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Randomized clinical trial: Nucleos(t)ide analogues improved survival of CHB-related HCC patients via reducing severity and progression of malignancy
BACKGROUND: The influence of nucleos(t)ide analogues (NAs) to treat Chronic hepatitis B (CHB) related hepatocellular carcinoma (HCC) remains to be explored. AIM: To investigate if NAs reduce the severity and progression of CHB-related HCC. RESULTS: Among 532 patients, there were 118 or 414 CHB-relat...
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/PMC5295451/ https://www.ncbi.nlm.nih.gov/pubmed/27329718 http://dx.doi.org/10.18632/oncotarget.10155 |
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author | Wang, Yun Xiang, Xiaogang Chen, Liwen Cao, Zhujun Bao, Rebecca Zhou, Huijuan Tang, Weiliang Lu, Jie Lin, Lanyi Xie, Qing Bao, Shisan Wang, Hui |
author_facet | Wang, Yun Xiang, Xiaogang Chen, Liwen Cao, Zhujun Bao, Rebecca Zhou, Huijuan Tang, Weiliang Lu, Jie Lin, Lanyi Xie, Qing Bao, Shisan Wang, Hui |
author_sort | Wang, Yun |
collection | PubMed |
description | BACKGROUND: The influence of nucleos(t)ide analogues (NAs) to treat Chronic hepatitis B (CHB) related hepatocellular carcinoma (HCC) remains to be explored. AIM: To investigate if NAs reduce the severity and progression of CHB-related HCC. RESULTS: Among 532 patients, there were 118 or 414 CHB-related HCC with or without NAs therapy, respectively. BCLC scores, serum level of ALT/AST and HBV DNA were compared. During follow-up, the survival period of CHB-related HCC patients with sustained NAs is significantly longer than that with NAs post-HCC and NAs naïve (p < 0.05). Factors significantly associated with the poor overall survival of CHB-related HCC include BCLC scores (hazard ratio, 1.84 [95% confidence interval, 1.57−2.15], p < 0.001), NAs post-HCC or NAs naïve (1.33 [1.07−1.65], p < 0.01), serum AST ≥ 40 IU/L (1.48 [1.03−2.12], p < 0.05) and HBV DNA ≥ 10(4) copies/ml (1.36 [1.01−1.83], p < 0.001). METHODS: Outcomes of 532 CHB-related HCC patients with/without NAs were investigated. Overall survival of CHB-related HCC patients, NAs naïve (n = 156), NAs received post-HCC (n = 258) and NAs sustained (n = 118) were determined. CONCLUSIONS: NAs reduced severity of CHB-related HCC patients. Sustained NAs is an important factor associated with the extended survival of CHB-related HCC patients. |
format | Online Article Text |
id | pubmed-5295451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-52954512017-02-08 Randomized clinical trial: Nucleos(t)ide analogues improved survival of CHB-related HCC patients via reducing severity and progression of malignancy Wang, Yun Xiang, Xiaogang Chen, Liwen Cao, Zhujun Bao, Rebecca Zhou, Huijuan Tang, Weiliang Lu, Jie Lin, Lanyi Xie, Qing Bao, Shisan Wang, Hui Oncotarget Clinical Research Paper BACKGROUND: The influence of nucleos(t)ide analogues (NAs) to treat Chronic hepatitis B (CHB) related hepatocellular carcinoma (HCC) remains to be explored. AIM: To investigate if NAs reduce the severity and progression of CHB-related HCC. RESULTS: Among 532 patients, there were 118 or 414 CHB-related HCC with or without NAs therapy, respectively. BCLC scores, serum level of ALT/AST and HBV DNA were compared. During follow-up, the survival period of CHB-related HCC patients with sustained NAs is significantly longer than that with NAs post-HCC and NAs naïve (p < 0.05). Factors significantly associated with the poor overall survival of CHB-related HCC include BCLC scores (hazard ratio, 1.84 [95% confidence interval, 1.57−2.15], p < 0.001), NAs post-HCC or NAs naïve (1.33 [1.07−1.65], p < 0.01), serum AST ≥ 40 IU/L (1.48 [1.03−2.12], p < 0.05) and HBV DNA ≥ 10(4) copies/ml (1.36 [1.01−1.83], p < 0.001). METHODS: Outcomes of 532 CHB-related HCC patients with/without NAs were investigated. Overall survival of CHB-related HCC patients, NAs naïve (n = 156), NAs received post-HCC (n = 258) and NAs sustained (n = 118) were determined. CONCLUSIONS: NAs reduced severity of CHB-related HCC patients. Sustained NAs is an important factor associated with the extended survival of CHB-related HCC patients. Impact Journals LLC 2016-06-18 /pmc/articles/PMC5295451/ /pubmed/27329718 http://dx.doi.org/10.18632/oncotarget.10155 Text en Copyright: © 2016 Wang 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 Wang, Yun Xiang, Xiaogang Chen, Liwen Cao, Zhujun Bao, Rebecca Zhou, Huijuan Tang, Weiliang Lu, Jie Lin, Lanyi Xie, Qing Bao, Shisan Wang, Hui Randomized clinical trial: Nucleos(t)ide analogues improved survival of CHB-related HCC patients via reducing severity and progression of malignancy |
title | Randomized clinical trial: Nucleos(t)ide analogues improved survival of CHB-related HCC patients via reducing severity and progression of malignancy |
title_full | Randomized clinical trial: Nucleos(t)ide analogues improved survival of CHB-related HCC patients via reducing severity and progression of malignancy |
title_fullStr | Randomized clinical trial: Nucleos(t)ide analogues improved survival of CHB-related HCC patients via reducing severity and progression of malignancy |
title_full_unstemmed | Randomized clinical trial: Nucleos(t)ide analogues improved survival of CHB-related HCC patients via reducing severity and progression of malignancy |
title_short | Randomized clinical trial: Nucleos(t)ide analogues improved survival of CHB-related HCC patients via reducing severity and progression of malignancy |
title_sort | randomized clinical trial: nucleos(t)ide analogues improved survival of chb-related hcc patients via reducing severity and progression of malignancy |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295451/ https://www.ncbi.nlm.nih.gov/pubmed/27329718 http://dx.doi.org/10.18632/oncotarget.10155 |
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