Continued Postoperative Use of Tumor Necrosis Factor-α Inhibitors for the Prevention of Crohn's Disease Recurrence.

Background/Aims: Many patients with Crohn's disease (CD) undergo intestinal resection during the disease course. Despite surgery, postoperative recurrence (POR) commonly occurs. Although postoperative use of tumor necrosis factor α (TNF-α) inhibitors is known to be effective in preventing POR, few studies have evaluated the effectiveness of continuing the same TNF-α inhibitors postoperatively in patients who received TNF-ɑ inhibitors before surgery.
Methods: This retrospective observational study was performed in a single tertiary medical center. We retrospectively reviewed patients who had undergone the first intestinal resection due to CD and divided them into two groups: TNF-α inhibitor users in both the preoperative and postoperative periods, and TNF-α inhibitor users in only the preoperative period. We compared the clinical outcomes between these two groups.
Results: In total, 45 patients who used TNF-α inhibitors preoperatively were recruited. Among them, TNF-α inhibitors were used postoperatively in 20 patients (44.4%). The baseline characteristics except age at diagnosis were similar in both groups. The rates of surgical and endoscopic recurrence were not different between the two groups, but the cumulative clinical recurrence rate was significantly lower in the postoperative TNF-α inhibitors group (log-rank p=0.003). In multivariate Cox regression analysis, postoperative TNF-α inhibitors use was significantly associated with a decreased risk of clinical recurrence (adjusted hazard ratio, 0.204; 95% confidence interval, 0.060 to 0.691; p=0.011). Conclusions: Continuing TNF-α inhibitors postoperatively in patients who were receiving TNF-α inhibitors before surgery significantly reduced the rate of clinical recurrence. For patients with CD who received TNF-α inhibitors preoperatively, continuing their use after surgery could be recommended.

INTRODUCTION

Crohn’s disease (CD) is a chronic inflammatory bowel disease with an unknown, complex pathophysiology associated with genetics, immunology, and environmental factors; there is no curative treatment for the disease.1 The incidence and prevalence of CD are rising globally, and the condition is associated with enormous economic and social burdens.2,3 Various types of medications, such as 5-aminosalicylic acids, immunomodulators (azathioprine, 6-mercaptopurine, and methotrexate), small molecules/biologic agents, such as tumor necrosis factor α (TNF-α) inhibitors, and biosimilars, have been used to improve the course of CD.4-6

Despite intensive medical treatment including new classes of medications, a significant number of patients with CD still require intestinal resection at some point in their disease course.7 Even patients who have previously received surgery might have to undergo repeated surgeries. In clinical practice, all possible treatment options, such as immunomodulators and biologics, are undertaken to delay surgery in the clinical course of CD.4

If patients must inevitably undergo surgery, effective postoperative management is an important step to reduce postoperative recurrence (POR). POR has become one of the major issues in the management of CD. Various factors are known to affect the POR of CD. Patient factors, such as smoking status and family history, and disease factors, such as age at disease onset, disease duration, disease extent, location, behavior, and surgery-related factors, are known to be associated with POR.1,7-11 Therefore, endeavors have been made to delay the disease course for preventing POR by early detection and management. Although the effectiveness of azathioprine has been proven for preventing POR, recent studies have reported that TNF-α inhibitors are superior to azathioprine in this regard.12-14 After risk assessment, postoperative prophylactic TNF-α inhibitors are commonly prescribed based on their proven efficacy in decreasing the rate of POR.15,16 However, most studies have focused on the preventive effects of TNF-α inhibitors for POR.17,18 Additionally, due to the concerns about immediate postoperative complications of TNF-α inhibitors, they are usually discontinued few weeks before elective surgery.19-23 After discontinuing TNF-α inhibitors before surgery, the decision to restart or discontinue them depend on each clinician’s assessment, due to the lack of evidence. Additionally, there have been few studies about the association between preoperative use of TNF-α inhibitors and POR. In this study, we investigated whether the same TNF-α inhibitors used postoperatively are effective in preventing POR in patients with CD who used TNF-α inhibitors before surgery.

MATERIALS AND METHODS

1. Study population

This was a retrospective observational study conducted in a single tertiary medical center in Korea (Severance Hospital, Yonsei University College of Medicine, Seoul). We retrospectively investigated patients who underwent the first intestinal resection due to CD between January 2010 and August 2020. In this study, appendectomy, stricture-plastic surgery, and perianal surgeries, such as fistulectomy, were not categorized as intestinal resection surgery due to CD.

2. Data collection

We retrospectively analyzed endoscopic, clinical, and surgical data of patients with CD. Although the data were collected retrospectively from electronic medical charts and colonoscopy or radiologic reports in our hospital, all clinical variables were prospectively recorded according to patient analysis. We investigated the patients’ age, age at diagnosis, sex, smoking history, family history, previous surgical history, and Montreal classification (A: age at diagnosis, L: disease location, B: disease behavior).11 We further investigated the events and dates of surgical, endoscopic, and clinical recurrences. The definitions of recurrences are described in “the definition of POR” section. We used the CD Activity Index (CDAI) to standardize patients’ disease activity.24 Physicians evaluated and calculated CDAI through history, physical examination, and laboratory findings during every patient visit. We investigated each patient’s medical records as well as endoscopic and surgery reports to analyze the histories of cumulative events such as additional surgery, hospitalization, disease exacerbation, and preoperative and postoperative medications for managing CD. All histories of prescribed medications, such as 5-aminosalicylic acids, immunomodulators (azathioprine, 6-mercaptopurine, methotrexate), and biologic agents were analyzed preoperatively and/or postoperatively. In this study, preoperative biologics use was defined as continuous, regular use (maintenance dose) of biologics before surgery. Continued use of biologics postoperatively was defined as starting biologics use within 3 months after surgery in consideration of the temporary perioperative discontinuation of biologic agents.18 Starting biologics after 3 months of surgery was not defined as continued use of biologics postoperatively. Concomitant immunomodulators were maintained after surgery in most patients if there were no contraindications such as leukopenia or combined infections. The data regarding this article can be shared upon request to the corresponding author.

3. Study design

In this study, we mainly focused on the POR (endoscopic, clinical, and surgical) according to the postoperative use of TNF-α inhibitors in patients with CD who were administered TNF-α inhibitors preoperatively. In other words, we divided patients who had undergone the first intestinal resection due to CD into two groups: TNF-α inhibitors users both in the preoperative and postoperative periods, and TNF-α inhibitors users only in preoperative period. We then compared the clinical outcomes while focusing on the endoscopic, clinical, and surgical recurrences between the two groups.

4. Definitions

1) Endoscopic recurrence

We analyzed the data of follow-up colonoscopies after surgery through electronic medical records and colonoscopic or radiologic reports and images. Endoscopic images were reviewed and categorized to show remission (Rutgeerts score of i0 or i1) or recurrence (Rutgeerts score i2 or more) according to the Rutgeerts score.25

2) Clinical recurrence

Clinical recurrence was defined as the first episode of symptomatic exacerbation of CD after surgery. In our study, a CDAI >200 was considered to indicate clinical recurrence.26 If clinical symptoms were exacerbated by other causes, such as infectious colitis and acute gastroenteritis, the condition was not considered as the clinical recurrence of CD.

3) Surgical recurrence

Surgical recurrence was defined as a condition requiring an additional intestinal resection during follow-up that was related to CD.26 Early postoperative complications, such as anastomotic leak, abscess drainage, or surgical site infections that occurred within 1 month after initial surgery were not considered as surgical recurrence. Moreover, surgeries performed for reasons other than CD, such as malignancies in the abdominal cavity or infections, were not regarded as surgical recurrence.

5. Statistical analysis

We analyzed the baseline characteristics using the Mann-Whitney U test for continuous variables and the chi-square test or the Fisher exact test for categorical variables. Non-normally distributed outcomes were presented as the median and interquartile range. The Kaplan-Meier survival analysis was used to estimate the cumulative recurrence rate in patients according to the variables. Univariable analysis was performed using the Cox proportional-hazards model to identify factors associated with increased risk of recurrences. Factors associated with recurrences with a p-value of less than 0.20 in the univariable analysis were entered in the multivariable model. Multivariable analysis was performed using the Cox regression model to control for multiple risk factors that could influence recurrence. Hazard ratios and corresponding 95% confidence intervals were calculated. Results were considered statistically significant at p-values <0.05. All statistical analyses were performed using SPSS version 20 software (IBM Corp., Armonk, NY, USA).

6. Ethical considerations

This study was performed in accordance with the ethical guidelines of the 1975 Declaration of Helsinki, and was approved by the Institutional Review Board of Severance Hospital, Seoul, South Korea (IRB number: 4-2020-1297). The informed consent was waived.

RESULTS

1. Baseline patient characteristics

We recruited patients with CD who had undergone the first intestinal resection in their disease course between January 2010 and August 2020. A total of 216 patients were selected through medical chart review. Among them, three cases related to colorectal cancer were excluded. Among 213 patients, a total of 109 patients were exposed to biologic agents. Among them, 55 patients were treated with biologic agents only postoperatively. Additionally, five patients with ineffective therapeutic dosage (in induction phase: two patients; discontinuation for long time [more than 3 months]: two patients; discontinuation due to side effects: one patient), one patient who changed biologic agents after surgery and three patients who maintained vedolizumab were excluded. We finally selected 45 patients who used preoperative TNF-α inhibitors with maintenance doses (Fig. 1). Postoperative TNF-α inhibitors were used in 20 patients, but not in the other 25 patients. Among the 20 patients, infliximab was most commonly used preoperatively (infliximab, n=13, 65.0%; adalimumab, n=7, 35.0%). After surgery, all the patients continued using the same TNF-α inhibitors (Table 1).

Fig. 1

Flowchart of patient inclusion.

TNF, tumor necrosis factor.

Table 1

Demographics and Clinical Characteristics of the Patients

Characteristic	Preoperative TNF-α inhibitors (+) (n=45)	With POT (n=20)	Without POT (n=25)	p-value
Male sex	28 (62.2)	14 (70.0)	14 (56.0)	0.336
Age at diagnosis, yr	24.0 (19.0–30.0)	22.0 (16.3–28.0)	25.0 (20.5–34.0)	0.053
Time from diagnosis to surgery, mo	80.0 (55.0–118.0)	71.5 (51.5–110.0)	92.0 (55.0–127.0)	0.607
Time from diagnosis to the first biologics, mo	51.0 (31.0–75.0)	53.5 (32.8–79.0)	45.0 (29.5–80.0)	0.508
Age (A)				0.012
A1 (<16 yr)	5 (11.1)	5 (25.0)	0
A2 (17–40 yr)	37 (82.2)	15 (75.0)	22 (88.0)
A3 (>40 yr)	3 (6.7)	0	3 (12.0)
Disease extent (L)				0.663
L1 (ileal)	8 (17.8)	3 (15.0)	5 (20.0)
L2 (colonic)	0	0	0
L3 (ileocolonic)	37 (82.2)	17 (85.0)	20 (80.0)
L4 (upper)	0	0	0
Disease characteristics				0.154
B1 (non-stricturing, non-penetrating)	10 (22.2)	6 (30.0)	4 (16.0)
B2 (stricturing)	12 (26.7)	7 (35.0)	5 (20.0)
B3 (penetrating)	23 (51.1)	7 (35.0)	16 (64.0)
Perianal disease	28 (62.2)	12 (60.0)	16 (64.0)	0.783
Smoking				0.657
Never-smoker	37 (82.2)	17 (85.0)	20 (80.0)
Former smoker	7 (15.6)	3 (15.0)	4 (16.0)
Current smoker	1 (2.2)	0	1 (4.0)
Smoking after surgery	0	0	0	NA
Appendectomy	5 (11.1)	3 (15.0)	2 (8.0)	0.458
Family history	2 (4.4)	0	2 (8.0)	0.196
Height, cm	168.0 (163.0–172.5)	167.5 (161.5–169.5)	170.0 (164.0–173.5)	0.243
Weight, kg	53.0 (48.0–61.0)	51.0 (42.0–61.8)	55.0 (50.0–61.0)	0.262
Surgical recurrence	4 (8.9)	1 (5.0)	3 (12.0)	0.412
Endoscopic recurrence	14/30 (46.7)	4/13 (30.8)	10/17 (58.8)	0.127
Clinical recurrence	22 (48.9)	3 (15.0)	19 (76.0)	<0.001
Mortality, No. (%)	1 (2.2)*	0	1 (4.0)*	0.366
Total number of preoperative biologic agents				0.241
1	31 (68.9)	16 (80.0)	15 (60.0)
2	12 (26.7)	4 (20.0)	8 (32.0)
3	2 (4.4)	0	2 (8.0)
TNF-α inhibitors just before surgery				0.540
Infliximab	27 (60.0)	13 (65.0)	14 (56.0)
Adalimumab	18 (40.0)	7 (35.0)	11 (44.0)
TNF-α inhibitors just after surgery	-		-	-
Infliximab		13 (65.0)
Adalimumab		7 (35.0)
Concomitant use of immunomodulators	31 (68.9)	16 (80.0)	15 (60.0)	0.150

Data are presented as number (%), median (IQR), or number/number (%).

TNF, tumor necrosis factor; POT, postoperative TNF-α inhibitors; IQR, interquartile range; NA, data not available for statistical analysis.

*Time from surgery to death, 13 months.

The baseline patient characteristics were similar except for the age at diagnosis (Table 1). On evaluating the age at diagnosis according to the Montreal classification, the proportion of A1 (age <16 years) was higher in postoperative TNF-α inhibitors users than in non-users (25.0% vs 0%, p=0.012). The total number and characteristics of biologics used preoperatively were not significantly different between the groups (p=0.241) (Table 1). Concomitant use of immunomodulatory agents was not significantly different between the groups (80.0% in postoperative TNF-α inhibitors users vs 60.0% in postoperative TNF-α inhibitors non-users, p=0.150) (Table 1).

2. Postoperative recurrence

We analyzed three classes of recurrence (endoscopic, clinical, and surgical recurrences). The rates of surgical and endoscopic recurrences were not significantly different between the two groups, but clinical recurrence was significantly lower in patients treated with postoperative biologics (n=3 [15.0%] vs n=19 [76.0%], p<0.001) (Table 1). The time from initial surgery to clinical recurrence was shorter than in surgical recurrence (31.5 months [range, 8.5 to 56.8] vs 93.0 months [range, 57.8 to 111.0]), although both the time from surgery to each recurrence and the time from diagnosis to each recurrence were not significantly different between groups (Table 2). The median CDAI was 289.5 (range, 245.0 to 320.0) at the point of clinical recurrence (Table 2). The median C-reactive protein at clinical recurrence was 10.6 mg/L (range, 4.5 to 19.0 mg/L), which was slightly higher than normal range (<10 mg/L).27

Table 2

Characteristics Related to Recurrences

Characteristics	Total (n=45)	With POT (n=20)	Without POT (n=25)	p-value
Clinical recurrence	22 (48.9)	3 (15.0)	19 (76.0)	<0.001
Time from surgery to CR, mo	31.5 (8.5–56.8)	60.0 (9.0–87.0)	31.0 (7.0–54.0)	0.315
Time from diagnosis to CR, mo	139.0 (81.5–176.3)	173.0 (158.0–259.0)	124.0 (62.0–172.0)	0.077
CDAI at CR	289.5 (245.0–320.0)	354.0 (234.0–391.0)	286.0 (246.0–313.0)	0.363
CRP at CR, mg/L	10.6 (4.5–19.0)	9.4 (6.8–26.9)	11.7 (2.8–17.5)	0.811
Surgical recurrence	4 (8.9)	1 (5.0)	3 (12.0)	0.412
Time from surgery to SR, mo	93.0 (57.8–111.0)	102.0	84.0 (49.0–114.0)	0.655
Time from diagnosis to SR, mo	180.5 (153.3–204.8)	172.0	189.0 (147.0–210.0)	0.655

Data are presented as number (%) or median (IQR).

TNF, tumor necrosis factor; POT, postoperative TNF-α inhibitors; CR, clinical recurrence; CDAI, Crohn’s Disease Activity Index; CRP, C-reactive protein; SR, surgical recurrence; IQR, interquartile range.

The Kaplan-Meier analysis revealed that the cumulative clinical recurrence rate was significantly lower in the postoperative TNF-α inhibitors group (log-rank p=0.003) (Fig. 2), but cumulative surgical recurrence rate was not significantly different between groups (log-rank p=0.941) (Fig. 2).

Fig. 2

Kaplan-Meier curves. (A) Cumulative clinical recurrence-free survival. (B) Cumulative surgical recurrence-free survival.

TNF, tumor necrosis factor.

In univariable and multivariable analyses with the Cox regression model, none of the factors were significantly related to surgical recurrence. For clinical recurrence, postoperative TNF-α inhibitors use was significantly associated with a decreased risk of clinical recurrence (adjusted hazard ratio, 0.204; 95% confidence interval, 0.060 to 0.691; p=0.011) (Table 3).

Table 3

Univariable and Multivariable Cox Regression Analyses for Recurrences

Variable	Univariable analysis			Multivariable analysis
	HR (95% CI)	p-value		Adjusted HR (95% CI)	p-value
Surgical recurrence
Early postop TNF-α inhibitors	0.922 (0.096–8.864)	0.944
Concomitant azathioprine	0.382 (0.054–2.719)	0.336
Time from diagnosis to initial surgery	1.002 (0.979–1.027)	0.849
Time from diagnosis to the first TNF-α inhibitors	1.021 (0.991–1.051)	0.169		1.021 (0.991–1.051)	0.169
Smoking history	NA*
Family history	NA*
Perianal disease	1.388 (0.144–13.348)	0.776
B3 (penetrating)	0.883 (0.124–6.269)	0.901
A1 (<16 yr)	NA*
Clinical recurrence
Early postop TNF-α inhibitors	0.194 (0.057–0.656)	0.008		0.204 (0.060–0.691)	0.011
Concomitant azathioprine	0.436 (0.186–1.023)	0.056		0.564 (0.228–1.393)	0.214
Time from diagnosis to initial surgery	1.006 (0.997–1.015)	0.177		1.003 (0.994–1.013)	0.501
Time from diagnosis to the first TNF-α inhibitors	1.004 (0.992–1.015)	0.544
Smoking history	1.425 (0.478–4.252)	0.526
Family history	1.300 (0.170–9.968)	0.801
Perianal disease	2.047 (0.753–5.562)	0.160		1.626 (0.562–4.708)	0.370
B3 (penetrating)	1.235 (0.527–2.890)	0.627
A1 (<16 yr)	0.370 (0.050–2.751)	0.331

HR, hazard ratio; CI, confidence interval; TNF, tumor necrosis factor.

*NA: data not available for statistical analysis due to the small number of surgical recurrences.

DISCUSSION

CD requires long-term medical and even surgical management due to its chronic relapsing-remitting disease course. Considering its long-term course, the most efficient methods to maintain disease remission and control disease exacerbation should be instituted. Inflammatory bowel disease specialists have considered surgery as an indispensable treatment option in managing CD, although intensive medical treatment should be administered before surgery to delay surgery to the maximum extent. However, if surgery is required due to symptom aggravation or loss of response to medical treatment, it is mandatory to set the right time for elective surgery through discussion with a surgical team.

For patients with CD, if surgery is inevitably performed, the first surgery might be a significant turning point to adjust treatment strategies. Even if surgery is successfully performed, it is well known that a substantial number of patients still need repeated surgeries during the course of the disease. Therefore, various methods and strategies to prevent POR based on risk models have been investigated. After assessing postoperative risk, step-up treatment is recommended according to ileo-colonoscopic findings. Especially for high-risk patients (smokers or those with perforating disease features or history of previous intestinal resection), earlier use of immunomodulators and biologic agents should be considered.7,8,28-30

There are a few important issues regarding POR in CD. One of the most interesting treatment strategies for patients with CD who have undergone surgery is the use of prophylactic biologic agents postoperatively to prevent POR.10,31-33 Although most studies proved that this strategy is effective in preventing recurrence in postoperative patients with CD, long-term investigation is necessary, especially in terms of side effects and costs.15 Another important issue is the perioperative use of biologic agents for POR. It is important that before elective surgery, biologics are stopped for some time due to concerns about postoperative complications such as delayed wound healing.19-21,34 There have been few studies about restarting or stopping TNF-α inhibitors after surgery in patients who were on preoperative TNF-α inhibitors in maintenance dose.

In our study, considering real-world practice, we retrospectively categorized patients who underwent their first intestinal resection and used TNF-α inhibitors preoperatively into two groups (postoperative use of TNF-α inhibitors vs no postoperative use of TNF-α inhibitors), and followed their disease courses while focusing on clinical endpoints (endoscopic, clinical, and surgical recurrences). To focus more on the long-term outcomes influenced by medical (TNF-α inhibitors) factors, we did not include the cases of early PORs by surgical factors. In this study, only four patients (8.9%) experienced surgical recurrence during the follow-up period. Although patients who continued using TNF-α inhibitors after surgery had a lower rate of surgical recurrence, the difference was not statistically significant, probably due to the small number of cases of surgical recurrence (1/20, 5.0% for postoperative TNF-α inhibitors users vs 3/25, 12.0% postoperative TNF-α inhibitors non-users; p=0.412). Additionally, this finding may be explained by the relatively short duration of follow-up (median duration of follow-up after the initial surgery was 48.0 months; interquartile range, 27.5 to 84.5 months).

For endoscopic recurrences, patients who maintained TNF-α inhibitors after surgery had a numerically lower rate of endoscopic recurrence, although this was not statistically significant (3/14, 30.8% with TNF-α inhibitors vs 10/17, 58.8% without TNF-α inhibitors; p=0.127).

In our study, more than 60% of patients were concomitantly treated with azathioprine. Immunomodulators, such as azathioprine, have been known to be effective in preventing POR, although the study results are conflicting.35,36 According to recent studies, azathioprine use after the detection of endoscopic recurrence was not inferior to immediate azathioprine use after surgery in terms of clinical outcomes.37,38 Besides biologic agents, further studies are needed to determine the role of immunomodulators in POR.

On the Kaplan-Meier analysis, clinical recurrence-free survival was significantly superior in those who used TNF-α inhibitors preoperatively and postoperatively compared to those without TNF-α inhibitors use after surgery (log-rank p=0.003). Moreover, continuing the use of TNF-α inhibitors postoperatively significantly reduced the risk of clinical recurrence on the multivariable Cox regression analysis (adjusted hazard ratio, 0.204; 95% confidence interval, 0.060 to 0.691; p=0.011).

Few studies have reported that postoperative use of TNF-α inhibitors reduced the occurrence of POR by aiding mucosal healing.39,40 Similarly, preoperative TNF-α inhibitors might improve clinical outcomes by aiding mucosal healing before surgery. In clinical practice, optimal medical treatments must be preceded to avoid surgery. However, there is a concern that the same TNF-α inhibitors might not be effective, especially if preoperative TNF-α inhibitors did not prevent surgery. In the state of maximal disease burden, no medical treatment would be effective; but if the disease burden is decreased by surgery, same TNF-α inhibitors might control remnant disease. Further studies are needed to prove the pathophysiology of the effects of preoperative and postoperative TNF-α inhibitors use in terms of preventing POR. Regueiro et al.41 reported that infliximab reduced endoscopic recurrence, although it did not reduce clinical recurrence at 76 and 104 weeks. The median time from initial surgery to clinical recurrences in our study was 31.5 months (interquartile range, 8.5 to 56.8 months), which was longer than that of the previous study (76 weeks). There is a possibility that infliximab might significantly reduce clinical recurrence if long-term follow-up was attained. In our study, the best clinical outcomes were shown in patients with both preoperative and postoperative TNF-α inhibitors use, suggesting that maintaining the same TNF-α inhibitors after surgery might be beneficial. Based on our study results, we suggest maintaining the same TNF-α inhibitors if TNF-α inhibitors were used preoperatively, and then performing early screening to evaluate and adjust medications. Furthermore, it might spare further possible treatment (biologics) options in the future. Long-term follow-up in prospective studies with a large cohort are required to prove our findings.

Our study had several limitations. First, this was a retrospective, single-center study, and variations in treatment strategies were quite small. In other words, there has been no consensus about continuing preoperatively used TNF-α inhibitors after surgery, and the decision was made based on each clinician’s perspective and expertise. A single-center design could be an advantage in terms of less variance in treatment strategies. Second, a small number of patients were enrolled, and the follow-up period was relatively short. This could explain the small number of surgical recurrences in our study. Third, inflammatory markers such as fecal calprotectin, C-reactive protein, erythrocyte sedimentation rate were not examined while analyzing recurrence. If biochemical markers could be combined with other parameters, it would be helpful to screen POR in the early stage. Fourth, in this retrospective study, we did not include the specific findings about endoscopic recurrence not to draw false results due to bias because not all the patients received postoperative colonoscopy exams at a specified time after surgery.

In conclusion, continuation of preoperatively administered TNF-α inhibitors significantly reduced the rate of clinical recurrence of CD after surgery. For patients with CD who were receiving TNF-α inhibitors before surgery, continuing rather than stopping TNF-α inhibitors after surgery could be recommended.