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用于识别急性淋巴细胞白血病患儿骨坏死风险的基因生物标志物

Genetic Biomarkers to Identify the Risk of Osteonecrosis in Children with Acute Lymphoblastic Leukemia.

作者信息

den Hoed Marissa A H, Pluijm Saskia M F, Uitterlinden André G, Pieters Rob, van den Heuvel-Eibrink Marry M

机构信息

Department of Pediatric Oncology/Hematology, Erasmus MC-Sophia Children's Hospital Rotterdam, Dr. Molewaterplein 60, 3015 GJ, Rotterdam, The Netherlands.

Princess Maxima Centre for Pediatric Oncology, Lundlaan 6, 3584 EA, Utrecht, The Netherlands.

出版信息

Mol Diagn Ther. 2016 Dec;20(6):519-522. doi: 10.1007/s40291-016-0226-z.

Abstract

Osteonecrosis is a disabling complication of treatment for pediatric acute lymphoblastic leukemia, and much effort has been made to predict which patients are prone to develop this disease. Multiple clinical and genetic factors have already been identified as being associated with osteonecrosis; however, a prediction model that combines pretreatment genetic biomarkers and clinical factors has not yet been designed. Such a prediction model can only be developed with continuing international collaborations and research efforts, including large genome-wide association studies.

摘要

骨坏死是儿童急性淋巴细胞白血病治疗中一种致残性并发症,人们已付出诸多努力来预测哪些患者容易患上这种疾病。多种临床和遗传因素已被确定与骨坏死有关;然而,尚未设计出一种将治疗前遗传生物标志物与临床因素相结合的预测模型。只有通过持续的国际合作和研究努力,包括大规模全基因组关联研究,才能开发出这样的预测模型。

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