TY - JOUR
T1 - A Treat-to-Target Update in Ulcerative Colitis
T2 - A Systematic Review
AU - Ungaro, Ryan
AU - Colombel, Jean Frédéric
AU - Lissoos, Trevor
AU - Peyrin-Biroulet, Laurent
N1 - Funding Information:
Guarantor of the article: Ryan Ungaro, MD, and Jean-Frédéric Colombel, MD. Specific author contributions: R.U. and L.P.-B.: screening of literature search output and study selection. All authors contributed to the conception and design, contributed to the critical review and revision of each draft of the manuscript, and approved the final version for submission. Financial support: Research support from Boehringer Ingelheim, Abbvie, and Pfizer. Supported by a Career Development Award from the Crohn’s and Colitis Foundation. R.U. has served as a consultant and/or advisory board member for Takeda, Pfizer, and Janssen. J.-F.C. has received grant support from AbbVie, Janssen Pharmaceuticals, and Takeda; has served as a speaker for AbbVie, Amgen, and Ferring Pharmaceuticals; has served as a consultant for AbbVie, Amgen, Boehringer Ingelheim, Celgene Corporation, Celltrion, Eli Lilly, Enterome, Ferring Pharmaceuticals, Genentech, Janssen Pharmaceuticals, MedImmune, Merck & Co., Pfizer, Protagonist, Second Genome, Seres Therapeutics, Shire, Takeda, and Theradiag; and is a shareholder of Genfit and Intestinal Biotech Development. T.L. is an employee of Takeda Pharmaceuticals U.S.A., Inc. L.P.-B. has received consulting fees from Merck, Abbott, Janssen, Gen-entech, Mitsubishi, Ferring, Norgine, Tillotts, Vifor, Shire, Therakos, Pharmacosmos, Pilège, BMS, UCB Pharma, Hospira, Celltrion, Takeda, Boehringer Ingelheim, Lilly, and Pfizer; and has received lecture fees from Merck, Abbott, Janssen, Ferring, Norgine, Tillotts, Vifor, Therakos, and HAC Pharma. Potential competing interests: R.U. has served as a consultant and/ or Advisory Board member for Takeda, Pfizer, and Janssen. J.-F.C. has received grant support from AbbVie, Janssen Pharmaceuticals, and Takeda; has served as a speaker for AbbVie, Amgen, and Ferring Pharmaceuticals; has served as a consultant for AbbVie, Amgen, Boehringer Ingelheim, Celgene Corporation, Celltrion, Eli Lilly, Enterome, Ferring Pharmaceuticals, Genentech, Janssen Pharmaceuticals, MedImmune, Merck & Co., Pfizer, Protagonist, Second Genome, Seres Therapeutics, Shire, Takeda, and Theradiag; and is a shareholder of Genfit and Intestinal Biotech Development. T.L. is an employee of Takeda Pharmaceuticals U.S.A., Inc. L.P.-B. has received consulting fees from Merck, Abbott, Janssen, Genentech, Mitsubishi, Ferring, Norgine, Tillotts, Vifor, Shire, Therakos, Phar-macosmos, Pilège, BMS, UCB Pharma, Hospira, Celltrion, Takeda, Boehringer Ingelheim, Lilly, and Pfizer; and has received lecture fees from Merck, Abbott, Janssen, Ferring, Norgine, Tillotts, Vifor, Therakos, and HAC Pharma. Medical writing and editing assistance for this article was provided by Reem Berro, PhD, Jessica Cardenas, PhD, and Katy Stevens, PhD, of inVentiv Medical Communications, LLC, and a Syneos Health Group company, respectively, and was supported by Takeda Pharmaceuticals U.S.A., Inc.
Publisher Copyright:
© 2019 by The American College of Gastroenterology. Unauthorized reproduction of this article is prohibited.
PY - 2019/6/1
Y1 - 2019/6/1
N2 - In 2015, the Selecting Therapeutic Targets in Inflammatory Bowel Disease (STRIDE) program proposed shifting the therapeutic focus on ulcerative colitis (UC) toward altering the natural history of the disease course by regularly monitoring objective measurements of disease activity and tailoring treatment accordingly. The therapeutic paradigm shift was well received in the research community and is often cited. However, new evidence on optimal UC treatment targets continues to accumulate since the time of the STRIDE guidelines. This systematic review summarizes the evidence accrued since the STRIDE UC recommendations, discusses the barriers for adoption of treat-to-target approaches in clinical practice in UC, and suggests directions for future research.METHODS:We systematically reviewed MEDLINE for studies from the time of the STRIDE systematic review up to March 31, 2018, that assessed the potential treatment targets identified by the STRIDE recommendations.RESULTS:Each potential treatment target literature search returned > 200 articles, which were then reviewed by 2 independent investigators for relevant studies. Selected studies of clinical factors, patient-reported outcomes, endoscopy, histology, imaging, and biomarkers and implications on treatment targets are summarized.CONCLUSIONS:It appears that the relative weight given to different therapeutic targets in the development and improvement of UC treatments could be optimized, with an increased emphasis on endoscopic and histological targets over clinical or symptomatic targets. For this evolution to occur, however, new research has to demonstrate that the treat-to-target approach will deliver on the promise of better long-term outcomes compared with current approaches.
AB - In 2015, the Selecting Therapeutic Targets in Inflammatory Bowel Disease (STRIDE) program proposed shifting the therapeutic focus on ulcerative colitis (UC) toward altering the natural history of the disease course by regularly monitoring objective measurements of disease activity and tailoring treatment accordingly. The therapeutic paradigm shift was well received in the research community and is often cited. However, new evidence on optimal UC treatment targets continues to accumulate since the time of the STRIDE guidelines. This systematic review summarizes the evidence accrued since the STRIDE UC recommendations, discusses the barriers for adoption of treat-to-target approaches in clinical practice in UC, and suggests directions for future research.METHODS:We systematically reviewed MEDLINE for studies from the time of the STRIDE systematic review up to March 31, 2018, that assessed the potential treatment targets identified by the STRIDE recommendations.RESULTS:Each potential treatment target literature search returned > 200 articles, which were then reviewed by 2 independent investigators for relevant studies. Selected studies of clinical factors, patient-reported outcomes, endoscopy, histology, imaging, and biomarkers and implications on treatment targets are summarized.CONCLUSIONS:It appears that the relative weight given to different therapeutic targets in the development and improvement of UC treatments could be optimized, with an increased emphasis on endoscopic and histological targets over clinical or symptomatic targets. For this evolution to occur, however, new research has to demonstrate that the treat-to-target approach will deliver on the promise of better long-term outcomes compared with current approaches.
UR - http://www.scopus.com/inward/record.url?scp=85067377733&partnerID=8YFLogxK
U2 - 10.14309/ajg.0000000000000183
DO - 10.14309/ajg.0000000000000183
M3 - Review article
C2 - 30908297
AN - SCOPUS:85067377733
SN - 0002-9270
VL - 114
SP - 874
EP - 883
JO - American Journal of Gastroenterology
JF - American Journal of Gastroenterology
IS - 6
ER -