Editorial
Copyright ©The Author(s) 2015.
World J Gastroenterol. Apr 28, 2015; 21(16): 4773-4778
Published online Apr 28, 2015. doi: 10.3748/wjg.v21.i16.4773
Table 1 Studies on the discontinuation of anti-tumor necrosis factor α therapy in inflammatory bowel disease
IBD typeAnti-TNFαtherapynMedian follow up, moSCR at the end of follow up, %Clinical benefit after re-introduction of anti-TNFαtherapy for relapse, %Ref.
CDIFX115285588[3]
CDIFX484935ND[4]
CDIFX53181296[7]
UCIFX28294071[7]
CDIFX or ADM121125555[11]
UCIFX51126594[13]
CDIFX or ADM371-44 (range)26 (1 yr)ND[10]
CDIFX or ADM171371100[9]
UCIFX34136590[9]
CDIFX10012052ND[6]
CDIFX or ADM861764 (1 yr)93[12]
CDIFX92472889[5]
Table 2 Risk factors for relapse after stopping anti-tumor necrosis factor α therapy for remission (clinical or endoscopic) in inflammatory bowel disease
Risk factorsRef.
Clinical or phenotypic
Corticosteroid use between 12 and 6 mo before baseline[3]
Male gender[3]
Absence of previous surgical resection[3]
Longer disease duration from diagnosis to first infliximab[7]
Previous biological therapy[11-13]
Dose intensification during the first year of anti-TNFα therapy[11]
Age at CD diagnosis ≥ 25 yr[6]
Ileocolonic disease at diagnosis[12]
Active smoking[5]
Previous antimetabolite failure[5]
Perianal disease[5]
Serological1
Hemoglobin levels ≤ 14.5 g/dL[3]
White blood count > 6 × 109/L[3]
High sensitive CRP ≥ 5 mg/L[3]
Infliximab trough levels ≥ 2 μg/mL[3]
Serum calprotectin > 5675 ng/mL[37]
Endoscopic1
CDEIS > 0[3]
Mucosal1
Lack of normalization of IL-17A and TNFα expression levels[10]
Microbiological1 (CD-associated dysbiosis)
Low rate of Faecalibacterium prausnitzii in fecal samples[38]
Low rate of Bacteroides in fecal samples[38]
Fecal1
Fecal calprotectin ≥ 300 μg/g[3]
Genetic
Fc gamma receptor IIIB-NA2/NA2 genotype (fistulising disease)[39]