Evidence map›Paper›PMID 36702552›Full record

ArticleJournal of Crohn's & colitis2023

Thioguanine is Effective as Maintenance Therapy for Inflammatory Bowel Disease: A Prospective Multicentre Registry Study.

Melek Simsek, Femke Schepers, Sigal Kaplan, Dirk van Asseldonk, Petra van Boeckel, Paul Boekema, Gerard Dijkstra, Herma Fidder, Ingrid Gisbertz, Frank Hoentjen and 10 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Journal of Crohn's & colitis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.1field-weighted citation impact, top 8% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 15 institutions in 3 countries.

Melek SimsekDepartment of Gastroenterology and Hepatology, AGEM Research Institute, Amsterdam University Medical Centre, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0001-8827-955X
Femke SchepersTeva Pharmaceutical Industries, Haarlem, The Netherlands.
Sigal KaplanTeva Pharmaceutical Industries Ltd, Netanya, Israel.
Dirk van AsseldonkDepartment of Gastroenterology and Hepatology, Noordwest ziekenhuisgroep, Alkmaar, The Netherlands.
Petra van BoeckelDepartment of Gastroenterology and Hepatology, Sint Antonius, Nieuwegein, The Netherlands.
Paul BoekemaDepartment of Gastroenterology and Hepatology, Maxima Medical Centre, Veldhoven, The Netherlands.
Gerard DijkstraDepartment of Gastroenterology and Hepatology, University Medical Centre Groningen, Groningen, The Netherlands.
Herma FidderDepartment of Gastroenterology and Hepatology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Ingrid GisbertzDepartment of Gastroenterology and Hepatology, Bernhoven Hospital, Uden, The Netherlands.
Frank HoentjenDepartment of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Bindia JharapDepartment of Gastroenterology and Hepatology, Meander Medical Centre, Amersfoort, The Netherlands.
Frank KubbenDepartment of Gastroenterology and Hepatology, Maasstad Hospital, Rotterdam, The Netherlands.
Marleen de LeestDepartment of Gastroenterology and Hepatology, Rijnstate Hospital, Arnhem, The Netherlands.
Maarten MeijssenDepartment of Gastroenterology and Hepatology, Isala Clinics, Zwolle, The Netherlands.
Ana PetrakTeva Pharmaceutical Industries, Haarlem, The Netherlands.
Else van de PoelTeva Pharmaceutical Industries, Haarlem, The Netherlands.
Maurice RusselDepartment of Gastroenterology and Hepatology, Medical Spectrum Twente, Enschede, The Netherlands.
Adriaan A van BodegravenDepartment of Gastroenterology, Geriatrics, Internal and Intensive Care Medicine (CO-MIK), Zuyderland Medical Centre, Heerlen-Sittard-Geleen, The Netherlands.
Chris J J MulderDepartment of Gastroenterology and Hepatology, AGEM Research Institute, Amsterdam University Medical Centre, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Nanne de BoerDepartment of Gastroenterology and Hepatology, AGEM Research Institute, Amsterdam University Medical Centre, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Teva Pharmaceuticals (Netherlands) · NLVrije Universiteit Amsterdam · NLRadboud University Nijmegen · NLIsala · NLMaasstad Ziekenhuis · NLMeander Medisch Centrum · NLMedisch Spectrum Twente · NLNoordwest Ziekenhuisgroep · NLRijnstate Hospital · NLSt. Antonius Ziekenhuis · NLTeva Pharmaceuticals (Israel) · ILUniversity Medical Center Groningen · NLUniversity Medical Center Utrecht · NLZiekenhuis Bernhoven · NLZuyderland Medisch Centrum · NL

Funding

TEVA Nederland B.V.
6 · The paper itself

Abstract

BACKGROUND AND

aimsThioguanine is a well-tolerated and effective therapy for inflammatory bowel disease [IBD] patients. Prospective effectiveness data are needed to substantiate the role of thioguanine as a maintenance therapy for IBD.

methodsIBD patients who previously failed azathioprine or mercaptopurine and initiated thioguanine were prospectively followed for 12 months starting when corticosteroid-free clinical remission was achieved (Harvey-Bradshaw Index [HBI] ≤ 4 or Simple Clinical Colitis Activity Index [SCCAI] ≤ 2). The primary endpoint was corticosteroid-free clinical remission throughout 12 months. Loss of clinical remission was defined as SCCAI > 2 or HBI > 4, need of surgery, escalation of therapy, initiation of corticosteroids or study discontinuation. Additional endpoints were adverse events, drug survival, physician global assessment [PGA] and quality of life [QoL].

resultsSustained corticosteroid-free clinical remission at 3, 6 or 12 months was observed in 75 [69%], 66 [61%] and 49 [45%] of 108 patients, respectively. Thioguanine was continued in 86 patients [80%] for at least 12 months. Loss of response [55%] included escalation to biologicals in 15%, corticosteroids in 10% and surgery in 3%. According to PGA scores, 82% of patients were still in remission after 12 months and QoL scores remained stable. Adverse events leading to discontinuation were reported in 11%, infections in 10%, myelo- and hepatotoxicity each in 6%, and portal hypertension in 1% of patients.

conclusionSustained corticosteroid-free clinical remission over 12 months was achieved in 45% of IBD patients on monotherapy with thioguanine. A drug continuation rate of 80%, together with favourable PGA and QoL scores, underlines the tolerability and effectiveness of thioguanine for IBD.

Indexed as

ColitisInflammatory Bowel DiseasesAzathioprineHumansImmunosuppressive AgentsMercaptopurineProspective StudiesQuality of LifeThioguanineAzathioprineImmunosuppressive AgentsMercaptopurineThioguanine6-thioguanine-nucleotidesazathioprineCrohn’s diseaseInflammatory bowel diseasemercaptopurinenodular regenerative hyperplasiathioguanineulcerative colitis

Identifiers

PMID36702552
PMCPMC10274302
OpenAlexW4318263853

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.