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High-dose nimotuzumab improves the survival rate of esophageal cancer patients who underwent radiotherapy

Nimotuzumab (h-R3) is a humanized monoclonal antibody that is safe to use against epidermal growth factor receptor (EGFR). However, the available information is insufficient about the dose effect of monoclonal antibody against epidermal growth factor receptor for the treatment of esophageal squamous...

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Autores principales: Wang, Chunyu, Fu, Xiaolong, Cai, Xuwei, Wu, Xianghua, Hu, Xichun, Fan, Min, Xiang, Jiaqing, Zhang, Yawei, Chen, Haiquan, Jiang, Guoliang, Zhao, Kuaile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4699509/
https://www.ncbi.nlm.nih.gov/pubmed/26766917
http://dx.doi.org/10.2147/OTT.S89592
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author Wang, Chunyu
Fu, Xiaolong
Cai, Xuwei
Wu, Xianghua
Hu, Xichun
Fan, Min
Xiang, Jiaqing
Zhang, Yawei
Chen, Haiquan
Jiang, Guoliang
Zhao, Kuaile
author_facet Wang, Chunyu
Fu, Xiaolong
Cai, Xuwei
Wu, Xianghua
Hu, Xichun
Fan, Min
Xiang, Jiaqing
Zhang, Yawei
Chen, Haiquan
Jiang, Guoliang
Zhao, Kuaile
author_sort Wang, Chunyu
collection PubMed
description Nimotuzumab (h-R3) is a humanized monoclonal antibody that is safe to use against epidermal growth factor receptor (EGFR). However, the available information is insufficient about the dose effect of monoclonal antibody against epidermal growth factor receptor for the treatment of esophageal squamous cell carcinoma (ESCC). We retrospectively recruited 66 patients with ESCC who were treated with h-R3 and chemoradiotherapy/radiotherapy. Patients who received more than 1,200 mg of h-R3 were classified as the high-dose group, and the remaining patients were classified as the low-dose group. The endpoint for efficacy was the overall survival. Differences in survival between the groups were analyzed using the log-rank test. The Cox proportional hazards model was used in multivariate analysis to identify independent prognostic factors. The low-dose and high-dose groups comprised 55 and eleven patients, respectively. The median follow-up time in the final analysis was 46 months. The high-dose group showed no increased incidence of toxicities compared to the low-dose group. The 1-, 2-, and 5-year overall survival rates in the low-dose and high-dose groups were 66.9%, 50.0%, 31.5% and 90.0%, 80.0%, 66.7%, respectively (P=0.04). Multivariate analyses showed that the high-dose group had better survival than the low-dose group (hazard ratio 0.28, 95% confidence interval 0.09–0.94, P=0.039). Taken together, high-dose h-R3 showed limited toxicity and improved survival in patients with ESCC.
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spelling pubmed-46995092016-01-13 High-dose nimotuzumab improves the survival rate of esophageal cancer patients who underwent radiotherapy Wang, Chunyu Fu, Xiaolong Cai, Xuwei Wu, Xianghua Hu, Xichun Fan, Min Xiang, Jiaqing Zhang, Yawei Chen, Haiquan Jiang, Guoliang Zhao, Kuaile Onco Targets Ther Original Research Nimotuzumab (h-R3) is a humanized monoclonal antibody that is safe to use against epidermal growth factor receptor (EGFR). However, the available information is insufficient about the dose effect of monoclonal antibody against epidermal growth factor receptor for the treatment of esophageal squamous cell carcinoma (ESCC). We retrospectively recruited 66 patients with ESCC who were treated with h-R3 and chemoradiotherapy/radiotherapy. Patients who received more than 1,200 mg of h-R3 were classified as the high-dose group, and the remaining patients were classified as the low-dose group. The endpoint for efficacy was the overall survival. Differences in survival between the groups were analyzed using the log-rank test. The Cox proportional hazards model was used in multivariate analysis to identify independent prognostic factors. The low-dose and high-dose groups comprised 55 and eleven patients, respectively. The median follow-up time in the final analysis was 46 months. The high-dose group showed no increased incidence of toxicities compared to the low-dose group. The 1-, 2-, and 5-year overall survival rates in the low-dose and high-dose groups were 66.9%, 50.0%, 31.5% and 90.0%, 80.0%, 66.7%, respectively (P=0.04). Multivariate analyses showed that the high-dose group had better survival than the low-dose group (hazard ratio 0.28, 95% confidence interval 0.09–0.94, P=0.039). Taken together, high-dose h-R3 showed limited toxicity and improved survival in patients with ESCC. Dove Medical Press 2015-12-30 /pmc/articles/PMC4699509/ /pubmed/26766917 http://dx.doi.org/10.2147/OTT.S89592 Text en © 2016 Wang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Wang, Chunyu
Fu, Xiaolong
Cai, Xuwei
Wu, Xianghua
Hu, Xichun
Fan, Min
Xiang, Jiaqing
Zhang, Yawei
Chen, Haiquan
Jiang, Guoliang
Zhao, Kuaile
High-dose nimotuzumab improves the survival rate of esophageal cancer patients who underwent radiotherapy
title High-dose nimotuzumab improves the survival rate of esophageal cancer patients who underwent radiotherapy
title_full High-dose nimotuzumab improves the survival rate of esophageal cancer patients who underwent radiotherapy
title_fullStr High-dose nimotuzumab improves the survival rate of esophageal cancer patients who underwent radiotherapy
title_full_unstemmed High-dose nimotuzumab improves the survival rate of esophageal cancer patients who underwent radiotherapy
title_short High-dose nimotuzumab improves the survival rate of esophageal cancer patients who underwent radiotherapy
title_sort high-dose nimotuzumab improves the survival rate of esophageal cancer patients who underwent radiotherapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4699509/
https://www.ncbi.nlm.nih.gov/pubmed/26766917
http://dx.doi.org/10.2147/OTT.S89592
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