• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

骨坏死:儿童急性淋巴细胞白血病(ALL)中一种与治疗相关的毒性反应——来自ALL-BFM 95试验的经验

Osteonecrosis: a treatment related toxicity in childhood acute lymphoblastic leukemia (ALL)--experiences from trial ALL-BFM 95.

作者信息

Bürger Britta, Beier Rita, Zimmermann Martin, Beck Jörn D, Reiter Alfred, Schrappe Martin

机构信息

Hannover Medical School, Department of Pediatric Hematology and Oncology, Hannover, Germany.

出版信息

Pediatr Blood Cancer. 2005 Mar;44(3):220-5. doi: 10.1002/pbc.20244.

DOI:10.1002/pbc.20244
PMID:15514916
Abstract

BACKGROUND

Osteonecrosis (ON) as a complication during treatment of acute lymphoblastic leukemia (ALL) has gained rising attention over the past decade. Corticosteroids, representing an essential element of antileukemic therapy, are known to induce ON, which in turn may cause significant morbidity. Due to spontaneous reporting of affected patients with ON, a group-wide evaluation was performed to determine incidence, risk factors, and morbidity for ON.

PROCEDURE

Patients were identified via spontaneous reporting to the study center and via questionnaire, addressing all 64 participating centers. We retrospectively analyzed 1,951 patients below 18 years of age who were treated according to trial ALL-BFM 95 between 01.01.1996 and 30.06.2000.

RESULTS

Thirty-one patients (14 male, 17 female) affected by ON were identified. The overall 5-year cumulative incidence for ON is 1.8%. The incidence for patients <10 years is 0.2%, whereas for patients >/=10 years it is 8.9% (P = 0.00) and 16.7% (P = 0.003) for patients >/=15 years. The majority (n = 20) showed ON in two or more joints, and the joints most commonly affected were knees (14 patients, 24 affected knees) and hips (11 patients, 20 affected joints). Thirteen out of 31 patients had to undergo surgery in the course of their disease.

CONCLUSIONS

Symptomatic ON is a rare event in patients treated with BFM-type chemotherapy with an overall 5-year cumulative incidence of 1.8%. The age group >/=10 years, and particularly adolescents >/=15 years have a significantly higher risk of developing ON.

摘要

背景

在过去十年中,作为急性淋巴细胞白血病(ALL)治疗期间的一种并发症,骨坏死(ON)日益受到关注。已知作为抗白血病治疗重要组成部分的皮质类固醇会诱发骨坏死,进而可能导致严重的发病情况。由于对骨坏死患者的自发报告,进行了一项全组评估以确定骨坏死的发病率、危险因素和发病情况。

程序

通过向研究中心的自发报告和问卷调查来确定患者,涉及所有64个参与中心。我们回顾性分析了1996年1月1日至2000年6月30日期间根据ALL - BFM 95试验接受治疗的1951名18岁以下患者。

结果

确定了31名受骨坏死影响的患者(14名男性,17名女性)。骨坏死的总体5年累积发病率为1.8%。年龄<10岁患者的发病率为0.2%,而年龄≥10岁患者的发病率为8.9%(P = 0.00),年龄≥15岁患者的发病率为16.7%(P = 0.003)。大多数患者(n = 20)在两个或更多关节出现骨坏死,最常受影响的关节是膝盖(14名患者,24个受影响膝盖)和髋关节(11名患者,20个受影响关节)。31名患者中有13名在病程中不得不接受手术。

结论

在接受BFM型化疗的患者中,有症状的骨坏死是一种罕见事件,总体5年累积发病率为1.8%。年龄≥10岁的年龄组,尤其是年龄≥15岁的青少年发生骨坏死的风险显著更高。

相似文献

1
Osteonecrosis: a treatment related toxicity in childhood acute lymphoblastic leukemia (ALL)--experiences from trial ALL-BFM 95.骨坏死:儿童急性淋巴细胞白血病(ALL)中一种与治疗相关的毒性反应——来自ALL-BFM 95试验的经验
Pediatr Blood Cancer. 2005 Mar;44(3):220-5. doi: 10.1002/pbc.20244.
2
Osteonecrosis: An emerging complication of intensive chemotherapy for childhood acute lymphoblastic leukemia.骨坏死:儿童急性淋巴细胞白血病强化化疗的一种新出现的并发症。
Haematologica. 2003 Jul;88(7):747-53.
3
Prognostic impact of age in children and adolescents with acute lymphoblastic leukemia: data from the trials ALL-BFM 86, 90, and 95.年龄对儿童和青少年急性淋巴细胞白血病的预后影响:来自ALL-BFM 86、90和95试验的数据。
Klin Padiatr. 2005 Nov-Dec;217(6):310-20. doi: 10.1055/s-2005-872515.
4
Joint preserving surgery for osteonecrosis and osteochondral defects after chemotherapy in childhood.儿童化疗后骨坏死和骨软骨缺损的保关节手术
Klin Padiatr. 2003 Nov-Dec;215(6):332-7. doi: 10.1055/s-2003-45495.
5
High body mass index increases the risk for osteonecrosis in children with acute lymphoblastic leukemia.高体重指数增加了急性淋巴细胞白血病患儿发生骨坏死的风险。
J Clin Oncol. 2007 Apr 20;25(12):1498-504. doi: 10.1200/JCO.2006.06.2539.
6
Methylenetetrahydrofolate reductase gene polymorphism and glucocorticoid intake in children with ALL and aseptic osteonecrosis.急性淋巴细胞白血病合并无菌性骨坏死患儿的亚甲基四氢叶酸还原酶基因多态性与糖皮质激素摄入情况
Klin Padiatr. 2003 Nov-Dec;215(6):327-31. doi: 10.1055/s-2003-45496.
7
Incidence of skeletal complications during treatment of childhood acute lymphoblastic leukemia: comparison of fracture risk with the General Practice Research Database.儿童急性淋巴细胞白血病治疗期间骨骼并发症的发生率:骨折风险与全科医学研究数据库的比较
Pediatr Blood Cancer. 2007 Jan;48(1):21-7. doi: 10.1002/pbc.20701.
8
Bone marrow oedema and aseptic osteonecrosis in children and adolescents with acute lymphoblastic leukaemia or non-Hodgkin-lymphoma treated with hyperbaric-oxygen-therapy (HBO): an approach to cure? -- BME/AON and hyperbaric oxygen therapy as a treatment modality.接受高压氧治疗(HBO)的急性淋巴细胞白血病或非霍奇金淋巴瘤儿童及青少年的骨髓水肿和无菌性骨坏死:一种治愈方法?——骨髓水肿/无菌性骨坏死与高压氧治疗作为一种治疗方式
Klin Padiatr. 2004 Nov-Dec;216(6):370-8. doi: 10.1055/s-2004-832341.
9
Skeletal morbidity in children receiving chemotherapy for acute lymphoblastic leukaemia.儿童急性淋巴细胞白血病化疗后的骨骼发病率。
Arch Dis Child. 2010 Oct;95(10):805-9. doi: 10.1136/adc.2009.172528. Epub 2010 Jun 24.
10
Impaired dexamethasone-related increase of anticoagulants is associated with the development of osteonecrosis in childhood acute lymphoblastic leukemia.地塞米松相关的抗凝剂增加受损与儿童急性淋巴细胞白血病骨坏死的发生有关。
Haematologica. 2008 Oct;93(10):1570-4. doi: 10.3324/haematol.12956. Epub 2008 Aug 12.

引用本文的文献

1
Assessment, diagnostic criteria, and outcome measures for non-femoral head lower limb avascular necrosis in children and adolescents: a scoping review.儿童和青少年非股骨头下肢缺血性坏死的评估、诊断标准及结局指标:一项范围综述
JBMR Plus. 2025 Jun 24;9(9):ziaf109. doi: 10.1093/jbmrpl/ziaf109. eCollection 2025 Sep.
2
Risk Factors for Corticosteroid-associated Osteonecrosis in Children: A National Database Study.儿童皮质类固醇相关骨坏死的危险因素:一项全国性数据库研究。
J Pediatr Soc North Am. 2025 May 23;12:100199. doi: 10.1016/j.jposna.2025.100199. eCollection 2025 Aug.
3
Glucocorticoid Therapy in Acute Lymphoblastic Leukemia: Navigating Short-Term and Long-Term Effects and Optimal Regimen Selection.
糖皮质激素治疗急性淋巴细胞白血病:短期和长期效应的探讨以及最佳方案的选择。
Curr Hematol Malig Rep. 2024 Aug;19(4):175-185. doi: 10.1007/s11899-024-00735-w. Epub 2024 Jun 13.
4
Physical impairments, activity limitations, and participation restrictions of childhood acute lymphoblastic leukemia survivors with and without hip osteonecrosis: a PETALE cohort study.有和没有髋部骨坏死的儿童急性淋巴细胞白血病幸存者的身体损伤、活动受限及参与限制:一项PETALE队列研究
J Cancer Surviv. 2024 May 24. doi: 10.1007/s11764-024-01585-4.
5
Pharmacovigilance for rare diseases: a bibliometrics and knowledge-map analysis based on web of science.罕见病药物警戒:基于 Web of Science 的文献计量学和知识图谱分析。
Orphanet J Rare Dis. 2023 Sep 26;18(1):303. doi: 10.1186/s13023-023-02915-y.
6
The incidence, risk factors, and outcomes of symptomatic avascular necrosis of bone among Chinese pediatric patients with acute lymphoblastic leukemia.中国儿童急性淋巴细胞白血病患者症状性骨缺血性坏死的发生率、危险因素和结局。
Cancer Med. 2023 May;12(9):10315-10325. doi: 10.1002/cam4.5762. Epub 2023 Mar 31.
7
[Osteonecrosis-severe side effect of treatment for acute lymphoblastic leukemia].[骨坏死——急性淋巴细胞白血病治疗的严重副作用]
Orthopadie (Heidelb). 2022 Oct;51(10):792-799. doi: 10.1007/s00132-022-04301-1. Epub 2022 Sep 7.
8
Risk factors for multi-joint disease in patients with glucocorticoid-induced osteonecrosis.糖皮质激素性骨坏死患者多关节病的危险因素。
Osteoporos Int. 2021 Oct;32(10):2095-2103. doi: 10.1007/s00198-021-05947-x. Epub 2021 Apr 20.
9
Prevalence of Osteopathologies in Children and Adolescents After Diagnosis of Acute Lymphoblastic Leukemia.急性淋巴细胞白血病诊断后儿童和青少年骨病的患病率
Front Pediatr. 2020 Aug 26;8:509. doi: 10.3389/fped.2020.00509. eCollection 2020.
10
British OsteoNEcrosis Study (BONES) protocol: a prospective cohort study to examine the natural history of osteonecrosis in older children, teenagers and young adults with acute lymphoblastic leukaemia and lymphoblastic lymphoma.英国骨坏死研究(BONES)方案:一项前瞻性队列研究,旨在研究急性淋巴细胞白血病和淋巴母细胞淋巴瘤的老年儿童、青少年和年轻成人中骨坏死的自然病程。
BMJ Open. 2019 May 22;9(5):e027204. doi: 10.1136/bmjopen-2018-027204.