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Effects of omeprazole in improving concurrent chemoradiotherapy efficacy in rectal cancer

AIM: To explore the effects of omeprazole on chemoradiotherapy efficacy and tumor recurrence in rectal cancer. METHODS: The medical data of 125 rectal cancer patients who received the same neoadjuvant chemoradiotherapy (CRT) followed by surgery were retrospectively collected. Patients who received o...

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Autores principales: Zhang, Jin-Liang, Liu, Min, Yang, Qing, Lin, Shi-Yong, Shan, Hong-Bo, Wang, Hui-Yun, Xu, Guo-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394521/
https://www.ncbi.nlm.nih.gov/pubmed/28465642
http://dx.doi.org/10.3748/wjg.v23.i14.2575
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author Zhang, Jin-Liang
Liu, Min
Yang, Qing
Lin, Shi-Yong
Shan, Hong-Bo
Wang, Hui-Yun
Xu, Guo-Liang
author_facet Zhang, Jin-Liang
Liu, Min
Yang, Qing
Lin, Shi-Yong
Shan, Hong-Bo
Wang, Hui-Yun
Xu, Guo-Liang
author_sort Zhang, Jin-Liang
collection PubMed
description AIM: To explore the effects of omeprazole on chemoradiotherapy efficacy and tumor recurrence in rectal cancer. METHODS: The medical data of 125 rectal cancer patients who received the same neoadjuvant chemoradiotherapy (CRT) followed by surgery were retrospectively collected. Patients who received omeprazole (OME) orally at a dose of 20 mg at least once daily for six days and/or intravenously at 40 mg a day were recognized as eligible OME users (EOU). Otherwise, patients were regarded as non-eligible OME users (non-EOU). Moreover, a preferred OME dose cut-off of 200 mg on tumor recurrence was obtained by receiver operating characteristic (ROC) curves. Patients were divided into two groups: the effective OME group (EOG, OME ≥ 200 mg) and the non-effective OME group (non-EOG, OME < 200 mg). RESULTS: The good response rate of CRT efficacy (50.8%) in EOU was significantly increased compared with non-EOU (30.6%) (P = 0.02). The recurrence rate in the EOG was 10.3%, which was significantly lower compared with 31.3% in non-EOG (P = 0.025). The good response rate of CRT efficacy in EOG was 55.2%, which was obviously higher compared with 36.5% in non-EOG, with a significant difference (P = 0.072). Multivariate Cox analysis demonstrated that OME (non-EOG and EOG) was an independent and significant impact factor for DFS (P = 0.048, HR = 0.30, 95%CI: 0.09-0.99). CONCLUSION: When applied as an adjuvant drug in cancer treatment for relieving common side effects of chemotherapy, omeprazole has a synergetic effect in improving CRT efficacy and decreasing rectal cancer recurrence.
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spelling pubmed-53945212017-05-02 Effects of omeprazole in improving concurrent chemoradiotherapy efficacy in rectal cancer Zhang, Jin-Liang Liu, Min Yang, Qing Lin, Shi-Yong Shan, Hong-Bo Wang, Hui-Yun Xu, Guo-Liang World J Gastroenterol Retrospective Study AIM: To explore the effects of omeprazole on chemoradiotherapy efficacy and tumor recurrence in rectal cancer. METHODS: The medical data of 125 rectal cancer patients who received the same neoadjuvant chemoradiotherapy (CRT) followed by surgery were retrospectively collected. Patients who received omeprazole (OME) orally at a dose of 20 mg at least once daily for six days and/or intravenously at 40 mg a day were recognized as eligible OME users (EOU). Otherwise, patients were regarded as non-eligible OME users (non-EOU). Moreover, a preferred OME dose cut-off of 200 mg on tumor recurrence was obtained by receiver operating characteristic (ROC) curves. Patients were divided into two groups: the effective OME group (EOG, OME ≥ 200 mg) and the non-effective OME group (non-EOG, OME < 200 mg). RESULTS: The good response rate of CRT efficacy (50.8%) in EOU was significantly increased compared with non-EOU (30.6%) (P = 0.02). The recurrence rate in the EOG was 10.3%, which was significantly lower compared with 31.3% in non-EOG (P = 0.025). The good response rate of CRT efficacy in EOG was 55.2%, which was obviously higher compared with 36.5% in non-EOG, with a significant difference (P = 0.072). Multivariate Cox analysis demonstrated that OME (non-EOG and EOG) was an independent and significant impact factor for DFS (P = 0.048, HR = 0.30, 95%CI: 0.09-0.99). CONCLUSION: When applied as an adjuvant drug in cancer treatment for relieving common side effects of chemotherapy, omeprazole has a synergetic effect in improving CRT efficacy and decreasing rectal cancer recurrence. Baishideng Publishing Group Inc 2017-04-14 2017-04-14 /pmc/articles/PMC5394521/ /pubmed/28465642 http://dx.doi.org/10.3748/wjg.v23.i14.2575 Text en ©The Author(s) 2017. 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
Zhang, Jin-Liang
Liu, Min
Yang, Qing
Lin, Shi-Yong
Shan, Hong-Bo
Wang, Hui-Yun
Xu, Guo-Liang
Effects of omeprazole in improving concurrent chemoradiotherapy efficacy in rectal cancer
title Effects of omeprazole in improving concurrent chemoradiotherapy efficacy in rectal cancer
title_full Effects of omeprazole in improving concurrent chemoradiotherapy efficacy in rectal cancer
title_fullStr Effects of omeprazole in improving concurrent chemoradiotherapy efficacy in rectal cancer
title_full_unstemmed Effects of omeprazole in improving concurrent chemoradiotherapy efficacy in rectal cancer
title_short Effects of omeprazole in improving concurrent chemoradiotherapy efficacy in rectal cancer
title_sort effects of omeprazole in improving concurrent chemoradiotherapy efficacy in rectal cancer
topic Retrospective Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394521/
https://www.ncbi.nlm.nih.gov/pubmed/28465642
http://dx.doi.org/10.3748/wjg.v23.i14.2575
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