Differences in clinical outcomes according to the time interval between the bridge to surgery stenting and surgery for left-sided malignant colorectal obstruction.

BACKGROUND: Self-expandable metal stent (SEMS) placement is commonly used as a bridge to surgery (BTS) for left-sided malignant colorectal obstruction (MCO). However, the optimal time interval between BTS stenting and surgery for left-sided MCO is unclear, and the results of previous studies are conflicting. This study aimed to determine the differences in clinical outcomes according to the time interval between BTS stenting and surgery in left-sided MCO.
METHODS: Data from 594 patients who underwent SEMS placement for MCO between January 2009 and December 2018 were reviewed. Among them, 148 patients who underwent SEMS placement as BTS treatment and curative surgery were enrolled. The enrolled patients were divided into three groups according to the interval between BTS stenting and surgery: group 1 (interval ≤2 weeks), group 2 (interval 2-3 weeks), and group 3 (interval >3 weeks).
RESULTS: Group 2 and 3 patients underwent significantly higher rates of laparoscopic surgery than those in group 1 (83.7, 81.0 vs. 53.2 %, respectively; P=0.003, P=0.003, respectively). Also, rates of stoma formation directly after resection were significantly higher in group 1 compared to groups 2 and 3 (21.3 vs 2.3, 6.9%, respectively; P=0.008, P=0.043, respectively). Bridging interval had no effect on SEMS-related complications, resection-related complications, 90-day mortality, permanent stoma formation, 3-year disease-free survival, and 3-year overall survival.
CONCLUSIONS: A bridging interval of > 2 weeks between BTS stenting and surgery for left-sided MCO is preferable for lower stoma formation rates and higher rates of laparoscopic approach operation, with no difference in short-term and long-term outcomes including complication, mortality, and survival.

Background

Colorectal cancer is the third-most common cancer worldwide, and its incidence in patients <50 years of age has been increasing [1]. Approximately 8–29% of patients with colorectal cancer experience malignant colorectal obstruction (MCO) and require emergency decompression [2, 3]. Classically, MCO has been treated with emergency surgery with stoma formation or primary resection. However, recent studies have reported that emergency surgery is associated with higher morbidity and mortality compared to elective surgery [4, 5]. Therefore, the need for alternative treatment options has emerged.

Since Dohmoto et al. first reported a case of self-expandable metal stent (SEMS) insertion for palliation of MCO [6], numerous studies have evaluated the efficacy of SEMS insertion in MCO. SEMS insertion can be performed for one of two purposes: to act as a bridge to surgery (BTS) or for palliation. In the former case, SEMS insertion has been accepted as a viable treatment option, especially for left-sided MCO. It shows a similar overall survival (OS) rate, lower complication rates, and lower stoma formation rates compared to emergency surgery [7-9]. Decompression with SEMS insertion allows bowel preparation, medical stabilization including repair of dehydration and electrolyte abnormalities, and optimization of concomitant conditions, all of which enhance bowel condition, nutrition, and inflammatory status in patients, thereby allowing elective one-stage surgery [10, 11]. However, the optimal time interval between SEMS placement and surgery remains unclear.

In 2014, the European Society of Gastrointestinal Endoscopy (ESGE) suggested 5–10 days as an optimum time interval between SEMS placement and operation when SEMS is used as BTS; however, this was based on low-quality evidence [12]. In 2020, the updated ESGE guideline suggested an interval of approximately 2 weeks, which was also based on low-quality evidence [7]. As there is no prospective comparative study concerning the time interval between SEMS placement and surgery, the guideline was based on retrospective studies and expert opinions. After the ESGE guidelines were updated in 2020, several studies have reported the optimal timing of surgery after SEMS placement. However, the data are conflicting.

In this study, we aimed to compare the short-term and long-term clinical outcomes according to the time interval between BTS stenting and surgery in left-sided MCO.

Materials and methods

Patient enrollment

A total of 594 patients who underwent SEMS placement for MCO between January 2009 and December 2018 at the Chonnam National University Hwasun Hospital and Chonnam National University Hospital were retrospectively reviewed. The eligibility criteria included (1) patients who were diagnosed with colonic obstruction using a combination of clinical and radiologic signs of obstruction, (2) histologically confirmed cancer, located in the left-sided colon (defined as splenic flexure, descending colon, or sigmoid colon), and (3) patients who had SEMS placement as a bridge to curative intent surgery. Exclusion criteria were (1) stage IV cancer or non-curative resection, (2) concurrent history of other cancers, (3) neoadjuvant chemotherapy, and (4) technical or clinical failure of SEMS placement. Finally, a total of 148 patients were enrolled in this study. Enrolled patients were divided into three groups according to bridging interval: (group 1, ≤2 weeks; group 2, 2–3 weeks; and group 3, >3 weeks). The range of intervals was based on the ESGE guidelines, which recommend a bridging interval of about 2 weeks. We compared the short- and long-term outcomes of patients divided by an interval of 2 weeks.

Procedure protocol

In our hospitals, patients with obstructive signs or symptoms such as abdominal pain, distension, and failure of gas passage underwent abdominal and chest computed tomography (CT) within 24 h of admission. Patients with signs of peritoneal irritation or hemodynamic instability were counseled to undergo surgery without stent placement. Every patient who underwent SEMS placement was assessed for technical and clinical success and complications. Technical success was defined as the successful placement of the SEMS over the obstruction site without any adverse events. Clinical success was defined as an improvement of obstructive symptoms and radiologic relief within 48 h after SEMS placement. The time for surgery was decided by the colorectal surgeons based on the patient’s general condition.

Operation characteristics and outcome measures

Operational characteristics included type of resection, the urgency of resection (emergency vs. elective), surgical approach (open vs. laparoscopic), stoma formation directly after resection, and operation time. Short-term treatment outcomes, including SEMS-related complications, operation-related complication rate, and 90-day mortality, were analyzed. Additionally, resection-related complications were classified according to the Clavien–Dindo classification (grades I, II vs. III, IV, and V) [13]. Grade >III indicated complications requiring surgical or endoscopic intervention. Regarding long-term treatment outcomes, the primary outcome parameters were 3-year disease-free survival (DFS) and 3-year OS rates.

Statistical analysis

Non-normally distributed variables were reported as medians (interquartile range [IQR]). The Mann–Whitney U test was used for comparisons between two groups and the Kruskal–Wallis test was used for comparisons between three groups. Categorical variables are expressed as frequencies and percentages. The Student’s t test, chi-square test, or analysis of variance was used as appropriate. Differences regarding disease-free and OS rates were assessed using the log-rank test. Using a logistic regression model, we determined predictive factors associated with recurrence and death. The Cox proportional hazards regression model with forward selection for variables that were significant in the univariate analysis for OS or DFS was used for multivariate analysis. The statistical significance was set at P < 0.05. All data were analyzed using Statistical Package for the Social Sciences, version 27.0 (SPSS Inc., Chicago, IL, USA).

Results

Baseline characteristics of enrolled patients according to bridging interval

A total of 148 patients were enrolled in this study. Forty-seven patients underwent surgery after a bridging interval of ≤2 weeks (group 1), 43 patients after 2–3 weeks (group 2), and 58 patients after >3 weeks (group 3). The baseline characteristics of the enrolled patients are summarized in Table 1. The median age was 68.0 years (IQR 55.0–78.0) in group 1, 66.0 years (IQR 56.0–76.0) in group 2, and 70.5 years (IQR 61.8–77.0) in group 3; no significant difference was found between the groups’ ages. There were also no significant differences in body mass index (BMI), American Society of Anesthesiologists (ASA) score, previous abdominal surgery history, primary tumor location, preoperative serum carcinoembryonic antigen (CEA) level, or adjuvant chemotherapy rates among the three groups. The interval from SEMS to operation was 10.0 days (IQR 8.0–12.0) in group 1, 18.0 days (IQR 17.0–20.0) in group 2, and 28.0 days (IQR 24.0–32.3) in group 3.

Table 1

Baseline characteristics of enrolled patients

	Totaln (%)	Bridging interval			P-value
		Group 1≤2 weeksn (%)	Group 22–3 weeksn (%)	Group 3>3 weeksn (%)	Overall	≤2 weeks vs. 2–3 weeks	2–3 weeks vs. >3 weeks	≤2 weeks vs. >3 weeks
Number of patients	148	47	43	58
Male sex	86 (58.1)	28 (59.6)	31 (72.1)	27 (46.6)	0.037	0.269	0.014	0.239
Age, median years (IQR years)	68.0 (58.0–77.0)	68.0 (55.0–78.0)	66.0 (56.0–76.0)	70.5 (61.8–77.0)	0.313	0.545	0.122	0.427
BMI, median kg/m2 (IQR kg/m2)	22.2 (20.0–24.9)	22.8 (20.6–25.0)	22.0 (20.2–24.8)	22.2 (19.3–25.0)	0.846	0.634	0.844	0.620
ASA score					0.119	0.679	0.066	0.253
ASA 1–2	132 (89.2)	43 (91.5)	43 (95.3)	48 (82.8)
ASA 3–4	16 (10.8)	4 (8.5)	2 (4.7)	10 (17.2)
Previous abdominal surgery	43 (29.1)	12 (25.5)	13 (30.2)	18 (31.0)	0.829	0.645	1.000	0.665
Primary tumor location					0.378	0.567	0.510	0.174
Splenic flexure	9 (6.1)	4 (8.5)	1 (2.3)	4 (6.9)
Descending colon	15 (10.1)	2 (4.3)	4 (9.3)	9 (15.5)
Sigmoido-descending junction	11 (7.4)	2 (4.3)	4 (9.3)	5 (8.6)
Sigmoid colon	75 (50.7)	28 (59.6)	24 (55.8)	23 (39.7)
Recto-sigmoid junction	38 (25.7)	11 (23.4)	10 (23.3)	17 (29.3)
Preoperative serum CEA, median ng/ml (IQR ng/ml) (n=146)	5.7 (3.2–13.6)	7.8 (4.3–15.3)	4.9 (2.5–9.8)	5.2 (2.7–11.7)	0.127	0.067	0.920	0.089
Adjuvant chemotherapy	116 (78.4)	38 (80.9)	35 (81.4)	43 (74.1)	0.633	1.000	0.475	0.488
Interval from SEMS to operation, median days (IQR days)	19.0 (12.0–25.8)	10.0 (8.0–12.0)	18.0 (17.0–20.0)	28.0 (24.0–32.3)	<0.001	<0.001	<0.001	<0.001
Pathologic results
T stage					0.894	1.000	0.832	0.664
1	1 (0.7)	1 (2.1)	0 (0.0)	0 (0.0)
3	101 (68.2)	32 (68.1)	30 (69.8)	39 (67.2)
4	46 (31.1)	14 (29.8)	13 (30.2)	19 (32.8)
N stage					0.139	0.037	0.139	0.756
0	66 (44.6)	18 (38.3)	24 (55.8)	24 (41.4)
1	54 (36.5)	22 (46.8)	9 (20.9)	23 (39.7)
2	28 (18.9)	7 (14.9)	10 (23.3)	11 (19.0)
Overall stage					0.205	0.138	0.164	0.842
2	66 (44.6)	18 (38.3)	24 (55.8)	24 (41.4)
3	82 (55.4)	29 (61.9)	19 (44.2)	34 (58.6)
Tumor size, median cm (IQR cm)	6.5 (5.5–7.5)	6.0 (5.0–6.5)	7.0 (6.0–8.0)	7.2 (7.0–8.0)	<0.001	<0.001	0.329	<0.001
Histologic grade					0.225	0.105	0.648	0.501
WD/MD	143 (96.6)	47 (100.0)	40 (93.0)	56 (96.6)
PD/Mucinous	5 (3.4)	0 (0.0)	3 (7.0)	2 (3.4)
Lymphovascular invasion	39 (26.4)	11 (23.4)	15 (34.9)	13 (22.4)	0.316	0.253	0.184	1.000
Perinueral invasion	97 (65.5)	29 (61.7)	29 (67.4)	39 (67.2)	0.841	0.661	1.000	0.682

IQR Interquartile range, BMI Body mass index, ASA American Society of Anesthesiologists, CEA Carcinoembryonic antigen, WD Well-differentiated, MD Moderately differentiated, PD Poorly differentiated

Operation characteristics

The operational characteristics are summarized in Table 2. 95.3% of group 2 and 98.3% of group 3 patients were discharged from the hospital during the bridging interval, which was significantly higher compared with group 1. Concerning urgency of resection, 10.6% of patients in group 1 underwent an emergency operation, which was significantly higher than in groups 2 and 3. Group 2 and group 3 patients underwent significantly higher rates of laparoscopic surgery than those in group 1 (83.7, 81.0 vs. 53.2%, respectively; P=0.003, P=0.003, respectively). Also, the rate of stoma formation directly after resection was significantly higher in group 1 (21.3%) compared with groups 2 (2.3%; P=0.008) and 3 (6.9%; P=0.043). There was no significant difference in the duration of surgery between the three groups.

Table 2

Perioperative characteristics of enrolled patients

	Totaln (%)	Bridging interval			P-value
		Group 1≤2 weeksn (%)	Group 22–3 weeksn (%)	Group 3>3 weeksn (%)	Overall	≤2 weeks vs. 2–3 weeks	2–3 weeks vs. >3 weeks	≤2 weeks vs. >3 weeks
Number of patients	148	47	43	58
Discharge from hospital during bridging interval	113 (79.0)	15 (31.9)	41 (95.3)	57 (98.3)	<0.001	<0.001	0.573	<0.001
Type of resection					0.028	0.063	0.361	0.024
Anterior resection	94 (63.5)	26 (55.3)	30 (69.8)	38 (65.5)
Low anterior resection	19 (12.8)	9 (19.1)	4 (9.3)	6 (10.3)
Left hemicolectomy	26 (17.6)	6 (12.8)	9 (21.0)	11 (19.0)
Subtotal colectomy	4 (2.7)	4 (8.5)	0 (0.0)	0 (0.)
Total colectomy	3 (2.0)	0 (0.0)	0 (0.0)	3 (5.2)
Hartmann’s operation	2 (1.4)	2 (4.3)	0 (0.0)	0 (0.0)
Urgency of resection					0.005	0.057	NA	0.016
Emergency	5 (3.4)	5 (10.6)	0 (0.0)	0 (0.0)
Elective	143 (96.6)	42 (89.4)	43 (100.0)	58 (100.0)
Surgical approach					0.001	0.003	0.797	0.003
Open	40 (27.0)	22 (46.8)	7 (16.3)	11 (19.0)
Laparoscopic	108 (73.0)	25 (53.2)	36 (83.7)	47 (81.0)
Stoma directly after resection	16 (10.8)	10 (21.3)	1 (2.3)	4 (6.9)	0.010	0.008	0.391	0.043
Operation time, median min (IQR min)	150.0 (120.0–198.8)	160.0 (125.0–205.0)	149.0 (110.0–190.0)	150.0 (125.0–201.3)	0.487	0.279	0.308	0.976

IQR Interquartile range

Short-term treatment outcomes

The short-term treatment outcomes are summarized in Table 3. 14.9% of group 1 patients had SEMS-related complications, including perforation (4.3%) and migration (10.6%). Seven percent of group 2 patients had SEMS-related complications, and 6.9% of group 3 patients had SEMS-related complications. Rates of operation-related complications within 90 days were 38.3% in group 1, 41.9% in group 2, and 37.9% in group 3, which were not significantly different. Postoperative complications classified according to the Clavien-Dindo classification [13] showed no significant difference among the three groups. There was no difference in a post-resection hospital stay or 90-day mortality between the groups. In addition, the interval from resection to adjuvant chemotherapy was not significantly different among the groups.

Table 3

Short-term treatment outcomes according to bridging interval

	Bridging interval				P-value
	Totaln (%)	Group 1≤2 weeksn (%)	Group 22–3 weekn (%)	Group 3>3 weeksn (%)	Overall	≤2 weeks vs. 2–3 weeks	2–3 weeks vs. >3 weeks	≤2 weeks vs. >3 weeks
Number of patients	148	47	43	58
SEMS-related complication	14 (9.5)	7 (14.9)	3 (7.0)	4 (6.9)	0.305	0.320	0.859	0.408
Perforation	2 (1.4)	2 (4.3)	0 (0.0)	0 (0.0)	0.182	0.495	NA	0.198
Migration	8 (5.4)	5 (10.6)	1 (2.3)	2 (3.4)	0.214	0.206	1.000	0.238
Pain	1 (0.7)	0 (0.0)	1 (2.3)	0 (0.0)	0.291	0.478	0.426	NA
Bleeding	1 (0.7)	0 (0.0)	1 (2.3)	0 (0.0)	0.291	0.478	0.426	NA
Fever	2 (1.4)	0 (0.0)	0 (0.0)	2 (3.4)	0.207	NA	0.334	0.326
Operation related complications within 90 days	58 (39.2)	18 (38.3)	18 (41.9)	22 (37.9)	0.932	0.830	0.837	1.000
Clavien–Dindo classification (n=58)					0.904	1.000	1.000	0.673
Grade 1–2	49 (84.5)	16 (88.9)	15 (83.3)	18 (81.8)
Grade 3–5	9 (15.5)	2 (11.1)	3 (16.7)	4 (18.2)
Post-resection hospital stays, median days (IQR days)	8.0 (7.0–11.8)	9.0 (7.0–13.0)	8.0 (7.0–11.0)	8.0 (7.0–10.0)	0.159	0.210	0.652	0.059
90-day mortality	2 (1.4)	0 (0.0)	0 (0.0)	2 (3.4)	0.334	NA	0.506	0.501
Interval from resection to adjuvant chemotherapy, median days (IQR days) (n=116)	34.5 (30.0–41.0)	32.0 (29.0–41.3)	36.0 (31.0–41.0)	34.0 (30.0–39.0)	0.470	0.331	0.269	0.666

SEMS Self-expandable metal stent, IQR Interquartile range

Long-term treatment outcomes

The long-term treatment outcomes are summarized in Table 4. The median follow-up duration was 45.0 months (IQR 27.0–60.0) in group 1, 45.0 months (IQR 31.0–59.0 in group 2, and 31.5 months (15.5–59.0) in group 3. No significant difference was observed in permanent stoma formation. The median DFS was 45.0 months (IQR 11.0–60.0) in group 1, 39.0 months (IQR 12.–58.0) in group 2, and 31.5 months (IQR 13.0–57.5) in group 3. Three-year DFS rates for groups 1, 2, and 3 were 75.3%, 65.7%, and 78.2%, respectively. Median OS was 43.0 months (IQR 23.0–70.0) in group 1, 42.0 months (IQR 25.0–62.0) in group 2, and 40.5 months (25.5–75.3) in group 3. Three-year OS rates for groups 1, 2, and 3 were 82.1%, 77.3%, and 79.0%, respectively. There was no significant difference in DFS, 3-year DFS, OS, or 3-year OS between the three groups.

Table 4

Long-term treatment outcomes according to bridging interval

	Bridging interval				P-value
	Totaln (%)	Group 1≤2 weeksn (%)	Group 22–3 weeksn (%)	Group 3>3 weeksn (%)	Overall	≤2 weeks vs. 2–3 weeks	2–3 weeks vs. >3 weeks	≤2 weeks vs. >3 weeks
Number of patients	148	47	43	58
Follow-up, median months (IQR months)	41.0 (23.0–59.0)	45.0 (27.0–60.0)	45.0 (31.0–59.0)	31.5 (15.5–59.0)	0.135	0.960	0.082	0.100
Duration of stoma, median days (IQR days) (n=16)	187.5 (114.5–260.0)	191.0 (142.3–267.5)	20.0 (20.0–20.0)	210.0 (18.5–487.0)	0.295	0.182	0.667	0.768
Permanent stoma at time of last follow–up	5 (3.4)	2 (4.3)	0 (0.0)	3 (5.2)	0.385	0.495	0.259	1.000
Recurrence	38 (25.7)	12 (25.5)	15 (34.9)	11 (19.0)	0.192	0.365	0.106	0.481
Death	47 (31.8)	17 (36.2)	12 (27.9)	18 (31.0)	0.716	0.500	0.827	0.678
Disease-free survival, median months (IQR days)	38.0 (13.0–59.0)	45.0 (11.0–60.0)	39.0 (12.0–58.0)	31.5 (13.0–57.5)	0.398	0.488	0.611	0.167
3-year disease free survival (%)	73.5	75.3	65.7	78.2	0.281	0.321	0.121	0.608
Overall survival, median months (IQR days)	42.0 (25.0–71.5)	43.0 (23.0–70.0)	42.0 (25.0–62.0)	40.5 (25.5–75.3)	0.962	0.811	0.966	0.816
3-year overall survival (%)	79.4	82.1	77.3	79.0	0.718	0.474	0.667	0.623

IQR Interquartile range

Univariate and multivariate logistic regression analyses of predictive factors for recurrence and death

Univariate and multivariate logistic regression analyses revealed no significant difference between recurrence and death in terms of the interval from SEMS insertion to resection. The presence of metastatic lymph nodes was associated with recurrence, with a hazard ratio of 1.387 (1.155–1666, P<0.001). In addition, age, stoma formation directly after resection, adjuvant chemotherapy, overall pathologic stage, metastatic lymph nodes, and perineural invasion were significantly associated with death (Table 5).

Table 5

Univariate and multivariate logistic regression analyses of predictive factors for recurrence and death

	Recurrence				Death
	Uni-variate analysis		Multi-variate analysis		Uni-variate analysis		Multi-variate analysis
	HR (95% CI)	P-value	HR (95% CI)	P-value	HR (95% CI)	P-value	HR (95% CI)	P-value
Male sex	0.855 (0.406–1.799)	0.680			0.846 (0.421–1.702)	0.639
Age, years	0.980 (0.952–1.009)	0.175			1.037 (1.005–1.069)	0.022	1.047 (1.000–1.096)	0.044
ASA 3–4	0.381 (0.082–1.760)	0.216	0.186 (0.022–1.586)	0.124	0.690 (0.210–2.265)	0.541
Preoperative serum CEA, ng/ml	1.029 (1.004–1.054)	0.020	1.024 (0.995–1.053)	0.101	1.035 (1.009–1.061)	0.009	1.027 (0.991–1.063)	0.142
Interval from SEMS to resection, days	0.977 (0.939–1.017)	0.252			1.012 (0.978–1.047)	0.492
Stoma directly after resection	2.879 (0.967–8.573)	0.057			5.189 (1.662–16.202)	0.005	6.617 (1.287–34.009)	0.024
Adjuvant chemotherapy	0.579 (0.248–1.351)	0.579	0.404 (0.149–1.094)	0.075	0.218 (0.096–0.496)	<0.001	0.151 (0.044–0.515)	0.003
Overall pathologic stage III	4.183 (1.761–9.935)	0.001			2.888 (1.365–6.107)	0.006	5.243 (1.548–17.757)	0.008
PD/Mucinous cancer	4.629 (0.743–28.835)	0.101			9.302 (1.010–85.672)	0.049	9.835 (0.770–125.638)	0.079
Metastatic LN, n	1.385 (1.172–1.636)	<0.001	1.387 (1.155–1.666)	<0.001	1.172 (1.046–1.313)	0.006	1.185 (1.004–1.400)	0.045
Lymphovascular invasion	2.337 (1.058–5.161)	0.036			1.054 (0.699–3.234)	0.296
Perineural invasion	3.692 (1.426–9.559)	0.007			1.027 (0.495–2.131)	0.942	0.271 (0.093–0.790)	0.017

ASA American Society of Anesthesiologists, CEA Carcinoembryonic antigen, SEMS Self-expandable metal stent, PD Poorly differentiated, LN Lymph node, HR Hazard ratio

Discussion

Patients with MCO often require emergency surgery. It often requires multiple-stage surgery as well as the formation of a stoma, which can reduce the patient’s quality of life severely [14]. Endoscopic decompression with SEMS can turn emergency surgery into a one-stage elective procedure, making it a viable option [7]. A number of studies have increased our understanding of SEMS as a BTS throughout the last decade. However, information on the appropriate time interval between stenting and surgery, as well as its influence, is lacking. There have been several studies recommending the time interval between SEMS placement and operation, but the results are conflicting and have limitations in several studies.

First, some studies recommended delayed surgery after SEMS placement. Akihisa et al. reported that an interval of <15 days was associated with postoperative complications after analyzing 47 patients [15]. Lee et al. reported that the rates of anastomotic leakage were significantly higher in patients who had <10 days interval between SEMS insertion and surgery [16]. Marnix et al. analyzed 168 patients with left-sided MCO, which included 94 patients who underwent SEMS insertion as a BTS. Patients were divided into three groups (ER group: emergency resection; early group; early BTS with <4 weeks interval; late group; late BTS with >4 weeks interval). A 90-day mortality was higher in the early group compared with the late group, and the late group had higher a 5-year recurrence-free survival rate than the late group. Surgical resection after a 4-week interval was an independent prognostic factor for OS. Therefore, a BTS interval of >4 weeks after SEMS placement was suggested for better short-term and long-term outcomes [17].

Other studies have suggested early surgery following the SEMS placement. A retrospective multicenter study performed by Malene et al. reported that time to resection > 18 days was associated with an increased risk of recurrence [18]. Kye et al. analyzed 174 patients who underwent surgery after SEMS placement for MCO. Patients were divided into three groups based on the interval between SEMS placement and surgery (group 1, ≤7 days; group 2, 8–14 days; and group 3, >14 days). The recurrence rate was significantly lower in group 1 compared with groups 2 and 3. The time interval between SEMS placement and surgery was an independent risk factor for disease-free survival. The authors therefore suggested an interval within 7 days to improve long-term outcome [19]. However, in the present study, the interval from SEMS to resection was not associated with recurrence nor death according to univariate and multivariate logistic regression analysis. Lim et al. reported that patients who underwent surgery within 2 weeks interval from SEMS placement had lower systemic recurrence rates after analyzing 53 patients [20]. Lastly, Sato et al. reported an interval longer than 16 days was an independent risk factor for poor relapse-free survival. An interval of >35 days was an independent risk factor for postoperative complications [21].

In the present study, short-term treatment outcomes, including operation-related complications within 90 days and 90-day mortality, were not statistically significantly different between the three groups. In addition, the interval from resection to adjuvant chemotherapy was not significantly different among the three groups. Although the difference was not statistically significant, group 1 had higher rates of SEMS-related complications, including perforation. In group 3, two patients had migration of the stent 10 days after stent insertion. Additionally, fever was documented 3 days after stent insertion in two patients who were cured with the use of antibiotics. In conclusion, all complications occurred within 3 weeks of SEMS insertion in the present study.

Long-term treatment outcomes, including recurrence, death, 3-year disease-free survival rate, and OS rate, were not significantly different between the three groups. This may be due to a small number of patients in each group. We also analyzed the short-term and long-term treatment outcomes of patients subdivided into two groups with an interval of 14 days (group 1: bridging interval <14 days, group 2: bridging interval ≥14 days), as some studies recommended delayed surgery because of high rates of operation-related complications when surgery was performed 10 to 15 days after SEMS insertion [15, 16]. However, there was no significant difference in short-term outcomes, including SEMS-related complication rates and resection-related complications within 90 days between the two groups. Moreover, there was no significant difference in the 3-year disease-free survival and OS rates between the two groups (Additional file 1).

Concerning the surgical approach (open vs. laparoscopy), a bridging interval of ≤2 weeks was associated with higher open surgery rates than bridging intervals of >2 weeks. Even after the exclusion of emergently operated patients due to stent-related complications, the result was similar. Previously, an interval of <16 days or <4 weeks has been associated with higher open surgery rates [17, 21]. Other studies reported no significant difference in the surgical approach according to bridging intervals. However, those studies showed a tendency for higher rates of open surgery in early surgery [20, 22].

There are only a few studies on stoma formation rates according to bridging intervals. Patients are very reluctant to undergo stoma formation as it compromises normal activity and can even result in psychological problems [23]. In a previous study, a bridging interval of 5–10 days was associated with a higher stoma formation rate compared with a bridging interval >10 days [22]. Others reported that the bridging interval was not significantly associated with the stoma formation rate [20]. In the present study, the stoma formation rate was significantly higher in the patients who had a bridging interval of ≤2 weeks. Even after removal of emergency-operated patients, group 1 still had higher stoma formation rates compared to group 2 (14.3 vs 2.3%, p value= 0.045).

The limitation of this study is that it is prone to selection bias because of its retrospective design. Therefore, this study should be interpreted with caution, and larger prospective studies are required to validate our findings.

Conclusion

A bridging interval of > 2 weeks between BTS stenting and surgery for left-sided MCO was significantly lower stoma formation rates and higher rates of laparoscopic approach operation than those of a bridging interval of <2 weeks. However, the bridging interval between BTS stenting and surgery was not associated with short-term and long-term outcomes including complication, mortality, and survival. Therefore, a bridging interval of > 2 weeks between BTS stenting and surgery for left-sided MCO is preferable for lower stoma formation rates and higher rates of laparoscopic approach operation.

Additional file 1. Comparison of treatment outcomes between bridging interval of <14 days and ≥14 days.