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儿童急性淋巴细胞白血病大剂量甲氨蝶呤化疗中药物监测应注意的几个问题 被引量:4

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作者 张华年
出处 《儿科药学杂志》 CAS 2010年第2期61-63,共3页 Journal of Pediatric Pharmacy
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参考文献19

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  • 10张华年,许琼,李晖,徐华,宋新文,汪洋.儿童急性淋巴细胞白血病甲氨蝶呤化疗方案优化的研究[J].中国医院药学杂志,2008,28(20):1776-1779. 被引量:5

二级参考文献11

  • 1徐卫群,汤永民,方澄清,宋华,石淑文,扬世隆,任鼎泰,沈红强,钱伯芹.大剂量甲氨蝶呤治疗儿童急性淋巴细胞白血病排泄延迟分析[J].中华血液学杂志,2005,26(1):15-18. 被引量:66
  • 2刘瑛,万伍卿,邓兵.大剂量甲氨蝶呤治疗急性淋巴细胞白血病的不良反应[J].实用儿科临床杂志,2006,21(3):170-171. 被引量:23
  • 3顾龙君.儿童急性淋巴细胞白血病诊疗建议(第三次修订草案)[J].中华儿科杂志,2006,44(5):392-395. 被引量:477
  • 4赵香兰 王建华 等.血清MTX7-OA-MTX的HPLC测定法及其与微生物法在大剂量MTX疗法监测应用中的比较[J].药物分析杂志,1988,8(5):278-278.
  • 5赵香兰,药物分析杂志,1988年,8卷,5期,278页
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  • 7Peter D, Maria J, Angela K, et al. Pharmacodynamic properties of methotrexate and aminotrexate during weekly therapy[J]. Cancer Chemother Pharmacol, 2005, 57: 826-834.
  • 8Evans WE, Crom WR, Abromowitch M, et al. Clinical phamacodynamic of high-dose methotrexate in acute lymphoblastic leukemia[J]. N Engl J Med, 1986,314:471-474.
  • 9Masson E, Relling MV, Synold TW, et al. Accumulation of methotrexate polyglutamates in lymphoblasts is a determinant of antileukemic effects in vivo : a rationale for high dose methotrexat[J]. J Clin Invest, 1996,97 : 73-80.
  • 10Galpin AJ, Schuetz JD, Massin E, et al. Differences in folypolyglutamatate sythetase and dihydrofolate reductase expression in human B-Lineage versus T-lineage leukemia lymphoblastic: mechanisms for lineage differences in methotrexate polyglutamylation and cytotoxicity[J]. Mol Pharmacol, 1997, 52,155-163.

共引文献38

同被引文献42

  • 1徐卫群,汤永民,方澄清,宋华,石淑文,扬世隆,任鼎泰,沈红强,钱伯芹.大剂量甲氨蝶呤治疗儿童急性淋巴细胞白血病排泄延迟分析[J].中华血液学杂志,2005,26(1):15-18. 被引量:66
  • 2刘瑛,万伍卿,邓兵.大剂量甲氨蝶呤治疗急性淋巴细胞白血病的不良反应[J].实用儿科临床杂志,2006,21(3):170-171. 被引量:23
  • 3顾龙君.儿童急性淋巴细胞白血病诊疗建议(第三次修订草案)[J].中华儿科杂志,2006,44(5):392-395. 被引量:477
  • 4周际昌.实用肿瘤内科学[M].2版.北京:人民卫生出版社,2002:343-346.
  • 5Fotoohi K,Skarby T,Soderhall S,et al.Interference of 7-hydroxy-methotrexate with the determination of methotrexate in plasma sam-ples from children with acute lymphoblastic leukemia employingroutine clinical assays[J].J Chromatogr B Analyt Technol BiomedLife Sci,2005,817(2):139-144.
  • 6Alnaim L.Therapeutic drug monitoring of cancer chemotherapy[J].J Oncol Pharm Pract,2007,13(4):207-221.
  • 7Treon SP,Chabner BA. Concepts in use of high - dose methotrex-ate therapy[ J]. Clin Chem,1996,42(8) : 1322.
  • 8Woessmann W, Seideraann K, Mann G, et al. The impact of themethotrexate administration schedule and dose in the treatment ofchildren and adolescents with B - cell neoplasms : a report of theBFM Group Study NHL-BFM95[ J]. Blood,2005 ,105(3) :948.
  • 9Millot F,Rubie H,Mazingue F,et al. Cerebrospinal fluid drug lev-els of leukemic children receiving intravenous 5 g/m2 methotrexate[J]. Leuk Lymphoma,1994,14( 1/2) : 141.
  • 10Rask C,Albertioni F,Bentzen S M,et al. Clinical and pharmacoki-netic risk factors for high - dose methotrexate - induced toxicity inchildren with acute lymphoblastic leukemia - a logistic regressionanalysis [J]. Acta Oncol,199Bt37(3) :277 -284.

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