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Treatment of pediatric refractory Crohn’s disease with thalidomide 被引量:15

Treatment of pediatric refractory Crohn’s disease with thalidomide
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摘要 AIM: To assess the efficacy and tolerability of thalidomide in pediatric Crohn's disease (CD). METHODS: Six patients with refractory CD received thalidomide at an initial dose of 2 mg/kg per day for one month, then increased to 3 mg/kg per day or decreased to 1 mg/kg per day, and again further reduced to 0.5 mg/kg per day, according to the individual patient's response to the drug. RESULTS: Remission was achieved within three months. Dramatic clinical improvement was demonstrated after thalidomide treatment. Endoscopic and pathological improvements were also observed after thalidomide treatment, which was well tolerated by all patients. CONCLUSION: Thalidomide is a useful drug for pediatric refractory CD. AIM: To assess the efficacy and tolerability of thalidomide in pediatric Crohn's disease (CD). METHODS: Six patients with refractory CD received thalidomide at an initial dose of 2 mg/kg per day for one month, then increased to 3 mg/kg per day or decreased to 1 mg/kg per day, and again further reduced to 0.5 mg/kg per day, according to the individual patient's response to the drug. RESULTS: Remission was achieved within three months. Dramatic clinical improvement was demonstrated after thalidomide treatment. Endoscopic and pathological improvements were also observed after thalidomide treatment, which was well tolerated by all patients. CONCLUSION: Thalidomide is a useful drug for pediat- ric refractory CD,
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第10期1286-1291,共6页 世界胃肠病学杂志(英文版)
关键词 Inflammatory bowel disease THALIDOMIDE Tumor necrosis factor-m CHILDREN 沙利度胺 治疗 小儿 药物反应 临床症状 耐受性 CD
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  • 1[1]Strober W,Nakamura K,Kitani A.The SAMP1/Yit mouse:another step closer to modeling human inflammatory bowel disease.J Clin Invest 2001; 107:667-670
  • 2[2]Bouma G,Strober W.The immunological and genetic basis of inflammatory bowel disease.Nat Rev Immunol 2003; 3:521-533
  • 3[3]Fiocchi C.Inflammatory bowel disease:etiology and pathogenesis.Gastroenterology 1998; 115:182-205
  • 4[4]Murch SH,Braegger CP,Walker-Smith JA,MacDonald TT.Location of tumour necrosis factor alpha by immunohistochemistry in chronic inflammatory bowel disease.Gut 1993;34:1705-1709
  • 5[5]Breese EJ,Michie CA,Nicholls SW,Murch SH,Williams CB,Domizio P,Walker-Smith JA,MacDonald TT.Tumor necrosis factor alpha-producing cells in the intestinal mucosa of children with inflammatory bowel disease.Gastroenterology 1994;106:1455-1466
  • 6[6]Braegger CP,Nicholls S,Murch SH,Stephens S,MacDonald TT.Tumour necrosis factor alpha in stool as a marker of intestinal inflammation.Lancet 1992; 339:89-91
  • 7[7]Powrie F,Leach MW,Mauze S,Menon S,Caddie LB,Coffman RL.Inhibition of Th1 responses prevents inflammatory bowel disease in scid mice reconstituted with CD45RBhi CD4+ T cells.Immunity 1994; 1:553-562
  • 8[8]Kosiewicz MM,Nast CC,Krishnan A,Rivera-Nieves J,Moskaluk CA,Matsumoto S,Kozaiwa K,Cominelli F.Th1-type responses mediate spontaneous ileitis in a novel murine model of Crohn's disease.J Clin Invest 2001; 107:695-702
  • 9[9]Van den Brande JM,Braat H,van den Brink GR,Versteeg HH,Bauer CA,Hoedemaeker I,van Montfrans C,Hommes DW,Peppelenbosch MP,van Deventer SJ.Infliximab but not etanercept induces apoptosis in lamina propria T-lymphocytes from patients with Crohn's disease.Gastroenterology 2003; 124:1774-1785
  • 10[10]Targan SR,Hanauer SB,van Deventer SJ,Mayer L,Present DH,Braakman T,DeWoody KL,Schaible TF,Rutgeerts PJ.A short-term study of chimeric monoclonal antibody cA2 to tumor necrosis factor alpha for Crohn's disease.Crohn's Disease cA2 Study Group.N Engl JMed 1997; 337:1029-1035

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