Reduction of peritoneal trauma by using nonsurgical gauze leads to less implantation metastasis of spilled tumor cells

被引:119
作者
van den Tol, RM [1 ]
van Rossen, EME [1 ]
van Eijck, CHJ [1 ]
Bonthuis, F [1 ]
Marquet, RL [1 ]
Jeekel, H [1 ]
机构
[1] Univ Hosp Dijkzigt, Dept Gen Surg, NL-3015 GD Rotterdam, Netherlands
关键词
D O I
10.1097/00000658-199802000-00014
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objectives To evaluate whether infliction of peritoneal trauma would promote tumor cell adherence to damaged peritoneal surfaces; to investigate whether peritoneal damage could promote tumor growth of extraperitoneal tumors; and to evaluate whether the amount of trauma correlated with the degree of tumor cell adherence and local and distant tumor growth. Background Data After potentially curative resection of colorectal carcinoma, the most common site for recurrence is locoregional. We previously demonstrated that surgical trauma induces a cascade of events leading to adhesion formation. The same mechanisms may be responsible for improved tumor cell adherence and growth facilitation in early local recurrence. Methods A reproducible rat model was used in which peritoneal damage was inflicted by standardized rubbing of the peritoneum with surgical gauzes of different texture. In the first experiment, tumor cell adherence and growth at traumatized and nontraumatized peritoneal sites were assessed semiquantitatively 3 weeks after perioperative intra-abdominal injection of CC-531 tumor cells. In the second experiment, the effect of peritoneal trauma on ectopic tumor growth was investigated (CC-531 implanted under the renal capsule). In the final experiment, we evaluated how soon after peritoneal traumatization tumor cell adhesion and growth-promoting factors were active and whether they could be passively transferred to naive nontraumatized abdominal cavities. Results A significant correlation between the amount of peritoneal trauma and the degree of tumor take at damaged peritoneal surfaces was found (p less than or equal to 0.018). Tumor take at remote peritoneal sites not directly traumatized was also significantly higher after severe trauma than after moderate trauma of the peritoneum (p less than or equal to 0.005). In addition, a significant correlation between the degree of peritoneal trauma and the growth of ectopic tumors under the renal capsule was observed (p less than or equal to 0.009). The final experiment demonstrated that within a few hours after infliction of peritoneal trauma, tumor growth-promoting effects could be passively transferred to naive recipients. Conclusions Surgical trauma is an important factor in the promotion of local recurrence. The enhancing effect of trauma is not restricted to the inflicted site but rather has a generalized character. Avoidance of unnecessary surgical trauma by using gentle techniques and materials is therefore indicated.
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页码:242 / 248
页数:7
相关论文
共 30 条
[1]   Laparoscopic surgery in the rat - Beneficial effect on body weight and tumor take [J].
Bouvy, ND ;
Marquet, RL ;
Hamming, JF ;
Jeekel, J ;
Bonjer, HJ .
SURGICAL ENDOSCOPY-ULTRASOUND AND INTERVENTIONAL TECHNIQUES, 1996, 10 (05) :490-494
[2]   PERITONEAL SEEDING FOLLOWING POTENTIALLY CURATIVE RESECTION OF COLONIC-CARCINOMA - IMPLICATIONS FOR ADJUVANT THERAPY [J].
BRODSKY, JT ;
COHEN, AM .
DISEASES OF THE COLON & RECTUM, 1991, 34 (08) :723-727
[3]   BLOOD-TRANSFUSIONS AND PROGNOSIS IN COLORECTAL-CANCER [J].
BUSCH, ORC ;
HOP, WCJ ;
VANPAPENDRECHT, MAWH ;
MARQUET, RL ;
JEEKEL, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (19) :1372-1376
[4]   GASTROINTESTINAL MALIGNANCY - RATIONALE FOR ADJUVANT THERAPY USING EARLY POSTOPERATIVE INTRAPERITONEAL CHEMOTHERAPY [J].
CUNLIFFE, WJ ;
SUGARBAKER, PH .
BRITISH JOURNAL OF SURGERY, 1989, 76 (10) :1082-1090
[5]  
DE JONG KP, 1995, HEPATOLOGY, V22, P1263
[6]  
EGGERMONT AMM, 1988, CANCER DETECT PREV, V12, P421
[7]  
EGGERMONT AMM, 1990, CANCER DETECT PREV, V14, P483
[8]  
EGGERMONT AMM, 1987, SURGERY, V102, P71
[9]  
FERMOR B, 1986, J NATL CANCER I, V76, P347
[10]  
FISHER B, 1967, CANCER, V20, P23, DOI 10.1002/1097-0142(1967)20:1<23::AID-CNCR2820200103>3.0.CO