The Effect of Metabolic Syndrome on the Outcome of Hepatitis B-Associated Hepatocellular Carcinoma Patients After Hepatectomy: A Multicenter Study
With changes in dietary patterns and modern lifestyles, the prevalence of metabolic syndrome (MetS) in hepatitis B virus (HBV)-associated hepatocellular carcinoma (HCC) patients is increasing. The purpose of our study is to explore the impact of MetS on the prognosis of HBV-associated HCC patients f...
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Published in | Frontiers in oncology Vol. 12; p. 811084 |
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Abstract | With changes in dietary patterns and modern lifestyles, the prevalence of metabolic syndrome (MetS) in hepatitis B virus (HBV)-associated hepatocellular carcinoma (HCC) patients is increasing. The purpose of our study is to explore the impact of MetS on the prognosis of HBV-associated HCC patients following radical hepatectomy.
Data on consecutive HCC patients who underwent radical hepatectomy were prospectively obtained and retrospectively analyzed from seven medical centers in west areas of China. Propensity score matching (PSM) analysis was conducted to balance the heterogeneity between MetS-HBV-HCC group and HBV-HCC group. Surgical outcomes have been contrasted between the two groups.
In 984 patients, 179 (18.19%) were diagnosed with MetS. Patients in the MetS-HBV-HCC group had higher CCI score (8.7 [0.0, 12.2] vs. 0.0 [0.0, 8.7],
= 0.048) and a higher rate of severe complications (Clavien-Dindo ≥3, 7.82% vs. 4.10%,
= 0.035), to be more precise: postoperative liver failure, hydrothorax, and hyperglycemia. Patients in the MetS-HBV-HCC group tended to have worse 5-year overall survival (OS) rate (61.45% vs. 69.94%,
= 0.027) and recurrence-free survival (RFS) rate (62.57% vs. 53.66%,
= 0.030), consistent with the results of the competing risk models. Last, MetS was identified to be an independent unfavorable prognostic factor in the multivariate analysis.
The involvement of MetS increased the risk of postoperative complications and worsens the overall survival and recurrence-free survival time, reminding us to be more prudent to face metabolic disorder among tumor patients. |
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AbstractList | With changes in dietary patterns and modern lifestyles, the prevalence of metabolic syndrome (MetS) in hepatitis B virus (HBV)-associated hepatocellular carcinoma (HCC) patients is increasing. The purpose of our study is to explore the impact of MetS on the prognosis of HBV-associated HCC patients following radical hepatectomy.Background and AimsWith changes in dietary patterns and modern lifestyles, the prevalence of metabolic syndrome (MetS) in hepatitis B virus (HBV)-associated hepatocellular carcinoma (HCC) patients is increasing. The purpose of our study is to explore the impact of MetS on the prognosis of HBV-associated HCC patients following radical hepatectomy.Data on consecutive HCC patients who underwent radical hepatectomy were prospectively obtained and retrospectively analyzed from seven medical centers in west areas of China. Propensity score matching (PSM) analysis was conducted to balance the heterogeneity between MetS-HBV-HCC group and HBV-HCC group. Surgical outcomes have been contrasted between the two groups.MethodsData on consecutive HCC patients who underwent radical hepatectomy were prospectively obtained and retrospectively analyzed from seven medical centers in west areas of China. Propensity score matching (PSM) analysis was conducted to balance the heterogeneity between MetS-HBV-HCC group and HBV-HCC group. Surgical outcomes have been contrasted between the two groups.In 984 patients, 179 (18.19%) were diagnosed with MetS. Patients in the MetS-HBV-HCC group had higher CCI score (8.7 [0.0, 12.2] vs. 0.0 [0.0, 8.7], p = 0.048) and a higher rate of severe complications (Clavien-Dindo ≥3, 7.82% vs. 4.10%, p = 0.035), to be more precise: postoperative liver failure, hydrothorax, and hyperglycemia. Patients in the MetS-HBV-HCC group tended to have worse 5-year overall survival (OS) rate (61.45% vs. 69.94%, p = 0.027) and recurrence-free survival (RFS) rate (62.57% vs. 53.66%, p = 0.030), consistent with the results of the competing risk models. Last, MetS was identified to be an independent unfavorable prognostic factor in the multivariate analysis.ResultsIn 984 patients, 179 (18.19%) were diagnosed with MetS. Patients in the MetS-HBV-HCC group had higher CCI score (8.7 [0.0, 12.2] vs. 0.0 [0.0, 8.7], p = 0.048) and a higher rate of severe complications (Clavien-Dindo ≥3, 7.82% vs. 4.10%, p = 0.035), to be more precise: postoperative liver failure, hydrothorax, and hyperglycemia. Patients in the MetS-HBV-HCC group tended to have worse 5-year overall survival (OS) rate (61.45% vs. 69.94%, p = 0.027) and recurrence-free survival (RFS) rate (62.57% vs. 53.66%, p = 0.030), consistent with the results of the competing risk models. Last, MetS was identified to be an independent unfavorable prognostic factor in the multivariate analysis.The involvement of MetS increased the risk of postoperative complications and worsens the overall survival and recurrence-free survival time, reminding us to be more prudent to face metabolic disorder among tumor patients.ConclusionThe involvement of MetS increased the risk of postoperative complications and worsens the overall survival and recurrence-free survival time, reminding us to be more prudent to face metabolic disorder among tumor patients. With changes in dietary patterns and modern lifestyles, the prevalence of metabolic syndrome (MetS) in hepatitis B virus (HBV)-associated hepatocellular carcinoma (HCC) patients is increasing. The purpose of our study is to explore the impact of MetS on the prognosis of HBV-associated HCC patients following radical hepatectomy. Data on consecutive HCC patients who underwent radical hepatectomy were prospectively obtained and retrospectively analyzed from seven medical centers in west areas of China. Propensity score matching (PSM) analysis was conducted to balance the heterogeneity between MetS-HBV-HCC group and HBV-HCC group. Surgical outcomes have been contrasted between the two groups. In 984 patients, 179 (18.19%) were diagnosed with MetS. Patients in the MetS-HBV-HCC group had higher CCI score (8.7 [0.0, 12.2] vs. 0.0 [0.0, 8.7], = 0.048) and a higher rate of severe complications (Clavien-Dindo ≥3, 7.82% vs. 4.10%, = 0.035), to be more precise: postoperative liver failure, hydrothorax, and hyperglycemia. Patients in the MetS-HBV-HCC group tended to have worse 5-year overall survival (OS) rate (61.45% vs. 69.94%, = 0.027) and recurrence-free survival (RFS) rate (62.57% vs. 53.66%, = 0.030), consistent with the results of the competing risk models. Last, MetS was identified to be an independent unfavorable prognostic factor in the multivariate analysis. The involvement of MetS increased the risk of postoperative complications and worsens the overall survival and recurrence-free survival time, reminding us to be more prudent to face metabolic disorder among tumor patients. Background and AimsWith changes in dietary patterns and modern lifestyles, the prevalence of metabolic syndrome (MetS) in hepatitis B virus (HBV)-associated hepatocellular carcinoma (HCC) patients is increasing. The purpose of our study is to explore the impact of MetS on the prognosis of HBV-associated HCC patients following radical hepatectomy.MethodsData on consecutive HCC patients who underwent radical hepatectomy were prospectively obtained and retrospectively analyzed from seven medical centers in west areas of China. Propensity score matching (PSM) analysis was conducted to balance the heterogeneity between MetS-HBV-HCC group and HBV-HCC group. Surgical outcomes have been contrasted between the two groups.ResultsIn 984 patients, 179 (18.19%) were diagnosed with MetS. Patients in the MetS-HBV-HCC group had higher CCI score (8.7 [0.0, 12.2] vs. 0.0 [0.0, 8.7], p = 0.048) and a higher rate of severe complications (Clavien–Dindo ≥3, 7.82% vs. 4.10%, p = 0.035), to be more precise: postoperative liver failure, hydrothorax, and hyperglycemia. Patients in the MetS-HBV-HCC group tended to have worse 5-year overall survival (OS) rate (61.45% vs. 69.94%, p = 0.027) and recurrence-free survival (RFS) rate (62.57% vs. 53.66%, p = 0.030), consistent with the results of the competing risk models. Last, MetS was identified to be an independent unfavorable prognostic factor in the multivariate analysis.ConclusionThe involvement of MetS increased the risk of postoperative complications and worsens the overall survival and recurrence-free survival time, reminding us to be more prudent to face metabolic disorder among tumor patients. |
Author | Zhu, Xinrui Shen, Junyi Jiang, Kangyi Wen, Tianfu Zhang, Yu Li, Chuan Xie, Fei Yu, Yu Dai, Junlong |
AuthorAffiliation | 1 Liver Transplantation Center, Department of Liver Surgery, West China Hospital , Chengdu , China 5 Department of Hepatobiliary Surgery, People’s Hospital of Leshan, Southwest Medical University , Leshan , China 3 Department of Hepatobiliary and Pancreatic Surgery, the First People’s Hospital of Neijiang City , Neijiang , China 2 Organ Transplantation Center, Sichuan Academy of Medical Sciences (Sichuan Provincial People’s Hospital), Chinese Academy of Sciences , Chengdu , China 4 Department of Hepatopancreatobiliary Surgery, the Second People’s Hospital of Yibin City , Yibin , China |
AuthorAffiliation_xml | – name: 5 Department of Hepatobiliary Surgery, People’s Hospital of Leshan, Southwest Medical University , Leshan , China – name: 2 Organ Transplantation Center, Sichuan Academy of Medical Sciences (Sichuan Provincial People’s Hospital), Chinese Academy of Sciences , Chengdu , China – name: 1 Liver Transplantation Center, Department of Liver Surgery, West China Hospital , Chengdu , China – name: 3 Department of Hepatobiliary and Pancreatic Surgery, the First People’s Hospital of Neijiang City , Neijiang , China – name: 4 Department of Hepatopancreatobiliary Surgery, the Second People’s Hospital of Yibin City , Yibin , China |
Author_xml | – sequence: 1 givenname: Junlong surname: Dai fullname: Dai, Junlong – sequence: 2 givenname: Xinrui surname: Zhu fullname: Zhu, Xinrui – sequence: 3 givenname: Junyi surname: Shen fullname: Shen, Junyi – sequence: 4 givenname: Yu surname: Zhang fullname: Zhang, Yu – sequence: 5 givenname: Fei surname: Xie fullname: Xie, Fei – sequence: 6 givenname: Yu surname: Yu fullname: Yu, Yu – sequence: 7 givenname: Kangyi surname: Jiang fullname: Jiang, Kangyi – sequence: 8 givenname: Tianfu surname: Wen fullname: Wen, Tianfu – sequence: 9 givenname: Chuan surname: Li fullname: Li, Chuan |
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Cites_doi | 10.1016/S0140-6736(05)66378-7 10.1158/1055-9965.EPI-19-0303 10.1002/hep.24397 10.1038/nrc.2016.89 10.1186/s12943-017-0646-3 10.2337/diab.37.12.1595 10.1080/00273171.2011.568786 10.1053/j.gastro.2018.08.065 10.5582/bst.2021.01094 10.1016/S0140-6736(09)61794-3 10.1002/ijc.32787 10.1038/pcan.2017.1 10.1172/JCI92035 10.5582/bst.2021.01287 10.1007/s10549-017-4131-x 10.1007/s11605-017-3629-1 10.1002/hep.27406 10.1136/gutjnl-2015-309501 10.1007/s11906-018-0812-z 10.2337/dc05-2179 10.1002/hep.29914 10.3390/ijms20030605 10.1002/cncr.24687 10.2147/OTT.S154848 10.1038/nrdp.2015.80 10.1111/jgh.12700 10.1016/j.jhep.2015.01.024 10.1158/1078-0432.CCR-14-0442 |
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Copyright | Copyright © 2022 Dai, Zhu, Shen, Zhang, Xie, Yu, Jiang, Wen and Li. Copyright © 2022 Dai, Zhu, Shen, Zhang, Xie, Yu, Jiang, Wen and Li 2022 Dai, Zhu, Shen, Zhang, Xie, Yu, Jiang, Wen and Li |
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Keywords | metabolic syndrome hepatectomy prognosis hepatocellular carcinoma HBV-associated HCC |
Language | English |
License | Copyright © 2022 Dai, Zhu, Shen, Zhang, Xie, Yu, Jiang, Wen and Li. 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. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This article was submitted to Gastrointestinal Cancers: Hepato Pancreatic Biliary Cancers, a section of the journal Frontiers in Oncology These authors have contributed equally to this work Edited by: Xin Chen, University of California, San Francisco, United States Reviewed by: Cheng Zhang, Anhui Medical University, China; Wei Tang, The University of Tokyo Hospital, Japan |
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SubjectTerms | HBV-associated HCC hepatectomy hepatocellular carcinoma metabolic syndrome Oncology prognosis |
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Title | The Effect of Metabolic Syndrome on the Outcome of Hepatitis B-Associated Hepatocellular Carcinoma Patients After Hepatectomy: A Multicenter Study |
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