Takada Joji, Kenno Sachiko, Aoki Takanori, Hamada Hiromi, Katsuki Yoshio
Department of Surgery, Nikko Memorial Hospital.
Gan To Kagaku Ryoho. 2009 Nov;36(12):2326-9.
The prognosis of most hepatic and lymph node metastases in AFP-producing gastric cancer is poor, and despite the use of multimodal therapy, the average survival period is reported to be approximately one year. Described here is one example in which intra-arterial chemotherapy for simultaneous hepatic metastases in AFP-producing gastric cancer achieved a marked improvement. The patient is a 65-year-old female. Distal gastrectomy was performed for Type II gastric cancer. L, type 2, 5.5x2.4 cm, tub 2>por 1, pT2 (MP), int, INF b, ly2, v1, pN1, pPM (-), pDM (-), pH1: stage IV. The AFP level before surgery was 801.4 ng/mL and lowered to 65.8 ng/mL after surgery, AFP-producing gastric cancer and simultaneous hepatic metastases (S4, single lesion) was diagnosed based upon imaging examinations. 5-FU+epirubicin+MMC (FEM)intra-arterial chemotherapy was started one month following surgery, but because CT showed multiple new hepatic lesions(S4, S5)four months following surgery, DSM therapy was performed with hepatic arterial injections of MMC 10 mg, DSM 300 mg. Dynamic CT showed a reduction in size of the tumors in both S4 and S5, and at five months following surgery, hepatic arterial infusion chemotherapy FP (CDDP 5 mg+5-FU 250 mg weekly) was started and performed 45 times in a 14-month period. During therapy, CR was achieved for the hepatic metastases and tumor marker levels were also normal. Because an introduction of contrast medium into the hepatic reservoir showed a narrowing of the hepatic artery and inflow of contrast medium into the splenic artery, arterial infusion was terminated. Following this, from the 20th month following surgery, S-1 (100 mg/day: 4 weeks administration, 2 weeks rest) was started and from the third course (50 mg/ day: 4 weeks administration, 2 weeks rest), and the patient is currently undergoing a sixth course. Currently, 2 years and 4 months after surgery, there have been no recurrences. This suggests the possibility that intra-arterial chemotherapy is an effective treatment method for hepatic metastases in AFP-producing gastric cancer.
大多数产生甲胎蛋白的胃癌肝转移和淋巴结转移预后较差,尽管采用了多模式治疗,但据报道平均生存期约为一年。本文介绍了一例通过动脉内化疗使产生甲胎蛋白的胃癌同时性肝转移获得显著改善的病例。患者为65岁女性。因II型胃癌行远端胃切除术。肿瘤大小为L,2型,5.5×2.4cm,组织学类型为tub2>por1,pT2(肌层浸润),组织学分级int,INF b,ly2,v1,pN1,pPM(-),pDM(-),pH1:IV期。术前甲胎蛋白水平为801.4ng/mL,术后降至65.8ng/mL,根据影像学检查诊断为产生甲胎蛋白的胃癌并同时性肝转移(S4,单个病灶)。术后1个月开始5-氟尿嘧啶+表柔比星+丝裂霉素(FEM)动脉内化疗,但术后4个月CT显示肝脏出现多个新病灶(S4、S5),遂行肝动脉注射丝裂霉素10mg、DSM 300mg的DSM治疗。动态CT显示S4和S5病灶均缩小,术后5个月开始肝动脉灌注化疗FP(顺铂5mg+5-氟尿嘧啶250mg每周),在14个月内进行了45次。治疗期间,肝转移灶达到完全缓解,肿瘤标志物水平也恢复正常。由于向肝储器内注入造影剂显示肝动脉狭窄且造影剂流入脾动脉,遂终止动脉灌注。此后,术后第20个月开始服用S-1(100mg/天:服用4周,休息2周),从第三疗程开始(50mg/天:服用4周,休息2周),目前患者正在接受第六疗程治疗。目前,术后2年4个月,无复发情况。这表明动脉内化疗可能是治疗产生甲胎蛋白的胃癌肝转移的有效方法。