Early intervention with biologic therapy in Crohn´s disease: how early is early?

医学 克罗恩病 干预(咨询) 疾病 内科学 精神科
作者
Joana Revés,André Mascarenhas,María José Temido,B Morão,Catarina Nascimento,Ana Rita Franco,Raquel R Mendes,Carolina Palmela,Cristina Chagas,Pedro Figueiredo,L Glória,Francisco Portela,Joana Torres
出处
期刊:Journal of Crohn's and Colitis [Oxford University Press]
卷期号:17 (11): 1752-1760 被引量:12
标识
DOI:10.1093/ecco-jcc/jjad089
摘要

Abstract Background Early biologic therapy within the first 18–24 months after diagnosis is associated with improved clinical outcomes in Crohn’s disease [CD]. However, the definition of the best time to initiate biologic therapy remains unclear. We aimed to assess if there is an optimal timing for early biologic therapy initiation. Methods This was a multicentre retrospective cohort study including newly diagnosed CD patients who started anti-tumour necrosis factor [TNF] therapy within 24 months from diagnosis. The timing of initiation of biologic therapy was categorised as ≤6, 7–12, 13–18, and 19–24 months. The primary outcome was CD-related complications defined as a composite of progression of Montreal disease behaviour, CD-related hospitalisations, or CD-related intestinal surgeries. Secondary outcomes included clinical, laboratory, endoscopic, and transmural remission. Results We included 141 patients where 54%, 26%, 11%, and 9% started biologic therapy at ≤6, 7–12, 13–18, and 19–24 months after diagnosis, respectively. A total of 34 patients [24%] reached the primary outcome: 8% had progression of disease behaviour, 15% were hospitalised, and 9% required surgery. There was no difference in the time to a CD-related complication according to the time of initiation of biologic therapy within the first 24 months. Clinical, endoscopic, and transmural remission was achieved in 85%, 50%, and 29%, respectively, but no differences were found according to the time of initiation of biologic therapy. Conclusion Starting anti-TNF therapy within the first 24 months after diagnosis was associated with a low rate of CD-related complications and high rates of clinical and endoscopic remission, although we found no differences with earlier initiation within this window of opportunity.
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