Sarcoma Unit, Royal Marsden NHS Foundation Trust, London, SW3 6JJ, UK.
The Institute of Cancer Research, London, SM2 5NG, UK.
Future Oncol. 2022 Aug;18(26):2967-2978. doi: 10.2217/fon-2022-0226. Epub 2022 Jul 26.
Over the past 20 years, the management of gastrointestinal stromal tumors has acted as an important model in the advancement of molecularly targeted therapies for solid tumors. The success of imatinib has established it as a lasting therapy in the management of early-stage and advanced disease in the first-line setting. Imatinib resistance inevitably develops, resulting in the need for further lines of therapy. Ripretinib is an orally administered switch-control tyrosine kinase inhibitor, specifically developed to target both primary and secondary KIT and PDGFRα resistance mutations. Herein, the authors discuss the molecular rationale, the preclinical evidence and the clinical use of ripretinib in the treatment of gastrointestinal stromal tumors in the advanced stages of disease.
在过去的 20 年中,胃肠道间质瘤的治疗管理为实体瘤的分子靶向治疗的发展提供了重要的范例。伊马替尼的成功确立了其在一线治疗中对早期和晚期疾病的持久治疗地位。伊马替尼耐药性不可避免地会发生,导致需要进一步的治疗方案。瑞派替尼是一种口服的开关控制酪氨酸激酶抑制剂,专门针对原发性和继发性 KIT 和 PDGFRα 耐药突变设计。本文作者讨论了瑞派替尼在治疗晚期胃肠道间质瘤中的分子原理、临床前证据和临床应用。