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The effect of apatinib in the treatment of sorafenib resistant metastatic hepatocellular carcinoma: A case report

RATIONALE: Most patients with hepatocellular carcinoma (HCC) have lost the chance of radical treatment at the time of their visit, and the prognosis of metastatic HCC is even worse. Sorafenib is currently regarded as a first-line systemic therapy in patients with advanced and metastatic HCC. Apatini...

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Autores principales: Han, Zonghong, He, Zhongming, Wang, Caoye, Wang, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310601/
https://www.ncbi.nlm.nih.gov/pubmed/30544412
http://dx.doi.org/10.1097/MD.0000000000013388
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author Han, Zonghong
He, Zhongming
Wang, Caoye
Wang, Qi
author_facet Han, Zonghong
He, Zhongming
Wang, Caoye
Wang, Qi
author_sort Han, Zonghong
collection PubMed
description RATIONALE: Most patients with hepatocellular carcinoma (HCC) have lost the chance of radical treatment at the time of their visit, and the prognosis of metastatic HCC is even worse. Sorafenib is currently regarded as a first-line systemic therapy in patients with advanced and metastatic HCC. Apatinib is a new inhibitor of vascular endothelial growth factor receptor 2 tyrosine kinase, which has been reported to be effective in some solid tumors. We herein report a case of apatinib in the treatment of the patient with metastatic HCC who was resistant to sorafenib. PATIENT CONCERNS: A 41-year-old Chinese man with a history of chronic hepatitis B had undergone an emergency partial hepatectomy for tumor ruptured. Despite the treatment with transcatheter arterial chemoembolization and sorafenib, the progression of tumor failed to control. DIAGNOSES: Although the patient had been treated with sorafenib (400 mg, twice daily) for 10 months, computed tomography documented radiological progression. INTERVENTIONS: Due to disease progression, failure of sorafenib and positive expression of vascular endothelial growth factor (VEGF), the drug regimen was changed to apatinib 250 mg once daily. Due to some degree of resistance, the dose was increased up to 425 mg once daily. OUTCOMES: The patient had a disease-free progression of 7 months at 250 mg apatinib. The dosage was adjusted to 425 mg due to drug resistance and the side effects were tolerable. The patient has survived a total of 19 months under apatinib. LESSONS: Apatinib may be a substitute for the HCC patients with sorafenib resistance in the future, especially for those with high expression of VEGF.
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spelling pubmed-63106012019-01-14 The effect of apatinib in the treatment of sorafenib resistant metastatic hepatocellular carcinoma: A case report Han, Zonghong He, Zhongming Wang, Caoye Wang, Qi Medicine (Baltimore) Research Article RATIONALE: Most patients with hepatocellular carcinoma (HCC) have lost the chance of radical treatment at the time of their visit, and the prognosis of metastatic HCC is even worse. Sorafenib is currently regarded as a first-line systemic therapy in patients with advanced and metastatic HCC. Apatinib is a new inhibitor of vascular endothelial growth factor receptor 2 tyrosine kinase, which has been reported to be effective in some solid tumors. We herein report a case of apatinib in the treatment of the patient with metastatic HCC who was resistant to sorafenib. PATIENT CONCERNS: A 41-year-old Chinese man with a history of chronic hepatitis B had undergone an emergency partial hepatectomy for tumor ruptured. Despite the treatment with transcatheter arterial chemoembolization and sorafenib, the progression of tumor failed to control. DIAGNOSES: Although the patient had been treated with sorafenib (400 mg, twice daily) for 10 months, computed tomography documented radiological progression. INTERVENTIONS: Due to disease progression, failure of sorafenib and positive expression of vascular endothelial growth factor (VEGF), the drug regimen was changed to apatinib 250 mg once daily. Due to some degree of resistance, the dose was increased up to 425 mg once daily. OUTCOMES: The patient had a disease-free progression of 7 months at 250 mg apatinib. The dosage was adjusted to 425 mg due to drug resistance and the side effects were tolerable. The patient has survived a total of 19 months under apatinib. LESSONS: Apatinib may be a substitute for the HCC patients with sorafenib resistance in the future, especially for those with high expression of VEGF. Wolters Kluwer Health 2018-12-10 /pmc/articles/PMC6310601/ /pubmed/30544412 http://dx.doi.org/10.1097/MD.0000000000013388 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Han, Zonghong
He, Zhongming
Wang, Caoye
Wang, Qi
The effect of apatinib in the treatment of sorafenib resistant metastatic hepatocellular carcinoma: A case report
title The effect of apatinib in the treatment of sorafenib resistant metastatic hepatocellular carcinoma: A case report
title_full The effect of apatinib in the treatment of sorafenib resistant metastatic hepatocellular carcinoma: A case report
title_fullStr The effect of apatinib in the treatment of sorafenib resistant metastatic hepatocellular carcinoma: A case report
title_full_unstemmed The effect of apatinib in the treatment of sorafenib resistant metastatic hepatocellular carcinoma: A case report
title_short The effect of apatinib in the treatment of sorafenib resistant metastatic hepatocellular carcinoma: A case report
title_sort effect of apatinib in the treatment of sorafenib resistant metastatic hepatocellular carcinoma: a case report
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310601/
https://www.ncbi.nlm.nih.gov/pubmed/30544412
http://dx.doi.org/10.1097/MD.0000000000013388
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