Molecular basis for primary and secondary tyrosine kinase inhibitor resistance in gastrointestinal stromal tumor

被引:0
作者
Mrinal M. Gounder
Robert G. Maki
机构
[1] Memorial Sloan-Kettering Cancer Center,
来源
Cancer Chemotherapy and Pharmacology | 2011年 / 67卷
关键词
GIST; Primary tyrosine kinase inhibitor resistance; Secondary tyrosine kinase inhibitor resistance; Nilotinib;
D O I
暂无
中图分类号
学科分类号
摘要
Small molecule kinase inhibitors have irrevocably altered cancer treatment. March 2010 marks the 10th anniversary of using imatinib in gastrointestinal stromal tumors (GIST), a cardinal example of the utility of such targeted therapy in a solid tumor. Before imatinib, metastatic GIST was frustrating to treat due to its resistance to standard cytotoxic chemotherapy. Median survival for patients with metastatic GIST improved from 19 to 60 months with imatinib. In treating patients with GIST, two patterns of tyrosine kinase inhibitor resistance have been observed. In the first, ~9–14% of patients have progression within 3 months of starting imatinib. These patients are classified as having primary or early resistance. Median progression-free survival (PFS) on imatinib is approximately 24 months; patients with later progression are classified as having secondary or acquired resistance. Primary studies and a meta-analysis of studies of imatinib in GIST patients have identified prognostic features that contribute to treatment failure. One of the strongest predictors for success of therapy is KIT or PDGFRA mutational status. Patients with KIT exon 11 mutant GIST have better response rates, PFS, and overall survival compared to other mutations. A great deal has been learned in the last decade about sensitivity and resistance of GIST to imatinib; however, many unanswered questions remain about secondary resistance mechanisms and clinical management in the third- and fourth-line setting. This review will discuss the role of dose effects, and early and late resistance to imatinib and their clinical implications. Patients intolerant to imatinib (5%) and those who progress on imatinib are treated with sunitinib. The mechanism of resistance to sunitinib is unknown at this time but is also appears related to growth of clones with secondary mutations in KIT. Third- and fourth-line treatments of GIST and with future treatment strategies are also discussed.
引用
收藏
页码:25 / 43
页数:18
相关论文
共 555 条
  • [1] Rubin BP(2001)KIT activation is a ubiquitous feature of gastrointestinal stromal tumors Cancer Res 61 8118-8121
  • [2] Singer S(2004)Biology of gastrointestinal stromal tumors: KIT mutations and beyond Cancer Invest 22 106-116
  • [3] Tsao C(1998)Gastrointestinal pacemaker cell tumor (GIPACT): gastrointestinal stromal tumors show phenotypic characteristics of the interstitial cells of Cajal Am J Pathol 152 1259-1269
  • [4] Duensing A(1995)W/kit gene required for interstitial cells of Cajal and for intestinal pacemaker activity Nature 373 347-349
  • [5] Lux ML(1989)Expression of c-kit gene products in known cellular targets of W mutations in normal and W mutant mice–evidence for an impaired c-kit kinase in mutant mice Genes Dev 3 816-826
  • [6] Ruiz R(1986)A new acute transforming feline retrovirus and relationship of its oncogene v-kit with the protein kinase gene family Nature 320 415-421
  • [7] Duensing A(1987)Human proto-oncogene c-kit: a new cell surface receptor tyrosine kinase for an unidentified ligand EMBO J 6 3341-3351
  • [8] Heinrich MC(2000)Immunohistochemical spectrum of GIST at different sites and their differential diagnosis with a reference to CD117 (KIT) Mod Pathol 13 1134-1142
  • [9] Fletcher CD(1997)Deficiency of c-kit + cells in patients with a myopathic form of chronic idiopathic intestinal pseudo-obstruction Am J Gastroenterol 92 332-334
  • [10] Fletcher JA(1995)Disturbed intestinal movement, bile reflux to the stomach, and deficiency of c-kit-expressing cells in Ws/Ws mutant rats Gastroenterology 109 456-464