Superior Efficacy of Infliximab Versus Adalimumab for First-Line Treatment of Crohn's Perianal Fistulae.


Journal

Digestive diseases and sciences
ISSN: 1573-2568
Titre abrégé: Dig Dis Sci
Pays: United States
ID NLM: 7902782

Informations de publication

Date de publication:
10 2023
Historique:
received: 19 02 2023
accepted: 26 07 2023
medline: 25 9 2023
pubmed: 4 8 2023
entrez: 4 8 2023
Statut: ppublish

Résumé

Crohn's disease perianal fistulae (CD-PAF) occur in 25% of patients and are notoriously challenging to manage. Tumor necrosis factor inhibitors are first line agents. The aim of this study was to compare infliximab (IFX) versus adalimumab (ADA) efficacy in CD-PAF healing over time. A retrospective study at two large-tertiary medical centers was performed. Inclusion criteria were actively draining CD-PAF and initial treatment with IFX or ADA following CD-PAF diagnosis. The primary endpoints were perianal fistula response and remission at 6 and 12 months. Secondary endpoints included biologic persistence over time and dose escalation at 6 and 12 months. Among 151 patients included in the study, 92 received IFX and 59 received ADA as first line agents after CD-PAF diagnosis. At 6 months, the 64.9% of the IFX group and 34.8% of the ADA group demonstrated CD-PAF clinical improvement (p < 0.01). Univariate and multivariate analyses demonstrated significant differences among the IFX and ADA groups for clinical response at 6-months and 12-months (p = 0.002 and p = 0.042, respectively). There were no factors that predicted response, with the exception of concomitant immunomodulator affecting the 6-month clinical response (p = 0.021). Biologic persistence, characterized by Kaplan Meier methods, was significantly longer in the IFX group compared to the ADA group (Log-rank p = 0.01). IFX induction and maintenance is associated with higher rates of response and remission in CD-PAF healing as well as higher treatment persistence compared to ADA. Additionally, our study supports the use of concomitant immunomodulator therapy for CD-PAF healing and remission.

Sections du résumé

BACKGROUND
Crohn's disease perianal fistulae (CD-PAF) occur in 25% of patients and are notoriously challenging to manage. Tumor necrosis factor inhibitors are first line agents.
AIMS
The aim of this study was to compare infliximab (IFX) versus adalimumab (ADA) efficacy in CD-PAF healing over time.
METHODS
A retrospective study at two large-tertiary medical centers was performed. Inclusion criteria were actively draining CD-PAF and initial treatment with IFX or ADA following CD-PAF diagnosis. The primary endpoints were perianal fistula response and remission at 6 and 12 months. Secondary endpoints included biologic persistence over time and dose escalation at 6 and 12 months.
RESULTS
Among 151 patients included in the study, 92 received IFX and 59 received ADA as first line agents after CD-PAF diagnosis. At 6 months, the 64.9% of the IFX group and 34.8% of the ADA group demonstrated CD-PAF clinical improvement (p < 0.01). Univariate and multivariate analyses demonstrated significant differences among the IFX and ADA groups for clinical response at 6-months and 12-months (p = 0.002 and p = 0.042, respectively). There were no factors that predicted response, with the exception of concomitant immunomodulator affecting the 6-month clinical response (p = 0.021). Biologic persistence, characterized by Kaplan Meier methods, was significantly longer in the IFX group compared to the ADA group (Log-rank p = 0.01).
CONCLUSION
IFX induction and maintenance is associated with higher rates of response and remission in CD-PAF healing as well as higher treatment persistence compared to ADA. Additionally, our study supports the use of concomitant immunomodulator therapy for CD-PAF healing and remission.

Identifiants

pubmed: 37540392
doi: 10.1007/s10620-023-08060-7
pii: 10.1007/s10620-023-08060-7
doi:

Substances chimiques

Infliximab B72HH48FLU
Adalimumab FYS6T7F842
Immunologic Factors 0
Biological Products 0
Tumor Necrosis Factor-alpha 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3994-4000

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Références

Mak WY, Mak OS, Lee CK et al. Significant medical and surgical morbidity in perianal Crohn’s disease: results from a territory-wide study. J. Crohn’s Colitis. 2018;12:1392–1398.
doi: 10.1093/ecco-jcc/jjx180.915
Panes J, Reinisch W, Rupniewska E et al. Burden and outcomes for complex perianal fistulas in Crohn’s disease: systematic review. World J. Gastroenterol. 2018;24:4821–4834.
doi: 10.3748/wjg.v24.i42.4821 pubmed: 30479468 pmcid: 6235801
Yarur AJ, Kanagala V, Stein DJ et al. Higher infliximab trough levels are associated with perianal fistula healing in patients with Crohn’s disease. Aliment. Pharmacol. Ther. 2017;45:933–940.
doi: 10.1111/apt.13970 pubmed: 28211593
Schwartz DA, Loftus EV, Tremaine WJ et al. The natural history of fistulizing Crohn’s disease in Olmsted County, Minnesota. Gastroenterology. 2002;122:875–880.
doi: 10.1053/gast.2002.32362 pubmed: 11910338
Adegbola SO, Dibley L, Sahnan K et al. Burden of disease and adaptation to life in patients with Crohn’s perianal fistula: a qualitative exploration. Health Qual Life Outcomes. 2020;18:370.
doi: 10.1186/s12955-020-01622-7 pubmed: 33218361 pmcid: 7678264
Vasudevan A, Bruining DH, Loftus EV, Faubion W, Ehman EC, Raffals L. Approach to medical therapy in perianal Crohn’s disease. World J. Gastroenterol. 2021;27:3693–3704.
doi: 10.3748/wjg.v27.i25.3693 pubmed: 34321838 pmcid: 8291021
Present DH, Rutgeerts P, Targan S et al. Infliximab for the treatment of fistulas in patients with Crohn’s disease. N. Engl. J. Med. 1999;340:1398–1405.
doi: 10.1056/NEJM199905063401804 pubmed: 10228190
Colombel J-F, Schwartz DA, Sandborn WJ et al. Adalimumab for the treatment of fistulas in patients with Crohn’s disease. Gut. 2009;58:940–948.
doi: 10.1136/gut.2008.159251 pubmed: 19201775
Hanauer SB, Sandborn WJ, Rutgeerts P et al. Human anti-tumor necrosis factor monoclonal antibody (Adalimumab) in crohn’s disease: the CLASSIC-I Trial. Gastroenterology. 2006;130:323–333.
doi: 10.1053/j.gastro.2005.11.030 pubmed: 16472588
Sandborn WJ, Rutgeerts P, Enns R et al. Adalimumab induction therapy for Crohn disease previously treated with infliximab: a randomized trial. Ann. Intern. Med. 2007;146:829–838.
doi: 10.7326/0003-4819-146-12-200706190-00159 pubmed: 17470824
Singh S, Proctor D, Scott FI, Falck-Ytter Y, Feuerstein JD. AGA technical review on the medical management of moderate to severe luminal and perianal fistulizing Crohn’s disease. Gastroenterology. 2021;160:2512-2556.e2519.
doi: 10.1053/j.gastro.2021.04.023 pubmed: 34051985
Sandborn WJ, Fazio VW, Feagan BG, Hanauer SB. AGA technical review on perianal Crohn’s disease. Gastroenterology. 2003;125:1508–1530.
doi: 10.1016/j.gastro.2003.08.025 pubmed: 14598268
Ji C-C, Takano S. Clinical efficacy of adalimumab versus infliximab and the factors associated with recurrence or aggravation during treatment of anal fistulas in Crohn’s disease. Intest Res 2017;15:182–186.
doi: 10.5217/ir.2017.15.2.182 pubmed: 28522947 pmcid: 5430009
Gisbert JP, Marín AC, McNicholl AG, Chaparro M. Systematic review with meta-analysis: the efficacy of a second anti-TNF in patients with inflammatory bowel disease whose previous anti-TNF treatment has failed. Aliment. Pharmacol. Ther. 2015;41:613–623.
doi: 10.1111/apt.13083 pubmed: 25652884
Taxonera C, Schwartz DA, García-Olmo D. Emerging treatments for complex perianal fistula in Crohn’s disease. World J. Gastroenterol. 2009;15:4263–4272.
doi: 10.3748/wjg.15.4263 pubmed: 19750568 pmcid: 2744181
Sands BE, Anderson FH, Bernstein CN et al. Infliximab maintenance therapy for fistulizing Crohn’s disease. N. Engl. J. Med. 2004;350:876–885.
doi: 10.1056/NEJMoa030815 pubmed: 14985485
Colombel JF, Sandborn WJ, Rutgeerts P et al. Adalimumab for maintenance of clinical response and remission in patients with Crohn’s disease: the CHARM trial. Gastroenterology. 2007;132:52–65.
doi: 10.1053/j.gastro.2006.11.041 pubmed: 17241859
Castaño-Milla C, Chaparro M, Saro C et al. Effectiveness of adalimumab in perianal fistulas in crohn’s disease patients naive to anti-TNF therapy. J. Clin. Gastroenterol. 2015;49:34–40.
doi: 10.1097/MCG.0000000000000169 pubmed: 25485513
De Gregorio M, Lee T, Krishnaprasad K et al. Higher anti-tumor necrosis factor-α levels correlate with improved radiologic outcomes in Crohn’s perianal fistulas. Clin. Gastroenterol. Hepatol. 2022;20:1306–1314.
doi: 10.1016/j.cgh.2021.07.053 pubmed: 34389484
Gu B, Venkatesh K, Williams AJ et al. Higher infliximab and adalimumab trough levels are associated with fistula healing in patients with fistulising perianal Crohn’s disease. World J. Gastroenterol. 2022;28:2597–2608.
doi: 10.3748/wjg.v28.i23.2597 pubmed: 35949350 pmcid: 9254145
Strik AS, Löwenberg M, Buskens CJ et al. Higher anti-TNF serum levels are associated with perianal fistula closure in Crohn’s disease patients. Scand. J. Gastroenterol. 2019;54:453–458.
doi: 10.1080/00365521.2019.1600014 pubmed: 31032686
Plevris N, Jenkinson PW, Arnott ID, Jones GR, Lees CW. Higher anti-tumor necrosis factor levels are associated with perianal fistula healing and fistula closure in Crohn’s disease. Eur. J. Gastroenterol. Hepatol. 2020;32:32–37.
doi: 10.1097/MEG.0000000000001561 pubmed: 31567638
Bouguen G, Siproudhis L, Gizard E et al. Long-term outcome of perianal fistulizing crohn’s disease treated with infliximab. Clin. Gastroenterol. Hepatol. 2013;11:975-981.e974.
doi: 10.1016/j.cgh.2012.12.042 pubmed: 23376316
Zhu M, Xu X, Feng Q et al. Effectiveness of infliximab on deep radiological remission in Chinese patients with perianal fistulizing Crohn’s disease. Dig. Dis. Sci. 2021;66:1658–1668.
doi: 10.1007/s10620-020-06398-w pubmed: 32524415

Auteurs

Laura Maas (L)

Division of Gastroenterology & Hepatology, Johns Hopkins University School of Medicine, 4940 Eastern Avenue, Baltimore, MD, 21224, USA. lmaas3@jh.edu.

Ruiyi Gao (R)

Division of Gastroenterology & Hepatology, Johns Hopkins University School of Medicine, 4940 Eastern Avenue, Baltimore, MD, 21224, USA.

Vivy Cusumano (V)

Division of Digestive Diseases, Center for Inflammatory Bowel Diseases, Vatche & Tamar Manoukian, UCLA School of Medicine, Los Angeles, CA, USA.

Ellen Spartz (E)

Division of Digestive Diseases, Center for Inflammatory Bowel Diseases, Vatche & Tamar Manoukian, UCLA School of Medicine, Los Angeles, CA, USA.

Reezwana Chowdhury (R)

Division of Gastroenterology & Hepatology, Johns Hopkins University School of Medicine, 4940 Eastern Avenue, Baltimore, MD, 21224, USA.

Mahesh Krishna (M)

Division of Gastroenterology & Hepatology, Johns Hopkins University School of Medicine, 4940 Eastern Avenue, Baltimore, MD, 21224, USA.

Mark Lazarev (M)

Division of Gastroenterology & Hepatology, Johns Hopkins University School of Medicine, 4940 Eastern Avenue, Baltimore, MD, 21224, USA.

Joanna Melia (J)

Division of Gastroenterology & Hepatology, Johns Hopkins University School of Medicine, 4940 Eastern Avenue, Baltimore, MD, 21224, USA.

Florin Selaru (F)

Division of Gastroenterology & Hepatology, Johns Hopkins University School of Medicine, 4940 Eastern Avenue, Baltimore, MD, 21224, USA.

Sowmya Sharma (S)

Division of Gastroenterology & Hepatology, Johns Hopkins University School of Medicine, 4940 Eastern Avenue, Baltimore, MD, 21224, USA.

Berkeley Limketkai (B)

Division of Digestive Diseases, Center for Inflammatory Bowel Diseases, Vatche & Tamar Manoukian, UCLA School of Medicine, Los Angeles, CA, USA.

Alyssa Parian (A)

Division of Gastroenterology & Hepatology, Johns Hopkins University School of Medicine, 4940 Eastern Avenue, Baltimore, MD, 21224, USA.

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