Evidence map›Paper›PMID 26670970›Full record

Trial reportJAMA2015

Autologous Hematopoetic Stem Cell Transplantation for Refractory Crohn Disease: A Randomized Clinical Trial.

Christopher J Hawkey, Matthieu Allez, Miranda M Clark, Myriam Labopin, James O Lindsay, Elena Ricart, Gerhard Rogler, Montserrat Rovira, Jack Satsangi, Silvio Danese and 19 more

Registry-linked trialOpen access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in JAMA, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00297193 (Autologous Stem Cell Transplantation for Crohn's Disease), which is not on this map. Cited by 77 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 6 pooled it
17.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00297193 phase3terminatednot on this map

Autologous Stem Cell Transplantation for Crohn's Disease: ASTIC

TypeinterventionalSponsorEuropean Society for Blood and Marrow TransplantationRan2006 to 2017Enrolled45ConditionsCrohn DiseaseArmsAutologous haematopoietic stem cell transplant
3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 6 syntheses or guidelines pooled it, 184 citations in OpenAlex.

  1. Guideline
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17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 20 institutions in 5 countries.

Christopher J HawkeyNottingham Digestive Diseases Centre, School of Clinical Sciences, Queens Medical Centre, Nottingham, United Kingdom.
Matthieu AllezAPHP, Hôpital Saint Louis, Department of Gastroenterology, INSERM UMRS 1160, Paris Diderot, Sorbonne Paris-Cité University, Paris, France.
Miranda M ClarkNottingham Digestive Diseases Centre, School of Clinical Sciences, Queens Medical Centre, Nottingham, United Kingdom.
Myriam LabopinEuropean Group for Blood and Marrow Transplantation, Paris, France.
James O LindsayCentre for Immunobiology, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
Elena RicartGastroenterology Department, Hospital Clinic, CIBER-EHD, Barcelona, Spain.
Gerhard RoglerDivision of Gastroenterology and Hepatology, University Hospital, University of Zurich, Zurich, Switzerland.
Montserrat RoviraHematology Department, Hospital Clinic, Barcelona, Spain.
Jack SatsangiGastro-intestinal Unit, Institute of Genetics and Molecular Medicine, Western General Hospital University of Edinburgh, Edinburgh, United Kingdom.
Silvio DaneseIBD Center, Humanitas Research Hospital, Rozzano, Milan, Italy.
Nigel RussellHaematology School of Medicine, University of Nottingham, Nottingham City Hospital, Nottingham, United Kingdom.
John GribbenCentre for Haemato-Oncology, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
Peter JohnsonDepartment of Haematology, Western General Hospital, Edinburgh, United Kingdom.
Jerome LargheroBiotherapies and Cell Therapy Unit, AP-HP Hôpital Saint-Louis, Paris 7 University, France.
Catherine ThieblemontHaematology/Transplantation, AP-HP Hôpital Saint-Louis, Paris 7 University, Paris, France.
Sandro ArdizzoneIBD Unit, Department of Gastroenterology, "L. Sacco" University Hospital, Milan, Italy.
Daan DierickxDepartment of Hematology, University hospitals Leuven, Gasthuisberg, Belgium University Hospital, Belgium.
Adalberto IbaticiDivisione Ematologia e Trapianto di Midollo, IRCCS San Martino-IST, Genova, Italy.
Timothy LittlewoodDepartment of Haematology, Oxford University Hospitals NHS Trust, Oxford, United Kingdom.
Francesco OnidaHematology-BMT Center, Fondazione IRCCS Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
Urs SchanzDivision of Hematology, University Hospital Zurich, Zurich, Switzerland.
Severine VermeireDepartment of Gastroenterology University Hospital Gasthuisberg Herestraat, Leuven, Belgium.
Jean-Frederic ColombelDepartment of Hepato-Gastroenterology, Hopital Huriez, Lille, France23Department of Gastroenterology, Icahn School of Medicine, New York, New York.
Jean-Paul JouetDepartement of Hematology, Hôpital Claude-Huriez, Lille, France.
Elizabeth ClarkEBMT Clinical Trials, European Group for Blood and Marrow Transplantation, London, United Kingdom.
Riccardo SaccardiEuropean Blood & Marrow Transplantation Group, Hematology Department, Careggi University Hospital, Florence, Italy.
Alan TyndallDepartment of Rheumatology, University Hospital, Basel, Switzerland.
Simon TravisTranslational Gastroenterology Unit, Oxford University Hospital, Oxford, United Kingdom.
Dominique FargeInternal Medicine and Vascular Disease Unit AP-HP Hôpital Saint-Louis, Paris 7 University, France.
Hôpital Claude Huriez · FRHospital Clínic de Barcelona · ESQueen Mary University of London · GBUniversité Paris Cité · FRUniversity Hospital of Zurich · CHAssistance Publique – Hôpitaux de Paris · FREcotaxie, Microenvironnement et développement lymphocytaireEuropean Society for Blood and Marrow Transplantation · FRIRCCS Humanitas Research Hospital · ITLuigi Sacco Hospital · ITNIHR Nottingham Digestive Diseases Biomedical Research Unit · GBNottingham City Hospital · GBOspedale Policlinico San Martino · ITOxford University Hospitals NHS Trust · GBQueen's Medical Centre · GBUniversity Hospital of Basel · CHUniversity of Edinburgh · GBUniversity of Milan · ITUniversity of Oxford · GBWestern General Hospital · GB

Funding

Chief Scientist Office ETM/137Chief Scientist Office ETM/75Medical Research Council G0600329Medical Research Council G0800675Medical Research Council G0800759
6 · The paper itself

Abstract

importanceCase reports and series suggest hematopoietic stem cell transplantation (HSCT) may benefit some patients with Crohn disease.

objectiveTo evaluate the effect of autologous HSCT on refractory Crohn disease. DESIGN, SETTING, AND

participantsParallel-group randomized clinical trial conducted in 11 European transplant units from July 2007 to September 2011, with follow-up through March 2013. Patients were aged 18 to 50 years with impaired quality of life from refractory Crohn disease not amenable to surgery despite treatment with 3 or more immunosuppressive or biologic agents and corticosteroids.

interventionsAll patients underwent stem cell mobilization before 1:1 randomization to immunoablation and HSCT (n = 23) or control treatment (HSCT deferred for 1 year [n = 22]). All were given standard Crohn disease treatment as needed. MAIN OUTCOMES AND MEASURES: Sustained disease remission at 1 year, a composite primary end point comprising clinical remission (Crohn Disease Activity Index (CDAI) <150 [range, 0-600]), no use of corticosteroids or immunosuppressive or biologic drugs for at least the last 3 months, and no endoscopic or radiological evidence of active (erosive) disease anywhere in the gastrointestinal (GI) tract. Secondary outcomes were individual components of the primary composite outcome and other measures of disease activity, laboratory results, quality of life and functional status, and GI tract imaging.

resultsTwenty-three patients underwent HSCT and 22 received standard Crohn disease treatment (controls). Sustained disease remission was achieved in 2 patients undergoing HSCT (8.7%) vs 1 control patient (4.5%) (absolute difference, 4.2% [95% CI, -14.2% to 22.6%]; P = .60). Fourteen patients undergoing HSCT (61%) vs 5 control patients (23%) had discontinued immunosuppressive or biologic agents or corticosteroids for at least 3 months (difference, 38.1% [95% CI, 9.3% to 59.3%]; P = .01). Ten vs 2 patients had a CDAI less than 150 (remission) at the final evaluation, 8 (34.8%) vs 2 (9.1%) for 3 or more months (difference, 25.7% [95% CI, 1.1% to 47.1%]; P = .052). Eight (34.8%) vs 2 (9.1%) patients were adjudicated free of active disease on endoscopy and radiology at final assessment (difference, 25.7% [95% CI, 1.1% to 47.1%]; P = .054). There were 76 serious adverse events in patients undergoing HSCT vs 38 in controls. One patient undergoing HSCT died. CONCLUSIONS AND RELEVANCE: Among adult patients with refractory Crohn disease not amenable to surgery who had impaired quality of life, HSCT, compared with conventional therapy, did not result in a statistically significant improvement in sustained disease remission at 1 year and was associated with significant toxicity. These findings do not support the widespread use of HSCT for patients with refractory Crohn disease.

trial registrationclinicaltrials.gov Identifier: NCT00297193.

Indexed as

Hematopoietic Stem Cell MobilizationAdultCrohn DiseaseFemaleHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedQuality of LifeRemission InductionTime FactorsTransplantation, AutologousTransplantation ConditioningTreatment Outcome

Identifiers

PMID26670970
OpenAlexW2202486845

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.