Sorafenib plus drug-eluting bead transarterial chemoembolization for early intrahepatic stage-progressed advanced hepatocellular carcinoma refractory to conventional transarterial chemoembolization
Purpose To investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the treatment of early intrahepatic stage-progressed advanced hepatocellular carcinoma (ISPA-HCC). Methods This study was approved by the ethics com...
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Published in | Journal of cancer research and clinical oncology Vol. 149; no. 5; pp. 1873 - 1882 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.05.2023
Springer Nature B.V |
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Abstract | Purpose
To investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the treatment of early intrahepatic stage-progressed advanced hepatocellular carcinoma (ISPA-HCC).
Methods
This study was approved by the ethics committees of six tertiary medical centers in China. Between October 2017 and October 2020, 213 patients with advanced HCC received either sorafenib combined with on-demand DEB-TACE (DTS group,
n
= 103) or sorafenib monotherapy (S group,
n
= 110). Overall survival (OS), time to progression (TTP), local tumor response, and adverse events (AEs) were compared between the two groups.
Results
The incidences of nause/vomiting, abdonimal pain, hyperbilirubinemia, fever and ALT/AST increasing were higher in the DTS group. The post-treatment partial response, objective response, and disease control rates were significantly higher in the DTS group than in the S group (51.5% vs. 23.6%; 56.3% vs. 25.5%; 77.7% vs. 56.4%, respectively). The median OS was significantly longer in the DTS group than in the S group [16.3 vs. 10.0 months; hazard ratio (HR) = 0.43;
P
< 0.001], as was the TTP (6.7 vs. 4.3 months; HR = 0.60;
P
= 0.001). In the DTS group, patients who received ≥ 2 sessions of DEB-TACE benefited more than those who received two sessions of DEB-TACE. Multivariate analysis revealed that the α-fetoprotein level and treatment allocation were independent predictors of OS and TTP.
Conclusion
The combination of sorafenib and DEB-TACE is safe and effective for the treatment of early ISPA-HCC. |
---|---|
AbstractList | To investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the treatment of early intrahepatic stage-progressed advanced hepatocellular carcinoma (ISPA-HCC).
This study was approved by the ethics committees of six tertiary medical centers in China. Between October 2017 and October 2020, 213 patients with advanced HCC received either sorafenib combined with on-demand DEB-TACE (DTS group, n = 103) or sorafenib monotherapy (S group, n = 110). Overall survival (OS), time to progression (TTP), local tumor response, and adverse events (AEs) were compared between the two groups.
The incidences of nause/vomiting, abdonimal pain, hyperbilirubinemia, fever and ALT/AST increasing were higher in the DTS group. The post-treatment partial response, objective response, and disease control rates were significantly higher in the DTS group than in the S group (51.5% vs. 23.6%; 56.3% vs. 25.5%; 77.7% vs. 56.4%, respectively). The median OS was significantly longer in the DTS group than in the S group [16.3 vs. 10.0 months; hazard ratio (HR) = 0.43; P < 0.001], as was the TTP (6.7 vs. 4.3 months; HR = 0.60; P = 0.001). In the DTS group, patients who received ≥ 2 sessions of DEB-TACE benefited more than those who received two sessions of DEB-TACE. Multivariate analysis revealed that the α-fetoprotein level and treatment allocation were independent predictors of OS and TTP.
The combination of sorafenib and DEB-TACE is safe and effective for the treatment of early ISPA-HCC. To investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the treatment of early intrahepatic stage-progressed advanced hepatocellular carcinoma (ISPA-HCC).PURPOSETo investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the treatment of early intrahepatic stage-progressed advanced hepatocellular carcinoma (ISPA-HCC).This study was approved by the ethics committees of six tertiary medical centers in China. Between October 2017 and October 2020, 213 patients with advanced HCC received either sorafenib combined with on-demand DEB-TACE (DTS group, n = 103) or sorafenib monotherapy (S group, n = 110). Overall survival (OS), time to progression (TTP), local tumor response, and adverse events (AEs) were compared between the two groups.METHODSThis study was approved by the ethics committees of six tertiary medical centers in China. Between October 2017 and October 2020, 213 patients with advanced HCC received either sorafenib combined with on-demand DEB-TACE (DTS group, n = 103) or sorafenib monotherapy (S group, n = 110). Overall survival (OS), time to progression (TTP), local tumor response, and adverse events (AEs) were compared between the two groups.The incidences of nause/vomiting, abdonimal pain, hyperbilirubinemia, fever and ALT/AST increasing were higher in the DTS group. The post-treatment partial response, objective response, and disease control rates were significantly higher in the DTS group than in the S group (51.5% vs. 23.6%; 56.3% vs. 25.5%; 77.7% vs. 56.4%, respectively). The median OS was significantly longer in the DTS group than in the S group [16.3 vs. 10.0 months; hazard ratio (HR) = 0.43; P < 0.001], as was the TTP (6.7 vs. 4.3 months; HR = 0.60; P = 0.001). In the DTS group, patients who received ≥ 2 sessions of DEB-TACE benefited more than those who received two sessions of DEB-TACE. Multivariate analysis revealed that the α-fetoprotein level and treatment allocation were independent predictors of OS and TTP.RESULTSThe incidences of nause/vomiting, abdonimal pain, hyperbilirubinemia, fever and ALT/AST increasing were higher in the DTS group. The post-treatment partial response, objective response, and disease control rates were significantly higher in the DTS group than in the S group (51.5% vs. 23.6%; 56.3% vs. 25.5%; 77.7% vs. 56.4%, respectively). The median OS was significantly longer in the DTS group than in the S group [16.3 vs. 10.0 months; hazard ratio (HR) = 0.43; P < 0.001], as was the TTP (6.7 vs. 4.3 months; HR = 0.60; P = 0.001). In the DTS group, patients who received ≥ 2 sessions of DEB-TACE benefited more than those who received two sessions of DEB-TACE. Multivariate analysis revealed that the α-fetoprotein level and treatment allocation were independent predictors of OS and TTP.The combination of sorafenib and DEB-TACE is safe and effective for the treatment of early ISPA-HCC.CONCLUSIONThe combination of sorafenib and DEB-TACE is safe and effective for the treatment of early ISPA-HCC. PURPOSE: To investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the treatment of early intrahepatic stage-progressed advanced hepatocellular carcinoma (ISPA-HCC). METHODS: This study was approved by the ethics committees of six tertiary medical centers in China. Between October 2017 and October 2020, 213 patients with advanced HCC received either sorafenib combined with on-demand DEB-TACE (DTS group, n = 103) or sorafenib monotherapy (S group, n = 110). Overall survival (OS), time to progression (TTP), local tumor response, and adverse events (AEs) were compared between the two groups. RESULTS: The incidences of nause/vomiting, abdonimal pain, hyperbilirubinemia, fever and ALT/AST increasing were higher in the DTS group. The post-treatment partial response, objective response, and disease control rates were significantly higher in the DTS group than in the S group (51.5% vs. 23.6%; 56.3% vs. 25.5%; 77.7% vs. 56.4%, respectively). The median OS was significantly longer in the DTS group than in the S group [16.3 vs. 10.0 months; hazard ratio (HR) = 0.43; P < 0.001], as was the TTP (6.7 vs. 4.3 months; HR = 0.60; P = 0.001). In the DTS group, patients who received ≥ 2 sessions of DEB-TACE benefited more than those who received two sessions of DEB-TACE. Multivariate analysis revealed that the α-fetoprotein level and treatment allocation were independent predictors of OS and TTP. CONCLUSION: The combination of sorafenib and DEB-TACE is safe and effective for the treatment of early ISPA-HCC. PurposeTo investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the treatment of early intrahepatic stage-progressed advanced hepatocellular carcinoma (ISPA-HCC).MethodsThis study was approved by the ethics committees of six tertiary medical centers in China. Between October 2017 and October 2020, 213 patients with advanced HCC received either sorafenib combined with on-demand DEB-TACE (DTS group, n = 103) or sorafenib monotherapy (S group, n = 110). Overall survival (OS), time to progression (TTP), local tumor response, and adverse events (AEs) were compared between the two groups.ResultsThe incidences of nause/vomiting, abdonimal pain, hyperbilirubinemia, fever and ALT/AST increasing were higher in the DTS group. The post-treatment partial response, objective response, and disease control rates were significantly higher in the DTS group than in the S group (51.5% vs. 23.6%; 56.3% vs. 25.5%; 77.7% vs. 56.4%, respectively). The median OS was significantly longer in the DTS group than in the S group [16.3 vs. 10.0 months; hazard ratio (HR) = 0.43; P < 0.001], as was the TTP (6.7 vs. 4.3 months; HR = 0.60; P = 0.001). In the DTS group, patients who received ≥ 2 sessions of DEB-TACE benefited more than those who received two sessions of DEB-TACE. Multivariate analysis revealed that the α-fetoprotein level and treatment allocation were independent predictors of OS and TTP.ConclusionThe combination of sorafenib and DEB-TACE is safe and effective for the treatment of early ISPA-HCC. Purpose To investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the treatment of early intrahepatic stage-progressed advanced hepatocellular carcinoma (ISPA-HCC). Methods This study was approved by the ethics committees of six tertiary medical centers in China. Between October 2017 and October 2020, 213 patients with advanced HCC received either sorafenib combined with on-demand DEB-TACE (DTS group, n = 103) or sorafenib monotherapy (S group, n = 110). Overall survival (OS), time to progression (TTP), local tumor response, and adverse events (AEs) were compared between the two groups. Results The incidences of nause/vomiting, abdonimal pain, hyperbilirubinemia, fever and ALT/AST increasing were higher in the DTS group. The post-treatment partial response, objective response, and disease control rates were significantly higher in the DTS group than in the S group (51.5% vs. 23.6%; 56.3% vs. 25.5%; 77.7% vs. 56.4%, respectively). The median OS was significantly longer in the DTS group than in the S group [16.3 vs. 10.0 months; hazard ratio (HR) = 0.43; P < 0.001], as was the TTP (6.7 vs. 4.3 months; HR = 0.60; P = 0.001). In the DTS group, patients who received ≥ 2 sessions of DEB-TACE benefited more than those who received two sessions of DEB-TACE. Multivariate analysis revealed that the α-fetoprotein level and treatment allocation were independent predictors of OS and TTP. Conclusion The combination of sorafenib and DEB-TACE is safe and effective for the treatment of early ISPA-HCC. |
Author | Wu, Yanqin Fan, Wenzhe Xue, Miao Zou, Xinhua Fan, Huishuang Yue, Shufan Li, Jiaping Zhu, Bowen Lu, Mingjian Wang, Hongyu Zheng, Xinlin Li, Fuliang Qiao, Liangliang Yuan, Guosheng |
Author_xml | – sequence: 1 givenname: Wenzhe surname: Fan fullname: Fan, Wenzhe organization: Department of Interventional Oncology, The First Affiliated Hospital of Sun Yat-Sen University – sequence: 2 givenname: Bowen surname: Zhu fullname: Zhu, Bowen organization: Department of Interventional Oncology, The First Affiliated Hospital of Sun Yat-Sen University – sequence: 3 givenname: Xinlin surname: Zheng fullname: Zheng, Xinlin organization: Department of Interventional Oncology, The First Affiliated Hospital of Sun Yat-Sen University – sequence: 4 givenname: Shufan surname: Yue fullname: Yue, Shufan organization: Department of Medical Ultrasound, The First Affiliated Hospital of Sun Yat-Sen University – sequence: 5 givenname: Mingjian surname: Lu fullname: Lu, Mingjian organization: Department of Radiology, Affiliated Cancer Hospital and Institute of Guangzhou Medical University – sequence: 6 givenname: Huishuang surname: Fan fullname: Fan, Huishuang organization: Interventional Department, Dongguan People’s Hospital – sequence: 7 givenname: Liangliang surname: Qiao fullname: Qiao, Liangliang organization: Department of Oncology, Jinshazhou Hospital of Guangzhou University of Chinese Medicine – sequence: 8 givenname: Fuliang surname: Li fullname: Li, Fuliang organization: Liver and Gall Surgical Department, Gaozhou People’s Hospital – sequence: 9 givenname: Guosheng surname: Yuan fullname: Yuan, Guosheng organization: Department of Gastroenterology, Nanfang Hospital – sequence: 10 givenname: Yanqin surname: Wu fullname: Wu, Yanqin organization: Department of Interventional Oncology, The First Affiliated Hospital of Sun Yat-Sen University – sequence: 11 givenname: Xinhua surname: Zou fullname: Zou, Xinhua organization: Department of Interventional Oncology, The First Affiliated Hospital of Sun Yat-Sen University – sequence: 12 givenname: Hongyu surname: Wang fullname: Wang, Hongyu organization: Department of Interventional Oncology, The First Affiliated Hospital of Sun Yat-Sen University – sequence: 13 givenname: Miao surname: Xue fullname: Xue, Miao organization: Department of Interventional Oncology, The First Affiliated Hospital of Sun Yat-Sen University – sequence: 14 givenname: Jiaping orcidid: 0000-0003-2927-8877 surname: Li fullname: Li, Jiaping email: lijiap@mail.sysu.edu.cn organization: Department of Interventional Oncology, The First Affiliated Hospital of Sun Yat-Sen University |
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Keywords | Hepatocellular carcinoma Stage progression Transarterial chemoembolization Sorafenib |
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To investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the... To investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the treatment... PurposeTo investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the... PURPOSE: To investigate the effectiveness and safety of the combination of sorafenib and drug-eluting bead transarterial chemoembolization (DEB-TACE) in the... |
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SubjectTerms | Cancer Research Carcinoma, Hepatocellular - drug therapy Chemoembolization Chemoembolization, Therapeutic - adverse effects China Disease control Drug delivery ethics fever hazard ratio Hematology Hepatocellular carcinoma hepatoma Humans Hyperbilirubinemia Inhibitor drugs Internal Medicine Liver cancer Liver Neoplasms - drug therapy Medicine Medicine & Public Health Multivariate analysis Oncology Original Article – Clinical Oncology Original – Clinical Oncology pain Patients Retrospective Studies Sorafenib Targeted cancer therapy Treatment Outcome Vomiting α-Fetoprotein |
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Title | Sorafenib plus drug-eluting bead transarterial chemoembolization for early intrahepatic stage-progressed advanced hepatocellular carcinoma refractory to conventional transarterial chemoembolization |
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