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晚期结直肠癌的治疗

Therapy for advanced colorectal cancer.

作者信息

Benson A B

机构信息

Clinical Investigation Program, Robert H. Lurie Cancer Center, Northwestern University, Chicago, IL 60611-2096, USA.

出版信息

Semin Oncol. 1998 Oct;25(5 Suppl 11):2-11.

PMID:9786311
Abstract

Although 5-fluorouracil (5-FU) has been used to treat advanced colorectal cancer for 45 years, the drug has only a modest response rate and impact on survival. Attempting to enhance 5-FU's activity, researchers have administered it in combination with biochemical modulators and changed its dosage schedules to increase dose intensity. The combination of 5-FU and leucovorin has been evaluated in many studies. Results of a meta-analysis comparing 5-FU administered by bolus injection with a combination of 5-FU and intravenous leucovorin indicate that the combination significantly increased response rates but failed to improve survival. Similarly, studies comparing different methods of 5-FU administration (bolus injection v prolonged infusion) have demonstrated improved response rates and decreased toxicity with prolonged infusion, but most have failed to demonstrate statistically significant improvements in survival. For patients with liver-dominant colorectal disease, researchers have investigated the administration of liver-directed therapy by techniques such as hepatic arterial infusion (HAI). Compared with systemic administration of fluoropyrimidines, HAI administration increased response rates, but no survival benefit was demonstrated. Both response and survival benefits were observed with HAI, however, in one trial comparing HAI with no treatment (palliative care) in previously untreated patients with liver metastases. This trial also demonstrated that HAI did not diminish quality of life. Intravenous fluoropyrimidine-based therapies continue to dominate as the first-line approach for patients with advanced colorectal cancer. Present and future clinical trials will determine the efficacy of 5-FU pro-drugs, regimens combining oral 5-FU and 5-ethynyluracil, thymidylate synthase inhibitors, and new 5-FU combination regimens (5-FU plus oxaliplatin [Eloxatine; Sanofi, New York, NY] or irinotecan [CPT-II, Camptosar; Pharmacia & Upjohn, Kalamazoo, MI], for example).

摘要

尽管5-氟尿嘧啶(5-FU)已用于治疗晚期结直肠癌45年,但该药物的缓解率和对生存率的影响都较为有限。为提高5-FU的活性,研究人员将其与生化调节剂联合使用,并改变给药方案以增加剂量强度。5-FU与亚叶酸的联合应用已在多项研究中得到评估。一项比较5-FU静脉推注与5-FU联合静脉亚叶酸的荟萃分析结果表明,联合用药显著提高了缓解率,但未能改善生存率。同样,比较5-FU不同给药方法(静脉推注与持续输注)的研究表明,持续输注可提高缓解率并降低毒性,但大多数研究未能证明生存率有统计学意义的提高。对于以肝脏为主的结直肠癌患者,研究人员通过肝动脉灌注(HAI)等技术研究了肝导向治疗的给药情况。与全身应用氟嘧啶相比,HAI给药提高了缓解率,但未显示出生存获益。然而,在一项将HAI与未治疗(姑息治疗)进行比较的试验中,在既往未治疗的肝转移患者中观察到了HAI治疗在缓解率和生存率方面的获益。该试验还表明,HAI并未降低生活质量。基于静脉氟嘧啶的治疗仍然是晚期结直肠癌患者的一线主要治疗方法。当前和未来的临床试验将确定5-FU前体药物、口服5-FU与5-乙炔基尿嘧啶联合方案、胸苷酸合成酶抑制剂以及新的5-FU联合方案(例如5-FU加奥沙利铂[乐沙定;赛诺菲,纽约,纽约州]或伊立替康[CPT-II,开普拓;法玛西亚公司,卡拉马祖,密歇根州])的疗效。

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Semin Oncol. 1998 Oct;25(5 Suppl 11):2-11.
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[Systemic chemotherapy for advanced colorectal cancer with liver metastasis].[晚期结直肠癌肝转移的全身化疗]
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Hepatic arterial infusion of oxaliplatin and intravenous LV5FU2 in unresectable liver metastases from colorectal cancer after systemic chemotherapy failure.在全身化疗失败后,对不可切除的结直肠癌肝转移患者进行肝动脉灌注奥沙利铂和静脉注射LV5FU2。
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Basic research supported developments of chemotherapy in nonresectable isolated colorectal liver metastases to a protocol of hepatic artery infusion using mitoxantrone, 5-FU + folinic acid and mitomycin C.基础研究推动了不可切除孤立性结直肠癌肝转移化疗的发展,形成了一种采用米托蒽醌、5-氟尿嘧啶+亚叶酸和丝裂霉素C的肝动脉灌注方案。
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Hepatic arterial infusion chemotherapy using fluorouracil followed by systemic therapy using oxaliplatin plus fluorouracil and leucovorin for patients with unresectable liver metastases from colorectal cancer.对于无法切除的结直肠癌肝转移患者,先采用氟尿嘧啶进行肝动脉灌注化疗,随后采用奥沙利铂加氟尿嘧啶和亚叶酸钙进行全身治疗。
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Regional and systemic therapies for advanced colorectal carcinoma: randomized clinical trial results.晚期结直肠癌的区域和全身治疗:随机临床试验结果
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[Results of hepatic arterial infusion chemotherapy with 5-FU and leucovorin for unresectable liver metastases from colorectal cancer].[5-氟尿嘧啶和亚叶酸钙肝动脉灌注化疗治疗不可切除的结直肠癌肝转移的结果]
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Hepatic arterial infusion after curative resection of colorectal cancer metastases: a meta-analysis of prospective clinical trials.
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J Gastrointest Surg. 2005 Feb;9(2):198-206. doi: 10.1016/j.gassur.2004.07.004.
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