ASTIC Autologous Stem Cell Transplantation for Crohn's Disease
Crohn Disease
About this trial
This is an interventional treatment trial for Crohn Disease focused on measuring Crohn's Disease, HSCT, Autologous, EBMT, ECCO
Eligibility Criteria
Inclusion Criteria: Inclusion criteria: mandatory Age between 18 and 50 years (Patients aged 50-65 can participate if specially approved by the Trial Steering Committee) Confirmed diagnosis of active Crohn's Disease Unsatisfactory course despite 3 immunosuppressive agents (usually azathioprine, methotrexate and infliximab) in addition to corticosteroids. Patients should have relapsing disease (i.e. >1 exacerbation/year) despite thiopurines, methotrexate and/or infliximab maintenance therapy or clear demonstration of intolerance / toxicity to these drugs. Impaired function and quality of life, compared to population means, on at least one of the following: IBDQ (Appendix 6) European Questionnaire of Life quality (EuroQOL-5D, Appendix 4) Impaired function on Karnofsky index (Appendix 7) Current problems unsuitable for surgery and patient at risk for developing short bowel syndrome. Informed consent Inclusion criteria: discretionary Wherever possible, diseased tissue should be accessible endoscopically for objective histological study but in the case of small bowel disease that is extensive but does not extend to duodenum or terminal ileum, participation without endoscopy is allowed. Smokers may enter the study provided they have received intensive counselling about smoking. Add patients with ileostomy/colostomy and patients with short bowel syndrome Exclusion Criteria: Pregnancy or unwillingness to use adequate contraception during the study Concomitant severe disease Diarrhoea due to short small or large bowel Infection or risk thereof Significant malnutrition: Body Mass Index (BMI) ≤18, serum albumin <20 g/l Previous poor compliance Concurrent enrolment in any other protocol using an investigational drug or hematopoietic growth factor up to four weeks before study entry. Lack of funding
Sites / Locations
- University Hospital Gasthuisberg
- University of Calgery
- Hopital Huriez Chru
- Hospital Sanin-Louis
- Dipatimento di Medicina Interna E Gastroenterologia
- Universita di Bologna Interna e Gastroenterologia Policlinico Saint Orsola
- Careggi Hospital
- Istituto Clinico Humanitas
- Fondazione IRCCS Ospedale Maggiore Policlinico Mangiagalli e Regina Elena
- L Sacco University Hopsital
- Casa Sollievo Della Sofferenza IRCCS Hospital
- Hospital Universitari Germans Trias I Pujol, Dept of Gastroenterology
- University Hospital
- Universitätsspital Zürich
- The John Radcliffe Hospital
- Western General Hospital
- Barts and the London NHS Trust
- City Hospital
- Nottingham Digestive Diseases Centre
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Transplant Arm
Delayed Transplant
Hematopoietic stem cell mobilisation followed, within 4 weeks, by high dose immunoablation and autologous stem cell transplantation
Hematopoietic stem cell mobilisation followed, after 59 weeks, by high dose immunoablation and autologous hematopoietic stem cell transplantation