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Circulating cytokines and outcome in metastatic colorectal cancer patients treated with regorafenib

BACKGROUND: Regorafenib is an oral small-molecule multikinase inhibitor approved in third or later line of treatment for patients with metastatic colorectal cancer (mCRC). Regorafenib has shown significant benefits in overall survival and progression free survival in two phase III trials compared to...

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Autores principales: Ricci, Vincenzo, Granetto, Cristina, Falletta, Antonella, Paccagnella, Matteo, Abbona, Andrea, Fea, Elena, Fabozzi, Teresa, Lo Nigro, Cristiana, Merlano, Marco Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081116/
https://www.ncbi.nlm.nih.gov/pubmed/32206180
http://dx.doi.org/10.4251/wjgo.v12.i3.301
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author Ricci, Vincenzo
Granetto, Cristina
Falletta, Antonella
Paccagnella, Matteo
Abbona, Andrea
Fea, Elena
Fabozzi, Teresa
Lo Nigro, Cristiana
Merlano, Marco Carlo
author_facet Ricci, Vincenzo
Granetto, Cristina
Falletta, Antonella
Paccagnella, Matteo
Abbona, Andrea
Fea, Elena
Fabozzi, Teresa
Lo Nigro, Cristiana
Merlano, Marco Carlo
author_sort Ricci, Vincenzo
collection PubMed
description BACKGROUND: Regorafenib is an oral small-molecule multikinase inhibitor approved in third or later line of treatment for patients with metastatic colorectal cancer (mCRC). Regorafenib has shown significant benefits in overall survival and progression free survival in two phase III trials compared to placebo in patients with mCRC who had progressed on previous therapy. AIM: To identify an immune profile that might specifically correlate with the outcome in patients treated with regorafenib. METHODS: Blood samples were collected from 17 patients before treatment with regorafenib and from 6 healthy volunteers. The proteins evaluated (TNF-α, TGF-β, VEGF, CCL-2, CCL-4, and CCL-5) were selected on the basis of their roles in angiogenesis and colorectal cancer pathogenesis. RESULTS: We found that TNF-α basal level was significantly higher in mCRC patients compared to healthy individuals. Non Responder (NR) patients showing progression of disease (n = 12) had higher basal level of TGF-β, TNF-α, VEGF, CCL-2 and CCL-5 compared to Responder (R) patients (complete response CR, n = 1; partial response PR, n = 1; Stable Disease SD, n = 3). On the contrary, plasma basal level of CCL-4 was higher in R compared to NR patients. High values of TGF-β and TNF-α negatively correlated with progression free survival. CONCLUSION: These results suggest a cytokine signature potentially able to discriminate between R and NR patients to treatment with regorafenib.
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spelling pubmed-70811162020-03-23 Circulating cytokines and outcome in metastatic colorectal cancer patients treated with regorafenib Ricci, Vincenzo Granetto, Cristina Falletta, Antonella Paccagnella, Matteo Abbona, Andrea Fea, Elena Fabozzi, Teresa Lo Nigro, Cristiana Merlano, Marco Carlo World J Gastrointest Oncol Retrospective Study BACKGROUND: Regorafenib is an oral small-molecule multikinase inhibitor approved in third or later line of treatment for patients with metastatic colorectal cancer (mCRC). Regorafenib has shown significant benefits in overall survival and progression free survival in two phase III trials compared to placebo in patients with mCRC who had progressed on previous therapy. AIM: To identify an immune profile that might specifically correlate with the outcome in patients treated with regorafenib. METHODS: Blood samples were collected from 17 patients before treatment with regorafenib and from 6 healthy volunteers. The proteins evaluated (TNF-α, TGF-β, VEGF, CCL-2, CCL-4, and CCL-5) were selected on the basis of their roles in angiogenesis and colorectal cancer pathogenesis. RESULTS: We found that TNF-α basal level was significantly higher in mCRC patients compared to healthy individuals. Non Responder (NR) patients showing progression of disease (n = 12) had higher basal level of TGF-β, TNF-α, VEGF, CCL-2 and CCL-5 compared to Responder (R) patients (complete response CR, n = 1; partial response PR, n = 1; Stable Disease SD, n = 3). On the contrary, plasma basal level of CCL-4 was higher in R compared to NR patients. High values of TGF-β and TNF-α negatively correlated with progression free survival. CONCLUSION: These results suggest a cytokine signature potentially able to discriminate between R and NR patients to treatment with regorafenib. Baishideng Publishing Group Inc 2020-03-15 2020-03-15 /pmc/articles/PMC7081116/ /pubmed/32206180 http://dx.doi.org/10.4251/wjgo.v12.i3.301 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Retrospective Study
Ricci, Vincenzo
Granetto, Cristina
Falletta, Antonella
Paccagnella, Matteo
Abbona, Andrea
Fea, Elena
Fabozzi, Teresa
Lo Nigro, Cristiana
Merlano, Marco Carlo
Circulating cytokines and outcome in metastatic colorectal cancer patients treated with regorafenib
title Circulating cytokines and outcome in metastatic colorectal cancer patients treated with regorafenib
title_full Circulating cytokines and outcome in metastatic colorectal cancer patients treated with regorafenib
title_fullStr Circulating cytokines and outcome in metastatic colorectal cancer patients treated with regorafenib
title_full_unstemmed Circulating cytokines and outcome in metastatic colorectal cancer patients treated with regorafenib
title_short Circulating cytokines and outcome in metastatic colorectal cancer patients treated with regorafenib
title_sort circulating cytokines and outcome in metastatic colorectal cancer patients treated with regorafenib
topic Retrospective Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081116/
https://www.ncbi.nlm.nih.gov/pubmed/32206180
http://dx.doi.org/10.4251/wjgo.v12.i3.301
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