Hyperthermic intraperitoneal chemotherapy in colorectal cancer

Background: This study evaluated the efficacy of hyperthermic intraperitoneal chemotherapy (HIPEC) in colorectal cancer with peritoneal metastases (pmCRC) in a large international data set of patients. Patients and Methods: Patients with pmCRC from 39 centres who underwent cytoreductive surgery with...

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Autores: Fisher, Oliver M., Brown, Chris, Esquivel, Jesus, Larsen, Stein G., Liauw, Winston, Alzahrani, Nayef A., Morris, David L., Kepenekian, Vahan, Sourrouille, Isabelle, Dumont, Frédéric, Tuech, Jean Jacques, Ceribelli, Cécilia, Doussot, Béranger, Sgarbura, Olivia, Alhosni, Mohammed, Quenet, Francois, Glehen, Olivier, Cashin, Peter H., Flatmark, Kjersti, Graf, Wilhelm, Takala, Heikki, Lowy, Andrew M., Chua, Terence, Pelz, Joerg, Baratti, Dario, Baumgartner, Joel M., Berri, Richard, Bretcha-Boix, Pedro, Deraco, Marcello, Flores-Ayala, Guillermo, Gomez-Portilla, Alberto, González-Moreno, Santiago, Goodman, Martin, Halkia, Evgenia, Kusamura, Shigeki, Moller, Mecker, Passot, Guillaume, Pocard, Marc, Salti, George, Sardi, Armando, Senthil, Maheswari, Spilioitis, John, Torres-Melero, Juan, Turaga, Kiran, Bereder, Jean Marc, Bernard, Jean Louis, Bakrin, Naoual, Carrère, Sébastien, Coget, Julien, Cotte, Eddy, Facy, Olivier, Gelli, Maximiliano, Gilly, François Noël, Ortega-Deballon, Pablo, Rat, Patrick, Rousset, Pascal, Thibaudeau, Emilie, Vaudoyer, Delphine
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universidad Francisco de Vitoria
Repositorio:DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
Idioma:inglés
OAI Identifier:oai:ddfv.ufv.es:10641/7245
Acceso en línea:https://hdl.handle.net/10641/7245
Access Level:acceso abierto
Palabra clave:Surgery
SDG 3 - Good Health and Well-being
Yes
yes
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spelling Hyperthermic intraperitoneal chemotherapy in colorectal cancerFisher, Oliver M.Brown, ChrisEsquivel, JesusLarsen, Stein G.Liauw, WinstonAlzahrani, Nayef A.Morris, David L.Kepenekian, VahanSourrouille, IsabelleDumont, FrédéricTuech, Jean JacquesCeribelli, CéciliaDoussot, BérangerSgarbura, OliviaAlhosni, MohammedQuenet, FrancoisGlehen, OlivierCashin, Peter H.Flatmark, KjerstiGraf, WilhelmTakala, HeikkiLowy, Andrew M.Chua, TerencePelz, JoergBaratti, DarioBaumgartner, Joel M.Berri, RichardBretcha-Boix, PedroDeraco, MarcelloFlores-Ayala, GuillermoGomez-Portilla, AlbertoGonzález-Moreno, SantiagoGoodman, MartinHalkia, EvgeniaKusamura, ShigekiMoller, MeckerPassot, GuillaumePocard, MarcSalti, GeorgeSardi, ArmandoSenthil, MaheswariSpilioitis, JohnTorres-Melero, JuanTuraga, KiranBereder, Jean MarcBernard, Jean LouisBakrin, NaoualCarrère, SébastienCoget, JulienCotte, EddyFacy, OlivierGelli, MaximilianoGilly, François NoëlOrtega-Deballon, PabloRat, PatrickRousset, PascalThibaudeau, EmilieVaudoyer, DelphineSurgerySDG 3 - Good Health and Well-beingYesyesBackground: This study evaluated the efficacy of hyperthermic intraperitoneal chemotherapy (HIPEC) in colorectal cancer with peritoneal metastases (pmCRC) in a large international data set of patients. Patients and Methods: Patients with pmCRC from 39 centres who underwent cytoreductive surgery with HIPEC between 1991 and 2018 were selected and compared for the HIPEC protocols received - oxaliplatin-HIPEC versus mitomycin-HIPEC. Following analysis of crude data, propensity-score matching (PSM) and Cox-proportional hazard modelling were performed. Outcomes of interest were overall survival (OS), recurrence-free survival (RFS) and the HIPEC dose-response effects (high versus low dose, dose intensification and double drug protocols) on OS, RFS and 90-day morbidity. Furthermore, the impact of the treatment time period was assessed. Results: Of 2760 patients, 2093 patients were included. Median OS was 43 months (95% c.i. 41 to 46 months) with a median RFS of 12 months (95% c.i. 12 to 13 months). The oxaliplatin-HIPEC group had an OS of 47 months (95% c.i. 42 to 53 months) versus 39 months (95% c.i. 36 to 43 months) in the mitomycin-HIPEC group (P = 0.002), aHR 0.77, 95% c.i. 0.67 to 0.90, P < 0.001. The OS benefit persisted after PSM of the oxaliplatin-HIPEC group and mitomycin-HIPEC group (48 months (95% c.i. 42 to 59 months) versus 40 months (95% c.i. 37 to 44 months)), P < 0.001, aHR 0.78 (95% c.i. 0.65 to 0.94), P = 0.009. Similarly, matched RFS was significantly higher for oxaliplatin-HIPEC versus others (13 months (95% c.i. 12 to 15 months) versus 11 months (95% c.i. 10 to 12 months, P = 0.02)). High-dose mitomycin-HIPEC protocols had similar OS compared to oxaliplatin-HIPEC. HIPEC dose intensification within each protocol resulted in improved survival. Oxaliplatin + irinotecan-HIPEC resulted in the most improved OS (61 months (95% c.i. 51 to 101 months)). Ninety-day mortality in both crude and PSM analysis was worse for mitomycin-HIPEC. There was no change in treatment effect depending on the analysed time period. Conclusions: Oxaliplatin-based HIPEC provided better outcomes compared to mitomycin-based HIPEC. High-dose mitomycin-HIPEC was similar to oxaliplatin-HIPEC. The 90-day mortality difference favours the oxaliplatin-HIPEC group. A trend for dose-response between low- and high-dose HIPEC was reported.Facultad de Medicina20242024-06-0120242024-06-01journal articlehttp://purl.org/coar/resource_type/c_6501info:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10641/7245reponame:DDFV. Repositorio Institucional de la Universidad Francisco de Vitoriainstname:Universidad Francisco de VitoriaInglésengopen accesshttp://purl.org/coar/access_right/c_abf2http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:ddfv.ufv.es:10641/72452026-06-11T12:44:57Z
dc.title.none.fl_str_mv Hyperthermic intraperitoneal chemotherapy in colorectal cancer
title Hyperthermic intraperitoneal chemotherapy in colorectal cancer
spellingShingle Hyperthermic intraperitoneal chemotherapy in colorectal cancer
Fisher, Oliver M.
Surgery
SDG 3 - Good Health and Well-being
Yes
yes
title_short Hyperthermic intraperitoneal chemotherapy in colorectal cancer
title_full Hyperthermic intraperitoneal chemotherapy in colorectal cancer
title_fullStr Hyperthermic intraperitoneal chemotherapy in colorectal cancer
title_full_unstemmed Hyperthermic intraperitoneal chemotherapy in colorectal cancer
title_sort Hyperthermic intraperitoneal chemotherapy in colorectal cancer
dc.creator.none.fl_str_mv Fisher, Oliver M.
Brown, Chris
Esquivel, Jesus
Larsen, Stein G.
Liauw, Winston
Alzahrani, Nayef A.
Morris, David L.
Kepenekian, Vahan
Sourrouille, Isabelle
Dumont, Frédéric
Tuech, Jean Jacques
Ceribelli, Cécilia
Doussot, Béranger
Sgarbura, Olivia
Alhosni, Mohammed
Quenet, Francois
Glehen, Olivier
Cashin, Peter H.
Flatmark, Kjersti
Graf, Wilhelm
Takala, Heikki
Lowy, Andrew M.
Chua, Terence
Pelz, Joerg
Baratti, Dario
Baumgartner, Joel M.
Berri, Richard
Bretcha-Boix, Pedro
Deraco, Marcello
Flores-Ayala, Guillermo
Gomez-Portilla, Alberto
González-Moreno, Santiago
Goodman, Martin
Halkia, Evgenia
Kusamura, Shigeki
Moller, Mecker
Passot, Guillaume
Pocard, Marc
Salti, George
Sardi, Armando
Senthil, Maheswari
Spilioitis, John
Torres-Melero, Juan
Turaga, Kiran
Bereder, Jean Marc
Bernard, Jean Louis
Bakrin, Naoual
Carrère, Sébastien
Coget, Julien
Cotte, Eddy
Facy, Olivier
Gelli, Maximiliano
Gilly, François Noël
Ortega-Deballon, Pablo
Rat, Patrick
Rousset, Pascal
Thibaudeau, Emilie
Vaudoyer, Delphine
author Fisher, Oliver M.
author_facet Fisher, Oliver M.
Brown, Chris
Esquivel, Jesus
Larsen, Stein G.
Liauw, Winston
Alzahrani, Nayef A.
Morris, David L.
Kepenekian, Vahan
Sourrouille, Isabelle
Dumont, Frédéric
Tuech, Jean Jacques
Ceribelli, Cécilia
Doussot, Béranger
Sgarbura, Olivia
Alhosni, Mohammed
Quenet, Francois
Glehen, Olivier
Cashin, Peter H.
Flatmark, Kjersti
Graf, Wilhelm
Takala, Heikki
Lowy, Andrew M.
Chua, Terence
Pelz, Joerg
Baratti, Dario
Baumgartner, Joel M.
Berri, Richard
Bretcha-Boix, Pedro
Deraco, Marcello
Flores-Ayala, Guillermo
Gomez-Portilla, Alberto
González-Moreno, Santiago
Goodman, Martin
Halkia, Evgenia
Kusamura, Shigeki
Moller, Mecker
Passot, Guillaume
Pocard, Marc
Salti, George
Sardi, Armando
Senthil, Maheswari
Spilioitis, John
Torres-Melero, Juan
Turaga, Kiran
Bereder, Jean Marc
Bernard, Jean Louis
Bakrin, Naoual
Carrère, Sébastien
Coget, Julien
Cotte, Eddy
Facy, Olivier
Gelli, Maximiliano
Gilly, François Noël
Ortega-Deballon, Pablo
Rat, Patrick
Rousset, Pascal
Thibaudeau, Emilie
Vaudoyer, Delphine
author_role author
author2 Brown, Chris
Esquivel, Jesus
Larsen, Stein G.
Liauw, Winston
Alzahrani, Nayef A.
Morris, David L.
Kepenekian, Vahan
Sourrouille, Isabelle
Dumont, Frédéric
Tuech, Jean Jacques
Ceribelli, Cécilia
Doussot, Béranger
Sgarbura, Olivia
Alhosni, Mohammed
Quenet, Francois
Glehen, Olivier
Cashin, Peter H.
Flatmark, Kjersti
Graf, Wilhelm
Takala, Heikki
Lowy, Andrew M.
Chua, Terence
Pelz, Joerg
Baratti, Dario
Baumgartner, Joel M.
Berri, Richard
Bretcha-Boix, Pedro
Deraco, Marcello
Flores-Ayala, Guillermo
Gomez-Portilla, Alberto
González-Moreno, Santiago
Goodman, Martin
Halkia, Evgenia
Kusamura, Shigeki
Moller, Mecker
Passot, Guillaume
Pocard, Marc
Salti, George
Sardi, Armando
Senthil, Maheswari
Spilioitis, John
Torres-Melero, Juan
Turaga, Kiran
Bereder, Jean Marc
Bernard, Jean Louis
Bakrin, Naoual
Carrère, Sébastien
Coget, Julien
Cotte, Eddy
Facy, Olivier
Gelli, Maximiliano
Gilly, François Noël
Ortega-Deballon, Pablo
Rat, Patrick
Rousset, Pascal
Thibaudeau, Emilie
Vaudoyer, Delphine
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
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author
dc.contributor.none.fl_str_mv Facultad de Medicina

dc.subject.none.fl_str_mv Surgery
SDG 3 - Good Health and Well-being
Yes
yes
topic Surgery
SDG 3 - Good Health and Well-being
Yes
yes
description Background: This study evaluated the efficacy of hyperthermic intraperitoneal chemotherapy (HIPEC) in colorectal cancer with peritoneal metastases (pmCRC) in a large international data set of patients. Patients and Methods: Patients with pmCRC from 39 centres who underwent cytoreductive surgery with HIPEC between 1991 and 2018 were selected and compared for the HIPEC protocols received - oxaliplatin-HIPEC versus mitomycin-HIPEC. Following analysis of crude data, propensity-score matching (PSM) and Cox-proportional hazard modelling were performed. Outcomes of interest were overall survival (OS), recurrence-free survival (RFS) and the HIPEC dose-response effects (high versus low dose, dose intensification and double drug protocols) on OS, RFS and 90-day morbidity. Furthermore, the impact of the treatment time period was assessed. Results: Of 2760 patients, 2093 patients were included. Median OS was 43 months (95% c.i. 41 to 46 months) with a median RFS of 12 months (95% c.i. 12 to 13 months). The oxaliplatin-HIPEC group had an OS of 47 months (95% c.i. 42 to 53 months) versus 39 months (95% c.i. 36 to 43 months) in the mitomycin-HIPEC group (P = 0.002), aHR 0.77, 95% c.i. 0.67 to 0.90, P < 0.001. The OS benefit persisted after PSM of the oxaliplatin-HIPEC group and mitomycin-HIPEC group (48 months (95% c.i. 42 to 59 months) versus 40 months (95% c.i. 37 to 44 months)), P < 0.001, aHR 0.78 (95% c.i. 0.65 to 0.94), P = 0.009. Similarly, matched RFS was significantly higher for oxaliplatin-HIPEC versus others (13 months (95% c.i. 12 to 15 months) versus 11 months (95% c.i. 10 to 12 months, P = 0.02)). High-dose mitomycin-HIPEC protocols had similar OS compared to oxaliplatin-HIPEC. HIPEC dose intensification within each protocol resulted in improved survival. Oxaliplatin + irinotecan-HIPEC resulted in the most improved OS (61 months (95% c.i. 51 to 101 months)). Ninety-day mortality in both crude and PSM analysis was worse for mitomycin-HIPEC. There was no change in treatment effect depending on the analysed time period. Conclusions: Oxaliplatin-based HIPEC provided better outcomes compared to mitomycin-based HIPEC. High-dose mitomycin-HIPEC was similar to oxaliplatin-HIPEC. The 90-day mortality difference favours the oxaliplatin-HIPEC group. A trend for dose-response between low- and high-dose HIPEC was reported.
publishDate 2024
dc.date.none.fl_str_mv 2024
2024-06-01
2024
2024-06-01
dc.type.none.fl_str_mv journal article
http://purl.org/coar/resource_type/c_6501
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://hdl.handle.net/10641/7245
url https://hdl.handle.net/10641/7245
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2

http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2

http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
instname:Universidad Francisco de Vitoria
instname_str Universidad Francisco de Vitoria
reponame_str DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
collection DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
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