Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Centre Léon Bérard, Lyon, 69008, France.
Future Oncol. 2024;20(27):1973-1982. doi: 10.1080/14796694.2024.2376521. Epub 2024 Sep 4.
Somatic activating mutations drive most gastrointestinal stromal tumors (GISTs). Disease progression eventually develops with first-line imatinib, commonly due to secondary mutations, and different kinase inhibitors have various levels of treatment efficacy dependent on specific acquired resistance mutations. Ripretinib is a broad-spectrum switch-control KIT/PDGFRA tyrosine kinase inhibitor for patients with advanced GIST who received prior treatment with three or more kinase inhibitors, including imatinib. Exploratory baseline circulating tumor DNA analysis from the second-line INTRIGUE trial determined that patients with advanced GIST previously treated with imatinib harboring primary exon 11 mutations and secondary resistance mutations restricted to exons 17/18 had greater clinical benefit with ripretinib versus sunitinib. We describe the rationale and design of INSIGHT (NCT05734105), an ongoing Phase III open-label study of ripretinib versus sunitinib in patients with advanced GIST previously treated with imatinib exclusively harboring exon 11 + 17/18 mutations detected by circulating tumor DNA. NCT05734105 (ClinicalTrials.gov).
体激活突变驱动大多数胃肠道间质瘤(GIST)。由于继发突变,一线伊马替尼最终会导致疾病进展,不同的激酶抑制剂对特定获得性耐药突变的治疗效果不同。 Ripretinib 是一种广谱开关控制 KIT/PDGFRA 酪氨酸激酶抑制剂,适用于先前接受过三种或更多激酶抑制剂(包括伊马替尼)治疗的晚期 GIST 患者。二线 INTRIGUE 试验的基线循环肿瘤 DNA 分析显示,先前接受过伊马替尼治疗且携带原发性外显子 11 突变和继发性耐药突变仅限于外显子 17/18 的晚期 GIST 患者,与舒尼替尼相比,接受 ripretinib 治疗具有更大的临床获益。我们描述了正在进行的、针对先前仅接受过伊马替尼治疗且携带由循环肿瘤 DNA 检测到的外显子 11+17/18 突变的晚期 GIST 患者的 ripretinib 与舒尼替尼的 III 期开放标签研究 INSIGHT(NCT05734105)的原理和设计。NCT05734105(ClinicalTrials.gov)。