Tumor Necrosis Factor Inhibitors May Have Limited Efficacy for Complex Perianal Fistulas Without Luminal Crohn's Disease.


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:
06 2020
Historique:
received: 11 06 2019
accepted: 12 10 2019
pubmed: 24 10 2019
medline: 21 10 2020
entrez: 24 10 2019
Statut: ppublish

Résumé

Complex perianal fistulas occurring in the absence of luminal inflammation (isolated perianal disease, IPD) may represent a specific phenotype of Crohn's disease (CD). We assessed the effectiveness of tumor necrosis factor (TNF)-antagonists in patients with IPD compared to those with perianal CD (PCD) with luminal inflammation. Patients were identified through our institutional radiology database and were classified as PCD or IPD based on the presence or absence of luminal inflammation by ileocolonoscopy and abdominal enterography. Consecutive adults (> 17 years) with recurrent IPD who were treated with TNF antagonists were matched by age and gender to patients with complex PCD (1:2 ratio). Fistula remission was defined as an absence of fistula drainage. Surgery-free survival was assessed by Cox proportional hazard models. Twenty-two patients with IPD treated with a TNF antagonist were compared with 44 matched patients with PCD. A similar proportion of patients with IPD and PCD were treated with concomitant immunomodulators (55% vs. 66%) and underwent examinations under anesthesia prior to therapy (36% vs. 46%). Fistula remission at 3, 6, and 12 months was lower for the IPD cohort: 9.5% versus 34%; 19% versus 39%; and 19% versus 43%. Surgical intervention after initiating anti-TNF therapy was more common for patients with IPD (HR 3.99: 95% CI, 1.62-9.83; p = 0.0026). Fewer patients with IPD achieved fistula remission, and more required surgical intervention after anti-TNF therapy, suggesting that TNF antagonists may not be as effective in these patients.

Sections du résumé

BACKGROUND
Complex perianal fistulas occurring in the absence of luminal inflammation (isolated perianal disease, IPD) may represent a specific phenotype of Crohn's disease (CD).
AIM
We assessed the effectiveness of tumor necrosis factor (TNF)-antagonists in patients with IPD compared to those with perianal CD (PCD) with luminal inflammation.
METHODS
Patients were identified through our institutional radiology database and were classified as PCD or IPD based on the presence or absence of luminal inflammation by ileocolonoscopy and abdominal enterography. Consecutive adults (> 17 years) with recurrent IPD who were treated with TNF antagonists were matched by age and gender to patients with complex PCD (1:2 ratio). Fistula remission was defined as an absence of fistula drainage. Surgery-free survival was assessed by Cox proportional hazard models.
RESULTS
Twenty-two patients with IPD treated with a TNF antagonist were compared with 44 matched patients with PCD. A similar proportion of patients with IPD and PCD were treated with concomitant immunomodulators (55% vs. 66%) and underwent examinations under anesthesia prior to therapy (36% vs. 46%). Fistula remission at 3, 6, and 12 months was lower for the IPD cohort: 9.5% versus 34%; 19% versus 39%; and 19% versus 43%. Surgical intervention after initiating anti-TNF therapy was more common for patients with IPD (HR 3.99: 95% CI, 1.62-9.83; p = 0.0026).
CONCLUSIONS
Fewer patients with IPD achieved fistula remission, and more required surgical intervention after anti-TNF therapy, suggesting that TNF antagonists may not be as effective in these patients.

Identifiants

pubmed: 31642006
doi: 10.1007/s10620-019-05905-y
pii: 10.1007/s10620-019-05905-y
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Gastrointestinal Agents 0
Tumor Necrosis Factor-alpha 0
Infliximab B72HH48FLU
Adalimumab FYS6T7F842

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1784-1789

Auteurs

Jeffrey D McCurdy (JD)

Division of Gastroenterology and Hepatology, The Ottawa Hospital, 737 Parkdale Ave, Suite 468, Ottawa, ON, K1Y 1J8, Canada. jmccurdy@toh.ca.
The Ottawa Hospital Research Institute, The Ottawa Hospital, Ottawa, ON, Canada. jmccurdy@toh.ca.

Simon Parlow (S)

Division of Gastroenterology and Hepatology, The Ottawa Hospital, 737 Parkdale Ave, Suite 468, Ottawa, ON, K1Y 1J8, Canada.

Yvonne Dawkins (Y)

Division of Gastroenterology and Hepatology, The Ottawa Hospital, 737 Parkdale Ave, Suite 468, Ottawa, ON, K1Y 1J8, Canada.

K Samji (K)

Department of Medical Imaging, The Ottawa Hospital, Ottawa, ON, Canada.

Glara Gaeun Rhee (GG)

Division of Gastroenterology and Hepatology, The Ottawa Hospital, 737 Parkdale Ave, Suite 468, Ottawa, ON, K1Y 1J8, Canada.

Lilianna Oliveira (L)

Division of Gastroenterology and Hepatology, The Ottawa Hospital, 737 Parkdale Ave, Suite 468, Ottawa, ON, K1Y 1J8, Canada.

Blair Macdonald (B)

Department of Medical Imaging, The Ottawa Hospital, Ottawa, ON, Canada.
The Ottawa Hospital Research Institute, The Ottawa Hospital, Ottawa, ON, Canada.

Elham Sabri (E)

The Ottawa Hospital Research Institute, The Ottawa Hospital, Ottawa, ON, Canada.

Sanjay Murthy (S)

Division of Gastroenterology and Hepatology, The Ottawa Hospital, 737 Parkdale Ave, Suite 468, Ottawa, ON, K1Y 1J8, Canada.
The Ottawa Hospital Research Institute, The Ottawa Hospital, Ottawa, ON, Canada.

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