Tajima Hidehiro, Kitagawa Hirohisa, Tsukada Tomoya, Okamoto Koichi, Nakanuma Shin-Ichi, Sakai Seisho, Makino Isamu, Furukawa Hiroyuki, Hayashi Hironori, Oyama Katsunobu, Inokuchi Masafumi, Nakagawara Hisatoshi, Miyashita Tomoharu, Itoh Hiroshi, Fujita Hideto, Takamura Hiroyuki, Ninomiya Itasu, Fushida Sachio, Fujimura Takashi, Ohta Tetsuo, Koda Wataru, Minami Tetsuya, Ryu Yasuji, Sanada Junichiro, Gabata Toshifumi, Matsui Osamu, Sai Yoshimichi
Department of Gastroenterological Surgery and, Division of Cancer Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Ishikawa 920-8641, Japan.
Department of Radiology, Division of Cancer Medicine, Graduate School of Medical Science, Kanazawa University, Kanazawa, Ishikawa 920-8641, Japan.
Mol Clin Oncol. 2013 Sep;1(5):869-874. doi: 10.3892/mco.2013.152. Epub 2013 Jul 23.
Hepatic metastasis is a common cause of treatment failure following resection of pancreatic cancer. In this study, we report our results of hepatic arterial infusion (HAI) chemotherapy with gemcitabine (GEM) plus 5-fluorouracil (5-FU) or oral S-1 treatment for postoperative liver metastases from pancreatic cancer. Seven patients with postoperative liver metastases from pancreatic cancer received HAI with GEM plus 5-FU or oral S-1 between October, 2008 and September, 2010 at Kanazawa University Hospital (Kanazawa, Japan). Three out of the 7 cases exhibited a partial response (PR) according to Response Evaluation Criteria in Solid Tumors (RECIST) and stable disease (SD) was achieved in 3 out of the 7 cases (response rate, 85.7%). A decrease in serum tumor marker CA 19-9 levels was observed after 10 HAI treatment cycles in 5 out of the 7 cases. The median time to treatment failure was 8 months (range, 0-17 months). Adverse events included grade 3 leukocytopenia in 1 case and anemia in all 7 cases, although 5 out of the 7 patients were anemic prior to HAI therapy. Grade 2 thrombocytopenia was also observed in 2 cases. Non-hematological events, such as nausea, diarrhea, liver injury or neuropathy and life-threatening toxicities were not reported; however, 6 patients (85.7%) developed catheter-related complications and the HAI catheter and subcutaneous implantable port system had to be removed. These findings demonstrated that HAI may deliver high doses of chemotherapeutic agents directly into the tumor vessels, producing increased regional levels with greater efficacy and a lower incidence/severity of systemic side effects. In conclusion, HAI chemotherapy is a safe and effective treatment for liver metastases from pancreatic cancer.
肝转移是胰腺癌切除术后治疗失败的常见原因。在本研究中,我们报告了吉西他滨(GEM)联合5-氟尿嘧啶(5-FU)肝动脉灌注(HAI)化疗或口服S-1治疗胰腺癌术后肝转移的结果。2008年10月至2010年9月期间,7例胰腺癌术后肝转移患者在日本金泽大学医院接受了GEM联合5-FU或口服S-1的HAI治疗。根据实体瘤疗效评价标准(RECIST),7例中有3例出现部分缓解(PR),7例中有3例病情稳定(SD)(缓解率为85.7%)。7例中有5例在10个HAI治疗周期后血清肿瘤标志物CA 19-9水平下降。治疗失败的中位时间为8个月(范围为0-17个月)。不良事件包括1例3级白细胞减少和所有7例贫血,尽管7例患者中有5例在HAI治疗前就已贫血。2例还观察到2级血小板减少。未报告恶心、腹泻、肝损伤或神经病变等非血液学事件以及危及生命的毒性反应;然而,6例患者(85.7%)出现了导管相关并发症,不得不移除HAI导管和皮下植入式端口系统。这些结果表明,HAI可将高剂量化疗药物直接输送至肿瘤血管,提高局部药物浓度,增强疗效,降低全身副作用的发生率和严重程度。总之,HAI化疗是治疗胰腺癌肝转移的一种安全有效的方法。