Nishida Toshirou, Wakasugi Masaki, Ueshima Shigeyuki
Dept. of Surgery, Osaka Police Hospital, Tennojiku, Osaka, Japan.
Gan To Kagaku Ryoho. 2012 Sep;39(9):1330-5.
GIST is driven by a gain-of-function mutation either in the KIT or PDGFRA gene. Atpresent , advanced and/or metastatic GIST is primarily treated by medical therapy of imatinib and sunitinib, both of which are re-imbursed by the government in Japan. Tumor responses are usually evaluated by contrast-enhanced CT scan with RECIST criteria, which cannot always predict patients with long SD showing similar prognostic effects to CR or PR. For early detection of drug activities, Choi's criteria with enhanced CT scan, as well as FDG-PET(or PET-CT), are considered to be useful. Choi's criteria also works for the early detection of resistance. When resistance and/or unmanagable adverse events are observed, early switching of drugs without any delay is recommended if there is another line of treatment.
胃肠道间质瘤(GIST)由KIT基因或血小板衍生生长因子受体α(PDGFRA)基因的功能获得性突变驱动。目前,晚期和/或转移性GIST主要通过伊马替尼和舒尼替尼进行药物治疗,这两种药物在日本均由政府报销。肿瘤反应通常采用RECIST标准通过增强CT扫描进行评估,该标准并不能总是预测出疾病稳定(SD)时间长且预后效果与完全缓解(CR)或部分缓解(PR)相似的患者。为了早期检测药物活性,采用增强CT扫描的Choi标准以及氟代脱氧葡萄糖正电子发射断层显像(FDG-PET,或PET-CT)被认为是有用的。Choi标准也可用于早期检测耐药性。当观察到耐药和/或无法控制的不良事件时,如果有其他治疗方案,建议立即尽早更换药物。