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2019 年 1.1 版李-佛美尼综合征医学指南

Medical guidelines for Li-Fraumeni syndrome 2019, version 1.1.

机构信息

Department of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.

Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.

出版信息

Int J Clin Oncol. 2021 Dec;26(12):2161-2178. doi: 10.1007/s10147-021-02011-w. Epub 2021 Oct 11.

DOI:10.1007/s10147-021-02011-w
PMID:34633580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8595164/
Abstract

Li-Fraumeni syndrome (LFS) is a hereditary tumor that exhibits autosomal dominant inheritance. LFS develops in individuals with a pathogenic germline variant of the cancer-suppressor gene, TP53 (individuals with TP53 pathogenic variant). The number of individuals with TP53 pathogenic variant among the general population is said to be 1 in 500 to 20,000. Meanwhile, it is found in 1.6% (median value, range of 0-6.7%) of patients with pediatric cancer and 0.2% of adult patients with cancer. LFS is diagnosed by the presence of germline TP53 pathogenic variants. However, patients can still be diagnosed with LFS even in the absence of a TP53 pathogenic variant if the familial history of cancers fit the classic LFS diagnostic criteria. It is recommended that TP53 genetic testing be promptly performed if LFS is suspected. Chompret criteria are widely used for the TP53 genetic test. However, as there are a certain number of cases of LFS that do not fit the criteria, if LFS is suspected, TP53 genetic testing should be performed regardless of the criteria. The probability of individuals with TP53 pathogenic variant developing cancer in their lifetime (penetrance) is 75% for men and almost 100% for women. The LFS core tumors (breast cancer, osteosarcoma, soft tissue sarcoma, brain tumor, and adrenocortical cancer) constitute the majority of cases; however, various types of cancers, such as hematological malignancy, epithelial cancer, and pediatric cancers, such as neuroblastoma, can also develop. Furthermore, approximately half of the cases develop simultaneous or metachronous multiple cancers. The types of TP53 pathogenic variants and factors that modify the functions of TP53 have an impact on the clinical presentation, although there are currently no definitive findings. There is currently no cancer preventive agent for individuals with TP53 pathogenic variant. Surgical treatments, such as risk-reducing bilateral mastectomy warrant further investigation. Theoretically, exposure to radiation could induce the onset of secondary cancer; therefore, imaging and treatments that use radiation should be avoided as much as possible. As a method to follow-up LFS, routine cancer surveillance comprising whole-body MRI scan, brain MRI scan, breast MRI scan, and abdominal ultrasonography (US) should be performed immediately after the diagnosis. However, the effectiveness of this surveillance is unknown, and there are problems, such as adverse events associated with a high rate of false positives, overdiagnosis, and sedation used during imaging as well as negative psychological impact. The detection rate of cancer through cancer surveillance is extremely high. Many cases are detected at an early stage, and treatments are low intensity; thus, cancer surveillance could contribute to an improvement in QOL, or at least, a reduction in complications associated with treatment. With the widespread use of genomic medicine, the diagnosis of LFS is unavoidable, and a comprehensive medical care system for LFS is necessary. Therefore, clinical trials that verify the feasibility and effectiveness of the program, comprising LFS registry, genetic counseling, and cancer surveillance, need to be prepared.

摘要

李-佛美尼综合征(Li-Fraumeni syndrome,LFS)是一种表现为常染色体显性遗传的遗传性肿瘤。LFS 发生在具有癌症抑制基因 TP53 种系变异的个体中(具有 TP53 致病性变异的个体)。一般人群中具有 TP53 致病性变异的个体数量据说为每 500 至 20000 人中 1 人。同时,在儿科癌症患者中发现了 1.6%(中位数,范围为 0-6.7%),在成年癌症患者中发现了 0.2%。LFS 通过存在种系 TP53 致病性变异来诊断。然而,如果家族癌症史符合经典 LFS 诊断标准,即使没有 TP53 致病性变异,患者仍可被诊断为 LFS。如果怀疑 LFS,则建议及时进行 TP53 基因检测。Chompret 标准广泛用于 TP53 基因检测。然而,由于存在一定数量不符合标准的 LFS 病例,如果怀疑 LFS,则无论标准如何,都应进行 TP53 基因检测。具有 TP53 致病性变异的个体一生中患癌症的概率(外显率)为男性 75%,女性几乎为 100%。LFS 核心肿瘤(乳腺癌、骨肉瘤、软组织肉瘤、脑肿瘤和肾上腺皮质癌)构成了大多数病例;然而,也可以发展各种类型的癌症,如血液恶性肿瘤、上皮癌和神经母细胞瘤等儿科癌症。此外,大约一半的病例会同时或先后发生多种癌症。TP53 致病性变异的类型和改变 TP53 功能的因素会影响临床表现,尽管目前尚无明确的发现。目前,没有针对具有 TP53 致病性变异的个体的癌症预防剂。有必要进一步研究风险降低的双侧乳房切除术等手术治疗。理论上,辐射暴露会引发继发性癌症;因此,应尽可能避免使用放射性成像和治疗。作为 LFS 随访的一种方法,应在诊断后立即进行全身 MRI 扫描、脑 MRI 扫描、乳腺 MRI 扫描和腹部超声(US)的常规癌症监测。然而,这种监测的效果尚不清楚,存在与高假阳性率、过度诊断、成像过程中使用镇静剂以及成像相关的负面心理影响等问题。通过癌症监测检测癌症的检出率极高。许多病例在早期被发现,且治疗强度较低;因此,癌症监测可能有助于提高 QOL,或至少减少与治疗相关的并发症。随着基因组医学的广泛应用,LFS 的诊断不可避免,需要建立 LFS 的综合医疗保健系统。因此,需要准备验证方案可行性和有效性的临床试验,包括 LFS 登记、遗传咨询和癌症监测。

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本文引用的文献

1
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Acta Neuropathol. 2020 Apr;139(4):669-687. doi: 10.1007/s00401-019-02055-3. Epub 2019 Aug 30.
2
Pediatric patients with cancer predisposition in Japan: Results of a questionnaire survey.日本癌症易感性儿科患者:问卷调查结果
Pediatr Blood Cancer. 2019 Oct;66(10):e27937. doi: 10.1002/pbc.27937. Epub 2019 Jul 19.
3
Germline pathogenic variants of 11 breast cancer genes in 7,051 Japanese patients and 11,241 controls.7051 例日本患者和 11241 例对照中 11 个乳腺癌基因的种系致病性变异。
Nat Commun. 2018 Oct 4;9(1):4083. doi: 10.1038/s41467-018-06581-8.
4
Whole-body magnetic resonance imaging of Li-Fraumeni syndrome patients: observations from a two rounds screening of Brazilian patients.Li-Fraumeni 综合征患者的全身磁共振成像:两轮巴西患者筛查的观察结果。
Cancer Imaging. 2018 Aug 14;18(1):27. doi: 10.1186/s40644-018-0162-8.
5
Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer.儿童癌症幸存者的后续肿瘤遗传风险。
J Clin Oncol. 2018 Jul 10;36(20):2078-2087. doi: 10.1200/JCO.2018.77.8589. Epub 2018 May 30.
6
The landscape of genomic alterations across childhood cancers.儿童癌症中基因组改变的全景。
Nature. 2018 Mar 15;555(7696):321-327. doi: 10.1038/nature25480. Epub 2018 Feb 28.
7
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J Clin Oncol. 2018 Feb 20;36(6):591-599. doi: 10.1200/JCO.2017.75.5215. Epub 2018 Jan 4.
8
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9
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BMC Anesthesiol. 2017 Oct 11;17(1):138. doi: 10.1186/s12871-017-0431-2.
10
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Fam Cancer. 2018 Apr;17(2):287-294. doi: 10.1007/s10689-017-0034-6.