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[结直肠癌外科辅助化疗的最新进展]

[Recent advances is surgical adjuvant chemotherapy for colorectal cancer].

作者信息

Kodaira S, Shatari T, Nozawa K

机构信息

First Dept. of Surgery, Teikyo University School of Medicine.

出版信息

Gan To Kagaku Ryoho. 2000 Dec;27(14):2201-8.

PMID:11142163
Abstract

To evaluate the significance of surgical adjuvant chemotherapy, randomized controlled trials (RCTs) of adjuvant chemotherapy after curative resection for colorectal cancer were reviewed. Several multi-drug systemic chemotherapies (MOF, MMC/FT, 5-FU, UFT p.o.) were useful as adjuvant treatment to improve survival or disease-free survival of patients with colorectal cancer. Moreover, a worldwide meta-analysis suggested that continuous intraportal 5-FU infusion improves survival. Combination chemotherapy trials utilizing 5-FU and levamisol (LEV) demonstrated a survival advantage in patients with high risk colon cancer. Recently, many RCTs have substantiated the benefits of treatment with 5-FU/Leucovorin (LV) and this treatment is widely used as adjuvant treatment for the patients with Dukes C resected colon cancer in Europe and the U.S.A. Now, with the increasing use of oral chemotherapy drugs, new trials comparing oral UFT/LV with intravenous 5-FU/LV are being implemented to investigate these drugs in terms of QOL, toxicity and cost. Furthermore, the new drug irinotecan (CPT-11) is now under investigation to see if it brings added efficacy to 5-FU/LV. In Japan, two major groups (N-SAS-CC and TAC-CR) are comparing surgery alone and UFT alone in patients with Dukes C colon and rectal cancer. From these results, surgical adjuvant chemotherapy seems to be effective in the treatment of patients with high risk colon cancer and those with rectal cancer.

摘要

为评估手术辅助化疗的意义,我们回顾了结肠癌根治性切除术后辅助化疗的随机对照试验(RCT)。几种多药全身化疗方案(MOF、MMC/FT、口服5-氟尿嘧啶、优福定)作为辅助治疗手段,对提高结肠癌患者的生存率或无病生存率有效。此外,一项全球荟萃分析表明,门静脉持续输注5-氟尿嘧啶可提高生存率。使用5-氟尿嘧啶和左旋咪唑(LEV)的联合化疗试验显示,高危结肠癌患者可从中获得生存优势。最近,许多随机对照试验证实了5-氟尿嘧啶/亚叶酸钙(LV)治疗的益处,在美国和欧洲,这种治疗方法被广泛用作Dukes C期结肠癌切除患者的辅助治疗。现在,随着口服化疗药物使用的增加,正在开展新的试验,比较口服优福定/亚叶酸钙与静脉注射5-氟尿嘧啶/亚叶酸钙,以研究这些药物在生活质量、毒性和成本方面的情况。此外,正在对新药伊立替康(CPT-11)进行研究,以确定其是否能增强5-氟尿嘧啶/亚叶酸钙的疗效。在日本,两个主要研究组(N-SAS-CC和TAC-CR)正在比较Dukes C期结肠癌和直肠癌患者单纯手术与单纯使用优福定的疗效。从这些结果来看,手术辅助化疗似乎对高危结肠癌患者和直肠癌患者的治疗有效。

相似文献

1
[Recent advances is surgical adjuvant chemotherapy for colorectal cancer].[结直肠癌外科辅助化疗的最新进展]
Gan To Kagaku Ryoho. 2000 Dec;27(14):2201-8.
2
[The current status of postoperative adjuvant chemotherapy for colorectal cancer].[结直肠癌术后辅助化疗的现状]
Gan To Kagaku Ryoho. 1997 Aug;24(10):1230-8.
3
[Progress in adjuvant therapy for colorectal cancer].[结直肠癌辅助治疗的进展]
Gan To Kagaku Ryoho. 2002 Dec;29(13):2488-97.
4
Postsurgical sequential methotrexate/5-FU and leucovorin on outpatient basis for advanced colorectal carcinoma.门诊使用甲氨蝶呤/5-氟尿嘧啶序贯疗法及亚叶酸钙治疗晚期结直肠癌
Hepatogastroenterology. 2001 Jan-Feb;48(37):128-32.
5
Five-year results of a randomized controlled trial of adjuvant chemotherapy for curatively resected colorectal carcinoma. The Colorectal Cancer Chemotherapy Study Group of Japan.根治性切除结直肠癌辅助化疗的随机对照试验五年结果。日本结直肠癌化疗研究组。
Jpn J Clin Oncol. 1995 Jun;25(3):91-103.
6
[Progress of adjuvant chemotherapy in colon cancer].[结肠癌辅助化疗的进展]
Gan To Kagaku Ryoho. 1996 Apr;23(5):554-9.
7
Adjuvant therapy for colorectal carcinoma.结直肠癌的辅助治疗。
Anticancer Res. 2002 Jul-Aug;22(4):2413-8.
8
[Review of comparative studies of postoperative adjuvant chemotherapy after curatively resected colorectal cancer in Japan].
Gan To Kagaku Ryoho. 2002 Sep;29(9):1532-9.
9
Importance of 5-fluorouracil dose-intensity in a double randomised trial on adjuvant portal and systemic chemotherapy for Dukes B2 and C colorectal cancer.5-氟尿嘧啶剂量强度在一项针对Dukes B2和C期结直肠癌辅助门静脉及全身化疗的双随机试验中的重要性
Anticancer Res. 2000 Nov-Dec;20(6C):4665-72.
10
Phase III Southwest Oncology Group 9415/Intergroup 0153 randomized trial of fluorouracil, leucovorin, and levamisole versus fluorouracil continuous infusion and levamisole for adjuvant treatment of stage III and high-risk stage II colon cancer.西南肿瘤协作组9415/肿瘤组0153的III期随机试验:氟尿嘧啶、亚叶酸钙和左旋咪唑对比氟尿嘧啶持续输注及左旋咪唑用于III期和高危II期结肠癌辅助治疗的研究
J Clin Oncol. 2005 Mar 20;23(9):1819-25. doi: 10.1200/JCO.2005.04.169.