TY - JOUR
T1 - Systematic review of effects of withdrawal of immunomodulators or biologic agents from patients with inflammatory bowel disease
AU - Torres, Joana
AU - Boyapati, Ray K.
AU - Kennedy, Nicholas A.
AU - Louis, Edouard
AU - Colombel, Jean Frédéric
AU - Satsangi, Jack
N1 - Funding Information:
The authors thank Rachel Pinotti, MLIS, in the Gustave L. and Janet W. Levy Library at the Icahn School of Medicine at Mount Sinai for her assistance in helping design the comprehensive search strategy for this project. The Biocycle project receives funding from the European Union''s Horizon 2020 research and innovation programme under grant agreement No. 633168 - BIOCYCLE (PHC-13-2014). Dr Nicholas A. Kennedy is funded by a Wellcome Trust Research Training Fellowship [Grant 097943]. The authors disclose the following: Joana Torres has received consultant fees from Abbvie. Nicholas A. Kennedy has received speaker fees from MSD and travel support from Abbvie. Edouard Louis has received fees for: Educational Grant: MSD, Abbvie. Speaker Fees: Abbvie, Ferring, MSD, Chiesi, Mitsubishi Pharma, Hospira, Janssen. Advisory Board: Abbvie, Ferring, MSD, Takeda, Mitsubishi Pharma, Celltrion. Jean-Frederic Colombel has served as consultant, advisory board member or speaker for Abbvie, ABScience, Amgen, Bristol Meyers Squibb, Celgene, Celltrion, Danone, Ferring, Genentech, Giuliani SPA, Given Imaging, Immune Pharmaceuticals, Janssen, Kyowa Kirin Pharma, Medimmune, Merck & Co., Millennium Pharmaceuticals Inc., Navigant Consulting, Neovacs, Nestle, Nutrition Science Partners Ltd., Pfizer Inc., Prometheus Laboratories, Protagonist, Receptos, Sanofi, Schering Plough Corporation, Second Genome, Shire, Takeda, Teva Pharmaceuticals, Tigenix, UCB Pharma, Vertex and Dr. August Wolff GmbH & Co. Jack Satsangi has received speaker fees from MSD, Takeda, and research support from Abbie Vie. Ray K. Boyapati has no conflicts to disclose.
Funding Information:
The Biocycle project receives funding from the European Union's Horizon 2020 research and innovation programme under grant agreement No. 633168 – BIOCYCLE (PHC-13-2014).
Funding Information:
Dr Nicholas A. Kennedy is funded by a Wellcome Trust Research Training Fellowship [Grant 097943].
Publisher Copyright:
© 2015 AGA Institute.
PY - 2015/12/1
Y1 - 2015/12/1
N2 - Little is known about the optimal duration of therapy with an anti-tumor necrosis factor (TNF) agent and/or an immunomodulator for patients with inflammatory bowel disease (IBD). We performed a systematic search of the literature to identify studies reporting after de-escalation (drug cessation or dose reduction) of anti-TNF agents and/or immunomodulators in patients in remission from IBD. Studies were reviewed according to the type of IBD and drug. Rates of relapse, factors associated with relapse, and response to re-treatment were determined. Our search yielded 6315 unique citations; we analyzed findings from 69 studies (18 on de-escalation [drug cessation or dose reduction] of immunomodulator monotherapy, 8 on immunomodulator de-escalation from combination therapy, and 43 on de-escalation of anti-TNF agents, including 3 during pregnancy) comprising 4672 patients. Stopping immunomodulator monotherapy after a period of remission was associated with high rates of relapse in patients with Crohn's disease or ulcerative colitis (approximately 75% of patients experienced a relapse within 5 years after therapy was stopped). Most studies of patients with Crohn's disease who discontinued an immunomodulator after combination therapy found that rates of relapse did not differ from those of patients who continued taking the drug (55%-60% had disease relapse 24 months after they stopped taking the immunomodulator). The only study in patients with ulcerative colitis supported continued immunomodulator use. Approximately 50% of patients who discontinued anti-TNF agents after combination therapy maintained remission 24 months later, but the proportion in remission decreased with time. Markers of disease activity, poor prognostic factors, and complicated or relapsing disease course were associated with future relapse. In conclusion, based on a systematic review, 50% or more of patients with IBD who cease therapy have a disease relapse. Further studies are required to accurately identify subgroups of patients who are good candidates for discontinuation of treatment. The decision to withdraw a drug should be made for each individual based on patient preference, disease markers, consequences of relapse, safety, and cost.
AB - Little is known about the optimal duration of therapy with an anti-tumor necrosis factor (TNF) agent and/or an immunomodulator for patients with inflammatory bowel disease (IBD). We performed a systematic search of the literature to identify studies reporting after de-escalation (drug cessation or dose reduction) of anti-TNF agents and/or immunomodulators in patients in remission from IBD. Studies were reviewed according to the type of IBD and drug. Rates of relapse, factors associated with relapse, and response to re-treatment were determined. Our search yielded 6315 unique citations; we analyzed findings from 69 studies (18 on de-escalation [drug cessation or dose reduction] of immunomodulator monotherapy, 8 on immunomodulator de-escalation from combination therapy, and 43 on de-escalation of anti-TNF agents, including 3 during pregnancy) comprising 4672 patients. Stopping immunomodulator monotherapy after a period of remission was associated with high rates of relapse in patients with Crohn's disease or ulcerative colitis (approximately 75% of patients experienced a relapse within 5 years after therapy was stopped). Most studies of patients with Crohn's disease who discontinued an immunomodulator after combination therapy found that rates of relapse did not differ from those of patients who continued taking the drug (55%-60% had disease relapse 24 months after they stopped taking the immunomodulator). The only study in patients with ulcerative colitis supported continued immunomodulator use. Approximately 50% of patients who discontinued anti-TNF agents after combination therapy maintained remission 24 months later, but the proportion in remission decreased with time. Markers of disease activity, poor prognostic factors, and complicated or relapsing disease course were associated with future relapse. In conclusion, based on a systematic review, 50% or more of patients with IBD who cease therapy have a disease relapse. Further studies are required to accurately identify subgroups of patients who are good candidates for discontinuation of treatment. The decision to withdraw a drug should be made for each individual based on patient preference, disease markers, consequences of relapse, safety, and cost.
KW - Cessation
KW - Crohn's disease
KW - Patient management
KW - Ulcerative colitis
UR - http://www.scopus.com/inward/record.url?scp=84952936248&partnerID=8YFLogxK
U2 - 10.1053/j.gastro.2015.08.055
DO - 10.1053/j.gastro.2015.08.055
M3 - Review article
C2 - 26381892
AN - SCOPUS:84952936248
SN - 0016-5085
VL - 149
SP - 1716
EP - 1730
JO - Gastroenterology
JF - Gastroenterology
IS - 7
ER -