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Late stage gastric cancer patients with extra gained HER2 positivity by dual block assessment may not show compromised efficacy to trastuzumab treatment

Dual block HER2 assessment can effectively increase the HER2 positive rate in resected specimens of gastric cancer (GC). The aim of this study is to explore whether GC patients with extra gained HER2 positivity by dual block assessment can benefit from trastuzumab therapy. Twenty-eight GC patients r...

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Autores principales: Xu, Chen, Liu, Yalan, Jiang, Dongxian, Ge, Xiaowen, Huang, Jie, Su, Jieakesu, Zhang, Xue, Lu, Shaohua, Ji, Yuan, Hou, Jun, Liu, Tianshu, Hou, Yingyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6914406/
https://www.ncbi.nlm.nih.gov/pubmed/31739285
http://dx.doi.org/10.18632/aging.102415
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author Xu, Chen
Liu, Yalan
Jiang, Dongxian
Ge, Xiaowen
Huang, Jie
Su, Jieakesu
Zhang, Xue
Lu, Shaohua
Ji, Yuan
Hou, Jun
Liu, Tianshu
Hou, Yingyong
author_facet Xu, Chen
Liu, Yalan
Jiang, Dongxian
Ge, Xiaowen
Huang, Jie
Su, Jieakesu
Zhang, Xue
Lu, Shaohua
Ji, Yuan
Hou, Jun
Liu, Tianshu
Hou, Yingyong
author_sort Xu, Chen
collection PubMed
description Dual block HER2 assessment can effectively increase the HER2 positive rate in resected specimens of gastric cancer (GC). The aim of this study is to explore whether GC patients with extra gained HER2 positivity by dual block assessment can benefit from trastuzumab therapy. Twenty-eight GC patients receiving gastrectomy prior to trastuzumab treatment were retrospectively analyzed. All the cases routinely accepted dual block HER2 assessment. The cases were divided into 2 cohorts based on HER2 status: cohort A with concordant HER2 results and cohort B with discordant HER2 results between the two blocks (cases with extra gained HER2 positivity). Response rate (RR), progress free survival (PFS) and overall survival (OS) were compared between the two cohorts. The results showed that no significant differences were found between the two cohorts in main clinicopathologic characteristics. No statistical difference was found in response rate (47.6% vs 57.1%) (P=1.0), either. The two cohorts did not demonstrate statistical differences in the PFS (10.5 months (95%CI 6.4-14.6) vs 8.0 months (95%CI 3.2-12.8), P=0.686) and the OS (23.3 months (95%CI 12.1-34.5) vs 20.0 months (95%CI 10.1-29.9), P=0.776). In conclusion, our study suggests that patients with extra gained HER2 positivity may not show compromised efficacy to trastuzumab treatment.
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spelling pubmed-69144062019-12-19 Late stage gastric cancer patients with extra gained HER2 positivity by dual block assessment may not show compromised efficacy to trastuzumab treatment Xu, Chen Liu, Yalan Jiang, Dongxian Ge, Xiaowen Huang, Jie Su, Jieakesu Zhang, Xue Lu, Shaohua Ji, Yuan Hou, Jun Liu, Tianshu Hou, Yingyong Aging (Albany NY) Research Paper Dual block HER2 assessment can effectively increase the HER2 positive rate in resected specimens of gastric cancer (GC). The aim of this study is to explore whether GC patients with extra gained HER2 positivity by dual block assessment can benefit from trastuzumab therapy. Twenty-eight GC patients receiving gastrectomy prior to trastuzumab treatment were retrospectively analyzed. All the cases routinely accepted dual block HER2 assessment. The cases were divided into 2 cohorts based on HER2 status: cohort A with concordant HER2 results and cohort B with discordant HER2 results between the two blocks (cases with extra gained HER2 positivity). Response rate (RR), progress free survival (PFS) and overall survival (OS) were compared between the two cohorts. The results showed that no significant differences were found between the two cohorts in main clinicopathologic characteristics. No statistical difference was found in response rate (47.6% vs 57.1%) (P=1.0), either. The two cohorts did not demonstrate statistical differences in the PFS (10.5 months (95%CI 6.4-14.6) vs 8.0 months (95%CI 3.2-12.8), P=0.686) and the OS (23.3 months (95%CI 12.1-34.5) vs 20.0 months (95%CI 10.1-29.9), P=0.776). In conclusion, our study suggests that patients with extra gained HER2 positivity may not show compromised efficacy to trastuzumab treatment. Impact Journals 2019-11-17 /pmc/articles/PMC6914406/ /pubmed/31739285 http://dx.doi.org/10.18632/aging.102415 Text en Copyright © 2019 Xu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Xu, Chen
Liu, Yalan
Jiang, Dongxian
Ge, Xiaowen
Huang, Jie
Su, Jieakesu
Zhang, Xue
Lu, Shaohua
Ji, Yuan
Hou, Jun
Liu, Tianshu
Hou, Yingyong
Late stage gastric cancer patients with extra gained HER2 positivity by dual block assessment may not show compromised efficacy to trastuzumab treatment
title Late stage gastric cancer patients with extra gained HER2 positivity by dual block assessment may not show compromised efficacy to trastuzumab treatment
title_full Late stage gastric cancer patients with extra gained HER2 positivity by dual block assessment may not show compromised efficacy to trastuzumab treatment
title_fullStr Late stage gastric cancer patients with extra gained HER2 positivity by dual block assessment may not show compromised efficacy to trastuzumab treatment
title_full_unstemmed Late stage gastric cancer patients with extra gained HER2 positivity by dual block assessment may not show compromised efficacy to trastuzumab treatment
title_short Late stage gastric cancer patients with extra gained HER2 positivity by dual block assessment may not show compromised efficacy to trastuzumab treatment
title_sort late stage gastric cancer patients with extra gained her2 positivity by dual block assessment may not show compromised efficacy to trastuzumab treatment
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6914406/
https://www.ncbi.nlm.nih.gov/pubmed/31739285
http://dx.doi.org/10.18632/aging.102415
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