Matsumoto Takashi, Shiota Masaki, Blas Leandro, Eto Masatoshi
Department of Urology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Cancer Manag Res. 2022 Aug 8;14:2389-2397. doi: 10.2147/CMAR.S326114. eCollection 2022.
Several studies have identified various targetable genomic alterations in prostate cancer, which accumulate during carcinogenesis and cancer progression. Genomic alterations in genes involved in DNA damage repair by homologous recombination repair may predict increased sensitivity to poly-ADP ribose polymerase (PARP) inhibitors. The Phase 3 PROfound trial has shown that treatment with the PARP inhibitor olaparib was associated with an improved radiographic progression-free survival and overall survival among patients with homologous recombination repair-deficient metastatic castration-resistant prostate cancer (mCRPC) after the treatment with androgen receptor targeting therapy, especially in men with or mutation. In Japan, olaparib was approved in December 2020 for the treatment of mCRPC with or mutation. In addition, genetic tests to detect or mutation to select patients who are likely to benefit from olaparib were also approved. This review summarizes the status of olaparib treatment for mCRPC, focusing on the situation in Japan.
多项研究已确定前列腺癌中存在各种可靶向的基因组改变,这些改变在致癌过程和癌症进展过程中不断积累。参与同源重组修复的DNA损伤修复相关基因的基因组改变可能预示着对聚ADP核糖聚合酶(PARP)抑制剂的敏感性增加。3期PROfound试验表明,在接受雄激素受体靶向治疗后,PARP抑制剂奥拉帕利治疗与同源重组修复缺陷型转移性去势抵抗性前列腺癌(mCRPC)患者的影像学无进展生存期和总生存期改善相关,尤其是在携带 或 突变的男性患者中。在日本,奥拉帕利于2020年12月获批用于治疗携带 或 突变的mCRPC。此外,检测 或 突变以选择可能从奥拉帕利中获益的患者的基因检测也已获批。本综述总结了奥拉帕利治疗mCRPC的现状,重点关注日本的情况。