Departments of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Medical Oncology, The Fourth Hospital of Hebei Medical University, Hebei, People's Republic of China.
Sci Rep. 2020 Feb 20;10(1):3080. doi: 10.1038/s41598-020-58366-z.
We performed two phase I trials of the histone deacetylase inhibitor vorinostat combined with either the vascular endothelial growth factor inhibitor pazopanib (NCT01339871) or the proteasome inhibitor ixazomib (NCT02042989) in patients with metastatic TP53 mutant solid tumors. Both trials followed a 3 + 3 dose-escalation design allowing for a dose expansion cohort of up to 14 additional patients with a specific tumor type. Patients had to have a confirmed TP53 mutation to be enrolled in NCT02042989. Among patients enrolled in NCT01339871, TP53 mutation status was determined for those for whom tumor specimens were available. The results of NCT01339871 were reported previously. Common treatment-related adverse events in NCT02042989 included anemia, thrombocytopenia, fatigue, nausea, vomiting, and diarrhea. Compared with patients with metastatic TP53 hotspot mutant solid tumors who were treated with ixazomib and vorinostat (n = 59), those who were treated with pazopanib and vorinostat (n = 11) had a significantly higher rate of clinical benefit, defined as stable disease lasting ≥6 months or an objective response (3.4% vs. 45%; p < 0.001), a significantly longer median progression-free survival duration (1.7 months [95% confidence interval (CI), 1.1-2.3] vs. 3.5 months [95% CI, 1.7-5.2]; p = 0.002), and a longer median overall survival duration (7.3 months [95% CI, 4.8-9.8] vs. 12.7 months [95% CI, 7.1-18.3]; p = 0.24). Our two phase I trials provide preliminary evidence supporting the use of antiangiogenisis-based therapy in patients with metastatic TP53 mutant solid tumors, especially in those with metastatic sarcoma or metastatic colorectal cancer.
我们进行了两项 I 期临床试验,评估组蛋白去乙酰化酶抑制剂伏立诺他联合血管内皮生长因子抑制剂帕唑帕尼(NCT01339871)或蛋白酶体抑制剂伊沙佐米(NCT02042989)治疗转移性 TP53 突变型实体瘤患者的疗效。两项试验均采用 3+3 剂量递增设计,允许对特定肿瘤类型的 14 名额外患者进行剂量扩展队列。NCT02042989 试验仅招募确认为 TP53 突变的患者。在 NCT01339871 中,对可获得肿瘤样本的患者进行 TP53 突变状态的评估。NCT01339871 的结果之前已经报道过。NCT02042989 中常见的治疗相关不良事件包括贫血、血小板减少、疲劳、恶心、呕吐和腹泻。与接受伊沙佐米和伏立诺他治疗的转移性 TP53 热点突变型实体瘤患者(n=59)相比,接受帕唑帕尼和伏立诺他治疗的患者(n=11)的临床获益率显著更高,定义为持续≥6 个月的稳定疾病或客观缓解(3.4%比 45%;p<0.001),无进展生存期显著延长(1.7 个月[95%置信区间(CI),1.1-2.3]比 3.5 个月[95% CI,1.7-5.2];p=0.002),总生存期也更长(7.3 个月[95% CI,4.8-9.8]比 12.7 个月[95% CI,7.1-18.3];p=0.24)。我们的两项 I 期试验提供了初步证据,支持在转移性 TP53 突变型实体瘤患者中使用抗血管生成治疗,尤其是转移性肉瘤或转移性结直肠癌患者。