Cargando…

Prognostic role of a new index (multi inflammatory index) in patients with metastatic colorectal cancer: results from the randomized ITACa trial

AIMS: We created a new index (Multi Inflammatory Index, MII) composed of an inflammatory index [neutrophil-to lymphocyte-ratio (NLR): MII-1; platelet-to-lymphocyte ratio (PLR): MII-2; or systemic immune-inflammation index (SII): MII-3] and C-reactive protein (CRP). Our aim was to evaluate the progno...

Descripción completa

Detalles Bibliográficos
Autores principales: Casadei Gardini, Andrea, Scarpi, Emanuela, Valgiusti, Martina, Monti, Manlio, Ruscelli, Silvia, Matteucci, Laura, Bartolini, Giulia, Vertogen, Bernadette, Pagan, Flavia, Rovesti, Giulia, Frassineti, Giovanni Luca, Passardi, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534088/
https://www.ncbi.nlm.nih.gov/pubmed/33062063
http://dx.doi.org/10.1177/1758835920958363
_version_ 1783590250148265984
author Casadei Gardini, Andrea
Scarpi, Emanuela
Valgiusti, Martina
Monti, Manlio
Ruscelli, Silvia
Matteucci, Laura
Bartolini, Giulia
Vertogen, Bernadette
Pagan, Flavia
Rovesti, Giulia
Frassineti, Giovanni Luca
Passardi, Alessandro
author_facet Casadei Gardini, Andrea
Scarpi, Emanuela
Valgiusti, Martina
Monti, Manlio
Ruscelli, Silvia
Matteucci, Laura
Bartolini, Giulia
Vertogen, Bernadette
Pagan, Flavia
Rovesti, Giulia
Frassineti, Giovanni Luca
Passardi, Alessandro
author_sort Casadei Gardini, Andrea
collection PubMed
description AIMS: We created a new index (Multi Inflammatory Index, MII) composed of an inflammatory index [neutrophil-to lymphocyte-ratio (NLR): MII-1; platelet-to-lymphocyte ratio (PLR): MII-2; or systemic immune-inflammation index (SII): MII-3] and C-reactive protein (CRP). Our aim was to evaluate the prognostic and/or predictive capacity of the MII in the randomized ITACa (Italian Trial in Advanced Colorectal Cancer) study on patients with metastatic colorectal cancer undergoing first-line chemotherapy. METHODS: Between November 2007 and March 2012, baseline NLR, PLR; SII and CRP were available for 131 patients, 66 receiving chemotherapy plus bevacizumab and 65 receiving chemotherapy alone. RESULTS: Patients with low (<25) MII-1 levels had a better outcome than those with high (⩾25) levels: median progression-free survival (PFS) was 12.4 versus 8.9 months [hazard ratio (HR) = 1.74, 95% confidence interval (CI) 1.21–2.51, p = 0.003] and median overall survival (OS) was 30.9 months versus 15.0 months (HR = 2.05, 95% CI 1.40–3.02, p = 0.0002), respectively. Similar results were obtained for patients with low (<1424) MII-2 levels compared with those with high (⩾1424) levels: median PFS was 12.6 versus 8.9 months (HR = 1.95, 95% CI 1.35–2.82, p = 0.0004) and median OS was 32.4 versus 14.6 months, respectively (HR = 2.42, 95% CI 1.64–3.57, p < 0.0001). Patients with low (<6068) MII-3 levels had a longer median PFS and OS than those with high (⩾6068) levels: 12.6 versus 8.9 months (HR = 1.91, 95% CI 1.33–2.76, p = 0.005) and 30.9 versus15.0 months (HR = 2.10, 95% CI 1.43–3.09, p = 0.0002), respectively. Following adjustment for clinical covariates, multivariate analysis confirmed all MII indexes as independent prognostic factors for predicting PFS and OS. CONCLUSION: All MII indexes appear to be useful as prognostic markers. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT01878422 (registration date: 07/06/2013) https://clinicaltrials.gov/ct2/show/NCT01878422
format Online
Article
Text
id pubmed-7534088
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-75340882020-10-14 Prognostic role of a new index (multi inflammatory index) in patients with metastatic colorectal cancer: results from the randomized ITACa trial Casadei Gardini, Andrea Scarpi, Emanuela Valgiusti, Martina Monti, Manlio Ruscelli, Silvia Matteucci, Laura Bartolini, Giulia Vertogen, Bernadette Pagan, Flavia Rovesti, Giulia Frassineti, Giovanni Luca Passardi, Alessandro Ther Adv Med Oncol Original Research AIMS: We created a new index (Multi Inflammatory Index, MII) composed of an inflammatory index [neutrophil-to lymphocyte-ratio (NLR): MII-1; platelet-to-lymphocyte ratio (PLR): MII-2; or systemic immune-inflammation index (SII): MII-3] and C-reactive protein (CRP). Our aim was to evaluate the prognostic and/or predictive capacity of the MII in the randomized ITACa (Italian Trial in Advanced Colorectal Cancer) study on patients with metastatic colorectal cancer undergoing first-line chemotherapy. METHODS: Between November 2007 and March 2012, baseline NLR, PLR; SII and CRP were available for 131 patients, 66 receiving chemotherapy plus bevacizumab and 65 receiving chemotherapy alone. RESULTS: Patients with low (<25) MII-1 levels had a better outcome than those with high (⩾25) levels: median progression-free survival (PFS) was 12.4 versus 8.9 months [hazard ratio (HR) = 1.74, 95% confidence interval (CI) 1.21–2.51, p = 0.003] and median overall survival (OS) was 30.9 months versus 15.0 months (HR = 2.05, 95% CI 1.40–3.02, p = 0.0002), respectively. Similar results were obtained for patients with low (<1424) MII-2 levels compared with those with high (⩾1424) levels: median PFS was 12.6 versus 8.9 months (HR = 1.95, 95% CI 1.35–2.82, p = 0.0004) and median OS was 32.4 versus 14.6 months, respectively (HR = 2.42, 95% CI 1.64–3.57, p < 0.0001). Patients with low (<6068) MII-3 levels had a longer median PFS and OS than those with high (⩾6068) levels: 12.6 versus 8.9 months (HR = 1.91, 95% CI 1.33–2.76, p = 0.005) and 30.9 versus15.0 months (HR = 2.10, 95% CI 1.43–3.09, p = 0.0002), respectively. Following adjustment for clinical covariates, multivariate analysis confirmed all MII indexes as independent prognostic factors for predicting PFS and OS. CONCLUSION: All MII indexes appear to be useful as prognostic markers. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT01878422 (registration date: 07/06/2013) https://clinicaltrials.gov/ct2/show/NCT01878422 SAGE Publications 2020-09-28 /pmc/articles/PMC7534088/ /pubmed/33062063 http://dx.doi.org/10.1177/1758835920958363 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Casadei Gardini, Andrea
Scarpi, Emanuela
Valgiusti, Martina
Monti, Manlio
Ruscelli, Silvia
Matteucci, Laura
Bartolini, Giulia
Vertogen, Bernadette
Pagan, Flavia
Rovesti, Giulia
Frassineti, Giovanni Luca
Passardi, Alessandro
Prognostic role of a new index (multi inflammatory index) in patients with metastatic colorectal cancer: results from the randomized ITACa trial
title Prognostic role of a new index (multi inflammatory index) in patients with metastatic colorectal cancer: results from the randomized ITACa trial
title_full Prognostic role of a new index (multi inflammatory index) in patients with metastatic colorectal cancer: results from the randomized ITACa trial
title_fullStr Prognostic role of a new index (multi inflammatory index) in patients with metastatic colorectal cancer: results from the randomized ITACa trial
title_full_unstemmed Prognostic role of a new index (multi inflammatory index) in patients with metastatic colorectal cancer: results from the randomized ITACa trial
title_short Prognostic role of a new index (multi inflammatory index) in patients with metastatic colorectal cancer: results from the randomized ITACa trial
title_sort prognostic role of a new index (multi inflammatory index) in patients with metastatic colorectal cancer: results from the randomized itaca trial
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534088/
https://www.ncbi.nlm.nih.gov/pubmed/33062063
http://dx.doi.org/10.1177/1758835920958363
work_keys_str_mv AT casadeigardiniandrea prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial
AT scarpiemanuela prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial
AT valgiustimartina prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial
AT montimanlio prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial
AT ruscellisilvia prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial
AT matteuccilaura prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial
AT bartolinigiulia prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial
AT vertogenbernadette prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial
AT paganflavia prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial
AT rovestigiulia prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial
AT frassinetigiovanniluca prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial
AT passardialessandro prognosticroleofanewindexmultiinflammatoryindexinpatientswithmetastaticcolorectalcancerresultsfromtherandomizeditacatrial