用于确诊ON,并根据Niinimäki分级系统对ON进行分级:结果:在纳入的 489 名患者中,两年内 sON 的累计发病率为 5.5%(n = 30)。年龄越大的患者发生 sON 的风险越高(赔率比 [OR] 1.25,95% 置信区间 [CI]:1.05-1.49,P<0.05):1.05-1.49, p 结论:本研究表明,sON 在小儿 HL 中与小儿 ALL 一样常见,其风险因素包括年龄较大、女性、高累积 GC 剂量和晚期 HL。未来HL治疗方案的制定应着眼于通过调整GC治疗来减轻ON的负担。
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来源期刊
Pediatric Blood & Cancer
Pediatric Blood & Cancer 医学-小儿科
CiteScore
4.90
自引率
9.40%
发文量
546
审稿时长
1.5 months
期刊介绍: Pediatric Blood & Cancer publishes the highest quality manuscripts describing basic and clinical investigations of blood disorders and malignant diseases of childhood including diagnosis, treatment, epidemiology, etiology, biology, and molecular and clinical genetics of these diseases as they affect children, adolescents, and young adults. Pediatric Blood & Cancer will also include studies on such treatment options as hematopoietic stem cell transplantation, immunology, and gene therapy.
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