Abstract
Viable intraluminal tumor cells can penetrate a clinically intact rodent colonic anastomosis and give rise to perianastomotic tumor growth. The aim of this study was to determine whether transanastomotic cell migration can be prevented by fibrin-based tissue sealant. Following distal colonic transection and reanastomosis with 5/0 silk sutures, Fischer F344 rats were randomly allocated to three experimental groups. In Group A, a circumferential ring of tissue sealant was placed around the serosal surface of the anastomosis; in Group B, sealant was limited to 50 percent of the anastomotic circumference; and, in Group C, no sealant was applied. All rats then had 10 5 Mtln 3 carcinoma cells injected into the proximal colonic lumen via a rectal catheter. The incidence of perianastomotic tumor at 21 days was significantly lower in Group A (3 of 14 animals) than in Group B (11 of 16 rats) (P =0.012; Fisher's exact test) or Group C (10 of 14 rats;P=0.011). A further experiment demonstrated that sealant did not protect the anastomosis when tumor cells were instilled directly into the peritoneal cavity. A topical carcinocidal action therefore appears unlikely, but our results suggest that a circumferential anastomotic ring of fibrin sealant forms an effective mechanical barrier preventing intraluminal tumor cells from reaching the peritoneal cavity.
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Gunderson LL, Sosin H. Areas of failure found at reoperation (second or symptomatic look) following “curative surgery” for adenocarcinoma of the rectum. Cancer 1974;34:1278–92.
Cass AW, Million RR, Pfaff WW. Patterns of recurrence following surgery alone for adenocarcinoma of the colon and rectum. Cancer 1976;37:2861–5.
Rao AR, Kagan AR, Chan PM, Gilbert HA, Nussbaum H, Hintz BL. Patterns of recurrence following curative resection alone for adenocarcinoma of the rectum and sigmoid colon. Cancer 1981;48:1492–5.
McDermott FT, Hughes ES, Pihl E, Johnson WR, Price AB. Local recurrence after potentially curative resection for rectal cancer in a series of 1008 patients. Br J Surg 1985;72:34–7.
Umpleby HC, Fermor B, Symes MO, Williamson RC. Viability of exfoliated colorectal cancer cells. Br J Surg 1984;71:659–63.
Umpleby HC, Williamson RC. Anastomotic recurrence in large bowel cancer. Br J Surg 1987;74: 873–8.
O'Dwyer PJ, Martin EW Jr. Viable intraluminal tumour cells and local/regional tumour growth in experimental colon cancer. Ann R Coll Surg Engl 1989;71:54–6.
McGregor JR, Galloway DJ, George WD. Intra-luminal tumour cells and peri-anastomotic tumour growth in experimental colonic surgery. Eur J Surg Oncol 1992;18:368–72.
Leather AJM, Yui CY, Baker LA,et al. Passage of shed intraluminal colorectal cancer cells across a sealed anastomosis (abstr). Br J Surg 1991;78:756.
Lawrance RJ, Loizidou ML, Cooper AJ, Alexander P, Taylor I. Importance of the omentum in the development of intra-abdominal metastases. Br J Surg 1991;78:117–9.
Akyol AM, Galloway DJ, George WD. Experimental study of anastomotic leaks and local tumour growth in the large bowel (abstr). Br J Surg 1991;78:1498.
Akyol AM, McGregor JR, Galloway DJ, Murray GD, George WD. Anastomotic leaks in colorectal cancer surgery: a risk factor for recurrence. Int J Colorectal Dis 1991;6:179–83.
Neri A, Welch D, Kawaguchi T, Nicolson GL. The development and biological properties of malignant cell sublines and clones of a spontaneously metastasising rat mammary carcinoma. J Natl Cancer Inst 1982;68:507–17.
Neri A, Nicolson GL. Phenotypic drift of metastatic and cell surface properties of mammary adenocarcinoma cell clones during growth in vitro. Int J Cancer 1981;28:731–8.
Phillips RK, Hittinger R, Blesovsky L, Fry JS, Fielding LP. Local recurrence following “curative” surgery for large bowel cancer. I. The overall picture. Br J Surg 1984;71:12–6.
Polk HC, Spratt JS. Recurrent colorectal carcinoma: detection, treatment and other considerations. Surgery 1971;69:9–23.
Welch JP, Donaldson GA. Detection and treatment of recurrent cancer of the colon and rectum. Am J Surg 1978;135:505–11.
Stulc JP, Petrelli NJ, Herrera L, Mittelman A. Anastomotic recurrence of adenocarcinoma of the colon. Arch Surg 1986;121:1077–80.
Heald RJ, Husband EM, Ryall RD. The mesorectum in rectal cancer—the clue to pelvic recurrence? Br J Surg 1982;69:613–6.
Heald RJ, Ryall RD. Recurrence and survival after total mesorectal excision for rectal cancer. Lancet 1986;1:1479–82.
Quirke P, Durdey P, Dixon MF, Williams NS. Local recurrence of rectal adenocarcinoma due to inadequate surgical resection. Histopathological study of lateral tumour spread and surgical excision. Lancet 1986;1:996–9.
Yu SK, Cohn I. Tumour implantation on colon mucosa. Arch Surg 1968;96:956–8.
Alexander JW, Altemier WK. Susceptibility of injured tissues to haematogenous metastases: an experimental study. Ann Surg 1964;159:933–44.
Fisher B, Fisher ER, Feduska N. Trauma and localisation of tumour cells. Cancer 1967;20:23–30.
Murphy P, Alexander P, Senior PV, Fleming J, Kirkham N, Taylor I. Mechanisms of organ selective tumour growth by bloodbourne cancer cells. Br J Cancer 1988;57:19–31.
Skipper D, Jeffrey MJ, Cooper AJ, Taylor I, Alexander P. Preferential growth of bloodbourne cancer cells in colonic anastomoses. Br J Cancer 1988;57:564–8.
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Supported by a grant from the Research Support Group of the Greater Glasgow Health Board.
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McGregor, J.R., Reinbach, D.H., Dahill, S.W. et al. Effect of fibrin sealant on perianastomotic tumor growth in an experimental model of colorectal cancer surgery. Dis Colon Rectum 36, 834–839 (1993). https://doi.org/10.1007/BF02047379
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DOI: https://doi.org/10.1007/BF02047379