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儿童基因组不稳定性疾病的癌症筛查和监测建议的最新进展。

Update on Recommendations for Cancer Screening and Surveillance in Children with Genomic Instability Disorders.

机构信息

Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada.

Princess Máxima Center for Pediatric Oncology and Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

出版信息

Clin Cancer Res. 2024 Nov 15;30(22):5009-5020. doi: 10.1158/1078-0432.CCR-24-1098.

Abstract

Genomic instability disorders are characterized by DNA or chromosomal instability, resulting in various clinical manifestations, including developmental anomalies, immunodeficiency, and increased risk of developing cancers beginning in childhood. Many of these genomic instability disorders also present with exquisite sensitivity to anticancer treatments such as ionizing radiation and chemotherapy, which may further increase the risk of second cancers. In July 2023, the American Association for Cancer Research held the second Childhood Cancer Predisposition Workshop, where multidisciplinary international experts discussed, reviewed, and updated recommendations for children with cancer predisposition syndromes. This article discusses childhood cancer risks and surveillance recommendations for the group of genomic instability disorders with predominantly recessive inheritance, including the DNA repair disorders ataxia telangiectasia, Nijmegen breakage syndrome, Fanconi anemia, xeroderma pigmentosum, Bloom syndrome, and Rothmund-Thomson syndrome, as well as the telomere biology disorders and mosaic variegated aneuploidy. Recognition of children with genomic instability disorders is important in order to make the proper diagnosis, enable genetic counseling, and inform cancer screening, cancer risk reduction, and choice of anticancer therapy.

摘要

基因组不稳定性疾病的特征是 DNA 或染色体不稳定性,导致各种临床表现,包括发育异常、免疫缺陷和儿童时期开始患癌症的风险增加。许多这些基因组不稳定性疾病也表现出对癌症治疗(如电离辐射和化疗)的高度敏感,这可能进一步增加第二癌症的风险。2023 年 7 月,美国癌症研究协会召开了第二次儿童癌症易感性研讨会,来自多个学科的国际专家讨论、审查和更新了儿童癌症易感性综合征的建议。本文讨论了主要为隐性遗传的基因组不稳定性疾病组的儿童癌症风险和监测建议,包括 DNA 修复障碍疾病共济失调毛细血管扩张症、范可尼贫血、着色性干皮病、布卢姆综合征和 Rothmund-Thomson 综合征,以及端粒生物学障碍和嵌合体不均一性。认识基因组不稳定性疾病的儿童很重要,以便做出正确的诊断、进行遗传咨询,并告知癌症筛查、降低癌症风险和选择抗癌治疗。

相似文献

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本文引用的文献

1
CT radiation exposure and cancer risk: from knowing to acting.CT辐射暴露与癌症风险:从认知到行动
Pediatr Radiol. 2024 Jul;54(8):1407-1409. doi: 10.1007/s00247-024-05949-x. Epub 2024 May 16.
5
Rothmund-Thomson syndrome, a disorder far from solved.罗思蒙德-汤姆森综合征,一种远未得到解决的病症。
Front Aging. 2023 Nov 10;4:1296409. doi: 10.3389/fragi.2023.1296409. eCollection 2023.
7
Ataxia-telangiectasia clinical trial landscape and the obstacles to overcome.共济失调毛细血管扩张症临床试验全景及需克服的障碍。
Expert Opin Investig Drugs. 2023 Jul-Dec;32(8):693-704. doi: 10.1080/13543784.2023.2249399. Epub 2023 Aug 28.

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