奥拉帕尼
医学
聚ADP核糖聚合酶
前列腺癌
PARP抑制剂
疾病
癌症研究
肿瘤科
前列腺
同源重组
内科学
癌症
生物信息学
聚合酶
基因
生物
遗传学
作者
Diego Teyssonneau,C. Dariane,Éric Barret,Jean-Baptiste Beauval,Laurent Beaugerie,G. Fiard,G. Fromont‐Hankard,G. Créhange,Mathieu Gauthé,A. Ruffion,Raphaële Renard‐Penna,Romain Mathiéu,Paul Sargos,Morgan Rouprêt,Guillaume Ploussard,Guilhem Roubaud
标识
DOI:10.1177/17588359241242959
摘要
Despite several improvements in outcomes, metastatic prostate cancer remains deadly. Alterations in the homologous recombination repair (HRR) pathway are associated with more aggressive disease. Olaparib and rucaparib, two poly-ADP-ribose polymerase (PARP) inhibitors, have received approval from the authorities of several countries for their anti-tumoral effects in patients with metastatic castration-resistant prostate cancers harboring HRR gene alterations, in particular BRCA2. More recently, it has been hypothesized that new hormonal therapies (NHTs) and PARP inhibitors (PARPi) could have synergistic actions and act independently of HRR deficiency. This review proposes to discuss the advantages and disadvantages of PARPi used as monotherapy or in combination with NHTs and whether there is a need for molecular selection.
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