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Treatment outcome of nimotuzumab plus chemotherapy in advanced cancer patients: a single institute experience
Nimotuzumab is a humanized anti-EGFR IgG1 monoclonal antibody and demonstrates a better safety profile than other anti-EGFR antibodies due to its intermediate affinity. Since it was approved in China for the treatment of nasopharyngeal cancer (NPC), it has been widely used in NPC and in many clinica...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078104/ https://www.ncbi.nlm.nih.gov/pubmed/27050148 http://dx.doi.org/10.18632/oncotarget.8516 |
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author | Xu, Shuping Ramos-Suzarte, Mayra Bai, Xianhong Xu, Binghe |
author_facet | Xu, Shuping Ramos-Suzarte, Mayra Bai, Xianhong Xu, Binghe |
author_sort | Xu, Shuping |
collection | PubMed |
description | Nimotuzumab is a humanized anti-EGFR IgG1 monoclonal antibody and demonstrates a better safety profile than other anti-EGFR antibodies due to its intermediate affinity. Since it was approved in China for the treatment of nasopharyngeal cancer (NPC), it has been widely used in NPC and in many clinical trials for other cancer types. However, the optimal dose and administration frequency of nimotuzumab that should be used and which kind of cancer patients will be more benefited from nimotuzumab is still unknown. In this retrospective study, 205 advanced cancer patients with colorectal cancer, esophageal cancer, head and neck cancer, gastric cancer, non-small cell lung cancer, or other cancers from mainland China, treated with nimotuzumab in combination with chemotherapy, were enrolled. Over 60% of these patients received nimotuzumab > 6 doses and ≥ 400 mg/week as maintenance therapy. It was well tolerated in real-life patients. This report demonstrates that age, sex and previous treatment might be potential predictive factors for survival, and patients received nimotuzumab > 6 doses and > 200 mg/week might benefit more from nimotuzumab therapy. Using these factors for stratification analysis may form a predictive differential clinical strategy for nimotuzumab to maximize the benefit in patients with different epithelial tumors. |
format | Online Article Text |
id | pubmed-5078104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-50781042016-10-28 Treatment outcome of nimotuzumab plus chemotherapy in advanced cancer patients: a single institute experience Xu, Shuping Ramos-Suzarte, Mayra Bai, Xianhong Xu, Binghe Oncotarget Clinical Research Paper Nimotuzumab is a humanized anti-EGFR IgG1 monoclonal antibody and demonstrates a better safety profile than other anti-EGFR antibodies due to its intermediate affinity. Since it was approved in China for the treatment of nasopharyngeal cancer (NPC), it has been widely used in NPC and in many clinical trials for other cancer types. However, the optimal dose and administration frequency of nimotuzumab that should be used and which kind of cancer patients will be more benefited from nimotuzumab is still unknown. In this retrospective study, 205 advanced cancer patients with colorectal cancer, esophageal cancer, head and neck cancer, gastric cancer, non-small cell lung cancer, or other cancers from mainland China, treated with nimotuzumab in combination with chemotherapy, were enrolled. Over 60% of these patients received nimotuzumab > 6 doses and ≥ 400 mg/week as maintenance therapy. It was well tolerated in real-life patients. This report demonstrates that age, sex and previous treatment might be potential predictive factors for survival, and patients received nimotuzumab > 6 doses and > 200 mg/week might benefit more from nimotuzumab therapy. Using these factors for stratification analysis may form a predictive differential clinical strategy for nimotuzumab to maximize the benefit in patients with different epithelial tumors. Impact Journals LLC 2016-03-31 /pmc/articles/PMC5078104/ /pubmed/27050148 http://dx.doi.org/10.18632/oncotarget.8516 Text en Copyright: © 2016 Xu et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Clinical Research Paper Xu, Shuping Ramos-Suzarte, Mayra Bai, Xianhong Xu, Binghe Treatment outcome of nimotuzumab plus chemotherapy in advanced cancer patients: a single institute experience |
title | Treatment outcome of nimotuzumab plus chemotherapy in advanced cancer patients: a single institute experience |
title_full | Treatment outcome of nimotuzumab plus chemotherapy in advanced cancer patients: a single institute experience |
title_fullStr | Treatment outcome of nimotuzumab plus chemotherapy in advanced cancer patients: a single institute experience |
title_full_unstemmed | Treatment outcome of nimotuzumab plus chemotherapy in advanced cancer patients: a single institute experience |
title_short | Treatment outcome of nimotuzumab plus chemotherapy in advanced cancer patients: a single institute experience |
title_sort | treatment outcome of nimotuzumab plus chemotherapy in advanced cancer patients: a single institute experience |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078104/ https://www.ncbi.nlm.nih.gov/pubmed/27050148 http://dx.doi.org/10.18632/oncotarget.8516 |
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