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Page 14 of 16                                                 Silk et al. Hepatoma Res 2020;6:73  I  http://dx.doi.org/10.20517/2394-5079.2020.61

               CONCLUSION
               Tyrosine kinase inhibitors have successfully extended the overall survival in patients with hepatocellular
               carcinoma [4-7] . However these treatments have been noted to cause severe side effects including liver
                                                                                         [68]
               toxicity, hypertension, gastrointestinal toxicity and the discussed cutaneous toxicities . These cutaneous
               toxicities tend to occur during the first and second months of treatment and can be managed with
               symptomatic treatment and dose reductions if necessary. Additional prophylactic measures can help
               prevent the manifestation of the some of most common cutaneous toxicities including HFRS and
               stomatitis. It is in these authors’ opinions on and others that the monitoring of TKI treated patients for
               cutaneous toxicities should be conducted every 2 weeks for the first few months of treatment and a baseline
               dermatological exam is also necessary [22,58,68] . A summary of recommendations for the management of
               cutaneous adverse events are displayed in Table 5. As cutaneous toxicities have also been seen with more
               recently developed TKIs, including Afatinib and Dorafenib, it appears as more TKIs are used to treat HCC
               that these cutaneous toxicities will remain as treatment side effects requiring careful management [69,70] .


               DECLARATIONS
               Authors’ contributions
               Made substantial contributions to conception and design of the review article: Silk T, Wu J

               Availability of data and materials
               Not applicable.

               Financial support and sponsorship
               None.

               Conflicts of interest
               All authors declared that there are no conflicts of interest.

               Ethical approval and consent to participate
               Not applicable.

               Consent for publication
               Not applicable.

               Copyright
               © The Author(s) 2020.


               REFERENCES
               1.   Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and
                   mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018;68:394-424.
               2.   Villanueva A. Hepatocellular carcinoma. N Engl J Med 2019;380:1450-62.
               3.   Llovet JM, Montal R, Sia D, Finn RS. Molecular therapies and precision medicine for hepatocellular carcinoma. Nat Rev Clin Oncol
                   2018;15:599-616.
               4.   Llovet JM, Ricci S, Mazzaferro V, Hilgard P, Gane E, et al; SHARP Investigators Study Group. Sorafenib in advanced hepatocellular
                   carcinoma. N Engl J Med 2008;359:378-90.
               5.   Bruix J, Qin S, Merle P, Granito A, Huang Y, et al. Regorafenib for patients with hepatocellular carcinoma who progressed on sorafenib
                   treatment (RESORCE): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet 2017;389:56-66.
               6.   Abou-Alfa GK, Meyer T, Cheng AL, El-Khoueiry AB, Rimassa L, et al. Cabozantinib in patients with advanced and progressing
                   hepatocellular carcinoma. N Engl J Med 2018;379:54-63.
               7.   Kudo M, Finn RS, Qin S, Han K, Ikeda K, et al. Lenvatinib versus sorafenib in first-line treatment of patients with unresectable
                   hepatocellular carcinoma: a randomised phase 3 non-inferiority trial. Lancet 2018;391:1163-73.
               8.   Reyes-Habito CM, Roh EK. Cutaneous reactions to chemotherapeutic drugs and targeted therapy for cancer: Part II. Targeted therapy. J
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