Early Postoperative Chemotherapy After Complete Cytoreduction and Hyperthermic Intraperitoneal Chemotherapy for Isolated Peritoneal Carcinomatosis of Colon Cancer: A Multicenter Study

Purpose The prognosis of peritoneal carcinomatosis (PC) from colorectal cancer has been improved with cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). However, benefits of postoperative chemotherapy (CT) are unclear. Methods This retrospective, multicenter study inc...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Annals of surgical oncology 2016-03, Vol.23 (3), p.863-869
Hauptverfasser: Maillet, Marianne, Glehen, Olivier, Lambert, Jerome, Goere, Diane, Pocard, Marc, Msika, Simon, Passot, Guillaume, Elias, Dominique, Eveno, Clarisse, Sabaté, Jean-Marc, Lourenco, Nelson, André, Thierry, Gornet, Jean-Marc
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 869
container_issue 3
container_start_page 863
container_title Annals of surgical oncology
container_volume 23
creator Maillet, Marianne
Glehen, Olivier
Lambert, Jerome
Goere, Diane
Pocard, Marc
Msika, Simon
Passot, Guillaume
Elias, Dominique
Eveno, Clarisse
Sabaté, Jean-Marc
Lourenco, Nelson
André, Thierry
Gornet, Jean-Marc
description Purpose The prognosis of peritoneal carcinomatosis (PC) from colorectal cancer has been improved with cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). However, benefits of postoperative chemotherapy (CT) are unclear. Methods This retrospective, multicenter study included 231 patients treated by CRS and HIPEC for isolated PC of colon cancer in four expert’s centers. Overall survival (OS), progression-free survival (PFS), and peritoneal recurrence-free survival (PRFS) were compared between patients with adjuvant CT (started within 3 months after surgery) and patients with surveillance only. Results After exclusion of 10 patients for early postoperative death (4 %), 221 patients were included (CT group: n  = 151; surveillance group: n  = 70). Main postoperative CT regimens (median of 6 cycles) were Folfox (28 %), Folfiri bevacizumab (24.5 %), Folfiri (16 %), and Folfiri cetuximab (12.5 %). The median OS after surgery was 43.3 months with no difference between CT and surveillance groups. In multivariate analysis, a low peritoneal cancer index ( p  
doi_str_mv 10.1245/s10434-015-4914-4
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1764702407</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1764702407</sourcerecordid><originalsourceid>FETCH-LOGICAL-c442t-7d2c0db90d91f43aa1d5f6ca87bfb83c70b84ed2443822c0c658bc07f22aaf753</originalsourceid><addsrcrecordid>eNp1kcFu1TAQRS0EoqXwAWyQJTZsUmzHSfzYPUWFPqmISsA6cuwxdeXYwXYq5cv4PRy9UhUkVuPxnHtnpIvQa0rOKePN-0QJr3lFaFPxHeUVf4JOaVN-eCvo0_Imrah2rG1O0IuUbgmhXU2a5-iEtVwQwcUp-nUho1vxdUg5zBBltneA-xuYQr4p7bzivckQcR-m2UEuszWHCHpR2QaPpdf4ci3CjZ6swgefiwqizcGDdH9bmRDxIQUnM2h8_QiSUVkfJplDsgkHU9a54t5LryB-wHv8eXHZKvDbKV_zoteX6JmRLsGr-3qGvn-8-NZfVldfPh36_VWlOGe56jRTRI87onfU8FpKqhvTKim60YyiVh0ZBQfNOK8FK6hqGzEq0hnGpDRdU5-hd0ffOYafC6Q8TDYpcE56CEsaaNfyjjBOuoK-_Qe9DUv05bqNqmtWKFYoeqRUDClFMMMc7STjOlAybKkOx1SHkuqwpTrwonlz77yME-gHxZ8YC8COQCoj_wPio9X_df0NM6uxnA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1763322402</pqid></control><display><type>article</type><title>Early Postoperative Chemotherapy After Complete Cytoreduction and Hyperthermic Intraperitoneal Chemotherapy for Isolated Peritoneal Carcinomatosis of Colon Cancer: A Multicenter Study</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Maillet, Marianne ; Glehen, Olivier ; Lambert, Jerome ; Goere, Diane ; Pocard, Marc ; Msika, Simon ; Passot, Guillaume ; Elias, Dominique ; Eveno, Clarisse ; Sabaté, Jean-Marc ; Lourenco, Nelson ; André, Thierry ; Gornet, Jean-Marc</creator><creatorcontrib>Maillet, Marianne ; Glehen, Olivier ; Lambert, Jerome ; Goere, Diane ; Pocard, Marc ; Msika, Simon ; Passot, Guillaume ; Elias, Dominique ; Eveno, Clarisse ; Sabaté, Jean-Marc ; Lourenco, Nelson ; André, Thierry ; Gornet, Jean-Marc ; BIG-RENAPE Working Group</creatorcontrib><description>Purpose The prognosis of peritoneal carcinomatosis (PC) from colorectal cancer has been improved with cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). However, benefits of postoperative chemotherapy (CT) are unclear. Methods This retrospective, multicenter study included 231 patients treated by CRS and HIPEC for isolated PC of colon cancer in four expert’s centers. Overall survival (OS), progression-free survival (PFS), and peritoneal recurrence-free survival (PRFS) were compared between patients with adjuvant CT (started within 3 months after surgery) and patients with surveillance only. Results After exclusion of 10 patients for early postoperative death (4 %), 221 patients were included (CT group: n  = 151; surveillance group: n  = 70). Main postoperative CT regimens (median of 6 cycles) were Folfox (28 %), Folfiri bevacizumab (24.5 %), Folfiri (16 %), and Folfiri cetuximab (12.5 %). The median OS after surgery was 43.3 months with no difference between CT and surveillance groups. In multivariate analysis, a low peritoneal cancer index ( p  &lt; 0.0001) and a long delay between diagnosis of CP and HIPEC ( p  = 0.001) were associated with increased OS. The median PFS and PRFS were 12.4 and 17 months, respectively. At 1 year, more patients were without progression ( p  = 0.001) or PC recurrence (0.0004) in the CT group, but with prolonged follow-up this difference was no longer significant. Conclusions Early postoperative CT does not improve OS after CRS and HIPEC for colon carcinomatosis. However, a transient effect on PFS and PRFS was observed. A subgroup of patients who may benefit more from CT remain to be defined.</description><identifier>ISSN: 1068-9265</identifier><identifier>EISSN: 1534-4681</identifier><identifier>DOI: 10.1245/s10434-015-4914-4</identifier><identifier>PMID: 26480848</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Chemotherapy, Cancer, Regional Perfusion ; Colonic Neoplasms - pathology ; Colonic Neoplasms - therapy ; Colorectal Cancer ; Combined Modality Therapy ; Cytoreduction Surgical Procedures ; Female ; Follow-Up Studies ; France - epidemiology ; Humans ; Hyperthermia, Induced ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Neoplasm Staging ; Oncology ; Peritoneal Neoplasms - secondary ; Peritoneal Neoplasms - therapy ; Postoperative Complications - drug therapy ; Postoperative Complications - epidemiology ; Prognosis ; Retrospective Studies ; Surgery ; Surgical Oncology ; Survival Rate</subject><ispartof>Annals of surgical oncology, 2016-03, Vol.23 (3), p.863-869</ispartof><rights>Society of Surgical Oncology 2015</rights><rights>Society of Surgical Oncology 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-7d2c0db90d91f43aa1d5f6ca87bfb83c70b84ed2443822c0c658bc07f22aaf753</citedby><cites>FETCH-LOGICAL-c442t-7d2c0db90d91f43aa1d5f6ca87bfb83c70b84ed2443822c0c658bc07f22aaf753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1245/s10434-015-4914-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1245/s10434-015-4914-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26480848$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Maillet, Marianne</creatorcontrib><creatorcontrib>Glehen, Olivier</creatorcontrib><creatorcontrib>Lambert, Jerome</creatorcontrib><creatorcontrib>Goere, Diane</creatorcontrib><creatorcontrib>Pocard, Marc</creatorcontrib><creatorcontrib>Msika, Simon</creatorcontrib><creatorcontrib>Passot, Guillaume</creatorcontrib><creatorcontrib>Elias, Dominique</creatorcontrib><creatorcontrib>Eveno, Clarisse</creatorcontrib><creatorcontrib>Sabaté, Jean-Marc</creatorcontrib><creatorcontrib>Lourenco, Nelson</creatorcontrib><creatorcontrib>André, Thierry</creatorcontrib><creatorcontrib>Gornet, Jean-Marc</creatorcontrib><creatorcontrib>BIG-RENAPE Working Group</creatorcontrib><title>Early Postoperative Chemotherapy After Complete Cytoreduction and Hyperthermic Intraperitoneal Chemotherapy for Isolated Peritoneal Carcinomatosis of Colon Cancer: A Multicenter Study</title><title>Annals of surgical oncology</title><addtitle>Ann Surg Oncol</addtitle><addtitle>Ann Surg Oncol</addtitle><description>Purpose The prognosis of peritoneal carcinomatosis (PC) from colorectal cancer has been improved with cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). However, benefits of postoperative chemotherapy (CT) are unclear. Methods This retrospective, multicenter study included 231 patients treated by CRS and HIPEC for isolated PC of colon cancer in four expert’s centers. Overall survival (OS), progression-free survival (PFS), and peritoneal recurrence-free survival (PRFS) were compared between patients with adjuvant CT (started within 3 months after surgery) and patients with surveillance only. Results After exclusion of 10 patients for early postoperative death (4 %), 221 patients were included (CT group: n  = 151; surveillance group: n  = 70). Main postoperative CT regimens (median of 6 cycles) were Folfox (28 %), Folfiri bevacizumab (24.5 %), Folfiri (16 %), and Folfiri cetuximab (12.5 %). The median OS after surgery was 43.3 months with no difference between CT and surveillance groups. In multivariate analysis, a low peritoneal cancer index ( p  &lt; 0.0001) and a long delay between diagnosis of CP and HIPEC ( p  = 0.001) were associated with increased OS. The median PFS and PRFS were 12.4 and 17 months, respectively. At 1 year, more patients were without progression ( p  = 0.001) or PC recurrence (0.0004) in the CT group, but with prolonged follow-up this difference was no longer significant. Conclusions Early postoperative CT does not improve OS after CRS and HIPEC for colon carcinomatosis. However, a transient effect on PFS and PRFS was observed. A subgroup of patients who may benefit more from CT remain to be defined.</description><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Chemotherapy, Cancer, Regional Perfusion</subject><subject>Colonic Neoplasms - pathology</subject><subject>Colonic Neoplasms - therapy</subject><subject>Colorectal Cancer</subject><subject>Combined Modality Therapy</subject><subject>Cytoreduction Surgical Procedures</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>France - epidemiology</subject><subject>Humans</subject><subject>Hyperthermia, Induced</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Oncology</subject><subject>Peritoneal Neoplasms - secondary</subject><subject>Peritoneal Neoplasms - therapy</subject><subject>Postoperative Complications - drug therapy</subject><subject>Postoperative Complications - epidemiology</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><subject>Survival Rate</subject><issn>1068-9265</issn><issn>1534-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kcFu1TAQRS0EoqXwAWyQJTZsUmzHSfzYPUWFPqmISsA6cuwxdeXYwXYq5cv4PRy9UhUkVuPxnHtnpIvQa0rOKePN-0QJr3lFaFPxHeUVf4JOaVN-eCvo0_Imrah2rG1O0IuUbgmhXU2a5-iEtVwQwcUp-nUho1vxdUg5zBBltneA-xuYQr4p7bzivckQcR-m2UEuszWHCHpR2QaPpdf4ci3CjZ6swgefiwqizcGDdH9bmRDxIQUnM2h8_QiSUVkfJplDsgkHU9a54t5LryB-wHv8eXHZKvDbKV_zoteX6JmRLsGr-3qGvn-8-NZfVldfPh36_VWlOGe56jRTRI87onfU8FpKqhvTKim60YyiVh0ZBQfNOK8FK6hqGzEq0hnGpDRdU5-hd0ffOYafC6Q8TDYpcE56CEsaaNfyjjBOuoK-_Qe9DUv05bqNqmtWKFYoeqRUDClFMMMc7STjOlAybKkOx1SHkuqwpTrwonlz77yME-gHxZ8YC8COQCoj_wPio9X_df0NM6uxnA</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Maillet, Marianne</creator><creator>Glehen, Olivier</creator><creator>Lambert, Jerome</creator><creator>Goere, Diane</creator><creator>Pocard, Marc</creator><creator>Msika, Simon</creator><creator>Passot, Guillaume</creator><creator>Elias, Dominique</creator><creator>Eveno, Clarisse</creator><creator>Sabaté, Jean-Marc</creator><creator>Lourenco, Nelson</creator><creator>André, Thierry</creator><creator>Gornet, Jean-Marc</creator><general>Springer International Publishing</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>7TO</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>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20160301</creationdate><title>Early Postoperative Chemotherapy After Complete Cytoreduction and Hyperthermic Intraperitoneal Chemotherapy for Isolated Peritoneal Carcinomatosis of Colon Cancer: A Multicenter Study</title><author>Maillet, Marianne ; Glehen, Olivier ; Lambert, Jerome ; Goere, Diane ; Pocard, Marc ; Msika, Simon ; Passot, Guillaume ; Elias, Dominique ; Eveno, Clarisse ; Sabaté, Jean-Marc ; Lourenco, Nelson ; André, Thierry ; Gornet, Jean-Marc</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-7d2c0db90d91f43aa1d5f6ca87bfb83c70b84ed2443822c0c658bc07f22aaf753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Chemotherapy, Cancer, Regional Perfusion</topic><topic>Colonic Neoplasms - pathology</topic><topic>Colonic Neoplasms - therapy</topic><topic>Colorectal Cancer</topic><topic>Combined Modality Therapy</topic><topic>Cytoreduction Surgical Procedures</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>France - epidemiology</topic><topic>Humans</topic><topic>Hyperthermia, Induced</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Neoplasm Staging</topic><topic>Oncology</topic><topic>Peritoneal Neoplasms - secondary</topic><topic>Peritoneal Neoplasms - therapy</topic><topic>Postoperative Complications - drug therapy</topic><topic>Postoperative Complications - epidemiology</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><topic>Survival Rate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maillet, Marianne</creatorcontrib><creatorcontrib>Glehen, Olivier</creatorcontrib><creatorcontrib>Lambert, Jerome</creatorcontrib><creatorcontrib>Goere, Diane</creatorcontrib><creatorcontrib>Pocard, Marc</creatorcontrib><creatorcontrib>Msika, Simon</creatorcontrib><creatorcontrib>Passot, Guillaume</creatorcontrib><creatorcontrib>Elias, Dominique</creatorcontrib><creatorcontrib>Eveno, Clarisse</creatorcontrib><creatorcontrib>Sabaté, Jean-Marc</creatorcontrib><creatorcontrib>Lourenco, Nelson</creatorcontrib><creatorcontrib>André, Thierry</creatorcontrib><creatorcontrib>Gornet, Jean-Marc</creatorcontrib><creatorcontrib>BIG-RENAPE Working Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maillet, Marianne</au><au>Glehen, Olivier</au><au>Lambert, Jerome</au><au>Goere, Diane</au><au>Pocard, Marc</au><au>Msika, Simon</au><au>Passot, Guillaume</au><au>Elias, Dominique</au><au>Eveno, Clarisse</au><au>Sabaté, Jean-Marc</au><au>Lourenco, Nelson</au><au>André, Thierry</au><au>Gornet, Jean-Marc</au><aucorp>BIG-RENAPE Working Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early Postoperative Chemotherapy After Complete Cytoreduction and Hyperthermic Intraperitoneal Chemotherapy for Isolated Peritoneal Carcinomatosis of Colon Cancer: A Multicenter Study</atitle><jtitle>Annals of surgical oncology</jtitle><stitle>Ann Surg Oncol</stitle><addtitle>Ann Surg Oncol</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>23</volume><issue>3</issue><spage>863</spage><epage>869</epage><pages>863-869</pages><issn>1068-9265</issn><eissn>1534-4681</eissn><abstract>Purpose The prognosis of peritoneal carcinomatosis (PC) from colorectal cancer has been improved with cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). However, benefits of postoperative chemotherapy (CT) are unclear. Methods This retrospective, multicenter study included 231 patients treated by CRS and HIPEC for isolated PC of colon cancer in four expert’s centers. Overall survival (OS), progression-free survival (PFS), and peritoneal recurrence-free survival (PRFS) were compared between patients with adjuvant CT (started within 3 months after surgery) and patients with surveillance only. Results After exclusion of 10 patients for early postoperative death (4 %), 221 patients were included (CT group: n  = 151; surveillance group: n  = 70). Main postoperative CT regimens (median of 6 cycles) were Folfox (28 %), Folfiri bevacizumab (24.5 %), Folfiri (16 %), and Folfiri cetuximab (12.5 %). The median OS after surgery was 43.3 months with no difference between CT and surveillance groups. In multivariate analysis, a low peritoneal cancer index ( p  &lt; 0.0001) and a long delay between diagnosis of CP and HIPEC ( p  = 0.001) were associated with increased OS. The median PFS and PRFS were 12.4 and 17 months, respectively. At 1 year, more patients were without progression ( p  = 0.001) or PC recurrence (0.0004) in the CT group, but with prolonged follow-up this difference was no longer significant. Conclusions Early postoperative CT does not improve OS after CRS and HIPEC for colon carcinomatosis. However, a transient effect on PFS and PRFS was observed. A subgroup of patients who may benefit more from CT remain to be defined.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>26480848</pmid><doi>10.1245/s10434-015-4914-4</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1068-9265
ispartof Annals of surgical oncology, 2016-03, Vol.23 (3), p.863-869
issn 1068-9265
1534-4681
language eng
recordid cdi_proquest_miscellaneous_1764702407
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Chemotherapy, Cancer, Regional Perfusion
Colonic Neoplasms - pathology
Colonic Neoplasms - therapy
Colorectal Cancer
Combined Modality Therapy
Cytoreduction Surgical Procedures
Female
Follow-Up Studies
France - epidemiology
Humans
Hyperthermia, Induced
Male
Medicine
Medicine & Public Health
Middle Aged
Neoplasm Staging
Oncology
Peritoneal Neoplasms - secondary
Peritoneal Neoplasms - therapy
Postoperative Complications - drug therapy
Postoperative Complications - epidemiology
Prognosis
Retrospective Studies
Surgery
Surgical Oncology
Survival Rate
title Early Postoperative Chemotherapy After Complete Cytoreduction and Hyperthermic Intraperitoneal Chemotherapy for Isolated Peritoneal Carcinomatosis of Colon Cancer: A Multicenter Study
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T14%3A53%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Early%20Postoperative%20Chemotherapy%20After%20Complete%20Cytoreduction%20and%20Hyperthermic%20Intraperitoneal%20Chemotherapy%20for%20Isolated%20Peritoneal%20Carcinomatosis%20of%20Colon%20Cancer:%20A%20Multicenter%20Study&rft.jtitle=Annals%20of%20surgical%20oncology&rft.au=Maillet,%20Marianne&rft.aucorp=BIG-RENAPE%20Working%20Group&rft.date=2016-03-01&rft.volume=23&rft.issue=3&rft.spage=863&rft.epage=869&rft.pages=863-869&rft.issn=1068-9265&rft.eissn=1534-4681&rft_id=info:doi/10.1245/s10434-015-4914-4&rft_dat=%3Cproquest_cross%3E1764702407%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1763322402&rft_id=info:pmid/26480848&rfr_iscdi=true