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Serum iron levels as a new biomarker in chemotherapy with leucovorin and fluorouracil plus oxaliplatin or leucovorin and fluorouracil plus irinotecan, with or without molecularly-targeted drugs

Serum iron levels have been reported to increase following the administration of various anticancer drugs. An increase in serum iron levels during therapy with leucovorin and fluorouracil plus oxaliplatin (FOLFOX) or leucovorin and fluorouracil plus irinotecan (FOLFIRI) was also observed. The aim of...

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Autores principales: OCHIAI, TAKUMI, NISHIMURA, KAZUHIKO, WATANABE, TOMOO, KITAJIMA, MASAYUKI, NAKATANI, AKINORI, INOU, TAKASHI, SHIBATA, HIDEKI, SATO, TSUYOSHI, KISHINE, KENJI, SEO, SHOUGO, OKUBO, SATOSHI, FUTAGAWA, SHUNJI, MASHIKO, SATOMI, NAGAOKA, ISAO
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916199/
https://www.ncbi.nlm.nih.gov/pubmed/24649250
http://dx.doi.org/10.3892/mco.2013.136
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author OCHIAI, TAKUMI
NISHIMURA, KAZUHIKO
WATANABE, TOMOO
KITAJIMA, MASAYUKI
NAKATANI, AKINORI
INOU, TAKASHI
SHIBATA, HIDEKI
SATO, TSUYOSHI
KISHINE, KENJI
SEO, SHOUGO
OKUBO, SATOSHI
FUTAGAWA, SHUNJI
MASHIKO, SATOMI
NAGAOKA, ISAO
author_facet OCHIAI, TAKUMI
NISHIMURA, KAZUHIKO
WATANABE, TOMOO
KITAJIMA, MASAYUKI
NAKATANI, AKINORI
INOU, TAKASHI
SHIBATA, HIDEKI
SATO, TSUYOSHI
KISHINE, KENJI
SEO, SHOUGO
OKUBO, SATOSHI
FUTAGAWA, SHUNJI
MASHIKO, SATOMI
NAGAOKA, ISAO
author_sort OCHIAI, TAKUMI
collection PubMed
description Serum iron levels have been reported to increase following the administration of various anticancer drugs. An increase in serum iron levels during therapy with leucovorin and fluorouracil plus oxaliplatin (FOLFOX) or leucovorin and fluorouracil plus irinotecan (FOLFIRI) was also observed. The aim of this study was to investigate the correlation between serum iron levels and prognosis in advanced colorectal cancer (CRC) patients treated with FOLFOX/FOLFIRI ± molecularly-targeted drugs. Serum iron levels were measured prior to and at 48 h after treatment with FOLFOX/FOLFIRI ± molecularly-targeted drugs in 72 advanced CRC patients, all of whom succumbed to the disease between December, 2005 and February, 2012. No patients received radiotherapy. Taking the median rate of increase in serum iron levels as the cut-off value in each therapy, the patients were divided into cohort I (increase rate greater than the cut-off value in at least one therapy) or cohort II (increase rate less than the cut-off value in all therapies). The χ(2) test and the t-test were used to compare patient characteristics between the two cohorts. Prognosis was evaluated between the two cohorts using the Kaplan-Meier method, the log-rank test and the Cox proportional hazards regression analysis. No significant bias in patient characteristics (including the frequency of chemotherapy or number of patients treated with molecularly-targeted drugs) was observed between the two cohorts. Serum iron levels were transiently elevated following treatment (P<0.001), returning to baseline within 2 weeks. Median survival time (MST) in cohort I (n=44) and cohort II (n=28) was 430 and 377 days, respectively. The MST was significantly higher in cohort I (P=0.0382). The multivariate analysis identified a small increase in serum iron levels as an independent risk factor for overall survival (OS). These results suggest that serum iron levels may be used as a new predictive factor in FOLFOX/FOLFIRI ± molecularly-targeted drug therapy. Serum iron levels may therefore prove to be a useful and convenient biomarker for OS in CRC patients.
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spelling pubmed-39161992014-03-19 Serum iron levels as a new biomarker in chemotherapy with leucovorin and fluorouracil plus oxaliplatin or leucovorin and fluorouracil plus irinotecan, with or without molecularly-targeted drugs OCHIAI, TAKUMI NISHIMURA, KAZUHIKO WATANABE, TOMOO KITAJIMA, MASAYUKI NAKATANI, AKINORI INOU, TAKASHI SHIBATA, HIDEKI SATO, TSUYOSHI KISHINE, KENJI SEO, SHOUGO OKUBO, SATOSHI FUTAGAWA, SHUNJI MASHIKO, SATOMI NAGAOKA, ISAO Mol Clin Oncol Articles Serum iron levels have been reported to increase following the administration of various anticancer drugs. An increase in serum iron levels during therapy with leucovorin and fluorouracil plus oxaliplatin (FOLFOX) or leucovorin and fluorouracil plus irinotecan (FOLFIRI) was also observed. The aim of this study was to investigate the correlation between serum iron levels and prognosis in advanced colorectal cancer (CRC) patients treated with FOLFOX/FOLFIRI ± molecularly-targeted drugs. Serum iron levels were measured prior to and at 48 h after treatment with FOLFOX/FOLFIRI ± molecularly-targeted drugs in 72 advanced CRC patients, all of whom succumbed to the disease between December, 2005 and February, 2012. No patients received radiotherapy. Taking the median rate of increase in serum iron levels as the cut-off value in each therapy, the patients were divided into cohort I (increase rate greater than the cut-off value in at least one therapy) or cohort II (increase rate less than the cut-off value in all therapies). The χ(2) test and the t-test were used to compare patient characteristics between the two cohorts. Prognosis was evaluated between the two cohorts using the Kaplan-Meier method, the log-rank test and the Cox proportional hazards regression analysis. No significant bias in patient characteristics (including the frequency of chemotherapy or number of patients treated with molecularly-targeted drugs) was observed between the two cohorts. Serum iron levels were transiently elevated following treatment (P<0.001), returning to baseline within 2 weeks. Median survival time (MST) in cohort I (n=44) and cohort II (n=28) was 430 and 377 days, respectively. The MST was significantly higher in cohort I (P=0.0382). The multivariate analysis identified a small increase in serum iron levels as an independent risk factor for overall survival (OS). These results suggest that serum iron levels may be used as a new predictive factor in FOLFOX/FOLFIRI ± molecularly-targeted drug therapy. Serum iron levels may therefore prove to be a useful and convenient biomarker for OS in CRC patients. D.A. Spandidos 2013-09 2013-05-30 /pmc/articles/PMC3916199/ /pubmed/24649250 http://dx.doi.org/10.3892/mco.2013.136 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
OCHIAI, TAKUMI
NISHIMURA, KAZUHIKO
WATANABE, TOMOO
KITAJIMA, MASAYUKI
NAKATANI, AKINORI
INOU, TAKASHI
SHIBATA, HIDEKI
SATO, TSUYOSHI
KISHINE, KENJI
SEO, SHOUGO
OKUBO, SATOSHI
FUTAGAWA, SHUNJI
MASHIKO, SATOMI
NAGAOKA, ISAO
Serum iron levels as a new biomarker in chemotherapy with leucovorin and fluorouracil plus oxaliplatin or leucovorin and fluorouracil plus irinotecan, with or without molecularly-targeted drugs
title Serum iron levels as a new biomarker in chemotherapy with leucovorin and fluorouracil plus oxaliplatin or leucovorin and fluorouracil plus irinotecan, with or without molecularly-targeted drugs
title_full Serum iron levels as a new biomarker in chemotherapy with leucovorin and fluorouracil plus oxaliplatin or leucovorin and fluorouracil plus irinotecan, with or without molecularly-targeted drugs
title_fullStr Serum iron levels as a new biomarker in chemotherapy with leucovorin and fluorouracil plus oxaliplatin or leucovorin and fluorouracil plus irinotecan, with or without molecularly-targeted drugs
title_full_unstemmed Serum iron levels as a new biomarker in chemotherapy with leucovorin and fluorouracil plus oxaliplatin or leucovorin and fluorouracil plus irinotecan, with or without molecularly-targeted drugs
title_short Serum iron levels as a new biomarker in chemotherapy with leucovorin and fluorouracil plus oxaliplatin or leucovorin and fluorouracil plus irinotecan, with or without molecularly-targeted drugs
title_sort serum iron levels as a new biomarker in chemotherapy with leucovorin and fluorouracil plus oxaliplatin or leucovorin and fluorouracil plus irinotecan, with or without molecularly-targeted drugs
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916199/
https://www.ncbi.nlm.nih.gov/pubmed/24649250
http://dx.doi.org/10.3892/mco.2013.136
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