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Water: A Simple Solution for Tumor Spillage

  • Translational Research and Biomarkers
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Abstract

Background

Although often proposed as a means to reduce the harmful consequences of tumor spill, water lavage has yet to be systematically evaluated in relevant in vitro and in vivo models. This study evaluates the mechanisms and utility of a single water lavage to improve the sequelae of tumor spill during laparotomy.

Methods

Murine colorectal tumor cell susceptibility to water-induced osmotic lysis was characterized in vitro. A reproducible model of tumor spill was established to recapitulate water or saline lavage during laparotomy. Analyses of tumor volumes calculated from noninvasive imaging were performed. The tumor volumes and survival of mice treated with water, normal saline, or sham laparotomy were assessed.

Results

Significant osmotic lysis of cultured murine colorectal cancer cells was observed after a brief exposure to water. Compared to saline or sham laparotomy, water lavage demonstrated superior clinical outcomes with a decrease in tumor burden and concomitant improvement in survival.

Conclusions

The use of water lavage during oncologic surgeries to reduce the sequelae of tumor spill is justified and strongly supported by our study. Data from our study raise several concerns regarding the mechanisms and efficacy of saline lavage. Clinically, the use of water lavage during laparotomy would be anticipated to reduce peritoneal disease burden with minimal toxicity or cost.

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References

  1. BookRags Biographies. http://www.bookrags.com/biography/anton-van-leeuwenhoek/.

  2. Lin CH, Hsieh HF, Yu JC, et al. Peritoneal lavage with distilled water during liver resection in patients with spontaneously ruptured hepatocellular carcinomas. J Surg Oncol. 2006;94:255–6.

    Article  PubMed  Google Scholar 

  3. Whiteside OJ, Tytherleigh MG, Thrush S, et al. Intra-operative peritoneal lavage—who does it and why? Ann R Coll Surg Engl. 2005;87:255–8.

    Article  PubMed  CAS  Google Scholar 

  4. Huguet EL, Keeling NJ. Distilled water peritoneal lavage after colorectal cancer surgery. Dis Colon Rectum. 2004;47:2114–9.

    Article  PubMed  Google Scholar 

  5. Morris PC, Scholten V. Osmotic lysis of tumor spill in ovarian cancer: a murine model. Am J Obstet Gynecol. 1996;175:1489–92.

    Article  PubMed  CAS  Google Scholar 

  6. Koppe MJ, Boerman OC, Oyen WJ, Bleichrodt RP. Peritoneal carcinomatosis of colorectal origin: incidence and current treatment strategies. Ann Surg. 2006;243:212–22.

    Article  PubMed  Google Scholar 

  7. Guller U, Zajac P, Schnider A, et al. Disseminated single tumor cells as detected by real-time quantitative polymerase chain reaction represent a prognostic factor in patients undergoing surgery for colorectal cancer. Ann Surg. 2002;236:768–75.

    Article  PubMed  Google Scholar 

  8. Oosterling SJ, van der Bij GJ, van Egmond M, van der Sijp JR. Surgical trauma and peritoneal recurrence of colorectal carcinoma. Eur J Surg Oncol. 2005;31:29–37.

    Article  PubMed  CAS  Google Scholar 

  9. Raa ST, Oosterling SJ, van der Kaaij NP, et al. Surgery promotes implantation of disseminated tumor cells, but does not increase growth of tumor cell clusters. J Surg Oncol. 2005;92:124–9.

    Article  PubMed  Google Scholar 

  10. Yamamoto S, Akasu T, Fujita S, Moriya Y. Long-term prognostic value of conventional peritoneal cytology after curative resection for colorectal carcinoma. Jpn J Clin Oncol. 2003;33:33–7.

    Article  PubMed  Google Scholar 

  11. Kanellos I, Demetriades H, Zintzaras E, et al. Incidence and prognostic value of positive peritoneal cytology in colorectal cancer. Dis Colon Rectum. 2003;46:535–9.

    Article  PubMed  CAS  Google Scholar 

  12. Wind P, Norklinger B, Roger V, et al. Long-term prognostic value of positive peritoneal washing in colon cancer. Scand J Gastroenterol. 1999;34:606–10.

    Article  PubMed  CAS  Google Scholar 

  13. Jayne DG, Fook S, Loi C, Seow-Choen F. Peritoneal carcinomatosis from colorectal cancer. Br J Surg. 2002;89:1545–50.

    Article  PubMed  CAS  Google Scholar 

  14. Altekruse SF, Kosary CL, Krapcho M, Neyman N, et al (eds). SEER cancer statistics review, 1975–2007. Bethesda, MD: National Cancer Institute; 2010.

  15. Park KG, Chetty U, Scott W, Miller W. The activity of locally applied cytotoxics to breast cancer cells in vitro. Ann R Coll Surg Engl. 1991;73:96–9.

    PubMed  CAS  Google Scholar 

  16. Pattana-arun J, Wolff BG. Benefits of povidone-iodine solution in colorectal operations: science or legend. Dis Colon Rectum. 2008;51:966–71.

    Article  PubMed  Google Scholar 

  17. Basha G, Ghirardi M, Geboes K, et al. Limitations of peritoneal lavage with antiseptics in prevention of recurrent colorectal cancer caused by tumor-cell seeding: experimental study in rats. Dis Colon Rectum. 2000;43:1713–8.

    Article  PubMed  CAS  Google Scholar 

  18. Basha G, Penninckx F, Yap P. Influence of blood components and faeces on the in vitro cancericidal activity of povidone-iodine. Br J Surg. 1998;85:534–7.

    Article  PubMed  CAS  Google Scholar 

  19. Stuntz M, Wilmoth G, Ong J, et al. Use of intraperitoneal 5-fluorouracil and chlorhexidine for prevention of recurrence of perforated colorectal carcinoma in a rat model. Dis Colon Rectum. 1997;40:1085–8.

    Article  PubMed  CAS  Google Scholar 

  20. Brundell S, Tucker K, Chatterton B, Hewett P. Influence of lavage timing on tumor cell burden during colonic resection. Dis Colon Rectum. 2003;46:460–6.

    Article  PubMed  Google Scholar 

  21. Brundell SM, Tucker K, Chatterton B, Hewett PJ. The effect of lavage on intraabdominal cell burden. Surg Endosc. 2002;16:1064–7.

    Article  PubMed  CAS  Google Scholar 

  22. Fermor B, Umpleby HC, Lever JV, et al. Proliferative and metastatic potential of exfoliated colorectal cancer cells. J Natl Cancer Inst. 1986;76:347–9.

    PubMed  CAS  Google Scholar 

  23. van der Bij GJ, Oosterling SJ, Beelen RH, et al. The perioperative period is an underutilized window of therapeutic opportunity in patients with colorectal cancer. Ann Surg. 2009;249:727–34.

    Article  PubMed  Google Scholar 

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Acknowledgment

The authors would like to thank Ree Dolnick, Daniel Fisher, and Jason Muhitch for their outstanding technical assistance. Supported by the U.S. National Institutes of Health (CA16056 to Roswell Park Cancer Institute).

Conflict of interest

The authors report no commercial interests or conflicts of interest regarding the contents of this manuscript.

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Correspondence to Joseph J. Skitzki MD.

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Ito, F., Camoriano, M., Seshadri, M. et al. Water: A Simple Solution for Tumor Spillage. Ann Surg Oncol 18, 2357–2363 (2011). https://doi.org/10.1245/s10434-011-1588-4

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  • DOI: https://doi.org/10.1245/s10434-011-1588-4

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