Crohn's disease (CD) is a chronic non-specific inflammatory disease of the intestine, and
anal fistula is the most common perianal lesion in CD. Active anal fistula refers to the
infection of the fistula, which causes perianal pain, discharge, redness, swelling, and
even fever in patients. Biologics are currently the most widely used drugs for treating
CD anal fistula. Studies with fistula healing as the main endpoint of observation show
that the clinical remission rate of fistula is about 50% at most. CD anal fistula is
difficult to treat, has a high recurrence rate, seriously affects the quality of life of
patients, and consumes a large amount of medical resources.
CD anal fistula is a special subtype of CD, and exploring CD anal fistula has very
important clinical significance. The incidence of anal fistula in Asian CD patients is
significantly higher than that in Western CD patients; the prognosis of CD patients with
anal fistula is worse, and the risk of intestinal stenosis or perforation is 3 to 4 times
higher than that of patients without anal fistula; approximately 10% of patients present
with anal fistula as the first manifestation of CD, and the symptoms of anal fistula most
affect the quality of life of patients during the course of the disease; the
susceptibility genes of CD anal fistula patients are different from those of other CD
patients, and the susceptibility genes of the Asian CD population are different from
those of the Western population. Our previous study included Han CD patients from
southern China for analysis and found that polymorphisms in the IRGM, AOX1, and NKX2-3
genes are associated with the development of anal fistula.Compared with the widely used
biologics for treating CD, small molecule drugs have great prospects. Biologics are
complex proteins that require injection for treatment, have immunogenicity, are prone to
secondary failure, and are relatively expensive. In contrast, small molecule drugs have a
relatively small molecular weight, are easier to pass through cell membranes; have a
short half-life and can be taken orally; have no antigenicity or immunogenicity, and have
better sustained efficacy; and have lower production costs.
Upadacitinib was approved for the treatment of CD on June 30, 2023, and it is the first
small molecule drug approved for CD treatment in China. The New England Journal of
Medicine recently published the results of a phase 3 clinical study of upadacitinib for
CD [8]: In the induction period study, the clinical remission rate of the upadacitinib 45
mg treatment group was higher than that of the placebo group (U-EXCEL study, 49.5% vs.
29.1%; U-EXCEED study, 38.9% vs. 21.1%), and the endoscopic response rate was also higher
than that of the placebo group (U-EXCEL study, 45.5% vs. 13.1%; U-EXCEED study, 34.6% vs.
3.5%); in the maintenance period study (U-ENDURE), the clinical remission rates (37.3%
and 47.6%) and endoscopic response rates (27.6% and 40.1%) of the upadacitinib 15 mg and
30 mg treatment groups at week 52 were both higher than those of the placebo group (15.1%
and 7.3%). The above study results show that upadacitinib is effective in treating
CD.However, as a new small molecule drug, the efficacy of upadacitinib for the special
subtype of CD anal fistula is not clear.
JAK/STAT is involved in innate and adaptive immunity. After activation, the signal is
rapidly transmitted from the membrane to the nucleus, and then cytokines are activated,
white blood cell transport is promoted, and cell proliferation is initiated, triggering
intestinal inflammation and playing an important role in the pathogenesis of CD. The
JAK/STAT signaling pathway may also be an important pathogenic mechanism of CD anal
fistula. Manreet et al. found that CD anal fistula patients have gene variations in the
JAK/STAT signaling pathway [9]. Upadacitinib targets and inhibits JAK1. Mechanistically,
it may be effective for CD anal fistula. At present, only post hoc subgroup analysis data
from the aforementioned three clinical studies on CD (not yet published) are available.
In these studies, the complete remission rates of patients with active fistulas treated
with different doses of upadacitinib at week 52 were 25% (3/12) and 10% (1/10),
respectively, which were superior to the placebo group (0%, 0/23 and 0/7). However, the
number of active fistula cases included in this post hoc subgroup analysis was relatively
small, and the study subjects were mostly Western populations. Therefore, more efficacy
data on this new small molecule drug for CD fistulas in the Chinese population are
needed.
Therefore, this study intends to include CD patients with active fistulas and use a
single-arm clinical study approach to explore the efficacy of upadacitinib in treating
Chinese CD fistula patients. This will prepare for subsequent randomized controlled
trials (RCTs) to further investigate the efficacy of different doses of upadacitinib in
treating fistulas and compare the efficacy of upadacitinib with other biological agents
in treating fistulas, and also provide more evidence-based medical evidence for the drug
selection of CD fistulas.
Our hospital is one of the largest inflammatory bowel disease centers in the country.
Additionally, due to the reputation of the anorectal surgery department, it has gathered
a large number of fistula patients, providing a guarantee for the number of cases in this
study.