Tajima Hidehiro, Ohta Tetsuo, Kitagawa Hirohisa, Sakai Seisho, Makino Isamu, Hayashi Hironori, Oyama Katsunobu, Nakagawara Hisatoshi, Fujita Hideto, Onishi Ichiro, Takamura Hiroyuki, Ninomiya Itasu, Fushida Sachio, Tani Takashi, Fujimura Takashi, Koda Wataru, Minami Tetsuya, Ryu Yasuji, Sanada Junichiro, Gabata Toshifumi, Matsui Osamu
Departments of Gastroenterologic Surgery, and.
Exp Ther Med. 2011 Mar;2(2):265-269. doi: 10.3892/etm.2011.190. Epub 2011 Jan 12.
Hepatic metastasis is a common cause of treatment failure after curative resection of pancreatic cancer. We report a pilot study of hepatic arterial infusion (HAI) chemotherapy with gemcitabine and 5-fluorouracil (5-FU) for postoperative liver metastases from pancreatic cancer. Five patients who had undergone curative resection of liver metastases from pancreatic cancer received HAI of gemcitabine and 5-FU between October 2008 and September 2010 at Kanazawa University Hospital. Gemcitabine at a dose of 800 mg was infused over 30 min via a bedside pump. After gemcitabine administration, 250 mg of 5-FU was infused continuously over 24 h on days 1-5, comprising one cycle of therapy. These treatment cycles were continued biweekly. In the evaluation according to RECIST criteria, a partial response was obtained in 2 of the 5 cases, with stable disease being achieved in the remaining 3 cases (response rate, 100%). In 4 of the 5 cases, a decrease in serum tumor marker CA19-9 was observed after 10 HAI treatment cycles. The median time to treatment failure was 10 months (range 3-17). As to adverse events, leukocytopenia was grade 3 in 1 of 4 affected cases and all 5 were anemic, although 4 of the 5 cases had anemia prior to HAI therapy. Grade 2 thrombocytopenia was observed in 2 cases. No nonhematologic events, such as nausea, diarrhea, liver injury and neuropathy, occurred. There were no life-threatening toxicities, but 4 cases (80%) developed catheter complications, and the HAI catheter and subcutaneous implantable port system had to be removed. HAI delivers high doses of chemotherapeutic agents directly into tumor vessels, producing increased regional levels with greater efficacy and a lower incidence/severity of systemic side effects. In conclusion, HAI chemotherapy is useful and safe for the treatment of malignancies confined to the liver.
肝转移是胰腺癌根治性切除术后治疗失败的常见原因。我们报告了一项关于吉西他滨和5-氟尿嘧啶(5-FU)肝动脉灌注(HAI)化疗用于胰腺癌术后肝转移的初步研究。2008年10月至2010年9月期间,5例接受过胰腺癌肝转移根治性切除的患者在金泽大学医院接受了吉西他滨和5-FU的HAI治疗。800mg吉西他滨通过床边泵在30分钟内输注完毕。给予吉西他滨后,在第1 - 5天连续24小时持续输注250mg 5-FU,构成一个治疗周期。这些治疗周期每两周进行一次。根据RECIST标准评估,5例中有2例获得部分缓解,其余3例病情稳定(缓解率100%)。5例中有4例在10个HAI治疗周期后血清肿瘤标志物CA19-9下降。治疗失败的中位时间为10个月(范围3 - 17个月)。关于不良事件,4例受影响病例中有1例白细胞减少为3级,所有5例均有贫血,尽管5例中有4例在HAI治疗前就已贫血。2例出现2级血小板减少。未发生恶心腹泻、肝损伤和神经病变等非血液学事件。没有危及生命的毒性反应,但4例(80%)出现导管并发症,不得不移除HAI导管和皮下植入式端口系统。HAI将高剂量化疗药物直接输送到肿瘤血管中,使局部药物浓度升高,疗效增强,全身副作用的发生率和严重程度降低。总之,HAI化疗对于局限于肝脏的恶性肿瘤的治疗是有效且安全的。