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Prediction of survival by neutropenia according to delivery schedule of oxaliplatin-5-Fluorouracil-leucovorin for metastatic colorectal cancer in a randomized international trial (EORTC 05963)

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Resumo:Circadian clocks control cellular proliferation and drug metabolism over the 24 h. However, circadian chronomodulated chemotherapy with 5-fluorouracil, leucovorin, and oxaliplatin (chronoFLO4) offered no survival benefit as compared with the non-time-stipulated FOLFOX2, in an international randomized trial involving patients with previously untreated metastatic colorectal cancer (EORTC 05963). The authors hypothesized that treatment near maximum tolerated dose could disrupt circadian clocks thus impairing the efficacy of chronoFLO4 but not of FOLFOX2. Patients with available data (N = 556) were categorized into three subgroups according to the worst grade (G) of neutropenia experienced during treatment. Distinct multivariate models with time-dependent covariates were constructed for each treatment schedule. Neutropenia incidence (all grades) was 33% on chronoFLO4 and 61% on FOLFOX2 (p < .0001), and G3-4 were 7% and 25%, respectively (p < .0001). Neutropenia was significantly more frequent in women than men on either schedule (FOLFOX2, p = .003; chronoFLO4, p = .04). Median survival was 20.7 mo in patients with G3-4 neutropenia versus 12.5 mo in neutropenia-free patients on FOLFOX2 (p < .0001). Corresponding figures were 13.7 and 19.4 mo, respectively, on chronoFLO4 (p = .36). Multivariate analysis confirmed occurrence of severe neutropenia independently predicted for better overall survival on FOLFOX2 (HR = 0.56; p = .015), and worse survival on chronoFLO4 (HR = 1.77, p = .06), with a significant interaction test (p < .0001). Prediction of better survival in neutropenic patients on FOLFOX2 supports the administration of conventional chemotherapy near maximum tolerated dose. The opposite trend shown here for chronoFLO4 supports the novel concept of jointly optimized hematologic tolerability and efficacy through personalized circadian-timed therapy.
Autores principais:Innominato, PF
Outros Autores:Giacchetti, S; Moreau, T; Carvalho, C, et al.
Assunto:Antineoplastic agents Colorectal neoplasms Neutropenia
Ano:2011
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Hospital Prof. Dr. Fernando Fonseca E.P.E.
Idioma:inglês
Origem:Repositório do Hospital Prof. Doutor Fernando Fonseca
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author Innominato, PF
author2 Giacchetti, S
Moreau, T
Carvalho, C, et al.
author2_role author
author
author
author_facet Innominato, PF
Giacchetti, S
Moreau, T
Carvalho, C, et al.
author_role author
contributor_name_str_mv Unidade Local de Saúde Amadora / Sintra
country_str PT
creators_json_txt [{\"Person.name\":\"Innominato, PF\"},{\"Person.name\":\"Giacchetti, S\"},{\"Person.name\":\"Moreau, T\"},{\"Person.name\":\"Carvalho, C, et al.\"}]
datacite.contributors.contributor.contributorName.fl_str_mv Unidade Local de Saúde Amadora / Sintra
datacite.creators.creator.creatorName.fl_str_mv Innominato, PF
Giacchetti, S
Moreau, T
Carvalho, C, et al.
datacite.date.Accepted.fl_str_mv 2011-01-01T00:00:00Z
datacite.date.available.fl_str_mv 2019-05-24T11:35:31Z
datacite.date.embargoed.fl_str_mv 2019-05-24T11:35:31Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_abf2
datacite.subjects.subject.fl_str_mv Antineoplastic agents
Colorectal neoplasms
Neutropenia
datacite.titles.title.fl_str_mv Prediction of survival by neutropenia according to delivery schedule of oxaliplatin-5-Fluorouracil-leucovorin for metastatic colorectal cancer in a randomized international trial (EORTC 05963)
dc.contributor.none.fl_str_mv Unidade Local de Saúde Amadora / Sintra
dc.creator.none.fl_str_mv Innominato, PF
Giacchetti, S
Moreau, T
Carvalho, C, et al.
dc.date.Accepted.fl_str_mv 2011-01-01T00:00:00Z
dc.date.available.fl_str_mv 2019-05-24T11:35:31Z
dc.date.embargoed.fl_str_mv 2019-05-24T11:35:31Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv http://hdl.handle.net/10400.10/2275
dc.language.none.fl_str_mv eng
dc.publisher.none.fl_str_mv Informa Healthcare
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.subject.none.fl_str_mv Antineoplastic agents
Colorectal neoplasms
Neutropenia
dc.title.fl_str_mv Prediction of survival by neutropenia according to delivery schedule of oxaliplatin-5-Fluorouracil-leucovorin for metastatic colorectal cancer in a randomized international trial (EORTC 05963)
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
description Circadian clocks control cellular proliferation and drug metabolism over the 24 h. However, circadian chronomodulated chemotherapy with 5-fluorouracil, leucovorin, and oxaliplatin (chronoFLO4) offered no survival benefit as compared with the non-time-stipulated FOLFOX2, in an international randomized trial involving patients with previously untreated metastatic colorectal cancer (EORTC 05963). The authors hypothesized that treatment near maximum tolerated dose could disrupt circadian clocks thus impairing the efficacy of chronoFLO4 but not of FOLFOX2. Patients with available data (N = 556) were categorized into three subgroups according to the worst grade (G) of neutropenia experienced during treatment. Distinct multivariate models with time-dependent covariates were constructed for each treatment schedule. Neutropenia incidence (all grades) was 33% on chronoFLO4 and 61% on FOLFOX2 (p < .0001), and G3-4 were 7% and 25%, respectively (p < .0001). Neutropenia was significantly more frequent in women than men on either schedule (FOLFOX2, p = .003; chronoFLO4, p = .04). Median survival was 20.7 mo in patients with G3-4 neutropenia versus 12.5 mo in neutropenia-free patients on FOLFOX2 (p < .0001). Corresponding figures were 13.7 and 19.4 mo, respectively, on chronoFLO4 (p = .36). Multivariate analysis confirmed occurrence of severe neutropenia independently predicted for better overall survival on FOLFOX2 (HR = 0.56; p = .015), and worse survival on chronoFLO4 (HR = 1.77, p = .06), with a significant interaction test (p < .0001). Prediction of better survival in neutropenic patients on FOLFOX2 supports the administration of conventional chemotherapy near maximum tolerated dose. The opposite trend shown here for chronoFLO4 supports the novel concept of jointly optimized hematologic tolerability and efficacy through personalized circadian-timed therapy.
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fulltext.url.fl_str_mv https://repositorio.hff.min-saude.pt/bitstreams/b199781b-e1e8-4390-a28f-01af844a617f/download
id rhff_fcf6b85ca8837578b00a05fa760587b5
identifier.url.fl_str_mv http://hdl.handle.net/10400.10/2275
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institution Hospital Prof. Dr. Fernando Fonseca E.P.E.
instname_str Hospital Prof. Dr. Fernando Fonseca E.P.E.
language eng
network_acronym_str rhff
network_name_str Repositório do Hospital Prof. Doutor Fernando Fonseca
oai_identifier_str oai:repositorio.hff.min-saude.pt:10400.10/2275
organization_str_mv urn:organizationAcronym:hff
person_str_mv Innominato, PF
Giacchetti, S
Moreau, T
Carvalho, C, et al.
publishDate 2011
publisher.none.fl_str_mv Informa Healthcare
reponame_str Repositório do Hospital Prof. Doutor Fernando Fonseca
repository_id_str urn:repositoryAcronym:rhff
service_str_mv urn:repositoryAcronym:rhff
spelling engInforma Healthcarept_PTCircadian clocks control cellular proliferation and drug metabolism over the 24 h. However, circadian chronomodulated chemotherapy with 5-fluorouracil, leucovorin, and oxaliplatin (chronoFLO4) offered no survival benefit as compared with the non-time-stipulated FOLFOX2, in an international randomized trial involving patients with previously untreated metastatic colorectal cancer (EORTC 05963). The authors hypothesized that treatment near maximum tolerated dose could disrupt circadian clocks thus impairing the efficacy of chronoFLO4 but not of FOLFOX2. Patients with available data (N = 556) were categorized into three subgroups according to the worst grade (G) of neutropenia experienced during treatment. Distinct multivariate models with time-dependent covariates were constructed for each treatment schedule. Neutropenia incidence (all grades) was 33% on chronoFLO4 and 61% on FOLFOX2 (p < .0001), and G3-4 were 7% and 25%, respectively (p < .0001). Neutropenia was significantly more frequent in women than men on either schedule (FOLFOX2, p = .003; chronoFLO4, p = .04). Median survival was 20.7 mo in patients with G3-4 neutropenia versus 12.5 mo in neutropenia-free patients on FOLFOX2 (p < .0001). Corresponding figures were 13.7 and 19.4 mo, respectively, on chronoFLO4 (p = .36). Multivariate analysis confirmed occurrence of severe neutropenia independently predicted for better overall survival on FOLFOX2 (HR = 0.56; p = .015), and worse survival on chronoFLO4 (HR = 1.77, p = .06), with a significant interaction test (p < .0001). Prediction of better survival in neutropenic patients on FOLFOX2 supports the administration of conventional chemotherapy near maximum tolerated dose. The opposite trend shown here for chronoFLO4 supports the novel concept of jointly optimized hematologic tolerability and efficacy through personalized circadian-timed therapy.application/pdfpt_PTPrediction of survival by neutropenia according to delivery schedule of oxaliplatin-5-Fluorouracil-leucovorin for metastatic colorectal cancer in a randomized international trial (EORTC 05963)Innominato, PFGiacchetti, SMoreau, TCarvalho, C, et al.HostingInstitutionOrganizationalUnidade Local de Saúde Amadora / Sintrae-mailmailto:repositorio@hff.min-saude.ptrepositorio@hff.min-saude.ptISSNIsPartOf1525-6073DOIIsPartOf10.3109/07420528.2011.5975322019-05-24T11:35:31Z20112011-01-01T00:00:00ZHandlehttp://hdl.handle.net/10400.10/2275http://purl.org/coar/access_right/c_abf2open accessAntineoplastic agentsColorectal neoplasmsNeutropenia888244 bytesliteraturehttp://purl.org/coar/resource_type/c_6501journal articlehttp://purl.org/coar/access_right/c_abf2application/pdffulltexthttps://repositorio.hff.min-saude.pt/bitstreams/b199781b-e1e8-4390-a28f-01af844a617f/downloadChronobiology internationalLondon
spellingShingle Prediction of survival by neutropenia according to delivery schedule of oxaliplatin-5-Fluorouracil-leucovorin for metastatic colorectal cancer in a randomized international trial (EORTC 05963)
Innominato, PF
Antineoplastic agents
Colorectal neoplasms
Neutropenia
status SINGLETON
subject.fl_str_mv Antineoplastic agents
Colorectal neoplasms
Neutropenia
title Prediction of survival by neutropenia according to delivery schedule of oxaliplatin-5-Fluorouracil-leucovorin for metastatic colorectal cancer in a randomized international trial (EORTC 05963)
title_full Prediction of survival by neutropenia according to delivery schedule of oxaliplatin-5-Fluorouracil-leucovorin for metastatic colorectal cancer in a randomized international trial (EORTC 05963)
title_fullStr Prediction of survival by neutropenia according to delivery schedule of oxaliplatin-5-Fluorouracil-leucovorin for metastatic colorectal cancer in a randomized international trial (EORTC 05963)
title_full_unstemmed Prediction of survival by neutropenia according to delivery schedule of oxaliplatin-5-Fluorouracil-leucovorin for metastatic colorectal cancer in a randomized international trial (EORTC 05963)
title_short Prediction of survival by neutropenia according to delivery schedule of oxaliplatin-5-Fluorouracil-leucovorin for metastatic colorectal cancer in a randomized international trial (EORTC 05963)
title_sort Prediction of survival by neutropenia according to delivery schedule of oxaliplatin-5-Fluorouracil-leucovorin for metastatic colorectal cancer in a randomized international trial (EORTC 05963)
topic Antineoplastic agents
Colorectal neoplasms
Neutropenia
topic_facet Antineoplastic agents
Colorectal neoplasms
Neutropenia
url http://hdl.handle.net/10400.10/2275
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