Journal of Minimally Invasive Surgery 2021; 24(3): 128-138
Published online September 15, 2021
https://doi.org/10.7602/jmis.2021.24.3.128
© The Korean Society of Endo-Laparoscopic & Robotic Surgery
Correspondence to : Yoon Suk Lee
Division of Colorectal Surgery, Department of General Surgery, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Korea
Tel: +82-2-2258-6095
Fax: +82-2-2258-2282
E-mail: yslee@catholic.ac.kr
ORCID:
https://orcid.org/0000-0002-1849-2774
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Purpose: The prognostic factors in obstructive colon cancer have not been clearly identified. We aimed to identify the prognostic factor to establish optimal treatment strategy in obstructive colon cancer.
Methods: Patients who underwent surgery for primary colon cancer in stages II and III with symptomatic obstruction from 2004 to 2010 in six hospitals were retrospectively collected. Clinicopathological and surgical outcomes were compared between stent insertion and emergent surgery group. Multiple regression analysis and survival curve analysis were used to identify the prognostic factors in symptomatic obstructive colon cancer.
Results: Among 210 patients, 168 patients (80.0%) underwent stent insertion followed by surgery and 42 patients (20.0%) underwent emergent surgery. Laparoscopic approach (55.4% vs. 23.8%, p < 0.001) and adequate lymph node (LN) harvest (≥12) (93.5% vs. 69.0%, p < 0.001) were significantly higher in stent insertion group. In multiple regression analysis, emergent surgery (hazard ratio [HR], 2.153; 95% confidence interval [CI], 1.031–4.495), vascular invasion (HR, 6.257; 95% CI, 2.784–14.061), and omitting adjuvant chemotherapy (HR, 3.107; 95% CI, 1.394–6.925) were independent poor prognostic factors in 5-year overall survival, and N stage (N1: HR, 3.095; 95% CI, 1.316–7.284; N2: HR, 4.156; 95% CI, 1.671–10.333) was the only poor prognostic factor in 5-year disease-free survival.
Conclusion: In symptomatic obstructive colon cancer, emergent surgery, N stage, vascular invasion, and omission of adjuvant chemotherapy were independent poor prognostic factors. Stent insertion is suggested as the initial treatment for symptomatic obstructive colon cancer, and adjuvant chemotherapy is recommended, especially when vascular invasion or LN metastasis is confirmed.
Keywords Colonic neoplasms, Intestinal obstruction, Self expandable metallic stents, Laparoscopy, Prognosis
Obstruction is one of the complications occurring in colon cancer, and up to 29% of colon cancers present with symptomatic obstruction, resulting in poor prognosis [1]. Symptomatic obstruction needs emergent management because of the risk of bowel perforation or peritonitis. In general, there are two treatment options for obstructive colon cancer; emergent surgical procedure with or without anastomosis and bridge-to-surgery following self-expanding metallic stent (SEMS) insertion [2,3].
Although some guidelines have recently been established for obstructive colon cancer, whether to perform SEMS insertion or emergent surgery remains controversial [4–7]. Recently, several studies have shown that the long-term outcome in SEMS insertion is comparable to that of emergent surgery, but the choice of treatment is still not clear because the prognostic factors of obstructive colon cancer have not been verified yet [8–12]. Identifying the prognostic factors is required to predict the long-term outcome and determine the treatment strategy. However, there are relatively few studies about prognostic risk evaluation including treatment strategies for obstructive colon cancer. The present study aimed to analyze the poor prognostic factors including both pathologic outcomes and treatment strategies in symptomatic obstructive colon cancer.
Flow diagram of patient selection is demonstrated in (Fig. 1). Patients who underwent curative resection for stage II, III colon cancer from January 2004 to December 2010 in the Catholic University of Korea Medical Center (Seoul St. Mary’s Hospital, Yeouido St. Mary’s Hospital, Incheon St. Mary’s Hospital, St. Vincent’s Hospital, Uijeongbu St. Mary’s Hospital, and Daejeon St. Mary’s Hospital) were retrospectively reviewed with medical records. A total of 1,785 patients were identified. We excluded 1,451 patients without colonic obstruction, 63 patients who had colonic obstruction without clinical symptom, 40 patients with evidence of perforation, and 21 patients with inadequate medical information were excluded. In final, 210 patients with symptomatic obstructive colon cancer were finally enrolled in the study. All patients were followed up with routine laboratory tests, imaging evaluation including chest and abdomen computed tomography (CT), and annual colonoscopy. The follow-up was completed in December 2015.
Patients’ data were collected from each hospital’s colon cancer patient registry including the demographic and clinicopathological characteristics, surgical outcomes, recurrence, and survival records. Patients were divided into two groups based on the initial treatment modality for the comparison analysis; SEMS insertion and emergent surgery.
The HANARO stent (M.I. Tech Corp., Ltd., Seoul, Korea) or the Niti-S stent (Taewoong Medical, Corp., Ltd., Gimpo, Korea) were used in all cases of SEMS insertion. Whether to perform SEMS insertion or emergent surgery was decided by each surgeon in consultation with an endoscopist. Complications such as perforation, stent expansion, and resolution of the bowel distension were checked serial plain abdominal films after the SEMS was inserted. Mechanical bowel preparation before surgery was performed if SEMS insertion was successful.
Oncological long-term outcomes were compared between two groups. The primary outcomes were 5-year overall survival (OS) and 5-year disease-free survival (DFS). The OS was defined as the time interval from the date of operation to the date of expire or last visit to the clinic. The DFS was defined as the time interval from the date of operation to the date of confirmation of cancer recurrence or last visit to the clinic. Subsequently, subgroup analysis in stages II and III colon cancer, respectively.
We defined symptomatic obstructive colon cancer as pathological confirmation of adenocarcinoma with clinical symptom of obstruction (abdominal distention, pain, tenderness, and no stool passage) and radiological finding of obstruction in CT scan or endoscopic finding of obstruction with failure of passing through tumor lesion. The right colon was defined as the cecum, ascending colon, hepatic flexure colon, and transverse colon, while the left colon was defined as the splenic flexure colon, descending colon, sigmoid colon, and rectosigmoid colon above the peritoneal reflection. The clinical success of SEMS insertion was defined as performing mechanical bowel preparation following the resolution of bowel distension. On the other hand, clinical failure was defined as the inability to perform bowel preparation due to unresolved obstruction and bowel perforation that occurred during or immediately after stent insertion.
The comparison for categorical variables was analyzed with the chi-square or Fisher exact test. The univariate prognostic significance of variables was determined using the Cox proportional hazard model. Variables resulted as significantly related to the survival rate in univariate analysis were consequently explored in multivariate analysis employing the Cox multiple regression model. Survival analyses were calculated using the Kaplan-Meier method and comparisons of survival curves were performed using the log-rank test. Significant value was defined as a p value less than 0.05. All statistical analyses were performed using IBM SPSS for Windows (version 24.0; IBM Corp., Armonk, NY, USA).
A total of 210 patients were included in this study. The median follow-up duration was 44 months with interquartile range of 17 to 61 months. The clinicopathological characteristics and surgical outcomes were compared in two groups and summarized in Table 1. The mean age of the patients was 65.8 ± 12.4 years and male-to-female ratio was 1.1:1. Among 210 patients, 168 patients (80.0%) were initially treated with SEMS insertion followed by elective surgery and 42 patients (20.0%) were treated with emergent surgery. Clinical success rate of SEMS insertion was 92.3%, and the failure of SEMS insertion were observed in 13 patients (7.8%). The bowel decompression after SEMS insertion was done in all cases. Older age (51.8% vs. 73.8%,
The outcomes of the univariate and multivariate analyses that were conducted to identify significant prognostic factors for OS and DFS in symptomatic obstructive colon cancer were demonstrated in Table 2 and 3, respectively. In terms of OS, emergent surgery (hazard ratio [HR], 2.176; 95% confidence interval [CI], 1.088–4.354;
Subgroup univariate analysis of OS and DFS in stage II and stage III were represented in Supplementary Table 1 and 2, respectively, and multivariate analyses of subgroups were summarized in Table 4. In stage II colon cancer, omitting adjuvant chemotherapy was the independent poor prognostic factor (HR, 3.133; 95% CI, 1.013–9.689;
Survival analyses using the Kaplan-Meier curve are shown in (Fig. 2). The survival rate was analyzed using the prognostic factors defined in multivariate analysis as the dependent variable; emergent surgery, N stage, vascular invasion, and omitting adjuvant chemotherapy. The 5-year OS rates were 85.7% and 71.4% in SEMS insertion and emergent surgery, respectively (
In this study, we have identified the prognostic factors for symptomatic obstructive colon cancer. Emergent surgery rather than SEMS insertion, presence of vascular invasion, and omission of adjuvant chemotherapy were the prognostic factors to lower the survival rates, where higher N stage appeared to be the significant prognostic factor for recurrence. Regarding SEMS insertion compared to emergent surgery, laparoscopic approach was more available and adequate LN dissection was more performed.
When emergent surgery is performed for obstructive colon cancer, laparotomy is more considered for the reason that severe bowel dilatation is present [11]. Our study also showed that emergent surgery had a higher rate of laparotomy approach than SEMS insertion (76.2% vs. 44.6%,
SEMS insertion has been reported to have superior short-term outcomes such as primary anastomosis rate and postoperative complications, as well as comparable long-term oncological outcomes compared to conventional emergent surgery [2,8–12]. Our study result showed a correlative outcome in 5-year OS rate (58.7% vs. 71.4%,
One of the prognostic factors for symptomatic obstructive colon cancer found in our results was the presence of vascular invasion. In recent, the significance of vascular invasion in colon cancer has been emphasized that its impact on prognosis is comparable to LN status (N stage). Qwaider et al. [25] stated that stage II colon cancer with extramural vascular invasion had worse OS than stage III colon cancer without vascular invasion (mean survival time, 94 ± 8 months vs. 127 ± 4 months;
One recent meta-analysis study reported that omitting adjuvant chemotherapy resulted in a higher recurrence rate in obstructive colon cancer [27]. Although adjuvant chemotherapy is highlighted in treatment guidelines of obstructive colon cancer, surgeons hesitate to recommend chemotherapy when patient is in old age and has poor performance status [7]. Not only found as the risk factor in entire group, omission of adjuvant chemotherapy appeared to be the risk factor for OS in stage II group and presented lower rate of 5-year OS (89.6% vs. 78.6%,
Our study had some limitations. Since the study was analyzed in retrospective approach, there are possibilities of unintended selection bias. A bias was induced by the fact that each surgeon decided whether to perform SEMS insertion or emergent surgery as the initial treatment and the time interval between SEMS insertion and followed surgery. There was also a bias that the surgeon decided whether to perform adjuvant chemotherapy in consideration of patient’s age and performance status. In addition, perioperative factors such as postoperative complications including leakage and infection, presence of stoma formation, and period of hospitalization were not analyzed in our study. Moreover, the lack of statistical analysis with nonobstructive colon cancer appeared to be another limitation and further research is required. However, our study has strong points that subgroup analysis dividing into stages II and III was conducted to reduce the bias, and multicenter analysis has been done to evaluate numerous, different patients.
In conclusion, this study demonstrated that N stage, emergent surgery, vascular invasion, and omitting adjuvant chemotherapy were associated with poor prognosis in symptomatic obstructive colon cancer. Therefore, we suggest SEMS insertion as the first treatment modality for symptomatic obstructive colon cancer and adjuvant chemotherapy should be performed after surgery, especially when LN metastasis or vascular invasion is identified.
Supplementary materials can be found via https://doi.org/10.7602/jmis.2021.24.3.128.
The study was performed in accordance with the ethical guidelines of the World Medical Association Declaration of Helsinki 2013. The study protocol was approved and monitored by the Institutional Review Board of the Ethics Committee of the College of Medicine, The Catholic University of Korea (No. XC14RIMI0056) and informed consent was wavied.
Conceptualization: JHB, YSL
Data curation: IKL, DSL, WKK, JHK, BHK, HMC, STO, SCL, YSL
Statistical analysis, Visualization: CHK, JHB
Investigation: JHB, CSL, SRH, IKL, DSL, WKK, JHK, BHK, HMC, STO, SCL, YSL
Methodology: CHK, JHB, YSL
Project administration, Supervision: YSL
Writing–original draft: CHK
Writing–review & editing: All authors
All authors read and approved the final manuscript.
All authors have no conflicts of interest to declare.
None.
Clinicopathological characteristics and surgical outcomes of symptomatic obstructive colon cancer
Variable | Total | SEMS insertion | Emergent surgery | |
---|---|---|---|---|
Patient | 210 (100) | 168 (80.0) | 42 (20.0) | |
Age (yr) | 0.010 | |||
≤65 | 92 (43.8) | 81 (48.2) | 11 (26.2) | |
>65 | 118 (56.2) | 87 (51.8) | 31 (73.8) | |
Sex | 0.534 | |||
Male | 111 (52.9) | 87 (51.8) | 24 (57.1) | |
Female | 99 (47.1) | 81 (48.2) | 18 (42.9) | |
Comorbidity | 0.622 | |||
No | 180 (85.7) | 145 (86.3) | 35 (83.3) | |
Yes | 30 (14.3) | 23 (13.7) | 7 (16.7) | |
Tumor location | <0.001 | |||
Right sided | 46 (21.9) | 27 (16.1) | 19 (45.2) | |
Left sided | 164 (78.1) | 141 (83.9) | 23 (54.8) | |
Stent procedure | ||||
Clinical success | 155 (92.3) | |||
Clinical failure | 13 (7.7) | |||
Surgical approach | <0.001 | |||
Laparoscopic | 103 (49.0) | 93 (55.4) | 10 (23.8) | |
Conventional | 107 (51.0) | 75 (44.6) | 32 (76.2) | |
Combined resection | 0.303 | |||
No | 176 (83.8) | 143 (85.1) | 33 (78.6) | |
Yes | 34 (16.2) | 25 (14.9) | 9 (21.4) | |
Stoma formation | 0.240 | |||
No | 190 (90.5) | 154 (91.7) | 36 (85.7) | |
Yes | 20 (9.5) | 14 (8.3) | 6 (14.3) | |
T stagea) | 0.643 | |||
3 | 175 (83.3) | 141 (83.9) | 34 (81.0) | |
4 | 35 (16.7) | 27 (16.1) | 8 (19.0) | |
N stage | 0.046 | |||
0 | 95 (45.2) | 70 (41.7) | 25 (59.5) | |
1 | 63 (30.0) | 53 (31.5) | 10 (23.8) | |
2 | 52 (24.8) | 45 (26.8) | 7 (16.7) | |
TNM stageb) | 0.038 | |||
II | 95 (45.2) | 70 (41.7) | 25 (59.5) | |
III | 115 (54.8) | 98 (58.3) | 17 (40.5) | |
LN harvest | <0.001 | |||
≥12 | 186 (88.6) | 157 (93.5) | 29 (69.0) | |
<12 | 24 (11.4) | 11 (6.5) | 13 (31.0) | |
Histologic type | 0.190 | |||
Well/moderate | 176 (83.8) | 138 (82.1) | 38 (90.5) | |
Poor/Muc/Sig | 34 (16.2) | 30 (17.9) | 4 (9.5) | |
Vascular invasion | 0.630 | |||
No | 191 (91.0) | 152 (90.5) | 39 (92.9) | |
Yes | 19 (9.0) | 16 (9.5) | 3 (7.1) | |
Lymphatic invasion | 0.188 | |||
No | 96 (45.7) | 73 (43.5) | 23 (18.1) | |
Yes | 114 (54.3) | 95 (56.5) | 19 (45.2) | |
Perineural invasion | 0.143 | |||
No | 140 (66.7) | 108 (64.3) | 32 (76.2) | |
Yes | 70 (33.3) | 60 (35.7) | 10 (23.8) | |
Adjuvant chemotherapy | 0.006 | |||
Yes | 163 (77.6) | 137 (81.5) | 26 (61.9) | |
No | 47 (22.4) | 31 (18.5) | 16 (38.1) | |
Recurrence | 0.755 | |||
No | 154 (73.3) | 124 (73.9) | 30 (71.4) | |
Yes | 56 (26.7) | 44 (26.2) | 12 (28.6) |
Data are expressed as number (%).
SEMS, self-expanding metallic stent; LN, lymph node; Muc, mucinous adenocarcinoma; Sig, signet-ring cell carcinoma.
a)No T1, T2 stage were presented. b)No stage I was presented.
Univariate and multivariate analysis of overall survival in symptomatic obstructive colon cancer
Variable | Totala) (n = 210) | Univariate | Multivariate | |||
---|---|---|---|---|---|---|
HR (95% CI) | HR (95% CI) | |||||
Age (yr) | ||||||
≤65 | 92 (43.8) | Reference | ||||
>65 | 118 (56.2) | 1.465 (0.746–2.876) | 0.265 | |||
Sex | ||||||
Male | 111 (52.9) | Reference | ||||
Female | 99 (47.1) | 0.670 (0.343–1.311) | 0.242 | |||
Initial treatment | ||||||
SEMS insertion | 168 (80.0) | Reference | Reference | |||
Emergent | 42 (20.0) | 2.176 (1.088–4.354) | 0.028 | 2.153 (1.031–4.495) | 0.041 | |
Tumor location | ||||||
Right sided | 46 (21.9) | Reference | ||||
Left sided | 164 (78.1) | 0.806 (0.367–1.771) | 0.591 | |||
Surgical approach | ||||||
Laparoscopic | 103 (49.0) | Reference | ||||
Conventional | 107 (51.0) | 1.366 (0.835–3.193) | 0.152 | |||
T stage | ||||||
3 | 175 (83.3) | Reference | ||||
4 | 20 (9.5) | 1.442 (0.657–3.165) | 0.361 | |||
N stage | ||||||
0 | 95 (45.2) | Reference | ||||
1 | 63 (30.0) | 1.356 (0.607–3.028) | 0.458 | |||
2 | 52 (24.8) | 1.756 (0.801–3.851) | 0.160 | |||
LN harvest | ||||||
≥12 | 186 (88.6) | Reference | ||||
<12 | 24 (11.4) | 2.118 (0.880–5.101) | 0.094 | |||
Histologic type | ||||||
Well/moderate | 176 (83.8) | Reference | ||||
Poor/Muc/Sig | 34 (16.2) | 1.299 (0.540–3.124) | 0.559 | |||
Vascular invasion | ||||||
No | 191 (91.0) | Reference | Reference | |||
Yes | 19 (9.0) | 3.944 (1.901–8.182) | <0.001 | 6.257 (2.784–14.061) | <0.001 | |
Lymphatic invasion | ||||||
No | 96 (45.7) | Reference | ||||
Yes | 114 (54.3) | 1.831 (0.915–3.663) | 0.088 | |||
Perineural invasion | ||||||
No | 140 (66.7) | Reference | ||||
Yes | 70 (33.3) | 1.394 (0.712–2.726) | 0.332 | |||
Adjuvant chemotherapy | ||||||
Yes | 163 (77.6) | Reference | Reference | |||
No | 47 (22.4) | 2.462 (1.208–5.020) | 0.013 | 3.107 (1.394–6.925) | 0.006 |
HR, hazard ratio; CI, confidence interval; SEMS, self-expanding metallic stent; LN, lymph node; Muc, mucinous adenocarcinoma; Sig, signet-ring cell carcinoma.
a)Number (%).
Univariate and multivariate analysis of disease-free survival in symptomatic obstructive colon cancer
Variable | Totala) (n = 210) | Univariate | Multivariate | |||
---|---|---|---|---|---|---|
HR (95% CI) | HR (95% CI) | |||||
Age (yr) | ||||||
≤65 | 92 (43.8) | Reference | ||||
>65 | 118 (56.2) | 1.250 (0.736–2.214) | 0.409 | |||
Sex | ||||||
Male | 111 (52.9) | Reference | ||||
Female | 99 (47.1) | 0.873 (0.515–1.479) | 0.613 | |||
Initial treatment | ||||||
SEMS insertion | 168 (80.0) | Reference | ||||
Emergent | 42 (20.0) | 1.248 (0.659–2.365) | 0.497 | |||
Tumor location | ||||||
Right sided | 46 (21.9) | Reference | ||||
Left sided | 164 (78.1) | 0.787 (0.423–1.465) | 0.450 | |||
Surgical approach | ||||||
Laparoscopic | 103 (49.0) | Reference | ||||
Conventional | 107 (51.0) | 1.486 (0.872–2.532) | 0.146 | |||
T stage | ||||||
3 | 175 (83.3) | Reference | ||||
4 | 20 (9.5) | 1.617 (0.883–2.962) | 0.119 | |||
N stage | ||||||
0 | 95 (45.2) | Reference | Reference | |||
1 | 63 (30.0) | 3.112 (1.490–6.498) | 0.003 | 3.095 (1.316–7.284) | 0.010 | |
2 | 52 (24.8) | 4.862 (2.389–9.896) | <0.001 | 4.156 (1.671–10.333) | 0.002 | |
LN harvest | ||||||
≥12 | 186 (88.6) | Reference | ||||
<12 | 24 (11.4) | 0.751 (0.272–2.078) | 0.581 | |||
Histologic type | ||||||
Well/moderate | 176 (83.8) | Reference | ||||
Poor/Muc/Sig | 34 (16.2) | 1.199 (0.587–2.446) | 0.619 | |||
Vascular invasion | ||||||
No | 191 (91.0) | Reference | Reference | |||
Yes | 19 (9.0) | 3.102 (1.602–6.005) | 0.001 | 1.750 (0.810–3.777) | 0.154 | |
Lymphatic invasion | ||||||
No | 96 (45.7) | Reference | Reference | |||
Yes | 114 (54.3) | 2.397 (1.342–4.282) | 0.003 | 0.934 (0.442–1.975) | 0.859 | |
Perineural invasion | ||||||
No | 140 (66.7) | Reference | Reference | |||
Yes | 70 (33.3) | 1.811 (1.069–3.071) | 0.027 | 1.176 (0.652–2.124) | 0.590 | |
Adjuvant chemotherapy | ||||||
Yes | 163 (77.6) | Reference | ||||
No | 47 (22.4) | 1.319 (0.665–2.617) | 0.429 |
HR, hazard ratio; CI, confidence interval; SEMS, self-expanding metallic stent; LN, lymph node; Muc, mucinous adenocarcinoma; Sig, signet-ring cell carcinoma.
a)Number (%).
Multivariate analysis of OS and DFS in symptomatic obstructive colon cancer stage II and stage III
Variable | Total (n = 95) | Stage II | Total (n = 115) | Stage III | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
OS | DFS | OS | DFS | |||||||||
HR (95% CI) | HR (95% CI) | HR (95% CI) | HR (95% CI) | |||||||||
Initial treatment | ||||||||||||
SEMS insertion | 70 (73.7) | Reference | Reference | |||||||||
Emergent | 25 (26.3) | 2.092 (0.684–6.400) | 0.196 | 2.702 (0.808–9.040) | 0.107 | |||||||
Surgical approach | ||||||||||||
Laparoscopic | 41 (43.2) | Reference | ||||||||||
Conventional | 54 (56.8) | 6.309 (0.782–50.923) | 0.084 | |||||||||
LN harvest | ||||||||||||
≥12 | 108 (93.9) | Reference | ||||||||||
<12 | 7 (6.1) | 5.166 (1.471–18.141) | 0.010 | |||||||||
Vascular invasion | ||||||||||||
No | 97 (84.3) | Reference | Reference | |||||||||
Yes | 18 (15.7) | 4.790 (2.061–11.135) | <0.001 | 2.159 (1.092–4.268) | 0.027 | |||||||
Adjuvant chemotherapy | ||||||||||||
Yes | 67 (70.5) | Reference | ||||||||||
No | 28 (29.5) | 3.133 (1.013–9.689) | 0.047 |
OS, overall survival; DFS, disease-free survival; HR, hazard ratio; CI, confidence interval; SEMS, self-expanding metallic stent; LN, lymph node.
Journal of Minimally Invasive Surgery 2021; 24(3): 128-138
Published online September 15, 2021 https://doi.org/10.7602/jmis.2021.24.3.128
Copyright © The Korean Society of Endo-Laparoscopic & Robotic Surgery.
Chang Hwan Kim1 , Jung Hoon Bae2 , Chul Seung Lee2 , Seung-Rim Han2 , In Kyu Lee2 , Dosang Lee2 , Won Kyung Kang3 , Ji Hoon Kim4 , Bong-Hyeon Kye5 , Hyeon-Min Cho5 , Seong Taek Oh6 , Sang Chul Lee7 , Yoon Suk Lee2
1Department of General Surgery, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
2Division of Colorectal Surgery, Department of General Surgery, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
3Division of Colorectal Surgery, Department of General Surgery, Yeouido St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
4Division of Colorectal Surgery, Department of General Surgery, Incheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
5Division of Colorectal Surgery, Department of General Surgery, St. Vincent’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
6Division of Colorectal Surgery, Department of General Surgery, Uijeongbu St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
7Division of Colorectal Surgery, Department of General Surgery, Daejeon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
Correspondence to:Yoon Suk Lee
Division of Colorectal Surgery, Department of General Surgery, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Korea
Tel: +82-2-2258-6095
Fax: +82-2-2258-2282
E-mail: yslee@catholic.ac.kr
ORCID:
https://orcid.org/0000-0002-1849-2774
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Purpose: The prognostic factors in obstructive colon cancer have not been clearly identified. We aimed to identify the prognostic factor to establish optimal treatment strategy in obstructive colon cancer.
Methods: Patients who underwent surgery for primary colon cancer in stages II and III with symptomatic obstruction from 2004 to 2010 in six hospitals were retrospectively collected. Clinicopathological and surgical outcomes were compared between stent insertion and emergent surgery group. Multiple regression analysis and survival curve analysis were used to identify the prognostic factors in symptomatic obstructive colon cancer.
Results: Among 210 patients, 168 patients (80.0%) underwent stent insertion followed by surgery and 42 patients (20.0%) underwent emergent surgery. Laparoscopic approach (55.4% vs. 23.8%, p < 0.001) and adequate lymph node (LN) harvest (≥12) (93.5% vs. 69.0%, p < 0.001) were significantly higher in stent insertion group. In multiple regression analysis, emergent surgery (hazard ratio [HR], 2.153; 95% confidence interval [CI], 1.031–4.495), vascular invasion (HR, 6.257; 95% CI, 2.784–14.061), and omitting adjuvant chemotherapy (HR, 3.107; 95% CI, 1.394–6.925) were independent poor prognostic factors in 5-year overall survival, and N stage (N1: HR, 3.095; 95% CI, 1.316–7.284; N2: HR, 4.156; 95% CI, 1.671–10.333) was the only poor prognostic factor in 5-year disease-free survival.
Conclusion: In symptomatic obstructive colon cancer, emergent surgery, N stage, vascular invasion, and omission of adjuvant chemotherapy were independent poor prognostic factors. Stent insertion is suggested as the initial treatment for symptomatic obstructive colon cancer, and adjuvant chemotherapy is recommended, especially when vascular invasion or LN metastasis is confirmed.
Keywords: Colonic neoplasms, Intestinal obstruction, Self expandable metallic stents, Laparoscopy, Prognosis
Obstruction is one of the complications occurring in colon cancer, and up to 29% of colon cancers present with symptomatic obstruction, resulting in poor prognosis [1]. Symptomatic obstruction needs emergent management because of the risk of bowel perforation or peritonitis. In general, there are two treatment options for obstructive colon cancer; emergent surgical procedure with or without anastomosis and bridge-to-surgery following self-expanding metallic stent (SEMS) insertion [2,3].
Although some guidelines have recently been established for obstructive colon cancer, whether to perform SEMS insertion or emergent surgery remains controversial [4–7]. Recently, several studies have shown that the long-term outcome in SEMS insertion is comparable to that of emergent surgery, but the choice of treatment is still not clear because the prognostic factors of obstructive colon cancer have not been verified yet [8–12]. Identifying the prognostic factors is required to predict the long-term outcome and determine the treatment strategy. However, there are relatively few studies about prognostic risk evaluation including treatment strategies for obstructive colon cancer. The present study aimed to analyze the poor prognostic factors including both pathologic outcomes and treatment strategies in symptomatic obstructive colon cancer.
Flow diagram of patient selection is demonstrated in (Fig. 1). Patients who underwent curative resection for stage II, III colon cancer from January 2004 to December 2010 in the Catholic University of Korea Medical Center (Seoul St. Mary’s Hospital, Yeouido St. Mary’s Hospital, Incheon St. Mary’s Hospital, St. Vincent’s Hospital, Uijeongbu St. Mary’s Hospital, and Daejeon St. Mary’s Hospital) were retrospectively reviewed with medical records. A total of 1,785 patients were identified. We excluded 1,451 patients without colonic obstruction, 63 patients who had colonic obstruction without clinical symptom, 40 patients with evidence of perforation, and 21 patients with inadequate medical information were excluded. In final, 210 patients with symptomatic obstructive colon cancer were finally enrolled in the study. All patients were followed up with routine laboratory tests, imaging evaluation including chest and abdomen computed tomography (CT), and annual colonoscopy. The follow-up was completed in December 2015.
Patients’ data were collected from each hospital’s colon cancer patient registry including the demographic and clinicopathological characteristics, surgical outcomes, recurrence, and survival records. Patients were divided into two groups based on the initial treatment modality for the comparison analysis; SEMS insertion and emergent surgery.
The HANARO stent (M.I. Tech Corp., Ltd., Seoul, Korea) or the Niti-S stent (Taewoong Medical, Corp., Ltd., Gimpo, Korea) were used in all cases of SEMS insertion. Whether to perform SEMS insertion or emergent surgery was decided by each surgeon in consultation with an endoscopist. Complications such as perforation, stent expansion, and resolution of the bowel distension were checked serial plain abdominal films after the SEMS was inserted. Mechanical bowel preparation before surgery was performed if SEMS insertion was successful.
Oncological long-term outcomes were compared between two groups. The primary outcomes were 5-year overall survival (OS) and 5-year disease-free survival (DFS). The OS was defined as the time interval from the date of operation to the date of expire or last visit to the clinic. The DFS was defined as the time interval from the date of operation to the date of confirmation of cancer recurrence or last visit to the clinic. Subsequently, subgroup analysis in stages II and III colon cancer, respectively.
We defined symptomatic obstructive colon cancer as pathological confirmation of adenocarcinoma with clinical symptom of obstruction (abdominal distention, pain, tenderness, and no stool passage) and radiological finding of obstruction in CT scan or endoscopic finding of obstruction with failure of passing through tumor lesion. The right colon was defined as the cecum, ascending colon, hepatic flexure colon, and transverse colon, while the left colon was defined as the splenic flexure colon, descending colon, sigmoid colon, and rectosigmoid colon above the peritoneal reflection. The clinical success of SEMS insertion was defined as performing mechanical bowel preparation following the resolution of bowel distension. On the other hand, clinical failure was defined as the inability to perform bowel preparation due to unresolved obstruction and bowel perforation that occurred during or immediately after stent insertion.
The comparison for categorical variables was analyzed with the chi-square or Fisher exact test. The univariate prognostic significance of variables was determined using the Cox proportional hazard model. Variables resulted as significantly related to the survival rate in univariate analysis were consequently explored in multivariate analysis employing the Cox multiple regression model. Survival analyses were calculated using the Kaplan-Meier method and comparisons of survival curves were performed using the log-rank test. Significant value was defined as a p value less than 0.05. All statistical analyses were performed using IBM SPSS for Windows (version 24.0; IBM Corp., Armonk, NY, USA).
A total of 210 patients were included in this study. The median follow-up duration was 44 months with interquartile range of 17 to 61 months. The clinicopathological characteristics and surgical outcomes were compared in two groups and summarized in Table 1. The mean age of the patients was 65.8 ± 12.4 years and male-to-female ratio was 1.1:1. Among 210 patients, 168 patients (80.0%) were initially treated with SEMS insertion followed by elective surgery and 42 patients (20.0%) were treated with emergent surgery. Clinical success rate of SEMS insertion was 92.3%, and the failure of SEMS insertion were observed in 13 patients (7.8%). The bowel decompression after SEMS insertion was done in all cases. Older age (51.8% vs. 73.8%,
The outcomes of the univariate and multivariate analyses that were conducted to identify significant prognostic factors for OS and DFS in symptomatic obstructive colon cancer were demonstrated in Table 2 and 3, respectively. In terms of OS, emergent surgery (hazard ratio [HR], 2.176; 95% confidence interval [CI], 1.088–4.354;
Subgroup univariate analysis of OS and DFS in stage II and stage III were represented in Supplementary Table 1 and 2, respectively, and multivariate analyses of subgroups were summarized in Table 4. In stage II colon cancer, omitting adjuvant chemotherapy was the independent poor prognostic factor (HR, 3.133; 95% CI, 1.013–9.689;
Survival analyses using the Kaplan-Meier curve are shown in (Fig. 2). The survival rate was analyzed using the prognostic factors defined in multivariate analysis as the dependent variable; emergent surgery, N stage, vascular invasion, and omitting adjuvant chemotherapy. The 5-year OS rates were 85.7% and 71.4% in SEMS insertion and emergent surgery, respectively (
In this study, we have identified the prognostic factors for symptomatic obstructive colon cancer. Emergent surgery rather than SEMS insertion, presence of vascular invasion, and omission of adjuvant chemotherapy were the prognostic factors to lower the survival rates, where higher N stage appeared to be the significant prognostic factor for recurrence. Regarding SEMS insertion compared to emergent surgery, laparoscopic approach was more available and adequate LN dissection was more performed.
When emergent surgery is performed for obstructive colon cancer, laparotomy is more considered for the reason that severe bowel dilatation is present [11]. Our study also showed that emergent surgery had a higher rate of laparotomy approach than SEMS insertion (76.2% vs. 44.6%,
SEMS insertion has been reported to have superior short-term outcomes such as primary anastomosis rate and postoperative complications, as well as comparable long-term oncological outcomes compared to conventional emergent surgery [2,8–12]. Our study result showed a correlative outcome in 5-year OS rate (58.7% vs. 71.4%,
One of the prognostic factors for symptomatic obstructive colon cancer found in our results was the presence of vascular invasion. In recent, the significance of vascular invasion in colon cancer has been emphasized that its impact on prognosis is comparable to LN status (N stage). Qwaider et al. [25] stated that stage II colon cancer with extramural vascular invasion had worse OS than stage III colon cancer without vascular invasion (mean survival time, 94 ± 8 months vs. 127 ± 4 months;
One recent meta-analysis study reported that omitting adjuvant chemotherapy resulted in a higher recurrence rate in obstructive colon cancer [27]. Although adjuvant chemotherapy is highlighted in treatment guidelines of obstructive colon cancer, surgeons hesitate to recommend chemotherapy when patient is in old age and has poor performance status [7]. Not only found as the risk factor in entire group, omission of adjuvant chemotherapy appeared to be the risk factor for OS in stage II group and presented lower rate of 5-year OS (89.6% vs. 78.6%,
Our study had some limitations. Since the study was analyzed in retrospective approach, there are possibilities of unintended selection bias. A bias was induced by the fact that each surgeon decided whether to perform SEMS insertion or emergent surgery as the initial treatment and the time interval between SEMS insertion and followed surgery. There was also a bias that the surgeon decided whether to perform adjuvant chemotherapy in consideration of patient’s age and performance status. In addition, perioperative factors such as postoperative complications including leakage and infection, presence of stoma formation, and period of hospitalization were not analyzed in our study. Moreover, the lack of statistical analysis with nonobstructive colon cancer appeared to be another limitation and further research is required. However, our study has strong points that subgroup analysis dividing into stages II and III was conducted to reduce the bias, and multicenter analysis has been done to evaluate numerous, different patients.
In conclusion, this study demonstrated that N stage, emergent surgery, vascular invasion, and omitting adjuvant chemotherapy were associated with poor prognosis in symptomatic obstructive colon cancer. Therefore, we suggest SEMS insertion as the first treatment modality for symptomatic obstructive colon cancer and adjuvant chemotherapy should be performed after surgery, especially when LN metastasis or vascular invasion is identified.
Supplementary materials can be found via https://doi.org/10.7602/jmis.2021.24.3.128.
The study was performed in accordance with the ethical guidelines of the World Medical Association Declaration of Helsinki 2013. The study protocol was approved and monitored by the Institutional Review Board of the Ethics Committee of the College of Medicine, The Catholic University of Korea (No. XC14RIMI0056) and informed consent was wavied.
Conceptualization: JHB, YSL
Data curation: IKL, DSL, WKK, JHK, BHK, HMC, STO, SCL, YSL
Statistical analysis, Visualization: CHK, JHB
Investigation: JHB, CSL, SRH, IKL, DSL, WKK, JHK, BHK, HMC, STO, SCL, YSL
Methodology: CHK, JHB, YSL
Project administration, Supervision: YSL
Writing–original draft: CHK
Writing–review & editing: All authors
All authors read and approved the final manuscript.
All authors have no conflicts of interest to declare.
None.
Table 1 . Clinicopathological characteristics and surgical outcomes of symptomatic obstructive colon cancer.
Variable | Total | SEMS insertion | Emergent surgery | |
---|---|---|---|---|
Patient | 210 (100) | 168 (80.0) | 42 (20.0) | |
Age (yr) | 0.010 | |||
≤65 | 92 (43.8) | 81 (48.2) | 11 (26.2) | |
>65 | 118 (56.2) | 87 (51.8) | 31 (73.8) | |
Sex | 0.534 | |||
Male | 111 (52.9) | 87 (51.8) | 24 (57.1) | |
Female | 99 (47.1) | 81 (48.2) | 18 (42.9) | |
Comorbidity | 0.622 | |||
No | 180 (85.7) | 145 (86.3) | 35 (83.3) | |
Yes | 30 (14.3) | 23 (13.7) | 7 (16.7) | |
Tumor location | <0.001 | |||
Right sided | 46 (21.9) | 27 (16.1) | 19 (45.2) | |
Left sided | 164 (78.1) | 141 (83.9) | 23 (54.8) | |
Stent procedure | ||||
Clinical success | 155 (92.3) | |||
Clinical failure | 13 (7.7) | |||
Surgical approach | <0.001 | |||
Laparoscopic | 103 (49.0) | 93 (55.4) | 10 (23.8) | |
Conventional | 107 (51.0) | 75 (44.6) | 32 (76.2) | |
Combined resection | 0.303 | |||
No | 176 (83.8) | 143 (85.1) | 33 (78.6) | |
Yes | 34 (16.2) | 25 (14.9) | 9 (21.4) | |
Stoma formation | 0.240 | |||
No | 190 (90.5) | 154 (91.7) | 36 (85.7) | |
Yes | 20 (9.5) | 14 (8.3) | 6 (14.3) | |
T stagea) | 0.643 | |||
3 | 175 (83.3) | 141 (83.9) | 34 (81.0) | |
4 | 35 (16.7) | 27 (16.1) | 8 (19.0) | |
N stage | 0.046 | |||
0 | 95 (45.2) | 70 (41.7) | 25 (59.5) | |
1 | 63 (30.0) | 53 (31.5) | 10 (23.8) | |
2 | 52 (24.8) | 45 (26.8) | 7 (16.7) | |
TNM stageb) | 0.038 | |||
II | 95 (45.2) | 70 (41.7) | 25 (59.5) | |
III | 115 (54.8) | 98 (58.3) | 17 (40.5) | |
LN harvest | <0.001 | |||
≥12 | 186 (88.6) | 157 (93.5) | 29 (69.0) | |
<12 | 24 (11.4) | 11 (6.5) | 13 (31.0) | |
Histologic type | 0.190 | |||
Well/moderate | 176 (83.8) | 138 (82.1) | 38 (90.5) | |
Poor/Muc/Sig | 34 (16.2) | 30 (17.9) | 4 (9.5) | |
Vascular invasion | 0.630 | |||
No | 191 (91.0) | 152 (90.5) | 39 (92.9) | |
Yes | 19 (9.0) | 16 (9.5) | 3 (7.1) | |
Lymphatic invasion | 0.188 | |||
No | 96 (45.7) | 73 (43.5) | 23 (18.1) | |
Yes | 114 (54.3) | 95 (56.5) | 19 (45.2) | |
Perineural invasion | 0.143 | |||
No | 140 (66.7) | 108 (64.3) | 32 (76.2) | |
Yes | 70 (33.3) | 60 (35.7) | 10 (23.8) | |
Adjuvant chemotherapy | 0.006 | |||
Yes | 163 (77.6) | 137 (81.5) | 26 (61.9) | |
No | 47 (22.4) | 31 (18.5) | 16 (38.1) | |
Recurrence | 0.755 | |||
No | 154 (73.3) | 124 (73.9) | 30 (71.4) | |
Yes | 56 (26.7) | 44 (26.2) | 12 (28.6) |
Data are expressed as number (%)..
SEMS, self-expanding metallic stent; LN, lymph node; Muc, mucinous adenocarcinoma; Sig, signet-ring cell carcinoma..
a)No T1, T2 stage were presented. b)No stage I was presented..
Table 2 . Univariate and multivariate analysis of overall survival in symptomatic obstructive colon cancer.
Variable | Totala) (n = 210) | Univariate | Multivariate | |||
---|---|---|---|---|---|---|
HR (95% CI) | HR (95% CI) | |||||
Age (yr) | ||||||
≤65 | 92 (43.8) | Reference | ||||
>65 | 118 (56.2) | 1.465 (0.746–2.876) | 0.265 | |||
Sex | ||||||
Male | 111 (52.9) | Reference | ||||
Female | 99 (47.1) | 0.670 (0.343–1.311) | 0.242 | |||
Initial treatment | ||||||
SEMS insertion | 168 (80.0) | Reference | Reference | |||
Emergent | 42 (20.0) | 2.176 (1.088–4.354) | 0.028 | 2.153 (1.031–4.495) | 0.041 | |
Tumor location | ||||||
Right sided | 46 (21.9) | Reference | ||||
Left sided | 164 (78.1) | 0.806 (0.367–1.771) | 0.591 | |||
Surgical approach | ||||||
Laparoscopic | 103 (49.0) | Reference | ||||
Conventional | 107 (51.0) | 1.366 (0.835–3.193) | 0.152 | |||
T stage | ||||||
3 | 175 (83.3) | Reference | ||||
4 | 20 (9.5) | 1.442 (0.657–3.165) | 0.361 | |||
N stage | ||||||
0 | 95 (45.2) | Reference | ||||
1 | 63 (30.0) | 1.356 (0.607–3.028) | 0.458 | |||
2 | 52 (24.8) | 1.756 (0.801–3.851) | 0.160 | |||
LN harvest | ||||||
≥12 | 186 (88.6) | Reference | ||||
<12 | 24 (11.4) | 2.118 (0.880–5.101) | 0.094 | |||
Histologic type | ||||||
Well/moderate | 176 (83.8) | Reference | ||||
Poor/Muc/Sig | 34 (16.2) | 1.299 (0.540–3.124) | 0.559 | |||
Vascular invasion | ||||||
No | 191 (91.0) | Reference | Reference | |||
Yes | 19 (9.0) | 3.944 (1.901–8.182) | <0.001 | 6.257 (2.784–14.061) | <0.001 | |
Lymphatic invasion | ||||||
No | 96 (45.7) | Reference | ||||
Yes | 114 (54.3) | 1.831 (0.915–3.663) | 0.088 | |||
Perineural invasion | ||||||
No | 140 (66.7) | Reference | ||||
Yes | 70 (33.3) | 1.394 (0.712–2.726) | 0.332 | |||
Adjuvant chemotherapy | ||||||
Yes | 163 (77.6) | Reference | Reference | |||
No | 47 (22.4) | 2.462 (1.208–5.020) | 0.013 | 3.107 (1.394–6.925) | 0.006 |
HR, hazard ratio; CI, confidence interval; SEMS, self-expanding metallic stent; LN, lymph node; Muc, mucinous adenocarcinoma; Sig, signet-ring cell carcinoma..
a)Number (%)..
Table 3 . Univariate and multivariate analysis of disease-free survival in symptomatic obstructive colon cancer.
Variable | Totala) (n = 210) | Univariate | Multivariate | |||
---|---|---|---|---|---|---|
HR (95% CI) | HR (95% CI) | |||||
Age (yr) | ||||||
≤65 | 92 (43.8) | Reference | ||||
>65 | 118 (56.2) | 1.250 (0.736–2.214) | 0.409 | |||
Sex | ||||||
Male | 111 (52.9) | Reference | ||||
Female | 99 (47.1) | 0.873 (0.515–1.479) | 0.613 | |||
Initial treatment | ||||||
SEMS insertion | 168 (80.0) | Reference | ||||
Emergent | 42 (20.0) | 1.248 (0.659–2.365) | 0.497 | |||
Tumor location | ||||||
Right sided | 46 (21.9) | Reference | ||||
Left sided | 164 (78.1) | 0.787 (0.423–1.465) | 0.450 | |||
Surgical approach | ||||||
Laparoscopic | 103 (49.0) | Reference | ||||
Conventional | 107 (51.0) | 1.486 (0.872–2.532) | 0.146 | |||
T stage | ||||||
3 | 175 (83.3) | Reference | ||||
4 | 20 (9.5) | 1.617 (0.883–2.962) | 0.119 | |||
N stage | ||||||
0 | 95 (45.2) | Reference | Reference | |||
1 | 63 (30.0) | 3.112 (1.490–6.498) | 0.003 | 3.095 (1.316–7.284) | 0.010 | |
2 | 52 (24.8) | 4.862 (2.389–9.896) | <0.001 | 4.156 (1.671–10.333) | 0.002 | |
LN harvest | ||||||
≥12 | 186 (88.6) | Reference | ||||
<12 | 24 (11.4) | 0.751 (0.272–2.078) | 0.581 | |||
Histologic type | ||||||
Well/moderate | 176 (83.8) | Reference | ||||
Poor/Muc/Sig | 34 (16.2) | 1.199 (0.587–2.446) | 0.619 | |||
Vascular invasion | ||||||
No | 191 (91.0) | Reference | Reference | |||
Yes | 19 (9.0) | 3.102 (1.602–6.005) | 0.001 | 1.750 (0.810–3.777) | 0.154 | |
Lymphatic invasion | ||||||
No | 96 (45.7) | Reference | Reference | |||
Yes | 114 (54.3) | 2.397 (1.342–4.282) | 0.003 | 0.934 (0.442–1.975) | 0.859 | |
Perineural invasion | ||||||
No | 140 (66.7) | Reference | Reference | |||
Yes | 70 (33.3) | 1.811 (1.069–3.071) | 0.027 | 1.176 (0.652–2.124) | 0.590 | |
Adjuvant chemotherapy | ||||||
Yes | 163 (77.6) | Reference | ||||
No | 47 (22.4) | 1.319 (0.665–2.617) | 0.429 |
HR, hazard ratio; CI, confidence interval; SEMS, self-expanding metallic stent; LN, lymph node; Muc, mucinous adenocarcinoma; Sig, signet-ring cell carcinoma..
a)Number (%)..
Table 4 . Multivariate analysis of OS and DFS in symptomatic obstructive colon cancer stage II and stage III.
Variable | Total (n = 95) | Stage II | Total (n = 115) | Stage III | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
OS | DFS | OS | DFS | |||||||||
HR (95% CI) | HR (95% CI) | HR (95% CI) | HR (95% CI) | |||||||||
Initial treatment | ||||||||||||
SEMS insertion | 70 (73.7) | Reference | Reference | |||||||||
Emergent | 25 (26.3) | 2.092 (0.684–6.400) | 0.196 | 2.702 (0.808–9.040) | 0.107 | |||||||
Surgical approach | ||||||||||||
Laparoscopic | 41 (43.2) | Reference | ||||||||||
Conventional | 54 (56.8) | 6.309 (0.782–50.923) | 0.084 | |||||||||
LN harvest | ||||||||||||
≥12 | 108 (93.9) | Reference | ||||||||||
<12 | 7 (6.1) | 5.166 (1.471–18.141) | 0.010 | |||||||||
Vascular invasion | ||||||||||||
No | 97 (84.3) | Reference | Reference | |||||||||
Yes | 18 (15.7) | 4.790 (2.061–11.135) | <0.001 | 2.159 (1.092–4.268) | 0.027 | |||||||
Adjuvant chemotherapy | ||||||||||||
Yes | 67 (70.5) | Reference | ||||||||||
No | 28 (29.5) | 3.133 (1.013–9.689) | 0.047 |
OS, overall survival; DFS, disease-free survival; HR, hazard ratio; CI, confidence interval; SEMS, self-expanding metallic stent; LN, lymph node..
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