Experimental assessment of the risk of tumor recurrence after laparoscopic surgery
Background: The aim of this experimental study was to evaluate the risk of tumor recurrence after laparoscopic cecal resection (LCR) of colonic carcinoma in the rat. Methods: The experimental cancer consisted of one million cells (DHK/K12), incorporated in an extracellular matrix, placed and secured...
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Published in: | Surgery Vol. 123; no. 4; pp. 427 - 431 |
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Main Authors: | , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
New York, NY
Mosby, Inc
01-04-1998
Elsevier |
Subjects: | |
Online Access: | Get full text |
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Summary: | Background: The aim of this experimental study was to evaluate the risk of tumor recurrence after laparoscopic cecal resection (LCR) of colonic carcinoma in the rat.
Methods: The experimental cancer consisted of one million cells (DHK/K12), incorporated in an extracellular matrix, placed and secured to the cecal serosa in 110 BD9 rats. Four weeks later, all animals were reoperated through a laparotomy to control tumor growth, and animals with diffuse carcinomatosis were excluded. Eligible animals were randomized either to laparoscopic cecal resection (group LCR,
n = 10), to open resection (group OCR,
n = 13), or to a control group without resection (group C,
n = 13). Resection was always considered as macrocopically complete. All animals were killed 4 weeks after the resection to determine the tumor recurrence and quantify carcinomatosis.
Results: We noted diffuse carcinomatosis in 70% of rats in groups C and LCR versus 23% in group OCR (
p = 0.038). For tumors noted as S- (not extending outside the serosa), diffuse carcinomatosis was observed in all animals of group C (3 of 3), in 6 of 8 in group LCR, and 0 of 6 in group OCR (
p = 0.004). The rate of port site or incisional metastases was not significantly different between groups.
Conclusions: These preliminary results demonstrated the deleterious impact of the laparoscopy for resection of large bowel malignancy. LCR increased significantly the incidence of a diffuse carcinomatosis even when performed for locally noninvasive tumors (S-). (Surgery 1998;123:427-31.) |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0039-6060 1532-7361 |
DOI: | 10.1016/S0039-6060(98)70164-3 |