Nannini Margherita, Rizzo Alessandro, Indio Valentina, Schipani Angela, Astolfi Annalisa, Pantaleo Maria Abbondanza
Division of Oncology, IRCSS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Department of Experimental, Diagnostic and Specialized Medicine, University of Bologna, Bologna, Italy.
Ther Adv Med Oncol. 2021 Jun 28;13:17588359211023278. doi: 10.1177/17588359211023278. eCollection 2021.
The medical management of advanced gastrointestinal stromal tumors (GIST) has improved with the development of tyrosine kinase inhibitors (TKIs) targeting and mutations. However, approximately 5-10% of GIST lack and mutations, and about a half are deficient in succinate dehydrogenase () that promotes carcinogenesis by the cytoplasmic accumulation of succinate. This rare group of GIST primarily occurs in the younger patients than other subtypes, and is frequently associated with hereditary syndromes. The role of TKIs in patients with -deficient GIST is controversial, with conflicting results; thus, there is an urgent need to uncover the disease mechanisms, treatment patterns, and responses to systemic therapy among these patients. Here, based on an extensive literature search, we have provided a rigorous overview of the current evidence on the medical treatment of -deficient GIST.
随着针对 和 突变的酪氨酸激酶抑制剂(TKIs)的发展,晚期胃肠道间质瘤(GIST)的医学管理得到了改善。然而,约5%-10%的GIST缺乏 和 突变,约一半缺乏琥珀酸脱氢酶(),其通过琥珀酸在细胞质中的积累促进致癌作用。这一罕见的GIST组主要发生在比其他亚型更年轻的患者中,并且经常与遗传综合征相关。TKIs在缺乏 的GIST患者中的作用存在争议,结果相互矛盾;因此,迫切需要揭示这些患者的疾病机制、治疗模式和对全身治疗的反应。在此,基于广泛的文献检索,我们对目前关于缺乏 的GIST医学治疗的证据进行了严格概述。