Utility of Cell-free Tumour DNA for Post-surgical Follow-up of Colorectal Cancer Patients
While efficient surgical treatment is the key to prolonged survival of patients with colorectal cancer, post-surgical follow-up is important for the early detection of relapsing disease or of disease progression. Current dispensarization, typically based on imaging CT, PET, MR, is frequently support...
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Veröffentlicht in: | Anticancer research 2012-05, Vol.32 (5), p.1621-1626 |
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creator | LEVY, Miroslav BENESOVA, Lucie LIPSKA, Ludmila BELSANOVA, Barbora MINARIKOVA, Petra VEPREKOVA, Gabriela ZAVORAL, Miroslav MINARIK, Marek |
description | While efficient surgical treatment is the key to prolonged survival of patients with colorectal cancer, post-surgical follow-up is important for the early detection of relapsing disease or of disease progression. Current dispensarization, typically based on imaging CT, PET, MR, is frequently supported by the observation of tumour markers (CEA, CA19-9). Due to their limited sensitivity and selectivity, better tools for monitoring of the disease are desirable. Tumour cell-free DNA (cfDNA) has been recently demonstrated as a new promising molecular marker for observation and early detection of disease progression.
We present results of post-surgical monitoring tumour cfDNA in the cases of seven patients suffering from advanced forms of CRC. We applied a mutation-based approach in which the total cfDNA was screened for a specific somatic mutation present in the primary tumour. We screened a panel of the most frequent somatic mutations covering the genes APC, KRAS, TP53, PIK3CA and BRAF. All patients were tested positive for tumour cfDNA prior to surgery. cfDNA was then evaluated within a week after surgery and subsequently in monthly intervals.
We present typical cases of colorectal cancer patients who underwent surgical treatment at different levels of radicality with or without adjuvant chemo/biotherapy. The tumour cfDNA status was found to be always closely correlated with the actual clinical status of the patient.
The cfDNA appears to be a viable tool for the monitoring of the clinical progression of CRC in patients with cfDNA positivity prior to surgery. |
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We present results of post-surgical monitoring tumour cfDNA in the cases of seven patients suffering from advanced forms of CRC. We applied a mutation-based approach in which the total cfDNA was screened for a specific somatic mutation present in the primary tumour. We screened a panel of the most frequent somatic mutations covering the genes APC, KRAS, TP53, PIK3CA and BRAF. All patients were tested positive for tumour cfDNA prior to surgery. cfDNA was then evaluated within a week after surgery and subsequently in monthly intervals.
We present typical cases of colorectal cancer patients who underwent surgical treatment at different levels of radicality with or without adjuvant chemo/biotherapy. The tumour cfDNA status was found to be always closely correlated with the actual clinical status of the patient.
The cfDNA appears to be a viable tool for the monitoring of the clinical progression of CRC in patients with cfDNA positivity prior to surgery.</description><identifier>ISSN: 0250-7005</identifier><identifier>EISSN: 1791-7530</identifier><identifier>PMID: 22593440</identifier><language>eng</language><publisher>Attiki: International Institute of Anticancer Research</publisher><subject>adenomatous polyposis coli ; Adjuvants ; Aged ; Biological and medical sciences ; CA-19-9 Antigen - blood ; Carcinoembryonic antigen ; Carcinoembryonic Antigen - blood ; Colorectal cancer ; Colorectal Neoplasms - blood ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - surgery ; Computed tomography ; Disease Progression ; DNA ; DNA, Neoplasm - blood ; Female ; Follow-Up Studies ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; K-Ras protein ; Male ; Medical sciences ; Middle Aged ; Mutation ; p53 protein ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Surgery ; Tomography, X-Ray Computed ; Tumors</subject><ispartof>Anticancer research, 2012-05, Vol.32 (5), p.1621-1626</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25927734$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22593440$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LEVY, Miroslav</creatorcontrib><creatorcontrib>BENESOVA, Lucie</creatorcontrib><creatorcontrib>LIPSKA, Ludmila</creatorcontrib><creatorcontrib>BELSANOVA, Barbora</creatorcontrib><creatorcontrib>MINARIKOVA, Petra</creatorcontrib><creatorcontrib>VEPREKOVA, Gabriela</creatorcontrib><creatorcontrib>ZAVORAL, Miroslav</creatorcontrib><creatorcontrib>MINARIK, Marek</creatorcontrib><title>Utility of Cell-free Tumour DNA for Post-surgical Follow-up of Colorectal Cancer Patients</title><title>Anticancer research</title><addtitle>Anticancer Res</addtitle><description>While efficient surgical treatment is the key to prolonged survival of patients with colorectal cancer, post-surgical follow-up is important for the early detection of relapsing disease or of disease progression. Current dispensarization, typically based on imaging CT, PET, MR, is frequently supported by the observation of tumour markers (CEA, CA19-9). Due to their limited sensitivity and selectivity, better tools for monitoring of the disease are desirable. Tumour cell-free DNA (cfDNA) has been recently demonstrated as a new promising molecular marker for observation and early detection of disease progression.
We present results of post-surgical monitoring tumour cfDNA in the cases of seven patients suffering from advanced forms of CRC. We applied a mutation-based approach in which the total cfDNA was screened for a specific somatic mutation present in the primary tumour. We screened a panel of the most frequent somatic mutations covering the genes APC, KRAS, TP53, PIK3CA and BRAF. All patients were tested positive for tumour cfDNA prior to surgery. cfDNA was then evaluated within a week after surgery and subsequently in monthly intervals.
We present typical cases of colorectal cancer patients who underwent surgical treatment at different levels of radicality with or without adjuvant chemo/biotherapy. The tumour cfDNA status was found to be always closely correlated with the actual clinical status of the patient.
The cfDNA appears to be a viable tool for the monitoring of the clinical progression of CRC in patients with cfDNA positivity prior to surgery.</description><subject>adenomatous polyposis coli</subject><subject>Adjuvants</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>CA-19-9 Antigen - blood</subject><subject>Carcinoembryonic antigen</subject><subject>Carcinoembryonic Antigen - blood</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - blood</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - surgery</subject><subject>Computed tomography</subject><subject>Disease Progression</subject><subject>DNA</subject><subject>DNA, Neoplasm - blood</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>K-Ras protein</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>p53 protein</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Surgery</subject><subject>Tomography, X-Ray Computed</subject><subject>Tumors</subject><issn>0250-7005</issn><issn>1791-7530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0M9LwzAUB_AgipvTf0F6EbwE8rNpj6O6KQz1sB08lbR9kUq61CRF9t8bdOLV04PH5z34fk_QnKqSYiU5OUVzwiTBihA5QxchvBOS52XBz9GMMVlyIcgcve5ib_t4yJzJKrAWGw-QbafBTT67e1pmxvnsxYWIw-Tf-lbbbOWsdZ94Gr9vnHUe2pj2ld63kLCOPexjuERnRtsAV8e5QLvV_bZ6wJvn9WO13OCRKRFx13BBy0YL2hFBRa4LTVgOYESnGFOm0I1QhglmpARNDdcMGtMyCtyUpVF8gW5__o7efUwQYj30oU1R9B7cFGpKmMhzQov_UCpJKkaJRK-PdGoG6OrR94P2h_q3uQRujkCH1IrxKX0f_pwsmVJc8C8raHcB</recordid><startdate>20120501</startdate><enddate>20120501</enddate><creator>LEVY, Miroslav</creator><creator>BENESOVA, Lucie</creator><creator>LIPSKA, Ludmila</creator><creator>BELSANOVA, Barbora</creator><creator>MINARIKOVA, Petra</creator><creator>VEPREKOVA, Gabriela</creator><creator>ZAVORAL, Miroslav</creator><creator>MINARIK, Marek</creator><general>International Institute of Anticancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7TM</scope></search><sort><creationdate>20120501</creationdate><title>Utility of Cell-free Tumour DNA for Post-surgical Follow-up of Colorectal Cancer Patients</title><author>LEVY, Miroslav ; BENESOVA, Lucie ; LIPSKA, Ludmila ; BELSANOVA, Barbora ; MINARIKOVA, Petra ; VEPREKOVA, Gabriela ; ZAVORAL, Miroslav ; MINARIK, Marek</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p274t-db3419ba41d04146a8a026eef4d7227f8ab47f242f55ea1f3a2ebfc21e3f99f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>adenomatous polyposis coli</topic><topic>Adjuvants</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>CA-19-9 Antigen - blood</topic><topic>Carcinoembryonic antigen</topic><topic>Carcinoembryonic Antigen - blood</topic><topic>Colorectal cancer</topic><topic>Colorectal Neoplasms - blood</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - surgery</topic><topic>Computed tomography</topic><topic>Disease Progression</topic><topic>DNA</topic><topic>DNA, Neoplasm - blood</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>K-Ras protein</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>p53 protein</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Surgery</topic><topic>Tomography, X-Ray Computed</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LEVY, Miroslav</creatorcontrib><creatorcontrib>BENESOVA, Lucie</creatorcontrib><creatorcontrib>LIPSKA, Ludmila</creatorcontrib><creatorcontrib>BELSANOVA, Barbora</creatorcontrib><creatorcontrib>MINARIKOVA, Petra</creatorcontrib><creatorcontrib>VEPREKOVA, Gabriela</creatorcontrib><creatorcontrib>ZAVORAL, Miroslav</creatorcontrib><creatorcontrib>MINARIK, Marek</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><jtitle>Anticancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LEVY, Miroslav</au><au>BENESOVA, Lucie</au><au>LIPSKA, Ludmila</au><au>BELSANOVA, Barbora</au><au>MINARIKOVA, Petra</au><au>VEPREKOVA, Gabriela</au><au>ZAVORAL, Miroslav</au><au>MINARIK, Marek</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Utility of Cell-free Tumour DNA for Post-surgical Follow-up of Colorectal Cancer Patients</atitle><jtitle>Anticancer research</jtitle><addtitle>Anticancer Res</addtitle><date>2012-05-01</date><risdate>2012</risdate><volume>32</volume><issue>5</issue><spage>1621</spage><epage>1626</epage><pages>1621-1626</pages><issn>0250-7005</issn><eissn>1791-7530</eissn><abstract>While efficient surgical treatment is the key to prolonged survival of patients with colorectal cancer, post-surgical follow-up is important for the early detection of relapsing disease or of disease progression. Current dispensarization, typically based on imaging CT, PET, MR, is frequently supported by the observation of tumour markers (CEA, CA19-9). Due to their limited sensitivity and selectivity, better tools for monitoring of the disease are desirable. Tumour cell-free DNA (cfDNA) has been recently demonstrated as a new promising molecular marker for observation and early detection of disease progression.
We present results of post-surgical monitoring tumour cfDNA in the cases of seven patients suffering from advanced forms of CRC. We applied a mutation-based approach in which the total cfDNA was screened for a specific somatic mutation present in the primary tumour. We screened a panel of the most frequent somatic mutations covering the genes APC, KRAS, TP53, PIK3CA and BRAF. All patients were tested positive for tumour cfDNA prior to surgery. cfDNA was then evaluated within a week after surgery and subsequently in monthly intervals.
We present typical cases of colorectal cancer patients who underwent surgical treatment at different levels of radicality with or without adjuvant chemo/biotherapy. The tumour cfDNA status was found to be always closely correlated with the actual clinical status of the patient.
The cfDNA appears to be a viable tool for the monitoring of the clinical progression of CRC in patients with cfDNA positivity prior to surgery.</abstract><cop>Attiki</cop><pub>International Institute of Anticancer Research</pub><pmid>22593440</pmid><tpages>6</tpages></addata></record> |
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subjects | adenomatous polyposis coli Adjuvants Aged Biological and medical sciences CA-19-9 Antigen - blood Carcinoembryonic antigen Carcinoembryonic Antigen - blood Colorectal cancer Colorectal Neoplasms - blood Colorectal Neoplasms - genetics Colorectal Neoplasms - surgery Computed tomography Disease Progression DNA DNA, Neoplasm - blood Female Follow-Up Studies Gastroenterology. Liver. Pancreas. Abdomen Humans K-Ras protein Male Medical sciences Middle Aged Mutation p53 protein Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Surgery Tomography, X-Ray Computed Tumors |
title | Utility of Cell-free Tumour DNA for Post-surgical Follow-up of Colorectal Cancer Patients |
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