Impact of primary tumour resection on survival of patients with colorectal cancer and synchronous metastases treated by chemotherapy: Results from the multicenter, randomised trial Fédération Francophone de Cancérologie Digestive 9601
Abstract Objective To assess the impact of primary tumour resection on overall survival (OS) of patients diagnosed with stage IV colorectal cancer (CRC). Design Among the 294 patients with non-resectable colorectal metastases enrolled in the Fédération Francophone de Cancérologie Digestive (FFCD) 96...
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creator | Ferrand, F Malka, D Bourredjem, A Allonier, C Bouché, O Louafi, S Boige, V Mousseau, M Raoul, J.L Bedenne, L Leduc, B Deguiral, P Faron, M Pignon, J.P Ducreux, M |
description | Abstract Objective To assess the impact of primary tumour resection on overall survival (OS) of patients diagnosed with stage IV colorectal cancer (CRC). Design Among the 294 patients with non-resectable colorectal metastases enrolled in the Fédération Francophone de Cancérologie Digestive (FFCD) 9601 phase III trial, which compared different first-line single-agent chemotherapy regimens, 216 patients (73%) presented with synchronous metastases at study entry and constituted the present study population. Potential baseline prognostic variables including prior primary tumour resection were assessed by univariate and multivariate Cox analyses. Progression-free survival (PFS) and OS curves were compared with the logrank test. Results Among the 216 patients with stage IV CRC (median follow-up, 33 months), 156 patients (72%) had undergone resection of their primary tumour prior to study entry. The resection and non-resection groups did not differ for baseline characteristics except for primary tumour location (rectum, 14% versus 35%; p = 0.0006). In multivariate analysis, resection of the primary was the strongest independent prognostic factor for PFS (hazard ratio (HR), 0.5; 95% confidence interval [CI], 0.4–0.8; p = 0.0002) and OS (HR, 0.4; CI, 0.3–0.6; p < 0.0001). Both median PFS (5.1 [4.6–5.6] versus 2.9 [2.2–4.1] months; p = 0.001) and OS (16.3 [13.7–19.2] versus 9.6 [7.4–12.5]; p < 0.0001) were significantly higher in the resection group. These differences in patient survival were maintained after exclusion of patients with rectal primary ( n = 43). Conclusion Resection of the primary tumour may be associated with longer PFS and OS in patients with stage IV CRC starting first-line, single-agent chemotherapy. |
doi_str_mv | 10.1016/j.ejca.2012.07.006 |
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Design Among the 294 patients with non-resectable colorectal metastases enrolled in the Fédération Francophone de Cancérologie Digestive (FFCD) 9601 phase III trial, which compared different first-line single-agent chemotherapy regimens, 216 patients (73%) presented with synchronous metastases at study entry and constituted the present study population. Potential baseline prognostic variables including prior primary tumour resection were assessed by univariate and multivariate Cox analyses. Progression-free survival (PFS) and OS curves were compared with the logrank test. Results Among the 216 patients with stage IV CRC (median follow-up, 33 months), 156 patients (72%) had undergone resection of their primary tumour prior to study entry. The resection and non-resection groups did not differ for baseline characteristics except for primary tumour location (rectum, 14% versus 35%; p = 0.0006). In multivariate analysis, resection of the primary was the strongest independent prognostic factor for PFS (hazard ratio (HR), 0.5; 95% confidence interval [CI], 0.4–0.8; p = 0.0002) and OS (HR, 0.4; CI, 0.3–0.6; p < 0.0001). Both median PFS (5.1 [4.6–5.6] versus 2.9 [2.2–4.1] months; p = 0.001) and OS (16.3 [13.7–19.2] versus 9.6 [7.4–12.5]; p < 0.0001) were significantly higher in the resection group. These differences in patient survival were maintained after exclusion of patients with rectal primary ( n = 43). Conclusion Resection of the primary tumour may be associated with longer PFS and OS in patients with stage IV CRC starting first-line, single-agent chemotherapy.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/j.ejca.2012.07.006</identifier><identifier>PMID: 22926014</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Aged ; Antineoplastic Agents - therapeutic use ; Biological and medical sciences ; Colorectal cancer ; Colorectal Neoplasms - mortality ; Colorectal Neoplasms - pathology ; Colorectal Neoplasms - therapy ; Digestive System Surgical Procedures ; Disease-Free Survival ; Female ; France ; Hematology, Oncology and Palliative Medicine ; Humans ; Kaplan-Meier Estimate ; Male ; Medical sciences ; Metastases ; Middle Aged ; Multivariate analysis ; Pharmacology. Drug treatments ; Primary tumour resection ; Proportional Hazards Models ; Treatment Outcome ; Tumors</subject><ispartof>European journal of cancer (1990), 2013-01, Vol.49 (1), p.90-97</ispartof><rights>Elsevier Ltd</rights><rights>2012 Elsevier Ltd</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c485t-b645f58b1f6af4f00884c9da4f106d5b3024297372bc2c6c78952f32bb6c6a033</citedby><cites>FETCH-LOGICAL-c485t-b645f58b1f6af4f00884c9da4f106d5b3024297372bc2c6c78952f32bb6c6a033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0959804912005679$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26821423$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22926014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ferrand, F</creatorcontrib><creatorcontrib>Malka, D</creatorcontrib><creatorcontrib>Bourredjem, A</creatorcontrib><creatorcontrib>Allonier, C</creatorcontrib><creatorcontrib>Bouché, O</creatorcontrib><creatorcontrib>Louafi, S</creatorcontrib><creatorcontrib>Boige, V</creatorcontrib><creatorcontrib>Mousseau, M</creatorcontrib><creatorcontrib>Raoul, J.L</creatorcontrib><creatorcontrib>Bedenne, L</creatorcontrib><creatorcontrib>Leduc, B</creatorcontrib><creatorcontrib>Deguiral, P</creatorcontrib><creatorcontrib>Faron, M</creatorcontrib><creatorcontrib>Pignon, J.P</creatorcontrib><creatorcontrib>Ducreux, M</creatorcontrib><title>Impact of primary tumour resection on survival of patients with colorectal cancer and synchronous metastases treated by chemotherapy: Results from the multicenter, randomised trial Fédération Francophone de Cancérologie Digestive 9601</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>Abstract Objective To assess the impact of primary tumour resection on overall survival (OS) of patients diagnosed with stage IV colorectal cancer (CRC). Design Among the 294 patients with non-resectable colorectal metastases enrolled in the Fédération Francophone de Cancérologie Digestive (FFCD) 9601 phase III trial, which compared different first-line single-agent chemotherapy regimens, 216 patients (73%) presented with synchronous metastases at study entry and constituted the present study population. Potential baseline prognostic variables including prior primary tumour resection were assessed by univariate and multivariate Cox analyses. Progression-free survival (PFS) and OS curves were compared with the logrank test. Results Among the 216 patients with stage IV CRC (median follow-up, 33 months), 156 patients (72%) had undergone resection of their primary tumour prior to study entry. The resection and non-resection groups did not differ for baseline characteristics except for primary tumour location (rectum, 14% versus 35%; p = 0.0006). In multivariate analysis, resection of the primary was the strongest independent prognostic factor for PFS (hazard ratio (HR), 0.5; 95% confidence interval [CI], 0.4–0.8; p = 0.0002) and OS (HR, 0.4; CI, 0.3–0.6; p < 0.0001). Both median PFS (5.1 [4.6–5.6] versus 2.9 [2.2–4.1] months; p = 0.001) and OS (16.3 [13.7–19.2] versus 9.6 [7.4–12.5]; p < 0.0001) were significantly higher in the resection group. These differences in patient survival were maintained after exclusion of patients with rectal primary ( n = 43). Conclusion Resection of the primary tumour may be associated with longer PFS and OS in patients with stage IV CRC starting first-line, single-agent chemotherapy.</description><subject>Aged</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - mortality</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Colorectal Neoplasms - therapy</subject><subject>Digestive System Surgical Procedures</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>France</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metastases</subject><subject>Middle Aged</subject><subject>Multivariate analysis</subject><subject>Pharmacology. Drug treatments</subject><subject>Primary tumour resection</subject><subject>Proportional Hazards Models</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Ut2q1DAQLqJ41qMv4IXkRvDCXSdpm7YigqyuHjgg-HMd0nR6NmvbrEm60kc6z3Gex3dwenZV8EIYCMl838yX-SZJHnNYceDyxW6FO6NXArhYQbECkHeSBS-LagllLu4mC6jyallCVp0lD0LYAUBRZnA_OROiEhJ4tkh-XvR7bSJzLdt722s_sTj2bvTMY0ATrRsYRRj9wR50d4vT0eIQA_th45YZ1zlPQMoZPRj0TA8NC9Ngtt4Nbgysx6gDBQYWPeqIDasnZrbYu7hFr_fTS_YJw9hRyda7ntEr6-lqDbVB_5x5Kul6G4gZvaVOm5vr5uba61t5G0obt9-6AVmDbE03ypGsK4vsrb3CEO0BWUUffpjca3UX8NHpPE--bt59WX9YXn58f7F-c7k0WZnHZS2zvM3LmrdSt1kLUJaZqRqdtRxkk9cpiExURVqI2ggjTVFWuWhTUdfSSA1pep48O9bde_d9JAGK1BvsOj0gjURxUaRZLkVZEFQcoca7EDy26uSD4qBmm9VOzTar2WYFhSKbifTkVH-se2z-UH77SoCnJ4AORnftPCIb_uJkKXgmZqGvjjikaRwsehUMmWuwsbOpqnH2_zpe_0M3nR0sdfyGE4Yd7dFAc1ZcBeKoz_NCzvvIBUAuiyr9Bf2X4yU</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Ferrand, F</creator><creator>Malka, D</creator><creator>Bourredjem, A</creator><creator>Allonier, C</creator><creator>Bouché, O</creator><creator>Louafi, S</creator><creator>Boige, V</creator><creator>Mousseau, M</creator><creator>Raoul, J.L</creator><creator>Bedenne, L</creator><creator>Leduc, B</creator><creator>Deguiral, P</creator><creator>Faron, M</creator><creator>Pignon, J.P</creator><creator>Ducreux, M</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20130101</creationdate><title>Impact of primary tumour resection on survival of patients with colorectal cancer and synchronous metastases treated by chemotherapy: Results from the multicenter, randomised trial Fédération Francophone de Cancérologie Digestive 9601</title><author>Ferrand, F ; Malka, D ; Bourredjem, A ; Allonier, C ; Bouché, O ; Louafi, S ; Boige, V ; Mousseau, M ; Raoul, J.L ; Bedenne, L ; Leduc, B ; Deguiral, P ; Faron, M ; Pignon, J.P ; Ducreux, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c485t-b645f58b1f6af4f00884c9da4f106d5b3024297372bc2c6c78952f32bb6c6a033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aged</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Colorectal cancer</topic><topic>Colorectal Neoplasms - mortality</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Colorectal Neoplasms - therapy</topic><topic>Digestive System Surgical Procedures</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>France</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metastases</topic><topic>Middle Aged</topic><topic>Multivariate analysis</topic><topic>Pharmacology. Drug treatments</topic><topic>Primary tumour resection</topic><topic>Proportional Hazards Models</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ferrand, F</creatorcontrib><creatorcontrib>Malka, D</creatorcontrib><creatorcontrib>Bourredjem, A</creatorcontrib><creatorcontrib>Allonier, C</creatorcontrib><creatorcontrib>Bouché, O</creatorcontrib><creatorcontrib>Louafi, S</creatorcontrib><creatorcontrib>Boige, V</creatorcontrib><creatorcontrib>Mousseau, M</creatorcontrib><creatorcontrib>Raoul, J.L</creatorcontrib><creatorcontrib>Bedenne, L</creatorcontrib><creatorcontrib>Leduc, B</creatorcontrib><creatorcontrib>Deguiral, P</creatorcontrib><creatorcontrib>Faron, M</creatorcontrib><creatorcontrib>Pignon, J.P</creatorcontrib><creatorcontrib>Ducreux, M</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>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of cancer (1990)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ferrand, F</au><au>Malka, D</au><au>Bourredjem, A</au><au>Allonier, C</au><au>Bouché, O</au><au>Louafi, S</au><au>Boige, V</au><au>Mousseau, M</au><au>Raoul, J.L</au><au>Bedenne, L</au><au>Leduc, B</au><au>Deguiral, P</au><au>Faron, M</au><au>Pignon, J.P</au><au>Ducreux, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of primary tumour resection on survival of patients with colorectal cancer and synchronous metastases treated by chemotherapy: Results from the multicenter, randomised trial Fédération Francophone de Cancérologie Digestive 9601</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>2013-01-01</date><risdate>2013</risdate><volume>49</volume><issue>1</issue><spage>90</spage><epage>97</epage><pages>90-97</pages><issn>0959-8049</issn><eissn>1879-0852</eissn><abstract>Abstract Objective To assess the impact of primary tumour resection on overall survival (OS) of patients diagnosed with stage IV colorectal cancer (CRC). Design Among the 294 patients with non-resectable colorectal metastases enrolled in the Fédération Francophone de Cancérologie Digestive (FFCD) 9601 phase III trial, which compared different first-line single-agent chemotherapy regimens, 216 patients (73%) presented with synchronous metastases at study entry and constituted the present study population. Potential baseline prognostic variables including prior primary tumour resection were assessed by univariate and multivariate Cox analyses. Progression-free survival (PFS) and OS curves were compared with the logrank test. Results Among the 216 patients with stage IV CRC (median follow-up, 33 months), 156 patients (72%) had undergone resection of their primary tumour prior to study entry. The resection and non-resection groups did not differ for baseline characteristics except for primary tumour location (rectum, 14% versus 35%; p = 0.0006). In multivariate analysis, resection of the primary was the strongest independent prognostic factor for PFS (hazard ratio (HR), 0.5; 95% confidence interval [CI], 0.4–0.8; p = 0.0002) and OS (HR, 0.4; CI, 0.3–0.6; p < 0.0001). Both median PFS (5.1 [4.6–5.6] versus 2.9 [2.2–4.1] months; p = 0.001) and OS (16.3 [13.7–19.2] versus 9.6 [7.4–12.5]; p < 0.0001) were significantly higher in the resection group. These differences in patient survival were maintained after exclusion of patients with rectal primary ( n = 43). Conclusion Resection of the primary tumour may be associated with longer PFS and OS in patients with stage IV CRC starting first-line, single-agent chemotherapy.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>22926014</pmid><doi>10.1016/j.ejca.2012.07.006</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Antineoplastic Agents - therapeutic use Biological and medical sciences Colorectal cancer Colorectal Neoplasms - mortality Colorectal Neoplasms - pathology Colorectal Neoplasms - therapy Digestive System Surgical Procedures Disease-Free Survival Female France Hematology, Oncology and Palliative Medicine Humans Kaplan-Meier Estimate Male Medical sciences Metastases Middle Aged Multivariate analysis Pharmacology. Drug treatments Primary tumour resection Proportional Hazards Models Treatment Outcome Tumors |
title | Impact of primary tumour resection on survival of patients with colorectal cancer and synchronous metastases treated by chemotherapy: Results from the multicenter, randomised trial Fédération Francophone de Cancérologie Digestive 9601 |
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