Evaluation and impact of residual disease in locally advanced cervical cancer after concurrent chemoradiation therapy: Results of a multicenter study

Abstract Background The aim of this study was to evaluate the diagnosis and impact of residual disease (RD) after concurrent chemoradiation therapy (CRT) in locally advanced cervical cancer (FIGO IB2-IVA). Methods This retrospective multicenter study included 159 patients who were treated with compl...

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Veröffentlicht in:European journal of surgical oncology 2013-12, Vol.39 (12), p.1428-1434
Hauptverfasser: Hequet, D, Marchand, E, Place, V, Fourchotte, V, De La Rochefordière, A, Dridi, S, Coutant, C, Lecuru, F, Bats, A-S, Koskas, M, Bretel, J-J, Bricou, A, Delpech, Y, Barranger, E
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container_end_page 1434
container_issue 12
container_start_page 1428
container_title European journal of surgical oncology
container_volume 39
creator Hequet, D
Marchand, E
Place, V
Fourchotte, V
De La Rochefordière, A
Dridi, S
Coutant, C
Lecuru, F
Bats, A-S
Koskas, M
Bretel, J-J
Bricou, A
Delpech, Y
Barranger, E
description Abstract Background The aim of this study was to evaluate the diagnosis and impact of residual disease (RD) after concurrent chemoradiation therapy (CRT) in locally advanced cervical cancer (FIGO IB2-IVA). Methods This retrospective multicenter study included 159 patients who were treated with completion surgery after CRT between 2006 and 2012. Magnetic resonance imaging (MRI) was performed 4–6 weeks after CRT and compared to pathological evidence of residual disease. Kaplan–Meier survival curves were plotted and univariate/multivariate analyses were performed to assess the association between RD and the outcome. Results Residual disease was present in 45.3% of the patients and detected by MRI in 57.1%. The MRI had a 29.2% false positive rate and an 11.1% false negative rate. The overall survival (OS) rates at 3 and 5 years were 78.6% (CI 95% [71%–86.9%]) and 76.5% (CI 95% [68.2%–85.7%]), respectively. The disease free survival (DFS) rates at 3 and 5 years were 73.4% (CI 95% [65.6%–82%]) and 71.1% (CI 95% [62.7%–80.1%]), respectively. RD greater than 10 mm decreased DFS (HR = 4.84, p  = 0.03), whereas RD between 1 and 10 mm (HR = 0.31, p  = 0.58) and less than 1 mm (HR = 0.37, p  = 0.54) had no impact on DFS. The OS was not changed by RD. Discussion The MRI accuracy value is not sufficient to select patients who might benefit from completion surgery. Residual disease over 10 mm decreased DFS but did not impact OS.
doi_str_mv 10.1016/j.ejso.2013.10.006
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Methods This retrospective multicenter study included 159 patients who were treated with completion surgery after CRT between 2006 and 2012. Magnetic resonance imaging (MRI) was performed 4–6 weeks after CRT and compared to pathological evidence of residual disease. Kaplan–Meier survival curves were plotted and univariate/multivariate analyses were performed to assess the association between RD and the outcome. Results Residual disease was present in 45.3% of the patients and detected by MRI in 57.1%. The MRI had a 29.2% false positive rate and an 11.1% false negative rate. The overall survival (OS) rates at 3 and 5 years were 78.6% (CI 95% [71%–86.9%]) and 76.5% (CI 95% [68.2%–85.7%]), respectively. The disease free survival (DFS) rates at 3 and 5 years were 73.4% (CI 95% [65.6%–82%]) and 71.1% (CI 95% [62.7%–80.1%]), respectively. RD greater than 10 mm decreased DFS (HR = 4.84, p  = 0.03), whereas RD between 1 and 10 mm (HR = 0.31, p  = 0.58) and less than 1 mm (HR = 0.37, p  = 0.54) had no impact on DFS. The OS was not changed by RD. Discussion The MRI accuracy value is not sufficient to select patients who might benefit from completion surgery. Residual disease over 10 mm decreased DFS but did not impact OS.</description><identifier>ISSN: 0748-7983</identifier><identifier>EISSN: 1532-2157</identifier><identifier>DOI: 10.1016/j.ejso.2013.10.006</identifier><identifier>PMID: 24183796</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; Advanced cervical cancer ; Aged ; Aged, 80 and over ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Carcinoma - diagnosis ; Carcinoma - therapy ; Chemoradiotherapy, Adjuvant ; Cisplatin - administration &amp; dosage ; Completion surgery ; Disease-Free Survival ; Dose Fractionation ; False Negative Reactions ; False Positive Reactions ; Female ; Fluorouracil - administration &amp; dosage ; Hematology, Oncology and Palliative Medicine ; Humans ; Hysterectomy ; Kaplan-Meier Estimate ; Magnetic Resonance Imaging ; Middle Aged ; Neoadjuvant Therapy ; Neoplasm, Residual ; Residual disease ; Retrospective Studies ; Surgery ; Survival Rate ; Uterine Cervical Neoplasms - diagnosis ; Uterine Cervical Neoplasms - therapy ; Young Adult</subject><ispartof>European journal of surgical oncology, 2013-12, Vol.39 (12), p.1428-1434</ispartof><rights>Elsevier Ltd</rights><rights>2013 Elsevier Ltd</rights><rights>Copyright © 2013 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-66a28772ab04805e9c9c4e49b01e35b00fc9a14b239a03847584562490a13f0b3</citedby><cites>FETCH-LOGICAL-c411t-66a28772ab04805e9c9c4e49b01e35b00fc9a14b239a03847584562490a13f0b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejso.2013.10.006$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3554,27933,27934,46004</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24183796$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hequet, D</creatorcontrib><creatorcontrib>Marchand, E</creatorcontrib><creatorcontrib>Place, V</creatorcontrib><creatorcontrib>Fourchotte, V</creatorcontrib><creatorcontrib>De La Rochefordière, A</creatorcontrib><creatorcontrib>Dridi, S</creatorcontrib><creatorcontrib>Coutant, C</creatorcontrib><creatorcontrib>Lecuru, F</creatorcontrib><creatorcontrib>Bats, A-S</creatorcontrib><creatorcontrib>Koskas, M</creatorcontrib><creatorcontrib>Bretel, J-J</creatorcontrib><creatorcontrib>Bricou, A</creatorcontrib><creatorcontrib>Delpech, Y</creatorcontrib><creatorcontrib>Barranger, E</creatorcontrib><title>Evaluation and impact of residual disease in locally advanced cervical cancer after concurrent chemoradiation therapy: Results of a multicenter study</title><title>European journal of surgical oncology</title><addtitle>Eur J Surg Oncol</addtitle><description>Abstract Background The aim of this study was to evaluate the diagnosis and impact of residual disease (RD) after concurrent chemoradiation therapy (CRT) in locally advanced cervical cancer (FIGO IB2-IVA). Methods This retrospective multicenter study included 159 patients who were treated with completion surgery after CRT between 2006 and 2012. Magnetic resonance imaging (MRI) was performed 4–6 weeks after CRT and compared to pathological evidence of residual disease. Kaplan–Meier survival curves were plotted and univariate/multivariate analyses were performed to assess the association between RD and the outcome. Results Residual disease was present in 45.3% of the patients and detected by MRI in 57.1%. The MRI had a 29.2% false positive rate and an 11.1% false negative rate. The overall survival (OS) rates at 3 and 5 years were 78.6% (CI 95% [71%–86.9%]) and 76.5% (CI 95% [68.2%–85.7%]), respectively. The disease free survival (DFS) rates at 3 and 5 years were 73.4% (CI 95% [65.6%–82%]) and 71.1% (CI 95% [62.7%–80.1%]), respectively. RD greater than 10 mm decreased DFS (HR = 4.84, p  = 0.03), whereas RD between 1 and 10 mm (HR = 0.31, p  = 0.58) and less than 1 mm (HR = 0.37, p  = 0.54) had no impact on DFS. The OS was not changed by RD. Discussion The MRI accuracy value is not sufficient to select patients who might benefit from completion surgery. 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Marchand, E ; Place, V ; Fourchotte, V ; De La Rochefordière, A ; Dridi, S ; Coutant, C ; Lecuru, F ; Bats, A-S ; Koskas, M ; Bretel, J-J ; Bricou, A ; Delpech, Y ; Barranger, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-66a28772ab04805e9c9c4e49b01e35b00fc9a14b239a03847584562490a13f0b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Advanced cervical cancer</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Carcinoma - diagnosis</topic><topic>Carcinoma - therapy</topic><topic>Chemoradiotherapy, Adjuvant</topic><topic>Cisplatin - administration &amp; dosage</topic><topic>Completion surgery</topic><topic>Disease-Free Survival</topic><topic>Dose Fractionation</topic><topic>False Negative Reactions</topic><topic>False Positive Reactions</topic><topic>Female</topic><topic>Fluorouracil - administration &amp; dosage</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Hysterectomy</topic><topic>Kaplan-Meier Estimate</topic><topic>Magnetic Resonance Imaging</topic><topic>Middle Aged</topic><topic>Neoadjuvant Therapy</topic><topic>Neoplasm, Residual</topic><topic>Residual disease</topic><topic>Retrospective Studies</topic><topic>Surgery</topic><topic>Survival Rate</topic><topic>Uterine Cervical Neoplasms - diagnosis</topic><topic>Uterine Cervical Neoplasms - therapy</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hequet, D</creatorcontrib><creatorcontrib>Marchand, E</creatorcontrib><creatorcontrib>Place, V</creatorcontrib><creatorcontrib>Fourchotte, V</creatorcontrib><creatorcontrib>De La Rochefordière, A</creatorcontrib><creatorcontrib>Dridi, S</creatorcontrib><creatorcontrib>Coutant, C</creatorcontrib><creatorcontrib>Lecuru, F</creatorcontrib><creatorcontrib>Bats, A-S</creatorcontrib><creatorcontrib>Koskas, M</creatorcontrib><creatorcontrib>Bretel, J-J</creatorcontrib><creatorcontrib>Bricou, A</creatorcontrib><creatorcontrib>Delpech, Y</creatorcontrib><creatorcontrib>Barranger, E</creatorcontrib><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 surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hequet, D</au><au>Marchand, E</au><au>Place, V</au><au>Fourchotte, V</au><au>De La Rochefordière, A</au><au>Dridi, S</au><au>Coutant, C</au><au>Lecuru, F</au><au>Bats, A-S</au><au>Koskas, M</au><au>Bretel, J-J</au><au>Bricou, A</au><au>Delpech, Y</au><au>Barranger, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation and impact of residual disease in locally advanced cervical cancer after concurrent chemoradiation therapy: Results of a multicenter study</atitle><jtitle>European journal of surgical oncology</jtitle><addtitle>Eur J Surg Oncol</addtitle><date>2013-12-01</date><risdate>2013</risdate><volume>39</volume><issue>12</issue><spage>1428</spage><epage>1434</epage><pages>1428-1434</pages><issn>0748-7983</issn><eissn>1532-2157</eissn><abstract>Abstract Background The aim of this study was to evaluate the diagnosis and impact of residual disease (RD) after concurrent chemoradiation therapy (CRT) in locally advanced cervical cancer (FIGO IB2-IVA). Methods This retrospective multicenter study included 159 patients who were treated with completion surgery after CRT between 2006 and 2012. Magnetic resonance imaging (MRI) was performed 4–6 weeks after CRT and compared to pathological evidence of residual disease. Kaplan–Meier survival curves were plotted and univariate/multivariate analyses were performed to assess the association between RD and the outcome. Results Residual disease was present in 45.3% of the patients and detected by MRI in 57.1%. The MRI had a 29.2% false positive rate and an 11.1% false negative rate. The overall survival (OS) rates at 3 and 5 years were 78.6% (CI 95% [71%–86.9%]) and 76.5% (CI 95% [68.2%–85.7%]), respectively. The disease free survival (DFS) rates at 3 and 5 years were 73.4% (CI 95% [65.6%–82%]) and 71.1% (CI 95% [62.7%–80.1%]), respectively. RD greater than 10 mm decreased DFS (HR = 4.84, p  = 0.03), whereas RD between 1 and 10 mm (HR = 0.31, p  = 0.58) and less than 1 mm (HR = 0.37, p  = 0.54) had no impact on DFS. The OS was not changed by RD. Discussion The MRI accuracy value is not sufficient to select patients who might benefit from completion surgery. Residual disease over 10 mm decreased DFS but did not impact OS.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>24183796</pmid><doi>10.1016/j.ejso.2013.10.006</doi><tpages>7</tpages></addata></record>
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subjects Adult
Advanced cervical cancer
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Carcinoma - diagnosis
Carcinoma - therapy
Chemoradiotherapy, Adjuvant
Cisplatin - administration & dosage
Completion surgery
Disease-Free Survival
Dose Fractionation
False Negative Reactions
False Positive Reactions
Female
Fluorouracil - administration & dosage
Hematology, Oncology and Palliative Medicine
Humans
Hysterectomy
Kaplan-Meier Estimate
Magnetic Resonance Imaging
Middle Aged
Neoadjuvant Therapy
Neoplasm, Residual
Residual disease
Retrospective Studies
Surgery
Survival Rate
Uterine Cervical Neoplasms - diagnosis
Uterine Cervical Neoplasms - therapy
Young Adult
title Evaluation and impact of residual disease in locally advanced cervical cancer after concurrent chemoradiation therapy: Results of a multicenter study
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