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Outcome of colon cancer initially presenting as colon perforation and obstruction
World Journal of Surgical Oncology volume 15, Article number: 164 (2017)
Emergency complications of colon cancer include perforation and obstruction which were recognized as poor prognostic factors. Few studies have directly compared the outcomes of these two groups. In this study, we evaluated mortality and morbidity in patients with colon cancer initially presenting as perforation and obstruction.
Newly diagnosed colon cancer cases initially presenting with perforation or obstruction at Tzu Chi General Hospital, Hualien, Taiwan, between 2009 and 2015 were included. Cases of iatrogenic perforation or perforation sites far away from the tumor sites and rectal (< 15 cm from the anal verge) cancer were excluded. Progression-free survival, local recurrence rate, distant metastasis rate, and overall survival were the evaluated outcomes.
Eighty-one patients met the selection criteria; 23 and 58 patients had perforation and obstruction, respectively, as the initial symptom. The median age was 72 years. The median tumor stage was stage IIIB. The 1-year and 3-year survival rates were 83.7 and 59.7%, respectively. The perforation group (PRG) and obstruction group (OBG) did not differ significantly in intensive care unit (ICU) stay rate (p = 0.147), sex (p = 0.45), comorbidities (heart, liver, and renal diseases and diabetes mellitus), median stage (p = 0.198), and overall survival (p = 0.328). However, PRG had a higher age at diagnosis (74 vs. 64 years, p = 0.037), a higher APACHE II score (12 vs. 7, p = 0.002), lower disease-free survival (p = 0.001), a higher recurrence rate (56.5 vs. 19%, p = 0.002), a higher distant metastasis rate (39.1 vs. 13.8%, p = 0.015), and a higher local recurrence rate (43.5 vs. 5.2%, p < 0.001) than did OBG. OBG had a higher two-stage operation rate (46.6 vs. 17.4%, p = 0.022). After adjustment for the tumor stage, comorbidity (chronic renal disease), body mass index (BMI), and adjuvant chemotherapy or radiotherapy in multivariate statistics, PRG had lower disease-free survival (p = 0.005) than OBG but overall survival was identical.
For colon cancer initially presenting as perforation or obstruction, the PRG had poorer progression-free survival, a higher local recurrence rate, and a higher distant metastasis rate than did OBG. Overall survival did not differ between these two groups.
Emergency complications of colon cancer include perforation and obstruction, and 15–40% of patients with colorectal cancer initially present these conditions . Colon cancer with perforation comprises 3–10% of the initial presentation of colon cancer, and that with obstruction comprises 8–40% [1,2,3,4]. These complications have indicated that poor prognostic factors influence outcomes [5,6,7,8,9,10,11]. Furthermore, in the European Society for Medical Oncology (2012) and National Comprehensive Cancer Network (2014) guidelines, colon cancer with perforation or obstruction is considered a poor prognostic factor along with T4 primary tumors, inadequately sampled nodes, lymphatic vessel invasion, and perineural invasion [12, 13]. However, few studies have directly compared the outcomes of perforation with those of obstruction in colon cancer. Moreover, most studies have pertained to rectal cancer, which has a different pathophysiology from that of colon cancer. In this study, we evaluated mortality and morbidity in patients with colon cancer initially presenting as perforation and obstruction.
We retrospectively reviewed medical records from 2009 to 2015. Newly diagnosed cases of colon cancer initially presenting as perforation or obstruction in Tzu Chi General Hospital, Hualien, Taiwan, were included. We reviewed and recorded the initial presenting symptoms, the length of intensive care unit (ICU) stay, imaging results, intraoperative results, operative methods, final pathological reports, tumor stage, APACHE (Acute Physiology and Chronic Health Evaluation) II score, adjuvant therapy, body mass index (BMI), comorbidities, local recurrence, distant metastasis, and survival time. Cases of iatrogenic perforations, distant perforation sites, and rectal cancers (< 15 cm from the anal verge) were excluded. Patients who did not return to the outpatient department after discharge were defined as lost follow-up and also excluded. The perforation group (PRG) included patients with a colon perforation at the primary cancer site, which was confirmed using images, pathological findings, and operative records (Fig. 1). Patients in the obstruction group (OBG) was assigned through clinical and radiological and intraoperative findings (complete obstruction) (Fig. 1). Local recurrence was defined as recurrent tumors in the original tumor bed. Distant recurrence was defined as recurrent tumors outside the peritoneal cavity. Overall survival was defined as the duration from operation to death or the last follow-up. Disease-free survival was defined as the duration from operation to cancer recurrence. Stage operation was defined as having undergone diversion surgery (colostomy or ileostomy) followed by an arranged definite surgery on another day.
The Mann–Whitney U test was used to calculate univariate continuous variables. The chi-squared test was used to calculate univariate categorical variables. The Kaplan–Meier curves and Cox proportional hazard models were used for survival analysis. We used IBM SPSS 22 (IBM Corporation, Armonk, NY, USA) for statistical analysis, and p < 0.05 was considered statistically significant.
In our hospital, 527 patients were diagnosed with colon cancer from 2009 to 2015. Among the 81 patients who met the inclusion criteria, 23 patients had perforation and 58 patients had obstruction as the initial symptom. The perforation and obstruction rates were 4.3 and 11%, respectively, in all colon cancers. The median age was 72 years (19–92 years), and the median tumor stage was stage IIIB (stages I–IVB). The male-to-female ratio was 51:30. The sigmoid colon was the most common tumor location (28 patients, 35%; Table 1), and 25 patients (30.9%) were admitted to ICUs. The median length of ICU stay was 3.5 days (1–83 days). The 1-year and 3-year survival rates were 83.7 and 59.7%, respectively.
The length of ICU stay, sex, comorbidities (heart, liver, and renal diseases and diabetes mellitus), median stage, and overall survival did not differ significantly between the two groups (Table 2; Fig. 2). However, the age at diagnosis was higher in OBG (74 vs. 64 years, p = 0.037), and OBG also had a higher APACHE II score (12 vs. 7, p = 0.002), a higher cancer recurrence rate (56.5 vs. 19%, p = 0.002), a higher distant metastasis rate (39.1 vs. 13.8%, p = 0.015), a higher local recurrent rate (43.5 vs. 5.2%, p = 0.022), and a poorer disease-free survival rate (p = 0.001; Table 2; Fig. 3). OBG had a higher two-stage operation rate (46.6 vs. 17.4%; Table 2) than did PRG. In multivariate statistics, after adjustment for the tumor stage, comorbidity (chronic renal disease), BMI (representing nutrition status), and treatment (chemotherapy or radiotherapy), PRG had a poorer disease-free survival (p = 0.005) than did OBG but the overall survival was identical in these two groups (Tables 4 and 6). A high tumor stage was associated with poor survival (p = 0.007). High BMI was also associated with poor survival (hazard ratio 2.26, p = 0.066; Tables 3 and 4). Patients receiving adjuvant chemotherapy or radiotherapy had improved survival (hazard ratio 0.202, p = 0.002) (Tables 3 and 4). The comparison between the results for PRG and OBG is listed in Table 5.
Emergency colorectal cancer surgeries are associated with poor outcomes . Obstruction and perforation are the two major factors. Chen et al. demonstrated that neoplastic bowel obstruction, but not bowel perforation at the tumor site, was associated with poor survival . Banaszkiewicz et al. reported increased rates of complications and mortality in these patient groups . Ho et al. reported that bowel obstruction and perforation were associated with poor disease survival in colorectal cancer . In our study, colon cancer with perforation or obstruction showed an overall 1-year survival rate of 83.7% and a 3-year survival rate of 59.7%. We found that the survival curve was very similar to that of stage IIIB colon cancer (Fig. 4) . The results can be explained by the following reasons: (1) increased age at diagnosis, (2) debility, (3) increased operative mortality, (4) advanced stage of disease at presentation, and (5) association with comorbidities (sepsis and acute kidney injury) [3, 18,19,20].
Our study focused on the comparison between colon cancer with perforation and that with obstruction. We defined the diagnoses of obstruction and perforation. We included patients with colon cancer and excluded patients with rectal cancer. Our results revealed that the overall survival did not differ significantly between obstruction and perforation in colon cancer. However, colon cancer with perforation had a poorer progression-free survival rate, a higher local recurrence rate, and a higher distant metastasis rate compared with colon cancer with obstruction (Table 6). Few studies have directly compared the prognosis of perforation and obstruction in colon cancer, and some studies did not offer clear definitions. Chen et al. compared complete bowel obstruction with bowel perforation at the site of tumor . The results revealed that bowel obstruction had poorer overall survival than did perforation. However, this study also involved patients with rectal cancer. Although Alvarez et al. indicated that the perforation group had a higher postsurgical mortality rate than did the obstruction group (29 vs. 11%, respectively), this study also included patients with rectal cancer . Biondo et al. published a study which might be the most specific study in comparing the survival rates between obstruction and perforation in colon cancer . Similarly to our study, this study excluded patients with rectal cancer and included 236 patients. The results revealed that tumor recurrence and overall survival did not differ significantly between patients with obstruction and those with perforation in colon cancer. However, the perforation group included patients who had bowel perforation because of distension (usually caused by obstruction). In our study, we only included bowel perforation at the tumor sites in the perforation group.
In our study, the obstruction group had a higher two-stage operation rate (46.6%) than did the perforation group. The perforation group also showed a two-stage operation rate of 17.4%. The reasons for performing two-stage operations might be as follows: (1) to allow complete resuscitation before surgery, (2) presence of peritonitis or severe sepsis, and (3) bowel distension with fecal contamination, which increases surgical difficulty. However, recent studies have suggested that one-stage curative emergency resection had similar perioperative morbidity, mortality, and long-term survival compared with two-stage operations [4, 11, 21]. However, in patients with compromised immunity, malnutrition, septic shock, or severe comorbidities (severe cardiopulmonary disease), two-stage operations were an option .
For colon cancer initially presenting as perforation or obstruction, the survival curve resembles stage IIIB colon cancer (3-year survival rate, 59.7 vs. 59.3%). Colon cancer with perforation had poorer progression-free survival, a higher local recurrence rate, and a higher distant metastasis rate compared with that with obstruction. The overall survival was identical. High tumor stage and high BMI were associated with poor survival. Patients who had received adjuvant chemotherapy or radiotherapy showed improved survival. We found a high rate of multiple-stage operations in our patient group, particularly in OBG. Further operative decisions might be adjusted to a one-stage curative tumor resection according to the current trend.
- APACHE II score:
Acute Physiology and Chronic Health Evaluation II score
Body mass index
Intensive care unit
Colon cancer with obstruction
Colon cancer with perforation
Biondo S, Martí-Ragué J, Kreisler E, et al. A prospective study of outcomes of emergency and elective surgeries for complicated colonic cancer. Am J Surg. 2005;189:377–83.
MacKenzie S, Thomson SR, Baker LW. Management options in malignant obstruction of the left colon. Surg Gynecol Obstet. 1992;174:337–45.
Crowder VHJ, Cohn IJ. Perforation in cancer of the colon and rectum. Dis Colon rectum. 1967;10:415–20.
McGregor JR, O’Dwyer PJ. The surgical management of obstruction and perforation of the left colon. Surg Gynecol Obstet. 1993;177:203–8.
Kızıltan R, Yılmaz Ö, Aras A, Çelik S, Kotan Ç. Factors affecting mortality in emergency surgery in cases of complicated colorectal cancer. Med Glas. 2016;13:62–7.
Quah H-M, Chou JF, Gonen M, et al. Identification of patients with high-risk stage II colon cancer for adjuvant therapy. Dis Colon rectum. 2008;51:503–7.
Alvarez JA, Baldonedo RF, Bear IG, Truán N, Pire G, Alvarez P. Presentation, treatment, and multivariate analysis of risk factors for obstructive and perforative colorectal carcinoma. Am J Surg. 2005;190:376–82.
Biondo S, Kreisler E, Millan M, et al. Differences in patient postoperative and long-term outcomes between obstructive and perforated colonic cancer. Am J Surg. 2008;195:427–32.
Chen et al. Obstruction and perforation in colorectal adenocarcinoma: an analysis of prognosis and current trends. Surgery. 2000;127:370–6.
Abdelrazeq AS, Scott N, Thorn C, et al. The impact of spontaneous tumour perforation on outcome following colon cancer surgery. Color Dis. 2008;10:775–80.
Teixeira F, Akaishi EH, Ushinohama AZ, et al. Can we respect the principles of oncologic resection in an emergency surgery to treat colon cancer? World J Emerg Surg. 2015;10:5.
Schmoll HJ, Van Cutsem E, Stein A, Valentini V, Glimelius B, Haustermans K, et al. ESMO Consensus Guidelines for management of patients with colon and rectal cancer. a personalized approach to clinical decision making. Ann Oncol Off J Eur Soc Med Oncol. 2012;23:2479–516.
Benson AB 3rd, Venook AP, Bekaii-Saab T, Chan E, Chen Y-J, Cooper HS, et al. Colon cancer, version 3.2014. J Natl Compr Cancer Netw. 2014;12:1028–59.
McArdle CS, Hole DJ. Emergency presentation of colorectal cancer is associated with poor 5-year survival. Br J Surg. 2004;91:605–9.
Banaszkiewicz Z, Woda L, Tojek K, Jarmocik P, Jawien A. Colorectal cancer with intestinal perforation—a retrospective analysis of treatment outcomes. Contemp Oncol (Poznan, Poland). 2014;18:414–8.
Ho YH, Siu SKK, Buttner P, Stevenson A, Lumley J, Stitz R. The effect of obstruction and perforation on colorectal cancer disease-free survival. World J Surg. 2010;34:1091–101.
Edge SB, Compton CC. The American Joint Committee on Cancer: the 7th edition of the AJCC cancer staging manual and the future of TNM. Ann Surg Oncol. 2010;17:1471–4.
Carraro PG, Segala M, Orlotti C, Tiberio G. Outcome of large-bowel perforation in patients with colorectal cancer. Dis Colon rectum. 1998;41:1421–6.
Mandava N, Kumar S, Pizzi WF, Aprile IJ. Perforated colorectal carcinomas. Am J Surg. 1996;172:236–8.
Cuffy M, Abir F, Audisio RA, Longo WE. Colorectal cancer presenting as surgical emergencies. Surg Oncol. 2004;13:149–57.
Runkel NS, Hinz U, Lehnert T, Buhr HJ, Herfarth C. Improved outcome after emergency surgery for cancer of the large intestine. Br J Surg. 1998;85:1260–5.
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The datasets used and analyzed during the current study are available from the corresponding authors on reasonable request.
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Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation: IRB 105–134-B
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Chen, T., Huang, Y. & Wang, G. Outcome of colon cancer initially presenting as colon perforation and obstruction. World J Surg Onc 15, 164 (2017). https://doi.org/10.1186/s12957-017-1228-y
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