儿童和青少年急性淋巴细胞白血病(ALL)强化治疗后骨坏死的发病率和转归

Incidence and outcome of osteonecrosis in children and adolescents after intensive therapy for acute lymphoblastic leukemia (ALL).

作者信息

Padhye Bhavna, Dalla-Pozza Luciano, Little David, Munns Craig

机构信息

Department of Oncology, The Children's Hospital at Westmead, Sydney, Australia.

Department Orthopaedics, The Children's Hospital at Westmead, Sydney, Australia.

出版信息

Cancer Med. 2016 May;5(5):960-7. doi: 10.1002/cam4.645. Epub 2016 Jan 20.

Abstract

Osteonecrosis (ON), a significant complication following treatment of acute lymphoblastic leukemia (ALL), has a profound impact on quality of life of ALL survivors. We studied incidence and outcome of ON in patients treated on or according to Australian and New Zealand Children's Haematology/ Oncology Group (ANZCHOG) study 8 at The Children's Hospital at Westmead. The study involved retrospective chart review of the patients. ON was defined by development of symptoms and confirmed by magnetic resonance imaging. From 2002-2011, 251 patients (143M, 108F, 59 Standard Risk (SR), 159 Medium Risk (MR) 5 High Risk (HR), and 28 Very high risk (VHR)) were treated according to study 8. Eighteen (7M, 11F, 2 SR, 12 MR, 4 VHR) patients developed ON (7.2%). Median age at diagnosis was 13.05 years(4.3-16.7). Incidence of ON in patients > 10 years at diagnosis was 29%. Six out of 18 patients developed ON after allogeneic stem cell transplantation. Median time from diagnosis to the development of ON following chemotherapy for ALL was 1.15 years (range 0.25-2.12). Most patients were treated with intravenous Zoledronic acid. At last follow-up, three patients had undergone arthroplasty, two patients were symptom free, and the remaining 13 patients reported persistent pain with activity. A majority of patients with ON of the hips had radiological progression. Overall, 7% of patients with ALL developed ON. Age >10 years was the most important risk factor. At last follow-up, 70% of patients had persistent symptoms. Although Zoledronic acid improved pain, most patients with ON of the hips had radiological progression.

摘要

骨坏死(ON)是急性淋巴细胞白血病(ALL)治疗后的一种严重并发症,对ALL幸存者的生活质量有深远影响。我们研究了在悉尼韦斯特米德儿童医院接受澳大利亚和新西兰儿童血液学/肿瘤学组(ANZCHOG)第8项研究治疗或参照该研究治疗的患者中ON的发生率和转归。该研究涉及对患者病历的回顾性分析。ON通过症状出现来定义,并经磁共振成像证实。2002年至2011年,根据第8项研究治疗了251例患者(143例男性,108例女性,59例标准风险(SR),159例中度风险(MR),5例高风险(HR),28例极高风险(VHR))。18例(7例男性,11例女性,2例SR,12例MR,4例VHR)患者发生了ON(7.2%)。诊断时的中位年龄为13.05岁(4.3 - 16.7岁)。诊断时年龄>10岁的患者中ON的发生率为29%。18例患者中有6例在异基因干细胞移植后发生ON。ALL化疗后从诊断到ON发生的中位时间为1.15年(范围0.25 - 2.12年)。大多数患者接受了静脉注射唑来膦酸治疗。在最后一次随访时,3例患者接受了关节置换术,2例患者无症状,其余13例患者报告活动时持续疼痛。大多数髋部ON患者有影像学进展。总体而言,7%的ALL患者发生了ON。年龄>10岁是最重要的危险因素。在最后一次随访时,70%的患者有持续症状。尽管唑来膦酸改善了疼痛,但大多数髋部ON患者有影像学进展。

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