Pons-Tostivint Elvire, Thibault Benoît, Guillermet-Guibert Julie
Centre de Recherches en Cancérologie de Toulouse (CRCT), Institut National de la Santé et de la Recherche Médicale (INSERM), Université Toulouse III Paul Sabatier, Toulouse, France; Laboratoire d'Excellence LABEX TouCAN, Toulouse, France.
Centre de Recherches en Cancérologie de Toulouse (CRCT), Institut National de la Santé et de la Recherche Médicale (INSERM), Université Toulouse III Paul Sabatier, Toulouse, France; Laboratoire d'Excellence LABEX TouCAN, Toulouse, France.
Trends Cancer. 2017 Jun;3(6):454-469. doi: 10.1016/j.trecan.2017.04.002. Epub 2017 May 14.
Targeting upstream phosphatidylinositol-3-kinases (PI3Ks) in the PI3K/Akt/mTOR pathway appears to be a promising therapy in solid cancers; however, first early clinical trials with PI3K inhibitors in monotherapy have been disappointing. A massive array of preclinical and clinical trials are currently evaluating combinations of PI3K inhibitors in targeted therapies. These combinations include co-treatments with drugs directed against other intra-/extracellular signaling molecules, nuclear hormone receptors, DNA damage repair enzymes, and immune modulators. We review the literature and pinpoint mechanisms of action in different genomic and organ contexts. Combinatorial approaches are potentially superior to monotherapies and should become alternative clinical strategies to treat cancer patients.
靶向PI3K/Akt/mTOR通路中的上游磷脂酰肌醇-3激酶(PI3K)似乎是实体癌中一种很有前景的治疗方法;然而,PI3K抑制剂单药治疗的首批早期临床试验结果令人失望。目前,大量的临床前和临床试验正在评估PI3K抑制剂在靶向治疗中的联合应用。这些联合应用包括与针对其他细胞内/外信号分子、核激素受体、DNA损伤修复酶和免疫调节剂的药物联合治疗。我们回顾了相关文献,并明确了在不同基因组和器官背景下的作用机制。联合治疗方法可能优于单药治疗,应成为治疗癌症患者的替代临床策略。