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ASTIC Autologous Stem Cell Transplantation for Crohn's Disease

Primary Purpose

Crohn Disease

Status
Terminated
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Autologous haematopoietic stem cell transplant
Sponsored by
European Society for Blood and Marrow Transplantation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn Disease focused on measuring Crohn's Disease, HSCT, Autologous, EBMT, ECCO

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Experimental

Arm Label

Transplant Arm

Delayed Transplant

Arm Description

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

Outcomes

Primary Outcome Measures

Proportion patients in sustained disease remission
To evaluate the potential clinical benefit of hematopoietic stem cell mobilisation followed by high dose immuno-ablation and autologous stem cell transplantation versus hematopoietic stem cell mobilisation only followed by best clinical practice in patients with Crohn' s disease.

Secondary Outcome Measures

patients who have not responded to immunosuppressant medication
To evaluate the safety of Hematopoietic Stem Cell Transplantation (HSCT) in Crohn's disease patients who have not responded to immunosuppressant medication

Full Information

First Posted
February 27, 2006
Last Updated
December 21, 2020
Sponsor
European Society for Blood and Marrow Transplantation
Collaborators
The Broad Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00297193
Brief Title
ASTIC Autologous Stem Cell Transplantation for Crohn's Disease
Official Title
Autologous Stem Cell Transplantation for Crohn's Disease: ASTIC
Study Type
Interventional

2. Study Status

Record Verification Date
August 2013
Overall Recruitment Status
Terminated
Why Stopped
For safety reasons the recruitment was halted prematurely. Patients on the trial continute to receive treatment and are being followed up as part the protocol.
Study Start Date
June 2006 (undefined)
Primary Completion Date
March 2013 (Actual)
Study Completion Date
March 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
European Society for Blood and Marrow Transplantation
Collaborators
The Broad Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Transplant study for patients with relapsing Crohn's disease demonstrating clear intolerance or toxicity to conventional treatment. The purpose of this study is to determine whether there is a potential clinical benefit of hematopoietic stem cell mobilisation followed by high dose immuno-ablation and autologous stem cell transplantation versus hematopoietic stem cell mobilisation only followed by best clinical practice.
Detailed Description
Open label, phase III, randomised, multicentre study comparing early transplantation procedure with transplantation carried out to the same protocol but delayed by one year. The status of patients undergoing early HSCT will be evaluated after one year and compared to those about to undergo delayed HSCT Patients will be randomised to: 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 All patients will be mobilised prior to randomisation. Those receiving early transplantation will be compared over the first year with those whose transplant has been delayed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn Disease
Keywords
Crohn's Disease, HSCT, Autologous, EBMT, ECCO

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Transplant Arm
Arm Type
Experimental
Arm Description
Hematopoietic stem cell mobilisation followed, within 4 weeks, by high dose immunoablation and autologous stem cell transplantation
Arm Title
Delayed Transplant
Arm Type
Experimental
Arm Description
Hematopoietic stem cell mobilisation followed, after 59 weeks, by high dose immunoablation and autologous hematopoietic stem cell transplantation
Intervention Type
Procedure
Intervention Name(s)
Autologous haematopoietic stem cell transplant
Intervention Description
All patients will be mobilised prior to randomisation. Those receiving early transplantation will be compared over the first year with those whose transplant has been delayed.
Primary Outcome Measure Information:
Title
Proportion patients in sustained disease remission
Description
To evaluate the potential clinical benefit of hematopoietic stem cell mobilisation followed by high dose immuno-ablation and autologous stem cell transplantation versus hematopoietic stem cell mobilisation only followed by best clinical practice in patients with Crohn' s disease.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
patients who have not responded to immunosuppressant medication
Description
To evaluate the safety of Hematopoietic Stem Cell Transplantation (HSCT) in Crohn's disease patients who have not responded to immunosuppressant medication
Time Frame
1 - 2 years
Other Pre-specified Outcome Measures:
Title
Impact of HSCT on health related, and generic, quality of life measures
Description
To evaluate the impact of HSCT on health related, and generic, quality of life measures
Time Frame
1 - 2 Years
Title
To identify factors predictive of success
Description
To identify factors predictive of success
Time Frame
1-2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher J Hawkey
Organizational Affiliation
Nottingham University Hospital - Wolfson Digestive Diseases Centre
Official's Role
Study Chair
Facility Information:
Facility Name
University Hospital Gasthuisberg
City
Leuven
State/Province
Herestraat 49
ZIP/Postal Code
3000
Country
Belgium
Facility Name
University of Calgery
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 2T9
Country
Canada
Facility Name
Hopital Huriez Chru
City
Lille
ZIP/Postal Code
59037
Country
France
Facility Name
Hospital Sanin-Louis
City
Paris
ZIP/Postal Code
75010
Country
France
Facility Name
Dipatimento di Medicina Interna E Gastroenterologia
City
Bologna
ZIP/Postal Code
40138
Country
Italy
Facility Name
Universita di Bologna Interna e Gastroenterologia Policlinico Saint Orsola
City
Bologna
ZIP/Postal Code
40138
Country
Italy
Facility Name
Careggi Hospital
City
Florence
ZIP/Postal Code
50134
Country
Italy
Facility Name
Istituto Clinico Humanitas
City
Milan
ZIP/Postal Code
20089
Country
Italy
Facility Name
Fondazione IRCCS Ospedale Maggiore Policlinico Mangiagalli e Regina Elena
City
Milan
ZIP/Postal Code
20122
Country
Italy
Facility Name
L Sacco University Hopsital
City
Milan
ZIP/Postal Code
20157
Country
Italy
Facility Name
Casa Sollievo Della Sofferenza IRCCS Hospital
City
San Giovanni Rotondo
ZIP/Postal Code
71013
Country
Italy
Facility Name
Hospital Universitari Germans Trias I Pujol, Dept of Gastroenterology
City
Badalona
ZIP/Postal Code
08916
Country
Spain
Facility Name
University Hospital
City
Basel
ZIP/Postal Code
CH-4031
Country
Switzerland
Facility Name
Universitätsspital Zürich
City
Zürich
ZIP/Postal Code
8091
Country
Switzerland
Facility Name
The John Radcliffe Hospital
City
Oxford
State/Province
Headington
ZIP/Postal Code
OX3 9DU
Country
United Kingdom
Facility Name
Western General Hospital
City
Edinburgh
ZIP/Postal Code
EH4 2XU
Country
United Kingdom
Facility Name
Barts and the London NHS Trust
City
London
ZIP/Postal Code
E1 1BB
Country
United Kingdom
Facility Name
City Hospital
City
Nottingham
ZIP/Postal Code
NG5 1PB
Country
United Kingdom
Facility Name
Nottingham Digestive Diseases Centre
City
Nottingham
ZIP/Postal Code
NG7 2UH
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
28497755
Citation
Lindsay JO, Allez M, Clark M, Labopin M, Ricart E, Rogler G, Rovira M, Satsangi J, Farge D, Hawkey CJ; ASTIC trial group; European Society for Blood and Marrow Transplantation Autoimmune Disease Working Party; European Crohn's and Colitis Organisation. Autologous stem-cell transplantation in treatment-refractory Crohn's disease: an analysis of pooled data from the ASTIC trial. Lancet Gastroenterol Hepatol. 2017 Jun;2(6):399-406. doi: 10.1016/S2468-1253(17)30056-0. Epub 2017 Apr 6.
Results Reference
derived
PubMed Identifier
26670970
Citation
Hawkey CJ, Allez M, Clark MM, Labopin M, Lindsay JO, Ricart E, Rogler G, Rovira M, Satsangi J, Danese S, Russell N, Gribben J, Johnson P, Larghero J, Thieblemont C, Ardizzone S, Dierickx D, Ibatici A, Littlewood T, Onida F, Schanz U, Vermeire S, Colombel JF, Jouet JP, Clark E, Saccardi R, Tyndall A, Travis S, Farge D. Autologous Hematopoetic Stem Cell Transplantation for Refractory Crohn Disease: A Randomized Clinical Trial. JAMA. 2015 Dec 15;314(23):2524-34. doi: 10.1001/jama.2015.16700.
Results Reference
derived

Learn more about this trial

ASTIC Autologous Stem Cell Transplantation for Crohn's Disease

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