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Table 10.1Studies on the withdrawal of anti-TNF-α therapiesAuthorsNumber of participants (n)Study designRelapse rateSignificant predictors of relapsePredictors evaluated but not found to be significantRecapture rateCDBrooks et al. [^52]86Prospective observational4.7% (3 months)Ileocolonic diseaseAge, gender, disease behavior, previous surgical resection, immunosuppression at start of anti-TNF-α treatment,disease duration, dose escalation of anti-TNF-α^agent, concomitant IMM, raised CRP93%18.6% (6 months)Previous anti-TNF-α^treatment(88% concomitant IMM)36% (1 year)Raised fecal calprotectinDomenech et al. [42]23Prospective observational (69% with concomitant IMM)31% (1 year)Perianal diseaseGender, smoking status, previous treatment with IFX, concomitant IMM, location, development of infusion acute reactions66% (1 year) for perianal diseaseLouis et al. (STORI) [41]115Prospective observational (100% with concomitant IMM)43.9% (1 year)Male, absence of surgical resection, elevated leucocyte count >6.0 × 109 /L,hemoglobin ≤ 145 g/LAge, smoking status, location, previous resection, disease duration, treatment duration88%15% (1 year) for those with ≤2 predictors of relapseC-reactive protein ≥5.0 mg/LFecal calprotectin ≥ 300 μg/gReenaers et al. (long-term follow-up of STORI trial) [^77]102/115 (long-term outcome)Prospective observational (100% with concomitant IMM)85% (median 8 years)Upper GI involvementNot reported (only abstract is available)40%Elevated leucocyte count > 6.0 × 109 /LH.H. Shim and C.H. Seow