Blay Jean-Yves, Le Cesne Axel, Cassier Philippe A, Ray-Coquard Isabelle L
Department of Medicine, Centre Leon Berard, Lyon 69008, France.
Discov Med. 2012 May;13(72):357-67.
Gastrointestinal stromal tumors (GIST) are the most frequent sarcoma and were recognized as distinct molecular entities in 1998. Following the identification of driving molecular alterations in KIT, imatinib was rapidly introduced for the treatment of GIST, and became the paradigm of molecularly targeted therapies for solid tumors. While surgery was the only known effective treatment in 1998, two drugs are approved by the FDA and EMA in 2012 for the treatment of localized and advanced forms of this disease. Imatinib has been shown to provide a high level of clinical efficacy in patients with advanced GIST, a median progression-free survival (PFS) of 2 years and median overall survival close to 5 years, with 20% patients progression-free after 10 years of treatment. Imatinib has also been proven to improve overall survival and reduce the risk of relapse in localized GIST at high risk for relapse after resection. Sunitinib is indicated in advanced GIST after failure of imatinib, and provided a median PFS close to 6 months after imatinib failure. However, there is an important variability in the molecular and genetic characteristics that drive the pathogenesis of GIST, allowing thus for the identification of distinct molecular subtypes of GIST with different prognosis and sensitivity to the targeted treatments. Different strategies are now recommended in these different molecular subtypes of GIST which must be recognized as different entities regarding sensitivity to tyrosine kinase inhibitors and treatment decisions. This fragmentation of a yet recently recognized disease entity illustrates to strong trend of fragmentation in nosology of cancers, even in rare tumors such as GIST. For this aspect also, GIST is again a paradigmatic model for oncology, as many tumors with a higher prevalence will be fragmented in different molecular subsets and are going to become rare disease in the years to come.
胃肠道间质瘤(GIST)是最常见的肉瘤,于1998年被确认为独特的分子实体。在确定了KIT基因的驱动分子改变后,伊马替尼迅速被引入用于治疗GIST,并成为实体瘤分子靶向治疗的典范。1998年时手术是唯一已知的有效治疗方法,而在2012年,两种药物被美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准用于治疗这种疾病的局部和晚期形式。伊马替尼已被证明在晚期GIST患者中具有较高的临床疗效,中位无进展生存期(PFS)为2年,中位总生存期接近5年,20%的患者在治疗10年后仍无进展。伊马替尼也已被证实可提高局部GIST在切除后复发高风险患者的总生存期并降低复发风险。舒尼替尼适用于伊马替尼治疗失败后的晚期GIST,在伊马替尼治疗失败后提供的中位PFS接近6个月。然而,驱动GIST发病机制的分子和遗传特征存在重要变异性,从而能够识别出具有不同预后和对靶向治疗敏感性的不同分子亚型GIST。现在针对这些不同分子亚型的GIST推荐了不同的策略,就对酪氨酸激酶抑制剂的敏感性和治疗决策而言,必须将它们视为不同的实体。这种对一个相对较新才被认识的疾病实体的细分说明了癌症分类学中细分的强烈趋势,即使在像GIST这样的罕见肿瘤中也是如此。就这一方面而言,GIST再次成为肿瘤学的典范模型,因为许多患病率较高的肿瘤将被细分为不同的分子亚群,并在未来几年成为罕见疾病。