Background. Release and circulation of tumor DNA could be favored by surger
y. No data is available for the effect of laparoscopy on this phenomenon. M
aterial and Methods: The aim of this study was to assess the impact of CO2
laparoscopy on circulating tumor DNA. Two xenografts of ovarian cancer were
obtained by intraperitoneal inoculation (IP) of IGR - OV1 or NIH: OVCAR-3
cells in nude rats. CO2 laparoscopy (L), gasless laparoscopy (GL), midline
laparotomy (ML) or general anesthesia as a control (C) were randomly carrie
d out when the tumor graft was present in the peritoneal cavity. A sterile
blood sample was taken in each case as soon as the experiment was completed
. DNA was subsequently extracted and amplified (PCR, primers HLA GH 26 and
HLA GH 27 specific for human DNA). In each model, we compared the influence
of each surgical approach on circulating tumor DNA. Statistics were perfor
med with the Wilcoxon test and Fisher exact test. 1: Results: Eighteen rats
were included in each group. Our protocol could detect an amount of tumor
DNA equivalent to 10 cells / ml of blood. This technique was specific. Circ
ulating tumor DNA was frequently observed in the IGR-OVl model (45 to 50 %)
, without significant difference between groups (p=0.6). In the NIH:OVCAR-3
model, the detection rate ranged froth 22 % (control group) to 64 % (gasle
ss group); but the overall comparison between the four groups was not signi
ficant (p = 0.2). Conclusion: In this experimental trial, CO2 laparoscopy h
ad no deleterious effect on circulating tumor DNA. Biologic characteristics
of tumors could also play a role.