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首页> 外文期刊>Journal of Clinical Oncology >Phase II trial of hepatic arterial infusion of fluorouracil and recombinant human interferon alfa-2b for liver metastases of colorectal cancer refractory to systemic fluorouracil and leucovorin.
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Phase II trial of hepatic arterial infusion of fluorouracil and recombinant human interferon alfa-2b for liver metastases of colorectal cancer refractory to systemic fluorouracil and leucovorin.

机译:肝动脉输注氟尿嘧啶和重组人干扰素α-2b治疗难治性全身氟尿嘧啶和亚叶酸的大肠癌肝转移的II期试验。

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PURPOSE: To determine the toxicity, response rate, and survival in patients treated with hepatic arterial infusion (HAI) of fluorouracil (5-FU) plus recombinant human interferon alfa-2b (rIFN-alpha 2b) (Intron-A; Schering-Plough, Inc, Kenilworth, NJ) for colorectal carcinoma (CRC) liver metastases refractory to systemic 5-FU plus leucovorin (LCV). PATIENTS AND METHODS: Forty-eight patients were given a 6-hour HAI of rIFN-alpha 2b 5 MU/m2 followed by an 18-hour HAI of 5-FU, 1,500 mg/m2 daily for 5 days. Twenty-nine patients were treated through percutaneously placed catheters and 19 through implantable infusion pumps (Shiley Infusaid Inc, Noorwood, MA). Treatment cycles were repeated every 28 to 35 days. RESULTS: There were three (6.6%) complete remissions (CRs) and 12 (26.6%) partial remissions (PRs), for a CR plus PR rate of 33.3% among 45 assessable patients (95% confidence interval [CI], 20% to 49%). The median response duration was 7 months, while median survival duration was 15 months. Grade 3 to 4 treatment-related toxic effects included mucositis (40%), neutropenia (42%), and thrombocytopenia (12%). No hepatobiliary toxicity was encountered in any of the patients. Treatment was discontinued because of progressive liver disease in 23 patients and extrahepatic progression in 16, while six patients continue treatment through an infusaid pump. CONCLUSION: HAI of 5-FU plus rIFN-alpha 2b is well tolerated, devoid of hepatobiliary toxicity, and can produce a response rate of 33.3% among patients refractory to bolus intravenous (IV) 5-FU plus LCV. The lack of hepatobiliary toxicity may permit salvage HAI with floxuridine (FUDR) in patients whose liver tumors fail to respond to HAI of 5-FU plus rIFN-alpha 2b. Because diarrhea was not a common side effect of HAI of 5-FU plus rIFN-alpha 2b, it would be of interest to investigate whether alternating HAI of 5-FU and rIFN-alpha 2b with systemic irinotecan (CPT-11) will decrease the incidence of both hepatic and extrahepatic disease progression.
机译:目的:确定氟尿嘧啶(5-FU)加重组人干扰素α-2b(rIFN-alpha 2b)经肝动脉输注(HAI)治疗的患者的毒性,反应率和生存率(Intron-A; Schering-Plough ,Inc,Kenilworth,NJ)用于全身性5-FU加亚叶酸(LCV)难治的大肠癌(CRC)肝转移。患者和方法:48位患者的rIFN-alpha 2b 5 MU / m2的HAI为6小时,随后每天以1500 mg / m2的5-FU进行18小时HAI,为期5天。通过经皮放置的导管治疗了29名患者,通过植入式输液泵(Shiley Infusaid Inc,Noorwood,MA)治疗了19名患者。每28至35天重复治疗周期。结果:45例可评估患者中,有3例(6.6%)完全缓解(CR)和12例(26.6%)部分缓解(PR),CR加PR率为33.3%(95%置信区间[CI],20%至49%)。中位缓解期为7个月,中位生存期为15个月。与治疗相关的3至4级毒性反应包括粘膜炎(40%),中性粒细胞减少症(42%)和血小板减少症(12%)。在任何患者中均未发生肝胆毒性。由于23例患者进行性肝病和16例肝外疾病进展而终止治疗,而6例患者通过输液泵继续治疗。结论:5-FU +rIFN-α2b的HAI耐受性良好,没有肝胆毒性,在静脉推注5-FU + LCV难治性患者中可产生33.3%的缓解率。肝胆毒性的缺乏可能允许使用氟尿苷(FUDR)挽救肝肿瘤不能对5-FU加rIFN-α2b的HAI产生反应的患者。由于腹泻不是5-FU加rIFN-alpha 2b的HAI的常见副作用,因此研究5-FU和rIFN-alpha 2b的HAI与系统性伊立替康(CPT-11)交替使用是否会降低腹泻是很有意义的。肝内和肝外疾病进展的发生率。

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