Finch Amy, Clark Roderick, Vesprini Danny, Lorentz Justin, Kim Raymond H, Thain Emily, Fleshner Neil, Akbari Mohammad R, Cybulski Cezary, Narod Steven A
Women's College Research Institute, Women's College Hospital, Toronto, Ontario, Canada.
Division of Urology, University of Toronto, Ontario, Canada.
NPJ Precis Oncol. 2022 Jun 22;6(1):43. doi: 10.1038/s41698-022-00282-8.
Most criteria for genetic testing for prostate cancer susceptibility require a prior diagnosis of prostate cancer, in particular cases with metastatic disease are selected. Advances in the field are expected to improve outcomes through tailored treatments for men with advanced prostate cancer with germline pathogenic variants, although these are not currently offered in the curative setting. A better understanding of the value of genetic testing for prostate cancer susceptibility in screening, for early detection and prevention is necessary. We review and summarize the literature describing germline pathogenic variants in genes associated with increased prostate cancer risk and aggressivity. Important questions include: what is our ability to screen for and prevent prostate cancer in a man with a germline pathogenic variant and how does knowledge of a germline pathogenic variant influence treatment of men with nonmetastatic disease, with hormone-resistant disease and with metastatic disease? The frequency of germline pathogenic variants in prostate cancer is well described, according to personal and family history of cancer and by stage and grade of disease. The role of these genes in aggressive prostate cancer is also discussed. It is timely to consider whether or not genetic testing should be offered to all men with prostate cancer. The goals of testing are to facilitate screening for early cancers in unaffected high-risk men and to prevent advanced disease in men with cancer.
大多数前列腺癌易感性基因检测标准都要求先诊断出前列腺癌,尤其会挑选有转移性疾病的病例。尽管目前在治愈性治疗中尚未提供针对携带种系致病变异的晚期前列腺癌男性的个性化治疗,但该领域的进展有望通过这种治疗改善治疗效果。有必要更好地了解前列腺癌易感性基因检测在筛查、早期检测和预防方面的价值。我们回顾并总结了描述与前列腺癌风险增加和侵袭性相关基因中的种系致病变异的文献。重要问题包括:我们对携带种系致病变异的男性进行前列腺癌筛查和预防的能力如何,以及种系致病变异的知识如何影响非转移性疾病、激素抵抗性疾病和转移性疾病男性的治疗?根据癌症的个人和家族病史以及疾病的分期和分级,前列腺癌中种系致病变异的频率已有充分描述。还讨论了这些基因在侵袭性前列腺癌中的作用。现在是时候考虑是否应该为所有前列腺癌男性提供基因检测了。检测的目标是便于在未受影响的高危男性中筛查早期癌症,并预防患癌男性的晚期疾病。