Nassif Haddad Elise, Javle Milind M, Yap Timothy A
Department of Sarcoma Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Department of Investigational Cancer Therapeutics, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Cancer. 2025 May 15;131(10):e35890. doi: 10.1002/cncr.35890.
In this issue of , Cecchini et al. report findings from a phase 2 open-label trial of olaparib in 30 patients with advanced cholangiocarcinoma and IDH1/2 mutations. While the trial did not meet its primary endpoint, a subset of patients experienced prolonged clinical benefit, highlighting the potential for alternative therapeutic strategies involving PARP inhibitors in future clinical trials.
在本期《 》中,塞奇尼等人报告了一项关于奥拉帕利的2期开放标签试验的结果,该试验纳入了30例晚期胆管癌且异柠檬酸脱氢酶1/2(IDH1/2)突变的患者。虽然该试验未达到其主要终点,但有一部分患者获得了延长的临床获益,这凸显了在未来临床试验中采用涉及聚(ADP-核糖)聚合酶(PARP)抑制剂的替代治疗策略的潜力。