Koyama Tomoki, Nimura Hiroshi, Kobayashi Katsutoshi, Marushima Hideki, Odaira Hironori, Kashimura Hirotaka, Mitsumori Norio, Yanaga Katsuhiko
Department of Surgery, The Jikei University School of Medicine, 3-25-8 Nishishinbashi, Minato-ku, Tokyo, 105-8461, Japan.
Gastric Cancer. 2006;9(3):235-9. doi: 10.1007/s10120-006-0368-5.
A 57-year-old man with gastrointestinal stromal tumor (GIST) of the stomach with peritoneal dissemination underwent gastrectomy. After surgery, he was treated with 400 mg/day of imatinib, without recurrence, for 26 months. At 26 months, the imatinib dose was reduced because of nausea, and 4 months after the dose reduction, recurrence of GIST was detected, for which surgical resection was performed again. The first surgical specimen had a mutation of exon 11 in the c-kit receptor gene. Intriguingly, the second surgical specimen had a novel mutation of exon 17, in addition to the above-mentioned mutation, in the c-kit receptor gene. Based on the result of molecular analysis, the novel mutation of exon 17, induced by longterm chemotherapy, was judged to have been responsible for the recurrence, which perhaps was triggered by the dose reduction of imatinib.
一名57岁患有胃胃肠道间质瘤(GIST)并伴有腹膜播散的男性接受了胃切除术。术后,他接受了每日400毫克伊马替尼的治疗,持续26个月无复发。在26个月时,由于恶心,伊马替尼剂量减少,剂量减少4个月后,检测到GIST复发,再次进行了手术切除。第一个手术标本的c-kit受体基因外显子11发生了突变。有趣的是,第二个手术标本除上述突变外,c-kit受体基因外显子17出现了新的突变。基于分子分析结果,长期化疗诱导的外显子17新突变被判定为复发的原因,这可能是由伊马替尼剂量减少引发的。