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      Clinical Significance of Adverse Events for Patients with Unresectable Hepatocellular Carcinoma Treated with Lenvatinib: A Multicenter Retrospective Study

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          Abstract

          We sought to investigate the clinical profile(s) associated with the discontinuation of lenvatinib (LEN) due to severe adverse events (DLSAE) in patients with unresectable hepatocellular carcinoma (HCC). This retrospective study enrolled 177 patients with HCC treated with LEN. Independent factors associated with DLSAE were advanced age, albumin-bilirubin (ALBI) grade 2, fatigue grade ≥ 3, and appetite loss ≥ 2. The overall survival (OS) in the group that did not require DLSAE was significantly longer compared to the group that did require DLSAE (median survival time (MST): not reached vs. 12.8 months, p < 0.001). Moreover, advanced age was the most important variable for DLSAE in a decision tree analysis. Hypertension and hand-foot-skin-reaction (HFSR) were also significantly associated with longer survival, and the occurrence of hypertension was the earliest predictor for improved prognosis, while appetite loss and development of grade ≥ 3 fatigue were predictive of a poor prognosis. We concluded that the appearance of hypertension has potential as an early surrogate marker to predict improved prognosis. Moreover, careful management to avoid discontinuation of treatment leads to longer survival in patients receiving LEN.

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          Outcomes of sequential treatment with sorafenib followed by regorafenib for HCC: Additional analyses from the phase III RESORCE trial

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            Systematic review: The model for end-stage liver disease--should it replace Child-Pugh's classification for assessing prognosis in cirrhosis?

            Prognosis in cirrhotic patients has had a resurgence of interest because of liver transplantation and new therapies for complications of end-stage cirrhosis. The model for end-stage liver disease score is now used for allocation in liver transplantation waiting lists, replacing Child-Turcotte-Pugh score. However, there is debate as whether it is better in other settings of cirrhosis. To review studies comparing the accuracy of model for end-stage liver disease score vs. Child-Turcotte-Pugh score in non-transplant settings. Transjugular intrahepatic portosystemic shunt studies (with 1360 cirrhotics) only one of five, showed model for end-stage liver disease to be superior to Child-Turcotte-Pugh to predict 3-month mortality, but not for 12-month mortality. Prognosis of cirrhosis studies (with 2569 patients) none of four showed significant differences between the two scores for either short- or long-term prognosis whereas no differences for variceal bleeding studies (with 411 cirrhotics). Modified Child-Turcotte-Pugh score, by adding creatinine, performed similarly to model for end-stage liver disease score. Hepatic encephalopathy and hyponatraemia (as an index of ascites), both components of Child-Turcotte-Pugh score, add to the prognostic performance of model for end-stage liver disease score. Based on current literature, model for end-stage liver disease score does not perform better than Child-Turcotte-Pugh score in non-transplant settings. Modified Child-Turcotte-Pugh and model for end-stage liver disease scores need further evaluation.
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              Disparities by Race, Age, and Sex in the Improvement of Survival for Major Cancers: Results From the National Cancer Institute Surveillance, Epidemiology, and End Results (SEER) Program in the United States, 1990 to 2010.

              Substantial progress has been made in cancer diagnosis and treatment, resulting in a steady improvement in cancer survival. The degree of improvement by age, race, and sex remains unclear.
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                Author and article information

                Journal
                Cancers (Basel)
                Cancers (Basel)
                cancers
                Cancers
                MDPI
                2072-6694
                11 July 2020
                July 2020
                : 12
                : 7
                : 1867
                Affiliations
                [1 ]Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan; niizeki_takashi@ 123456kurume-u.ac.jp (T.N.); shirono_tomotake@ 123456med.kurume-u.ac.jp (T.S.); noda_yuu@ 123456med.kurume-u.ac.jp (Y.N.); kamachi_naoki@ 123456med.kurume-u.ac.jp (N.K.); okamura_shyuusuke@ 123456kurume-u.ac.jp (S.O.); nakano_masahito@ 123456kurume-u.ac.jp (M.N.); ryoko@ 123456med.kurme-u.ac.jp (R.K.); takumi@ 123456med.kurume-u.ac.jp (T.K.); hirokoga@ 123456med.kurume-u.ac.jp (H.K.); tori@ 123456med.kurume-u.ac.jp (T.T.)
                [2 ]Iwamoto Internal Medical Clinic, Kitakyusyu 802-0832, Japan; ttttyama2@ 123456yahoo.co.jp
                [3 ]Department of Gastroenterology and Hepatology, Yanagawa Hospital, Fukuoka 832-0077, Japan; suga516@ 123456med.kurume-u.ac.jp
                [4 ]Department of Gastroenterology and Hepatology, Miyama, Fukuoka 839-0295, Japan; mazzo6528@ 123456me.com
                [5 ]Department of Gastroenterology and Hepatology, Omuta City Hospital, Fukuoka 836-8567, Japan; hisyo@ 123456ghp.omuta.fukuoka.jp
                Author notes
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0003-2068-8386
                https://orcid.org/0000-0002-2662-6779
                https://orcid.org/0000-0002-3375-180X
                https://orcid.org/0000-0002-7064-4325
                Article
                cancers-12-01867
                10.3390/cancers12071867
                7408786
                32664489
                d08d1db2-e013-4f4d-8745-19db75d0fd46
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 20 June 2020
                : 09 July 2020
                Categories
                Article

                lenvatinib,adverse events,molecular target agents,hepatocellular carcinoma

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