癌症基因检测

Q4 Medicine Onkologie (Czech Republic) Pub Date : 2022-08-24 DOI:10.36290/xon.2022.037
J. Soukupová
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引用次数: 3

摘要

,种系突变的基因检测可以为患者的家庭提供有针对性的基因咨询,识别有风险的个体,并对患者及其检测呈阳性的健康亲属进行适当的监测管理。BRCA1和BRCA2基因的种系和体细胞突变也可能在考虑特异性聚ADP核糖聚合酶抑制剂(PARPi)的适应症中发挥作用。BRCA1和BRCA2的体细胞突变在另外5-9%的癌症女性中发现。种系和体细胞突变的同时检测将有助于更有效地识别一种PARPi维持治疗的潜在候选患者,同时也能检测出特别是乳腺癌和卵巢癌癌症高风险的健康亲属。
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Genetic testing in ovarian cancer
, genetic testing of germline mutations allows targeted genetic counselling in the patient`s family, identification of individuals at risk and appropriate surveillance management of the patient and her positively tested healthy relatives. Germline as well as somatic mutations in BRCA1 and BRCA2 genes may also play a role in the consideration of the indication of a specific poly-ADP-ribose polymerase inhibitor (PARPi). Somatic mutations in BRCA1 and BRCA2 are found in an additional 5–9% of women with ovarian cancer. Simultaneous testing for germline and somatic mutations will allow for more efficient identification of patients who are potential candidates for one type of PARPi maintenance therapy, while also detecting healthy relatives at high risk of developing breast and ovarian cancer in particular.
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来源期刊
Onkologie (Czech Republic)
Onkologie (Czech Republic) Medicine-Oncology
CiteScore
0.10
自引率
0.00%
发文量
43
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