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儿童造血系统恶性肿瘤遗传易感性监测建议的更新。

Update on Recommendations for Surveillance for Children with Predisposition to Hematopoietic Malignancy.

机构信息

University of Utah-Huntsman Cancer Institute, Primary Children's Hospital, Salt Lake City, Utah.

St. Jude Children's Research Hospital, Memphis, Tennessee.

出版信息

Clin Cancer Res. 2024 Oct 1;30(19):4286-4295. doi: 10.1158/1078-0432.CCR-24-0685.

Abstract

Children harboring certain germline gene variants have an increased risk of developing myelodysplastic syndrome (MDS) and other hematopoietic malignancies (HM), such as leukemias and lymphomas. Recent studies have identified an expanding number of these predisposition genes, with variants most prevalent in children with MDS but also found in children with other HM. For some hematopoietic malignancy predispositions (HMP), specifically those with a high risk of MDS, early intervention through hematopoietic stem cell transplantation can favorably impact overall survival, providing a rationale for rigorous surveillance. A multidisciplinary panel of experts at the 2023 AACR Childhood Cancer Predisposition Workshop reviewed the latest advances in the field and updated prior 2017 surveillance recommendations for children with HMP. In addition to general guidance for all children with HMP, which includes annual physical examination, education about the signs and symptoms of HM, consultation with experienced providers, and early assessment by a hematopoietic stem cell transplantation specialist, the panel provided specific recommendations for individuals with a higher risk of MDS based on the affected gene. These recommendations include periodic and comprehensive surveillance for individuals with those syndromes associated with higher risk of MDS, including serial bone marrow examinations to monitor for morphologic changes and deep sequencing for somatic changes in genes associated with HM progression. This approach enables close monitoring of disease evolution based on the individual's genetic profile. As more HMP-related genes are discovered and the disorders' natural histories are better defined, these personalized recommendations will serve as a foundation for future guidelines in managing these conditions.

摘要

儿童携带某些种系基因突变会增加患骨髓增生异常综合征(MDS)和其他血液系统恶性肿瘤(HM)的风险,如白血病和淋巴瘤。最近的研究已经确定了越来越多的这些易感基因,这些变体在 MDS 患儿中最为常见,但也在其他 HM 患儿中发现。对于某些血液系统恶性肿瘤易感性(HMP),特别是那些 MDS 风险较高的患者,通过造血干细胞移植进行早期干预可以显著影响总生存率,为严格监测提供了依据。在 2023 年 AACR 儿童癌症易感性研讨会上,一个多学科专家组审查了该领域的最新进展,并更新了之前 2017 年针对 HMP 儿童的监测建议。除了针对所有 HMP 儿童的一般指导(包括每年进行体检、教育他们了解 HM 的症状和体征、咨询有经验的提供者以及由造血干细胞移植专家进行早期评估)外,专家组还根据受影响的基因,为 MDS 风险较高的个体提供了具体建议。这些建议包括对那些与 MDS 风险较高相关的综合征的个体进行定期和全面监测,包括连续进行骨髓检查以监测形态学变化,以及对与 HM 进展相关的基因进行体细胞突变的深度测序。这种方法可以根据个体的遗传特征密切监测疾病的演变。随着更多的 HMP 相关基因被发现,并且这些疾病的自然史得到更好的定义,这些个性化建议将成为未来管理这些疾病的指南的基础。

本文引用的文献

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MECOM Deficiency: from Bone Marrow Failure to Impaired B-Cell Development.MECOM 缺陷:从骨髓衰竭到 B 细胞发育受损。
J Clin Immunol. 2023 Aug;43(6):1052-1066. doi: 10.1007/s10875-023-01545-0. Epub 2023 Jul 5.

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