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How Much Time Should Be Waited and What Are the Main Findings to Evaluate the Hepatocellular Carcinoma Response to Regorafenib? A Real-Life Experience

dc.contributor.authorKawanami, Gustavo Hideki
dc.contributor.authorKatsuda, Leopoldo
dc.contributor.authorRocha, Thiara Barcelos [UNESP]
dc.contributor.authorDa Silva Yamashiro, Fabio
dc.contributor.authorPelafsky, Leonardo [UNESP]
dc.contributor.authorQi, Xingshun
dc.contributor.authorRomeiro, Fernando Gomes [UNESP]
dc.contributor.institutionFundação Para O Desenvolvimento Médico e Hospitalar Hospital Estadual de Bauru
dc.contributor.institutionBauru
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionGeneral Hospital of Northern Theater Command (Formerly General Hospital of Shenyang Military Area)
dc.date.accessioned2021-06-25T11:03:07Z
dc.date.available2021-06-25T11:03:07Z
dc.date.issued2021-01-01
dc.description.abstractBackground. Hepatocellular carcinoma is a relevant cause of mortality worldwide, mainly among patients who have a prior liver disease. In spite of clear recommendations regarding surveillance and screening methods, most patients are still diagnosed only when they are no longer candidates to curative treatment modalities, while others do not achieve the goals of such treatments, thus increasing the need of anticancer drugs. Moreover, when cirrhotic patients begin to receive these drugs, many types of adverse events are seen as a reason to withdrawal, even when there are findings suggesting a good response to the treatment. Case Summary. This case report is about a cirrhotic patient who received many types of treatment, from surgery and chemoembolization during early stages to first- and second-line systemic therapy when the disease turned to be advanced. Since he had no signs of liver dysfunction and suffered tumor progression during sorafenib treatment, regorafenib was initiated. The main findings that make this case important are the adverse events after taking this second-line agent, which would certainly be considered unacceptable and would lead to the drug withdrawal. The reasons why regorafenib was maintained are explained based on clinical and imaging findings, showing how this decision led to an excellent response. Conclusions. The knowledge of the main adverse events described in the pilot clinical trials can avoid unnecessary withdrawal of regorafenib. In addition, some clinical and imaging findings can be deemed as predictors of good response to tyrosine kinase inhibitors.en
dc.description.affiliationFundação Para O Desenvolvimento Médico e Hospitalar Hospital Estadual de Bauru
dc.description.affiliationImagem Diagnósticos Médicos Bauru
dc.description.affiliationGastroenterology Division Department of Internal Medicine Universidade Estadual Paulista (UNESP)
dc.description.affiliationSurgery Department Faculdade de Medicina de Botucatu Universidade Estadual Paulista (UNESP)
dc.description.affiliationDepartment of Gastroenterology General Hospital of Northern Theater Command (Formerly General Hospital of Shenyang Military Area)
dc.description.affiliationUnespGastroenterology Division Department of Internal Medicine Universidade Estadual Paulista (UNESP)
dc.description.affiliationUnespSurgery Department Faculdade de Medicina de Botucatu Universidade Estadual Paulista (UNESP)
dc.identifierhttp://dx.doi.org/10.1155/2021/6219896
dc.identifier.citationCanadian Journal of Gastroenterology and Hepatology, v. 2021.
dc.identifier.doi10.1155/2021/6219896
dc.identifier.issn2291-2797
dc.identifier.issn2291-2789
dc.identifier.scopus2-s2.0-85100960020
dc.identifier.urihttp://hdl.handle.net/11449/207911
dc.language.isoeng
dc.relation.ispartofCanadian Journal of Gastroenterology and Hepatology
dc.sourceScopus
dc.titleHow Much Time Should Be Waited and What Are the Main Findings to Evaluate the Hepatocellular Carcinoma Response to Regorafenib? A Real-Life Experienceen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0002-9448-6739[6]
unesp.author.orcid0000-0002-9394-6895[7]

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