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[Therapeutic effect of sequential doses of methotrexate (MTX) and 5-fluorouracil (5-FU) in advanced gastric cancer: comparison of intermediate-dose MTX with high-dose MTX].

作者信息

Akazawa S, Nakajima T, Kitagawa H, Nakagawa T, Kanda Y, Futatsuki K, Suda Y, Yoshida S, Honda T

出版信息

Gan To Kagaku Ryoho. 1985 Jan;12(1):91-8.

PMID:3966810
Abstract

Twenty-one patients were treated with sequential doses of MTX and 5-FU so as to be classified by MTX dosage into an intermediate MTX-dose group and a high MTX-dose group. In the intermediate-dose MTX group, the drug was given at a dosage of 100 mg/m2 intravenously (i.v.) and followed 1 hour later by 5-FU at 800 mg/m2 i.v. (dripping for 1 hour); the drugs were recycled every 1 week. In the high-dose MTX group, the drug was administered at a dose of 1.5 g/m2 i.v. (dripping for 2 hours) and followed 1 hour later by 5-FU at 1.5 g/m2 i.v. (dripping for 2 hours); the drugs were recycled every 2-3 weeks. Average MTX concentrations in serum at the start of 5-FU administration were 1.69 X 10(-5) and 1.33 X 10(-4) mol/l/h in the intermediate and high-dose MTX groups, respectively. Six (50%) of 12 patients adequately treated with intermediate-dose MTX had a partial response (PR), and one (14.3%) of 7 evaluable patients treated with high-dose MTX had a PR. Major toxicity included diarrhea (33.3%) in the intermediate-dose MTX group and hair loss (71.4%) in the high-dose MTX group. Hematological toxicity was mild in MTX group: six (50%) of 12 patients had a granulocyte count nadir less than 1,000/microliters and one (8.3%) of 12 patients had a platelet count nadir less than 10(5)/microliters in the intermediate-dose MTX group. Five (71.4%) of 7 patients had a granulocyte nadir less than 1,000/microliters and two (28.6%) of 7 patients had a platelet count nadir less than 10(5)/microliters in the high-dose MTX group.

摘要

相似文献

1
[Therapeutic effect of sequential doses of methotrexate (MTX) and 5-fluorouracil (5-FU) in advanced gastric cancer: comparison of intermediate-dose MTX with high-dose MTX].
Gan To Kagaku Ryoho. 1985 Jan;12(1):91-8.
2
[Sequential methotrexate-5-fluorouracil (MTX-5-FU) treatment of patients with advanced gastric and colorectal cancer. Sequential Methotrexate-5-FU Study Group].
Gan To Kagaku Ryoho. 1987 Aug;14(8):2482-90.
3
[Intra-aortic infusion therapy with sequential methotrexate (MTX) and 5-FU in advanced gastric carcinoma].
Gan To Kagaku Ryoho. 1986 May;13(5):1927-33.
4
A phase II study of sequential methotrexate and 5-fluorouracil chemotherapy in previously treated gastric cancer: a report from the Gastrointestinal Oncology Group of the Japan Clinical Oncology Group, JCOG 9207 trial.序贯甲氨蝶呤和5-氟尿嘧啶化疗用于既往治疗过的胃癌的II期研究:日本临床肿瘤学会胃肠道肿瘤学组的报告,JCOG 9207试验
Jpn J Clin Oncol. 2008 Jun;38(6):432-7. doi: 10.1093/jjco/hyn043. Epub 2008 May 30.
5
[A new sequential chemotherapy of methotrexate with 5-fluorouracil against advanced colo-rectal cancer].
Gan To Kagaku Ryoho. 1993 Apr;20(5):603-9.
6
[Low-dose methotrexate and sequential 5-FU treatment in advanced gastric cancer].
Gan To Kagaku Ryoho. 1984 Nov;11(11):2408-13.
7
[Clinical evaluation of sequential MTX/5-FU therapy for gastric cancer].[甲氨蝶呤/氟尿嘧啶序贯疗法治疗胃癌的临床评估]
Gan To Kagaku Ryoho. 1995 Jul;22(8):994-1000.
8
Comparison of methotrexate and sequential methotrexate-5-fluorouracil for patients with recurrent squamous cell carcinoma of the oral cavity.甲氨蝶呤与序贯甲氨蝶呤-5-氟尿嘧啶治疗复发性口腔鳞状细胞癌患者的比较。
Chemioterapia. 1987 Dec;6(6):390-2.
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[Sequential chemotherapy with methotrexate and 5-fluorouracil for advanced gastric cancer].[甲氨蝶呤与5-氟尿嘧啶序贯化疗用于晚期胃癌]
Gan To Kagaku Ryoho. 1998 Mar;25(4):541-6.
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Phase II study of sequential methotrexate and 5-fluorouracil chemotherapy against peritoneally disseminated gastric cancer with malignant ascites: a report from the Gastrointestinal Oncology Study Group of the Japan Clinical Oncology Group, JCOG 9603 Trial.甲氨蝶呤与5-氟尿嘧啶序贯化疗治疗伴有恶性腹水的腹膜播散性胃癌的II期研究:日本临床肿瘤学会胃肠肿瘤研究组JCOG 9603试验报告
Jpn J Clin Oncol. 2004 Jun;34(6):316-22. doi: 10.1093/jjco/hyh063.

引用本文的文献

1
Chemotherapy for advanced gastric cancer.晚期胃癌的化疗
Cochrane Database Syst Rev. 2017 Aug 29;8(8):CD004064. doi: 10.1002/14651858.CD004064.pub4.