Laparoscopic-assisted vs. open colectomy for colorectal cancer: influence on neoplastic cell mobilization
Laparoscopic surgery for treatment of colorectal cancer has been suggested to enhance tumor dissemination. Recently, molecular techniques have been developed to detect micrometastatic disease in patients with solid tumors, with a higher accuracy than cytologic or immunohistochemical approaches. This...
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creator | Bessa, Xavier Castells, Antoni Lacy, Antonio M. Elizalde, J.Ignasi Delgado, Salvadora Boix, Loreto Piñol, Virgínia Pellisé, Maria García-Valdecasas, Juan C. Piqué, Josep M. |
description | Laparoscopic surgery for treatment of colorectal cancer has been suggested to enhance tumor dissemination. Recently, molecular techniques have been developed to detect micrometastatic disease in patients with solid tumors, with a higher accuracy than cytologic or immunohistochemical approaches. This study was undertaken to investigate the potential harmful effects of laparoscopic-assisted colectomy on neoplastic cell mobilization in patients with resectable colorectal cancer. Fifty patients with nonmetastatic colorectal cancer were randomly assigned to laparoscopic-assisted (LAC, n = 26) or open (OC, n = 24) colectomy. Peripheral venous blood samples were obtained preoperatively, immediately after tumor removal, and 24 hours later. In 10 patients from each treatment group, portal blood and peritoneal fluid samples were also obtained before and after resection. Neoplastic cells were detected by means of reverse transcriptase-polymerase chain reaction targeted to carcinoembryonic antigen (CEA) transcription. CEA mRNA was detected in peripheral venous blood samples from 35 of 50 colorectal cancer patients preoperatively. Among those 15 baseline-negative patients, four experienced conversion 24 hours after tumor resection (2 [33%] of 6 in the LAC group vs. 2 [22%] of 9 in the OC group; NS). At that time point, clearance of CEA mRNA expression was observed in 14 of the 35 baseline-positive patients (9 [45%] of 20 in the LAC group vs. 5 [33%] of 15 in the OC group; NS). In addition, only one patient in the LAC group with baseline-negative CEA mRNA expression experienced portal blood conversion after tumor removal, although his peripheral blood level remained negative. Finally, baseline peritoneal fluid CEA mRNA expression was never detected, but one patient in each group became positive postoperatively. These results confirm that preoperative and perioperative mobilization of neoplastic cells is a frequent occurrence in patients with colorectal cancer, but the surgical approach (LAC vs. OC) does not seem to be a determining factor. |
doi_str_mv | 10.1016/S1091-255X(01)80015-9 |
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Recently, molecular techniques have been developed to detect micrometastatic disease in patients with solid tumors, with a higher accuracy than cytologic or immunohistochemical approaches. This study was undertaken to investigate the potential harmful effects of laparoscopic-assisted colectomy on neoplastic cell mobilization in patients with resectable colorectal cancer. Fifty patients with nonmetastatic colorectal cancer were randomly assigned to laparoscopic-assisted (LAC, n = 26) or open (OC, n = 24) colectomy. Peripheral venous blood samples were obtained preoperatively, immediately after tumor removal, and 24 hours later. In 10 patients from each treatment group, portal blood and peritoneal fluid samples were also obtained before and after resection. Neoplastic cells were detected by means of reverse transcriptase-polymerase chain reaction targeted to carcinoembryonic antigen (CEA) transcription. CEA mRNA was detected in peripheral venous blood samples from 35 of 50 colorectal cancer patients preoperatively. Among those 15 baseline-negative patients, four experienced conversion 24 hours after tumor resection (2 [33%] of 6 in the LAC group vs. 2 [22%] of 9 in the OC group; NS). At that time point, clearance of CEA mRNA expression was observed in 14 of the 35 baseline-positive patients (9 [45%] of 20 in the LAC group vs. 5 [33%] of 15 in the OC group; NS). In addition, only one patient in the LAC group with baseline-negative CEA mRNA expression experienced portal blood conversion after tumor removal, although his peripheral blood level remained negative. Finally, baseline peritoneal fluid CEA mRNA expression was never detected, but one patient in each group became positive postoperatively. These results confirm that preoperative and perioperative mobilization of neoplastic cells is a frequent occurrence in patients with colorectal cancer, but the surgical approach (LAC vs. OC) does not seem to be a determining factor.</description><identifier>ISSN: 1091-255X</identifier><identifier>EISSN: 1873-4626</identifier><identifier>DOI: 10.1016/S1091-255X(01)80015-9</identifier><identifier>PMID: 11309650</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Ascitic Fluid - cytology ; Biomarkers, Tumor - blood ; Biomarkers, Tumor - genetics ; carcinoembryonic antigen ; Carcinoembryonic Antigen - blood ; Carcinoembryonic Antigen - genetics ; circulating neoplastic cells ; Colectomy - adverse effects ; Colectomy - methods ; Colonoscopy - adverse effects ; Colonoscopy - methods ; Colorectal cancer ; Colorectal Neoplasms - surgery ; Female ; Gene Expression Regulation, Neoplastic - genetics ; Humans ; Laparoscopic colectomy ; Laparoscopy - adverse effects ; Laparoscopy - methods ; Male ; Medical research ; Middle Aged ; Neoplasm Seeding ; Pilot Projects ; Proctoscopy - adverse effects ; Proctoscopy - methods ; RNA, Messenger - analysis ; RNA, Neoplasm - analysis ; Time Factors ; Transcription, Genetic - genetics</subject><ispartof>Journal of gastrointestinal surgery, 2001-01, Vol.5 (1), p.66-73</ispartof><rights>2001</rights><rights>The Society for Surgery of the Alimentary Tract, Inc. 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-58207db97f32a09059749e6b0682d68ac7697d3aba0d83c5dc5f0c7fd5d02f633</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11309650$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bessa, Xavier</creatorcontrib><creatorcontrib>Castells, Antoni</creatorcontrib><creatorcontrib>Lacy, Antonio M.</creatorcontrib><creatorcontrib>Elizalde, J.Ignasi</creatorcontrib><creatorcontrib>Delgado, Salvadora</creatorcontrib><creatorcontrib>Boix, Loreto</creatorcontrib><creatorcontrib>Piñol, Virgínia</creatorcontrib><creatorcontrib>Pellisé, Maria</creatorcontrib><creatorcontrib>García-Valdecasas, Juan C.</creatorcontrib><creatorcontrib>Piqué, Josep M.</creatorcontrib><title>Laparoscopic-assisted vs. open colectomy for colorectal cancer: influence on neoplastic cell mobilization</title><title>Journal of gastrointestinal surgery</title><addtitle>J Gastrointest Surg</addtitle><description>Laparoscopic surgery for treatment of colorectal cancer has been suggested to enhance tumor dissemination. Recently, molecular techniques have been developed to detect micrometastatic disease in patients with solid tumors, with a higher accuracy than cytologic or immunohistochemical approaches. This study was undertaken to investigate the potential harmful effects of laparoscopic-assisted colectomy on neoplastic cell mobilization in patients with resectable colorectal cancer. Fifty patients with nonmetastatic colorectal cancer were randomly assigned to laparoscopic-assisted (LAC, n = 26) or open (OC, n = 24) colectomy. Peripheral venous blood samples were obtained preoperatively, immediately after tumor removal, and 24 hours later. In 10 patients from each treatment group, portal blood and peritoneal fluid samples were also obtained before and after resection. Neoplastic cells were detected by means of reverse transcriptase-polymerase chain reaction targeted to carcinoembryonic antigen (CEA) transcription. CEA mRNA was detected in peripheral venous blood samples from 35 of 50 colorectal cancer patients preoperatively. Among those 15 baseline-negative patients, four experienced conversion 24 hours after tumor resection (2 [33%] of 6 in the LAC group vs. 2 [22%] of 9 in the OC group; NS). At that time point, clearance of CEA mRNA expression was observed in 14 of the 35 baseline-positive patients (9 [45%] of 20 in the LAC group vs. 5 [33%] of 15 in the OC group; NS). In addition, only one patient in the LAC group with baseline-negative CEA mRNA expression experienced portal blood conversion after tumor removal, although his peripheral blood level remained negative. Finally, baseline peritoneal fluid CEA mRNA expression was never detected, but one patient in each group became positive postoperatively. These results confirm that preoperative and perioperative mobilization of neoplastic cells is a frequent occurrence in patients with colorectal cancer, but the surgical approach (LAC vs. OC) does not seem to be a determining factor.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Ascitic Fluid - cytology</subject><subject>Biomarkers, Tumor - blood</subject><subject>Biomarkers, Tumor - genetics</subject><subject>carcinoembryonic antigen</subject><subject>Carcinoembryonic Antigen - blood</subject><subject>Carcinoembryonic Antigen - genetics</subject><subject>circulating neoplastic cells</subject><subject>Colectomy - adverse effects</subject><subject>Colectomy - methods</subject><subject>Colonoscopy - adverse effects</subject><subject>Colonoscopy - methods</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - surgery</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic - genetics</subject><subject>Humans</subject><subject>Laparoscopic colectomy</subject><subject>Laparoscopy - adverse effects</subject><subject>Laparoscopy - methods</subject><subject>Male</subject><subject>Medical research</subject><subject>Middle Aged</subject><subject>Neoplasm Seeding</subject><subject>Pilot Projects</subject><subject>Proctoscopy - adverse effects</subject><subject>Proctoscopy - methods</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Neoplasm - analysis</subject><subject>Time Factors</subject><subject>Transcription, Genetic - genetics</subject><issn>1091-255X</issn><issn>1873-4626</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqFkV1rFTEQhoNYbK3-BCUgiF5sndmcfHkjUvyCA72ognchm2QhZXezJruF9teb7TkieONVZuCZycszhLxAuEBA8e4aQWPTcv7zDeBbBYC80Y_IGSrJmp1oxeNa_0FOydNSbiojAdUTcorIQAsOZyTu7WxzKi7N0TW2lFiW4OltuaBpDhN1aQhuSeMd7VPeupRrbwfq7ORCfk_j1A9rqDVNE51CmgdbluioC8NAx9TFId7bJabpGTnp7VDC8-N7Tn58_vT98muzv_ry7fLjvnFM49Jw1YL0nZY9ay1o4FrudBAdCNV6oayTQkvPbGfBK-a4d7wHJ3vPPbS9YOycvD7snXP6tYaymDGWLY2t6dZipASuBJMVfPUPeJPWPNVsBhFbJnetwkrxA-WqpZJDb-YcR5vvDILZLmEeLmE2zQbQPFzC6Dr38rh97cbg_04d1VfgwwEIVcZtDNkUFzeRPm6KjU_xP1_8BrcKmWk</recordid><startdate>20010101</startdate><enddate>20010101</enddate><creator>Bessa, Xavier</creator><creator>Castells, Antoni</creator><creator>Lacy, Antonio M.</creator><creator>Elizalde, J.Ignasi</creator><creator>Delgado, Salvadora</creator><creator>Boix, Loreto</creator><creator>Piñol, Virgínia</creator><creator>Pellisé, Maria</creator><creator>García-Valdecasas, Juan C.</creator><creator>Piqué, Josep M.</creator><general>Elsevier Inc</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20010101</creationdate><title>Laparoscopic-assisted vs. open colectomy for colorectal cancer: influence on neoplastic cell mobilization</title><author>Bessa, Xavier ; 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Recently, molecular techniques have been developed to detect micrometastatic disease in patients with solid tumors, with a higher accuracy than cytologic or immunohistochemical approaches. This study was undertaken to investigate the potential harmful effects of laparoscopic-assisted colectomy on neoplastic cell mobilization in patients with resectable colorectal cancer. Fifty patients with nonmetastatic colorectal cancer were randomly assigned to laparoscopic-assisted (LAC, n = 26) or open (OC, n = 24) colectomy. Peripheral venous blood samples were obtained preoperatively, immediately after tumor removal, and 24 hours later. In 10 patients from each treatment group, portal blood and peritoneal fluid samples were also obtained before and after resection. Neoplastic cells were detected by means of reverse transcriptase-polymerase chain reaction targeted to carcinoembryonic antigen (CEA) transcription. CEA mRNA was detected in peripheral venous blood samples from 35 of 50 colorectal cancer patients preoperatively. Among those 15 baseline-negative patients, four experienced conversion 24 hours after tumor resection (2 [33%] of 6 in the LAC group vs. 2 [22%] of 9 in the OC group; NS). At that time point, clearance of CEA mRNA expression was observed in 14 of the 35 baseline-positive patients (9 [45%] of 20 in the LAC group vs. 5 [33%] of 15 in the OC group; NS). In addition, only one patient in the LAC group with baseline-negative CEA mRNA expression experienced portal blood conversion after tumor removal, although his peripheral blood level remained negative. Finally, baseline peritoneal fluid CEA mRNA expression was never detected, but one patient in each group became positive postoperatively. These results confirm that preoperative and perioperative mobilization of neoplastic cells is a frequent occurrence in patients with colorectal cancer, but the surgical approach (LAC vs. OC) does not seem to be a determining factor.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11309650</pmid><doi>10.1016/S1091-255X(01)80015-9</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Ascitic Fluid - cytology Biomarkers, Tumor - blood Biomarkers, Tumor - genetics carcinoembryonic antigen Carcinoembryonic Antigen - blood Carcinoembryonic Antigen - genetics circulating neoplastic cells Colectomy - adverse effects Colectomy - methods Colonoscopy - adverse effects Colonoscopy - methods Colorectal cancer Colorectal Neoplasms - surgery Female Gene Expression Regulation, Neoplastic - genetics Humans Laparoscopic colectomy Laparoscopy - adverse effects Laparoscopy - methods Male Medical research Middle Aged Neoplasm Seeding Pilot Projects Proctoscopy - adverse effects Proctoscopy - methods RNA, Messenger - analysis RNA, Neoplasm - analysis Time Factors Transcription, Genetic - genetics |
title | Laparoscopic-assisted vs. open colectomy for colorectal cancer: influence on neoplastic cell mobilization |
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