Cargando…
Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Predictors of Outcomes in Patients With Unresectable Hepatocellular Carcinoma Undergoing Transarterial Chemoembolization Plus Sorafenib
Objectives: To investigate the predictive value of inflammatory biomarkers in patients with unresectable hepatocellular carcinoma (HCC) for outcomes following the combination treatment of transarterial chemoembolization (TACE) plus sorafenib. Materials and Methods: A total of 314 (270 male and 44 fe...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8194392/ https://www.ncbi.nlm.nih.gov/pubmed/34124139 http://dx.doi.org/10.3389/fmolb.2021.624366 |
_version_ | 1783706408167931904 |
---|---|
author | Zhang, Lei Yan, Zhi-Ping Hou, Zhong-Heng Huang, Peng Yang, Min-Jie Zhang, Shuai Zhang, Shen Zhang, Shao-Hua Zhu, Xiao-Li Ni, Cai-Fang Li, Qiang |
author_facet | Zhang, Lei Yan, Zhi-Ping Hou, Zhong-Heng Huang, Peng Yang, Min-Jie Zhang, Shuai Zhang, Shen Zhang, Shao-Hua Zhu, Xiao-Li Ni, Cai-Fang Li, Qiang |
author_sort | Zhang, Lei |
collection | PubMed |
description | Objectives: To investigate the predictive value of inflammatory biomarkers in patients with unresectable hepatocellular carcinoma (HCC) for outcomes following the combination treatment of transarterial chemoembolization (TACE) plus sorafenib. Materials and Methods: A total of 314 (270 male and 44 female) treatment-naïve patients with unresectable HCC treated by TACE plus sorafenib between January 2011 and December 2018 were enrolled in the retrospective study. The primary outcome was overall survival (OS). The secondary outcome was progression-free survival (PFS). Neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) were obtained within 3–7 days before the initial TACE and the median value of the NLR and PLR was considered as the cut-off value. Results: The median value of NLR and PLR was 2.42 and 100, respectively. The median OS and PFS of the entire cohort were 18.7 months (95% CI: 16.8–20.6) and 9.1 months (95% CI: 8.5–9.8), respectively. The low NLR and PLR group showed improved OS and PFS compared with the high NLR and PLR group [21.8 months (95% CI: 15.2–28.5) vs. 15.4 months (95% CI: 12.4–18.3), p < 0.0001; 21.6 months (95% CI: 15.8–27.5) vs. 14.9 months (95% CI: 11.9–17.8), p = 0.00027, respectively]. In addition, the low NLR and PLR group also provided a longer PFS than the high NLR and PLR group [10.4 months (95% CI: 8.9–12.0) vs. 8.1 months (95% CI: 7.1–9.2), p = 0.00022; 10.3 months (95% CI: 8.6–11.9) vs. 8.2 months (95% CI: 7.2–9.2), p < 0.0001, respectively]. High NLR and PLR at baseline were predictive factors of poor OS (p = 0.02 and p = 0.004) and PFS (p = 0.045 and p = 0.005). Conclusion: This study showed the prognostic value of quantitative inflammatory biomarkers in correlation with OS and PFS in unresectable HCC patients undergoing TACE plus sorafenib treatment. |
format | Online Article Text |
id | pubmed-8194392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81943922021-06-12 Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Predictors of Outcomes in Patients With Unresectable Hepatocellular Carcinoma Undergoing Transarterial Chemoembolization Plus Sorafenib Zhang, Lei Yan, Zhi-Ping Hou, Zhong-Heng Huang, Peng Yang, Min-Jie Zhang, Shuai Zhang, Shen Zhang, Shao-Hua Zhu, Xiao-Li Ni, Cai-Fang Li, Qiang Front Mol Biosci Molecular Biosciences Objectives: To investigate the predictive value of inflammatory biomarkers in patients with unresectable hepatocellular carcinoma (HCC) for outcomes following the combination treatment of transarterial chemoembolization (TACE) plus sorafenib. Materials and Methods: A total of 314 (270 male and 44 female) treatment-naïve patients with unresectable HCC treated by TACE plus sorafenib between January 2011 and December 2018 were enrolled in the retrospective study. The primary outcome was overall survival (OS). The secondary outcome was progression-free survival (PFS). Neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) were obtained within 3–7 days before the initial TACE and the median value of the NLR and PLR was considered as the cut-off value. Results: The median value of NLR and PLR was 2.42 and 100, respectively. The median OS and PFS of the entire cohort were 18.7 months (95% CI: 16.8–20.6) and 9.1 months (95% CI: 8.5–9.8), respectively. The low NLR and PLR group showed improved OS and PFS compared with the high NLR and PLR group [21.8 months (95% CI: 15.2–28.5) vs. 15.4 months (95% CI: 12.4–18.3), p < 0.0001; 21.6 months (95% CI: 15.8–27.5) vs. 14.9 months (95% CI: 11.9–17.8), p = 0.00027, respectively]. In addition, the low NLR and PLR group also provided a longer PFS than the high NLR and PLR group [10.4 months (95% CI: 8.9–12.0) vs. 8.1 months (95% CI: 7.1–9.2), p = 0.00022; 10.3 months (95% CI: 8.6–11.9) vs. 8.2 months (95% CI: 7.2–9.2), p < 0.0001, respectively]. High NLR and PLR at baseline were predictive factors of poor OS (p = 0.02 and p = 0.004) and PFS (p = 0.045 and p = 0.005). Conclusion: This study showed the prognostic value of quantitative inflammatory biomarkers in correlation with OS and PFS in unresectable HCC patients undergoing TACE plus sorafenib treatment. Frontiers Media S.A. 2021-05-28 /pmc/articles/PMC8194392/ /pubmed/34124139 http://dx.doi.org/10.3389/fmolb.2021.624366 Text en Copyright © 2021 Zhang, Yan, Hou, Huang, Yang, Zhang, Zhang, Zhang, Zhu, Ni and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Zhang, Lei Yan, Zhi-Ping Hou, Zhong-Heng Huang, Peng Yang, Min-Jie Zhang, Shuai Zhang, Shen Zhang, Shao-Hua Zhu, Xiao-Li Ni, Cai-Fang Li, Qiang Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Predictors of Outcomes in Patients With Unresectable Hepatocellular Carcinoma Undergoing Transarterial Chemoembolization Plus Sorafenib |
title | Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Predictors of Outcomes in Patients With Unresectable Hepatocellular Carcinoma Undergoing Transarterial Chemoembolization Plus Sorafenib |
title_full | Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Predictors of Outcomes in Patients With Unresectable Hepatocellular Carcinoma Undergoing Transarterial Chemoembolization Plus Sorafenib |
title_fullStr | Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Predictors of Outcomes in Patients With Unresectable Hepatocellular Carcinoma Undergoing Transarterial Chemoembolization Plus Sorafenib |
title_full_unstemmed | Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Predictors of Outcomes in Patients With Unresectable Hepatocellular Carcinoma Undergoing Transarterial Chemoembolization Plus Sorafenib |
title_short | Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratios as Predictors of Outcomes in Patients With Unresectable Hepatocellular Carcinoma Undergoing Transarterial Chemoembolization Plus Sorafenib |
title_sort | neutrophil-to-lymphocyte and platelet-to-lymphocyte ratios as predictors of outcomes in patients with unresectable hepatocellular carcinoma undergoing transarterial chemoembolization plus sorafenib |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8194392/ https://www.ncbi.nlm.nih.gov/pubmed/34124139 http://dx.doi.org/10.3389/fmolb.2021.624366 |
work_keys_str_mv | AT zhanglei neutrophiltolymphocyteandplatelettolymphocyteratiosaspredictorsofoutcomesinpatientswithunresectablehepatocellularcarcinomaundergoingtransarterialchemoembolizationplussorafenib AT yanzhiping neutrophiltolymphocyteandplatelettolymphocyteratiosaspredictorsofoutcomesinpatientswithunresectablehepatocellularcarcinomaundergoingtransarterialchemoembolizationplussorafenib AT houzhongheng neutrophiltolymphocyteandplatelettolymphocyteratiosaspredictorsofoutcomesinpatientswithunresectablehepatocellularcarcinomaundergoingtransarterialchemoembolizationplussorafenib AT huangpeng neutrophiltolymphocyteandplatelettolymphocyteratiosaspredictorsofoutcomesinpatientswithunresectablehepatocellularcarcinomaundergoingtransarterialchemoembolizationplussorafenib AT yangminjie neutrophiltolymphocyteandplatelettolymphocyteratiosaspredictorsofoutcomesinpatientswithunresectablehepatocellularcarcinomaundergoingtransarterialchemoembolizationplussorafenib AT zhangshuai neutrophiltolymphocyteandplatelettolymphocyteratiosaspredictorsofoutcomesinpatientswithunresectablehepatocellularcarcinomaundergoingtransarterialchemoembolizationplussorafenib AT zhangshen neutrophiltolymphocyteandplatelettolymphocyteratiosaspredictorsofoutcomesinpatientswithunresectablehepatocellularcarcinomaundergoingtransarterialchemoembolizationplussorafenib AT zhangshaohua neutrophiltolymphocyteandplatelettolymphocyteratiosaspredictorsofoutcomesinpatientswithunresectablehepatocellularcarcinomaundergoingtransarterialchemoembolizationplussorafenib AT zhuxiaoli neutrophiltolymphocyteandplatelettolymphocyteratiosaspredictorsofoutcomesinpatientswithunresectablehepatocellularcarcinomaundergoingtransarterialchemoembolizationplussorafenib AT nicaifang neutrophiltolymphocyteandplatelettolymphocyteratiosaspredictorsofoutcomesinpatientswithunresectablehepatocellularcarcinomaundergoingtransarterialchemoembolizationplussorafenib AT liqiang neutrophiltolymphocyteandplatelettolymphocyteratiosaspredictorsofoutcomesinpatientswithunresectablehepatocellularcarcinomaundergoingtransarterialchemoembolizationplussorafenib |