TY - JOUR
T1 - Thioguanine is Effective as Maintenance Therapy for Inflammatory Bowel Disease
T2 - A Prospective Multicentre Registry Study
AU - Simsek, Melek
AU - Schepers, Femke
AU - Kaplan, Sigal
AU - van Asseldonk, Dirk
AU - van Boeckel, Petra
AU - Boekema, Paul
AU - Dijkstra, Gerard
AU - Fidder, Herma
AU - Gisbertz, Ingrid
AU - Hoentjen, Frank
AU - Jharap, Bindia
AU - Kubben, Frank
AU - de Leest, Marleen
AU - Meijssen, Maarten
AU - Petrak, Ana
AU - van de Poel, Else
AU - Russel, Maurice
AU - van Bodegraven, Adriaan A.
AU - Mulder, Chris J. J.
AU - de Boer, Nanne
N1 - Funding Information: This work was supported by TEVA Nederland B.V. Publisher Copyright: © 2023 The Author(s). Published by Oxford University Press on behalf of European Crohn's and Colitis Organisation.
PY - 2023/6/1
Y1 - 2023/6/1
N2 - Background and Aims: Thioguanine 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. Methods: IBD 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]. Results: Sustained 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. Conclusion: Sustained 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.
AB - Background and Aims: Thioguanine 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. Methods: IBD 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]. Results: Sustained 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. Conclusion: Sustained 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.
KW - 6-thioguanine-nucleotides
KW - Crohn's disease
KW - Inflammatory bowel disease
KW - azathioprine
KW - mercaptopurine
KW - nodular regenerative hyperplasia
KW - thioguanine
KW - ulcerative colitis
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85161812372&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/36702552
UR - http://www.scopus.com/inward/record.url?scp=85161812372&partnerID=8YFLogxK
U2 - https://doi.org/10.1093/ecco-jcc/jjad013
DO - https://doi.org/10.1093/ecco-jcc/jjad013
M3 - Article
C2 - 36702552
SN - 1873-9946
VL - 17
SP - 933
EP - 942
JO - Journal of Crohn's and Colitis
JF - Journal of Crohn's and Colitis
IS - 6
ER -