Hepatic arterial infusion chemotherapy using fluorouracil, epirubicin, and mitomycin C for patients with liver metastases from gastric cancer after treatment failure of systemic S-1 plus cisplatin

被引:13
|
作者
Seki, Hiroshi [1 ]
Ohi, Hiroyuki [1 ]
Ozaki, Toshirou [1 ]
Yabusaki, Hiroshi [2 ]
机构
[1] Niigata Canc Ctr Hosp, Dept Diagnost Radiol, Niigata 9518566, Japan
[2] Niigata Canc Ctr Hosp, Dept Surg Gastroenterol, Niigata 9518566, Japan
关键词
Interventional therapy; liver; metastases; abdomen/GI; angiography; catheters; SIDE-HOLE CATHETER; COLORECTAL-CANCER; RADIOFREQUENCY ABLATION; ADENOCARCINOMA; SURVIVAL; TRIAL; EPIDEMIOLOGY; MULTICENTER; PLACEMENT; THERAPY;
D O I
10.1177/0284185115603247
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: For patients with liver metastases from gastric cancer (LMGC), combination chemotherapy with fluoropyrimidines and platinum agents has been recognized as standard treatment. However, the prognosis of hepatic progression after first-line treatment failure remains poor. When hepatic progression occurs, hepatic arterial infusion (HAI) chemotherapy may be helpful for preventing disease progression. Purpose: To retrospectively assess the feasibility and efficacy of HAI chemotherapy using 5-fluorouracil, epirubicin, and mitomycin C (FEM) for patients with LMGC after failure of systemic S-1 plus cisplatin. Material and Methods: We reviewed the records of patients who received HAI chemotherapy using FEM for LMGC that progressed during systemic S-1 plus cisplatin treatment while extrahepatic disease was decreased or did not appear. HAI chemotherapy was given as second-line therapy using 5-fluorouracil (330 mg/m(2) weekly), epirubicin (30 or 40 mg/m(2) every 4 weeks), and mitomycin C (2.7 mg/m(2) biweekly). Results: Fourteen patients were analyzed. Toxicity of HAI chemotherapy was generally mild. The objective response rate was 42.9%, including a complete response rate of 14.3%. Median times to hepatic and extrahepatic progression were 9.2 and 7.4 months, respectively. Of 12 patients with documented progression after HAI chemotherapy, 10 patients (83.3%) received additional treatment, including irinotecan or taxanes. Overall, median survival was 12.7 months. Conclusion: Our findings suggest that HAI chemotherapy using FEM is a feasible and effective treatment for patients with LMGC after failure of systemic S-1 plus cisplatin. HAI chemotherapy employed in the second-line setting is useful for achieving long-term disease control of LMGC.
引用
收藏
页码:781 / 788
页数:8
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