Cassier Philippe A, Dufresne Armelle, Arifi Samia, El Sayadi Hiba, Ray-Coquard Isabelle, Bringuier Pierre-Paul, Scoazec Jean-Yves, Alberti Laurent, Blay Jean-Yves
Conticanet Network of Excellence (LSH-060188), Département de Medicine, Centre Léon Bérard, 28 Rue Laennec, 69008 Lyon, France.
Curr Gastroenterol Rep. 2008 Dec;10(6):555-61. doi: 10.1007/s11894-008-0102-z.
Gastrointestinal stromal tumors (GIST) are rare tumors of mesenchymal origin that may arise anywhere along the gastrointestinal tract or in the peritoneum. In most cases, GIST harbor mutations of KIT or PDGFRA. Imatinib mesylate (IM), a small-molecule tyrosine kinase inhibitor developed for the treatment of chronic myeloid leukemia, has been shown to be active against these mutations and has significant activity in patients with metastatic GIST. However, resistance to IM emerges after a median of 24 months of treatment. Sunitinib malate (SU) has been approved for the treatment of patients with IM-resistant advanced GIST, but the median progression-free survival in this setting is only 6 months. This article reviews the current knowledge regarding IM and SU resistance in GIST, as well as the available options for the management of GIST resistant to IM and SU.
胃肠道间质瘤(GIST)是一种罕见的间叶源性肿瘤,可发生于胃肠道的任何部位或腹膜。在大多数情况下,GIST存在KIT或PDGFRA基因突变。甲磺酸伊马替尼(IM)是一种开发用于治疗慢性粒细胞白血病的小分子酪氨酸激酶抑制剂,已被证明对这些突变有效,并且在转移性GIST患者中具有显著活性。然而,治疗中位24个月后会出现对IM的耐药性。苹果酸舒尼替尼(SU)已被批准用于治疗对IM耐药的晚期GIST患者,但在此情况下的中位无进展生存期仅为6个月。本文综述了目前关于GIST中IM和SU耐药性的知识,以及对IM和SU耐药的GIST的可用管理方案。