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S-1诱导的、对5'-DFUR难治的胃癌肺转移的长期完全消退:一项药代动力学研究的病例报告

S-1-induced, prolonged complete regression of lung metastasis from gastric cancer refractory to 5'-DFUR: a case report with pharmacokinetic study.

作者信息

Ueda Yuji, Yamagishi Hisakazu, Yamashita Tetsuro, Itoh Norio, Itoi Hirosumi, Shirasaka Tetsuhiko, Ajani Jaffer A

机构信息

Department of Surgery and Oncology of the Digestive System, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Japan.

出版信息

Jpn J Clin Oncol. 2004 May;34(5):282-6. doi: 10.1093/jjco/hyh044.

Abstract

S-1 is an oral fluoropyrimidine reported to be most active for gastric cancer. However, few studies have documented a complete response (CR) of lung metastasis to S-1 treatment. We describe a 66-year-old woman in whom S-1 induced complete regression of lung metastasis from gastric cancer, that had been refractory to another oral fluoropyrimidine, 5'-deoxy-5-fluorouridine (5'-DFUR). After preoperative chemotherapy with a combination of etoposide, adriamycin and cisplatin and with methotrexate plus 5-fluorouracil, the patient underwent a total gastrectomy with lower esophagectomy for advanced diffuse-type gastric cancer with invasion of the esophagus in May 1993. She received postoperative adjuvant chemotherapy with 5'-DFUR (600 mg/day) for 3 years. However, a solitary metastasis to the left lung was detected in November 1996 and she underwent partial resection of the left lung. Chemotherapy with 5'-DFUR was reinitiated after operation, but re-metastasis to the left lung with elevation of the serum carcinoembryonic antigen (CEA) level was diagnosed in June 1999. Treatment with S-1 was started in August. S-1 was given orally in a dose of 100 mg/day for 28 consecutive days, followed by a 14-day recovery; treatment was repeated every 6 weeks. The metastatic lesion in the left lung completely regressed after two courses of S-1 and the serum CEA level returned to the normal range. The patient received a total of 10 courses of S-1. The dose of S-1 was reduced to 80 mg/day from the sixth course because of grade 2 skin rash. Pharmacokinetic studies after administration of S-1 revealed high and prolonged plasma 5-FU levels. Nearly 4 years have passed since complete regression of the lung metastasis. This may be the first report to document a prolonged complete response of lung metastasis from gastric cancer induced by single-agent chemotherapy with S-1.

摘要

S-1是一种口服氟嘧啶,据报道对胃癌活性最强。然而,很少有研究记录S-1治疗对肺转移瘤的完全缓解(CR)情况。我们报告一名66岁女性,S-1使她的胃癌肺转移灶完全消退,该转移灶对另一种口服氟嘧啶5'-脱氧-5-氟尿苷(5'-DFUR)难治。1993年5月,患者在接受依托泊苷、阿霉素和顺铂联合以及甲氨蝶呤加5-氟尿嘧啶的术前化疗后,因晚期弥漫型胃癌侵犯食管行全胃切除加食管下段切除术。她接受了为期3年的术后辅助化疗,使用5'-DFUR(600毫克/天)。然而,1996年11月检测到左肺单发转移,她接受了左肺部分切除术。术后重新开始使用5'-DFUR化疗,但1999年6月诊断为左肺再次转移且血清癌胚抗原(CEA)水平升高。8月开始使用S-1治疗。S-1口服给药,剂量为100毫克/天,连续服用28天,随后休息14天;每6周重复治疗。经过两个疗程的S-1治疗后,左肺转移灶完全消退,血清CEA水平恢复正常范围。患者共接受了10个疗程的S-1治疗。由于2级皮疹,从第六个疗程起S-1剂量减至80毫克/天。S-1给药后的药代动力学研究显示血浆5-氟尿嘧啶水平高且持续时间长。自肺转移灶完全消退以来已过去近4年。这可能是首篇记录单药S-1化疗诱导胃癌肺转移长期完全缓解的报告。

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