Abstract
Background
Obstruction (OBSTR) and perforation (PERF) in colorectal cancer impact adversely upon outcomes, and cancer-related survival may also be affected. However, data are sparse, particularly on disease-free survival (DFS) where the cancer is both obstructed and perforated (OBS-PERF).
Methods
Data were extracted from a prospectively collected database of 1876 colorectal cancer patients managed and followed up at the Royal Brisbane Hospital from 1984 to 2004. The patients who had curative surgery (n = 1426) were classified as OBSTR (n = 153), PERF (n = 53), OBS-PERF (n = 19), and uncomplicated (UNCOM; n = 1201). Kaplan-Meier survival and Cox proportional hazard analyses were performed.
Results
Postoperative mortality within 30 days of surgery was 1.5% (n = 22) and the overall complication rate was 40.8% (n = 582). However, only 7.2% (n = 102) required reoperations. The median survival time was 71 (IQR = 64.9–77.1) months and the median follow-up for DFS was 37.5 (IQR 14–68) months. The overall recurrence rate was 32.7% (n = 466), the local recurrence rate was 9.4% (n = 135), and local and distant recurrences occurred in the same patient in 4.7% (n = 67). Male gender, OBSTR, PERF, OBS-PERF, emergency operation, major medical and surgical complications, reoperation, TNM staging, tumor grading, and tumor venous invasion adversely affected DFS (p < 0.05). Multivariate analysis showed that OBS-PERF (p = 0.008), major medical complications (p = 0.011), reoperation (p = 0.018), TNM staging (p < 0.001), grading (p = 0.018), and venous invasion (p = 0.002) were independently associated with a poorer DFS.
Conclusions
OBS-PERF colorectal cancer is associated with a poorer DFS, which may be worse than either OBSTR or PERF alone.
Similar content being viewed by others
References
Australian Institute of Health and Welfare (2006) Cancer in Australia: an overview, 2006. Cat. No. Can 32, Canberra, AIHW
McArdle CS, McMillan DC, Hole DJ (2006) The impact of blood loss, obstruction and perforation on survival in patients undergoing curative resection for colon cancer. Br J Surg 93:483–488
Phillips RK, Hittinger R, Fry JS et al (1985) Malignant large bowel obstruction. Br J Surg 72:296–302
Scott NA, Jeacock J, Kingston RD (1995) Risk factors in patients presenting as an emergency with colorectal cancer. Br J Surg 82:321–323
Carraro PG, Segala M, Cesana BM et al (2001) Obstructing colonic cancer: failure and survival patterns over a ten-year follow-up after one-stage curative surgery. Dis Colon Rectum 44:243–250
Carraro PG, Segala M, Orlotti C et al (1998) Outcome of large-bowel perforation in patients with colorectal cancer. Dis Colon Rectum 41:1421–1426
Chen HS, Sheen-Chen SM (2000) Obstruction and perforation in colorectal adenocarcinoma: an analysis of prognosis and current trends. Surgery 127:370–376
McArdle CS, Hole DJ (2004) Emergency presentation of colorectal cancer is associated with poor 5-year survival. Br J Surg 91:605–609
Jestin P, Nilsson J, Huergren M et al (2005) Emergency surgery for colorectal cancer in a defined population. Br J Surg 92:94–100
Welch J, Donaldson GA (1974) Management of severe obstruction of large bowel due to malignant disease. Am J Surg 127:492–499
Ohman U (1982) Prognosis in patients with obstructing colorectal carcinoma. Am J Surg 143:742–747
Hughes ES (1966) Mortality of large bowel obstruction. Br J Surg 53:593–594
Irvin TT, Greaney MG (1977) Treatment of colonic cancer presenting with intestinal obstruction. Br J Surg 64:741–744
Chapuis PH, Dent OF, Fisher R et al (1985) A multivariate analysis of clinical and pathological variables in prognosis after resection of large bowel cancer. Br J Surg 72:698–702
Crowder VH Jr, Cohn I Jr (1967) Perforation in cancer of the colon and rectum 10:415–420
Staib L, Link KH, Blatx A et al (2002) Surgery of colorectal cancer: surgical morbidity and five- and ten-year results in 2400 patients–monoinstitutional experience. World J Surg 26:59–66
Lee IK, Sung NY, Lee SC et al (2007) The survival rate and prognostic factors in 26 perforated colorectal cancer patients. Int J Colorectal Dis 22:467–473
Wu ZY, Wan J, Zhao G et al (2008) Risk factors for local recurrence of middle and lower rectal carcinoma after curative resection. World J Gastroenterol 14:4805–4809
Link KH, Saghan TA, Morschel M et al (2005) Colon cancer: survival after curative surgery. Langenbecks Arch Surg 390:83–93
Crozier JE, Leitch EF, McKee RF et al (2000) Relationship between emergency presentation, systemic response, and cancer specific survival in patients undergoing potentially curative surgery for colon cancer. Am J Surg 174:544–549
McMillan DC, Wotherspoon HA, Fearon KC et al (1995) Prospective study of tumour recurrence and the acute-phase response after apparently curative colorectal cancer surgery. Am J Surg 170:319–322
McMillan DC, Canna K, McArdle CS (2003) Systemic inflammatory response predicts survival following curative resection of colorectal cancer. Br J Surg 90:215–219
Canna K, McMillan DC, McKee RF et al (2004) Evaluation of a cumulative prognostic score based on systemic inflammatory response based on the systemic inflammatory surgery for colorectal cancer. Br J Cancer 90:1707–1709
Kraemer M, Wiratkapun MD, Seow-Choen F et al (2001) Stratifying risk factors for follow-up: a comparison of recurrent and nonrecurrent colorectal cancer. Dis Colon Rectum 44:815–821
Thomson WH, Foy CJ, Longman RJ (2008) The nature of local recurrence after colorectal cancer recurrence. Colorectal Dis 10:69–74
Hall NR, Finan PJ, Brown S et al (2000) Comparison of prognosis in cancer of the colon and rectum. Colorectal Dis 2:159–164
Mulcahy HE, Skelly MM, Husain A (1996) Long-term outcome following curative surgery for malignant large bowel obstruction. Br J Surg 83:46–50
Diggs JC, Xu F, Diaz M et al (2007) Failure to screen: predictors and burden of emergency colorectal cancer resection. Am J Manag Care 13:157–164
Rabeneck L, Paszzt LF, Li C (2006) Risk factors for obstruction, perforation, or emergency admission at presentation in patients with colorectal cancer: a population-based study. Am J Gastroenterol 101:1098–1103
Kingston RD, Walsh SH, Jeacock J (1993) Physical status is the principal determinant of outcome after emergency admission of patients with colorectal cancer. Ann R Coll Surg Engl 75:335–338
Yancik R, Wesley MN, Ries LA et al (1998) Comorbidity and age as predictors of risk for early mortality of male and female colon carcinoma patients: a population-based study. Cancer 82:2123–2134
Bass G, Fleming C, Conneely J et al (2009) Emergency first presentation of colorectal cancer predicts significantly poorer outcomes: review of 365 consecutive Irish patients. Dis Colon Rectum 52:678–684
Alvarez JA, Baldnedo RF, Bear IG (2005) Presentation, treatment, and multivariate analysis of risk factors for obstructive and perforative colorectal carcinoma. Am J Surg 190:376–382
Bokey EL, Chapuis PH, Fung C et al (1995) Postoperative morbidity and mortality following resection of the colon and rectum for cancer. Dis Colon Rectum 38:480–486
Tentes AA, Mirelis CG, Kakoliris S et al (2009) Results of surgery for colorectal carcinoma with obstruction. Langenbecks Arch Surg 394:46–53
Biondo S, Kreisler E, Millan M et al (2008) Differences in patient postoperative and long-term outcomes between obstructive and perforated cancer. Am J Surg 195:427–432
Kagda FH, Nyam DC, Ho Y-H et al (1999) Surgery may be curative for patients with a localized perforation of rectal carcinoma. Br J Surg 86:1448–1450
Cheynel N, Coetet M, Lepage C (2009) Incidence, patterns of failure, and prognosis of perforated colorectal cancers in a well-defined population. Dis Colon Rectum 52:406–411
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Ho, YH., Siu, S.K.K., Buttner, P. et al. The Effect of Obstruction and Perforation on Colorectal Cancer Disease-Free Survival. World J Surg 34, 1091–1101 (2010). https://doi.org/10.1007/s00268-010-0443-2
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00268-010-0443-2