National Cancer Center Hospital East, Surgery , 6-5-1 Kashiwanoha, Kashiwa, 277-8577 , Japan.
Expert Opin Pharmacother. 2014 Oct;15(14):1979-89. doi: 10.1517/14656566.2014.937707. Epub 2014 Jul 3.
Gastrointestinal stromal tumor (GIST) is the most common sarcoma of the gastrointestinal tract. Proliferation of GIST is driven by activating mutations in the KIT or PDGFRA genes that found in most sporadic GISTs. Surgery is the main remedial measure for primary GIST, and imatinib is the principal therapeutic of choice for unresectable or metastatic GIST. Imatinib revolutionized treatment for unresectable or metastatic GISTs; however, resistance to imatinib has inevitably developed for most GIST patients.
PubMed was searched to find biological studies of GIST and clinical trials of molecularly targeted agents on unresectable or metastatic GISTs, and the key papers found have been reviewed. In this paper, the standard therapy which includes imatinib, sunitinib and regorafenib for unresectable or metastatic GIST has been reviewed and molecular mechanisms of resistance for tyrosine kinase inhibitors (TKIs) have been postulated and discussed. Treatment measures for resistant GIST and therapeutic choices after the standard therapy have also been described.
The standard therapy for unresectable or metastatic GISTs is first-line imatinib, second-line sunitinib and third-line regorafenib. After standard therapy, best supportive care or clinical trials is recommended in the guidelines. However, patients may benefit from continuation of TKIs beyond disease progression and from rechallenge of TKIs used previously.
胃肠道间质瘤(GIST)是胃肠道最常见的肉瘤。GIST 的增殖是由 KIT 或 PDGFRA 基因的激活突变驱动的,这些突变存在于大多数散发性 GIST 中。手术是原发性 GIST 的主要治疗措施,伊马替尼是不可切除或转移性 GIST 的主要治疗选择。伊马替尼彻底改变了不可切除或转移性 GIST 的治疗方法;然而,大多数 GIST 患者不可避免地对伊马替尼产生了耐药性。
通过检索 PubMed 中的 GIST 生物学研究和不可切除或转移性 GIST 的分子靶向药物临床试验,对找到的关键论文进行了综述。在本文中,对包括伊马替尼、舒尼替尼和瑞戈非尼在内的不可切除或转移性 GIST 的标准治疗进行了综述,并推测和讨论了酪氨酸激酶抑制剂(TKI)的耐药分子机制。还描述了耐药 GIST 的治疗措施和标准治疗后的治疗选择。
不可切除或转移性 GIST 的标准治疗是一线伊马替尼、二线舒尼替尼和三线瑞戈非尼。在指南中,建议在标准治疗后进行最佳支持治疗或临床试验。然而,患者可能会受益于疾病进展后继续使用 TKI 以及重新使用之前使用过的 TKI。