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Impact of nutritional status in the era of FOLFOX/FIRI-based chemotherapy

BACKGROUND: The nutritional status plays a pivotal role during anticancer therapy. This study analyzed whether nutritional status influences the outcomes in the era of FOLFOX/FIRI therapy. METHODS: The patients were divided into two groups according to whether the nutritional status was well (serum...

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Autores principales: Okada, Shunji, Yamazaki, Shintaro, Kaiga, Teruo, Funada, Tomoya, Kochi, Mitsugu, Takayama, Tadatoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571622/
https://www.ncbi.nlm.nih.gov/pubmed/28836976
http://dx.doi.org/10.1186/s12957-017-1226-0
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author Okada, Shunji
Yamazaki, Shintaro
Kaiga, Teruo
Funada, Tomoya
Kochi, Mitsugu
Takayama, Tadatoshi
author_facet Okada, Shunji
Yamazaki, Shintaro
Kaiga, Teruo
Funada, Tomoya
Kochi, Mitsugu
Takayama, Tadatoshi
author_sort Okada, Shunji
collection PubMed
description BACKGROUND: The nutritional status plays a pivotal role during anticancer therapy. This study analyzed whether nutritional status influences the outcomes in the era of FOLFOX/FIRI therapy. METHODS: The patients were divided into two groups according to whether the nutritional status was well (serum albumin level ≥ 3.8 g/dL or a ≥ 1.0 g/dL increase as compared with the value before chemotherapy) or not before and 2 and 6 months after the start of chemotherapy. Chemotherapy-related adverse events (AE), treatment effect, and compliance were evaluated according to the nutritional status. The progression-free survival (PFS) and overall survival (OS) were assessed based on the nutritional status at 6 months. RESULTS: Between 2010 and 2013, data on 108 consecutive patients were analyzed. At 2 months after chemotherapy, the hematotoxicic AE and the value of tumor markers did not differ significantly. The non-hematotoxic AE were less frequent in patients in the well-nourished group (grade 2, 15.9 vs. 38.5%, p < 0.01). Based on the nutritional status at 6 months after chemotherapy, the hematotoxicic AE (grade 3, 9 vs. 19.5%, p = 0.03) and non-hematotoxic AE (grade 2, 31.3 vs. 51.2%, p = 0.04; grade 3, 6.0 vs. 24.4%, p < 0.01) were less frequent, and the median CEA value (5.3 vs. 27.75 mg/L, p < 0.01) was significantly lower in the well-nourished group. The median PFS (364 vs. 233 days, p < 0.01) and 5-year OS (26.5 vs. 11.1%, p = 0.01) are significantly better in the well-nourished group. CONCLUSIONS: The well-nourished at initial 6 months may predict a better treatment response and fewer adverse events in FOLFOX/FIRI chemotherapy.
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spelling pubmed-55716222017-08-30 Impact of nutritional status in the era of FOLFOX/FIRI-based chemotherapy Okada, Shunji Yamazaki, Shintaro Kaiga, Teruo Funada, Tomoya Kochi, Mitsugu Takayama, Tadatoshi World J Surg Oncol Research BACKGROUND: The nutritional status plays a pivotal role during anticancer therapy. This study analyzed whether nutritional status influences the outcomes in the era of FOLFOX/FIRI therapy. METHODS: The patients were divided into two groups according to whether the nutritional status was well (serum albumin level ≥ 3.8 g/dL or a ≥ 1.0 g/dL increase as compared with the value before chemotherapy) or not before and 2 and 6 months after the start of chemotherapy. Chemotherapy-related adverse events (AE), treatment effect, and compliance were evaluated according to the nutritional status. The progression-free survival (PFS) and overall survival (OS) were assessed based on the nutritional status at 6 months. RESULTS: Between 2010 and 2013, data on 108 consecutive patients were analyzed. At 2 months after chemotherapy, the hematotoxicic AE and the value of tumor markers did not differ significantly. The non-hematotoxic AE were less frequent in patients in the well-nourished group (grade 2, 15.9 vs. 38.5%, p < 0.01). Based on the nutritional status at 6 months after chemotherapy, the hematotoxicic AE (grade 3, 9 vs. 19.5%, p = 0.03) and non-hematotoxic AE (grade 2, 31.3 vs. 51.2%, p = 0.04; grade 3, 6.0 vs. 24.4%, p < 0.01) were less frequent, and the median CEA value (5.3 vs. 27.75 mg/L, p < 0.01) was significantly lower in the well-nourished group. The median PFS (364 vs. 233 days, p < 0.01) and 5-year OS (26.5 vs. 11.1%, p = 0.01) are significantly better in the well-nourished group. CONCLUSIONS: The well-nourished at initial 6 months may predict a better treatment response and fewer adverse events in FOLFOX/FIRI chemotherapy. BioMed Central 2017-08-24 /pmc/articles/PMC5571622/ /pubmed/28836976 http://dx.doi.org/10.1186/s12957-017-1226-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Okada, Shunji
Yamazaki, Shintaro
Kaiga, Teruo
Funada, Tomoya
Kochi, Mitsugu
Takayama, Tadatoshi
Impact of nutritional status in the era of FOLFOX/FIRI-based chemotherapy
title Impact of nutritional status in the era of FOLFOX/FIRI-based chemotherapy
title_full Impact of nutritional status in the era of FOLFOX/FIRI-based chemotherapy
title_fullStr Impact of nutritional status in the era of FOLFOX/FIRI-based chemotherapy
title_full_unstemmed Impact of nutritional status in the era of FOLFOX/FIRI-based chemotherapy
title_short Impact of nutritional status in the era of FOLFOX/FIRI-based chemotherapy
title_sort impact of nutritional status in the era of folfox/firi-based chemotherapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571622/
https://www.ncbi.nlm.nih.gov/pubmed/28836976
http://dx.doi.org/10.1186/s12957-017-1226-0
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