TY - JOUR
T1 - Autologous haematopoietic stem cell transplantation without CD34 + cell selection in refractory Crohn's disease
AU - Cassinotti, Andrea
AU - Annaloro, C.
AU - Ardizzone, S.
AU - Onida, F.
AU - Della Volpe, A.
AU - Clerici, M.
AU - Usardi, P.
AU - Greco, S.
AU - Maconi, G.
AU - Bianchi Porro, G.
AU - Lambertenghi Deliliers, G.
PY - 2008/2
Y1 - 2008/2
N2 - Objectives: Autologous haematopoietic stem cell transplantation (HSCT) with CD34+ cell selection has recently been used in the treatment of refractory Crohn's disease, showing good safety and promising efficacy. We investigated the safety and efficacy of HSCT with unselected peripheral blood stem cells (PBSCs) in moderate-severe refractory Crohn's disease. Patients: Four patients (three male, one female; age range 26-45 years) with active moderate-severe Crohn's disease (median Crohn's Disease Activity Index (CDAI) 319, range 272-345), refractory or intolerant to multiple drugs including infliximab, were enrolled. Interventions: Unselected PBSCs were collected after mobilisation with cyclophosphamide (CTX) 1.5 g/m2 and granulocyte-colony stimulating factor (G-CSF) 10 μg/kg. The conditioning regimen included CTX 50 mg/kg on days -5 to -2 and rabbit anti-thymocyte globulin (ATG) 2.5 mg/kg on days -4 to -2. Main outcome measures: Primary endpoints were toxicity and clinical remission (CDAI
AB - Objectives: Autologous haematopoietic stem cell transplantation (HSCT) with CD34+ cell selection has recently been used in the treatment of refractory Crohn's disease, showing good safety and promising efficacy. We investigated the safety and efficacy of HSCT with unselected peripheral blood stem cells (PBSCs) in moderate-severe refractory Crohn's disease. Patients: Four patients (three male, one female; age range 26-45 years) with active moderate-severe Crohn's disease (median Crohn's Disease Activity Index (CDAI) 319, range 272-345), refractory or intolerant to multiple drugs including infliximab, were enrolled. Interventions: Unselected PBSCs were collected after mobilisation with cyclophosphamide (CTX) 1.5 g/m2 and granulocyte-colony stimulating factor (G-CSF) 10 μg/kg. The conditioning regimen included CTX 50 mg/kg on days -5 to -2 and rabbit anti-thymocyte globulin (ATG) 2.5 mg/kg on days -4 to -2. Main outcome measures: Primary endpoints were toxicity and clinical remission (CDAI
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U2 - 10.1136/gut.2007.128694
DO - 10.1136/gut.2007.128694
M3 - Article
C2 - 17895357
AN - SCOPUS:38549137308
VL - 57
SP - 211
EP - 217
JO - Gut
JF - Gut
SN - 0017-5749
IS - 2
ER -