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dc.contributor.authorKumar, Shashank
dc.contributor.authorPandey, Abhay Kumar
dc.date.accessioned2024-01-16T14:23:21Z
dc.date.available2024-01-16T14:23:21Z
dc.date.issued2023-01-18T00:00:00
dc.identifier.issn17187729
dc.identifier.urihttps://doi.org/10.3390/curroncol30020105
dc.identifier.urihttp://kr.cup.edu.in/handle/32116/2912
dc.description.abstractHepatocellular carcinoma (HCC) is one of the most prevalent and lethal cancers, representing a serious worldwide health concern. The recurrence incidence of hepatocellular carcinoma (HCC) following surgery or ablation is as high as 70%. Thus, the clinical applicability of standard surgery and other locoregional therapy to improve the outcomes of advanced HCC is restricted and far from ideal. The registered trials did not identify a treatment that prolonged recurrence-free survival, the primary outcome of the majority of research. Several investigator-initiated trials have demonstrated that various treatments extend patients� recurrence-free or overall survival after curative therapies. In the past decade, targeted therapy has made significant strides in the treatment of advanced HCC. These targeted medicines produce antitumour effects via specific signals, such as anti-angiogenesis or advancement of the cell cycle. As a typical systemic treatment option, it significantly improves the prognosis of this fatal disease. In addition, the combination of targeted therapy with an immune checkpoint inhibitor is redefining the paradigm of advanced HCC treatment. In this review, we focused on the role of approved targeted medicines and potential therapeutic targets in unresectable HCC. � 2023 by the authors.en_US
dc.language.isoen_USen_US
dc.publisherMDPIen_US
dc.subjectclinical trialen_US
dc.subjectliver canceren_US
dc.subjectrecurrenceen_US
dc.subjectsurvivalen_US
dc.subjecttherapeutic targeten_US
dc.titlePotential Molecular Targeted Therapy for Unresectable Hepatocellular Carcinomaen_US
dc.typeReviewen_US
dc.identifier.doi10.3390/curroncol30020105
dc.title.journalCurrent Oncologyen_US
dc.type.accesstypeOpen Accessen_US


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