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接受肉瘤治疗的儿科患者的骨矿物质密度不足。

Bone mineral density deficits in pediatric patients treated for sarcoma.

作者信息

Kaste Sue C, Ahn Hyunah, Liu Tiebin, Liu Wei, Krasin Matthew J, Hudson Melissa M, Spunt Sheri L

机构信息

Department of Radiological Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

出版信息

Pediatr Blood Cancer. 2008 May;50(5):1032-8. doi: 10.1002/pbc.21281.

Abstract

BACKGROUND

Children treated for sarcoma are at risk of treatment-associated deficits in bone mineral density (BMD). We investigated the severity of risk factors for BMD deficits in this patient population.

PROCEDURE

Using signed-rank test and logistic regression analysis, we retrospectively analyzed the relation of treatment variables and other potential risk factors to BMD (using quantitative computed tomography (QCT)) of 99 patients treated for pediatric sarcoma who had completed therapy at least 1 year previously.

RESULTS

The study group (38% rhabdomyosarcoma (RMS), 25% osteosarcoma (OS), 24% Ewing-family tumors, and 12% non-rhabdomyosarcoma soft-tissue sarcoma (NRSTS)) represented 22% of the sarcoma survivors treated between 1982 and 2003 who remained in follow-up at St. Jude. These patients underwent QCT between July 1, 1997 and February 5, 2003. Their median age was 8.7 years (range, 0.2-21.3 years) at diagnosis and 17.4 years (range, 3.3-30.2 years) at the time of BMD measurement; 58% were male and 82% Caucasian. Median BMD Z-score was -0.75 (range, -3.33-3.02), and median BMD was 168.0 mg/cc (range, 89.2-264.8 mg/cc). Risk of BMD deficit increased significantly with younger age at diagnosis (P = 0.044) and higher cumulative cyclophosphamide dose (P = 0.007). Patients with lower extremity primary disease had a significantly lower risk of BMD deficits than others. We found no association between BMD and body habitus, primary disease, lifestyle factors, or endocrinopathy.

CONCLUSION

A significant subset of sarcoma survivors are at risk of BMD deficits warranting prospective study of BMD to verify our results and refine risk factors contributing to BMD deficits.

摘要

背景

接受肉瘤治疗的儿童存在骨矿物质密度(BMD)与治疗相关的缺陷风险。我们调查了该患者群体中BMD缺陷风险因素的严重程度。

程序

我们使用符号秩检验和逻辑回归分析,回顾性分析了99例至少在1年前完成治疗的小儿肉瘤患者的治疗变量和其他潜在风险因素与BMD(使用定量计算机断层扫描(QCT))之间的关系。

结果

研究组(38%为横纹肌肉瘤(RMS),25%为骨肉瘤(OS),24%为尤因家族肿瘤,12%为非横纹肌肉瘤软组织肉瘤(NRSTS))占1982年至2003年间在圣裘德接受随访的肉瘤幸存者的22%。这些患者在1997年7月1日至2003年2月5日期间接受了QCT检查。他们诊断时的中位年龄为8.7岁(范围为0.2 - 21.3岁),BMD测量时的中位年龄为17.4岁(范围为3.3 - 30.2岁);58%为男性,82%为白种人。BMD Z评分中位数为 -0.75(范围为 -3.33 - 3.02),BMD中位数为168.0 mg/cc(范围为89.2 - 264.8 mg/cc)。诊断时年龄越小(P = 0.044)和累积环磷酰胺剂量越高(P = 0.007),BMD缺陷风险显著增加。下肢原发性疾病患者的BMD缺陷风险明显低于其他患者。我们发现BMD与身体形态、原发性疾病、生活方式因素或内分泌病之间无关联。

结论

相当一部分肉瘤幸存者存在BMD缺陷风险,需要对BMD进行前瞻性研究以验证我们的结果并完善导致BMD缺陷的风险因素。

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