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

IF 10 1区 医学 Q1 ONCOLOGY Clinical Cancer Research Pub Date : 2024-09-12 DOI:10.1158/1078-0432.ccr-24-1098
Yoshiko Nakano,Roland P Kuiper,Kim E Nichols,Christopher C Porter,Harry Lesmana,Julia Meade,Christian P Kratz,Lucy A Godley,Luke D Maese,Maria Isabel Achatz,Payal P Khincha,Sharon A Savage,Andrea S Doria,Mary-Louise C Greer,Vivian Y Chang,Lisa L Wang,Sharon E Plon,Michael F Walsh
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Abstract

Genomic instability disorders are characterized by DNA or chromosomal instability resulting in various clinical manifestations including developmental anomalies, immunodeficiency, and increased risk to develop 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 of 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 will discuss 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 anti-cancer therapy.
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基因组不稳定性疾病儿童癌症筛查和监测建议的更新。
基因组不稳定性疾病的特点是 DNA 或染色体不稳定,导致各种临床表现,包括发育异常、免疫缺陷和从儿童时期开始罹患癌症的风险增加。其中许多基因组不稳定疾病还表现为对电离辐射和化疗等抗癌治疗非常敏感,这可能会进一步增加罹患第二种癌症的风险。2023 年 7 月,美国癌症研究协会举办了第二届儿童癌症易感性研讨会,多学科国际专家在会上讨论、审查并更新了针对儿童癌症易感性综合征的建议。本文将讨论以隐性遗传为主的一组基因组不稳定性疾病的儿童癌症风险和监测建议,这些疾病包括 DNA 修复疾病共济失调性毛细血管扩张症、奈梅根断裂综合征、范可尼贫血症、色素沉着病、布鲁姆综合征和罗斯蒙特-汤姆森综合征,以及端粒生物学疾病和镶嵌变异非整倍体。识别患有基因组不稳定性疾病的儿童非常重要,这有助于做出正确诊断,提供遗传咨询,并为癌症筛查、降低癌症风险和选择抗癌疗法提供依据。
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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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