We are analyzing https://link.springer.com/article/10.1007/s11523-017-0484-7.

Title:
Sorafenib: A Review in Hepatocellular Carcinoma | Targeted Oncology
Description:
Sorafenib (Nexavar®) is currently the only systemic agent approved for use in hepatocellular carcinoma (HCC). Its approval was based on the results of the pivotal SHARP and Sorafenib Asia-Pacific (AP) trials in Child-Pugh (CP) class A patients with advanced HCC, which showed significantly longer median overall survival (OS) and time to radiological progression (TTP) with sorafenib 400 mg twice daily than with placebo, with no significant between-group difference in the median time to symptomatic progression (TTSP). Subsequent results from real-world studies such as GIDEON also support the use of sorafenib in HCC, including in carefully selected CP class B patients, although the median OS achieved in these patients appears relatively short. Sorafenib has a well characterized tolerability and safety profile, with strategies available to prevent and manage adverse effects such as hand-foot skin reactions. In conclusion, sorafenib remains an important option for the treatment of HCC.
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28 years and 1 months (reg. 1997-05-29).

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Keywords {🔍}

sorafenib, article, pubmed, google, scholar, hepatocellular, carcinoma, cas, patients, advanced, study, oncol, cancer, phase, clin, gideon, trial, analysis, treatment, clinical, hcc, safety, liver, iii, hepatol, randomized, central, abstract, results, access, practice, chen, suppl, efficacy, kudo, content, therapeutic, tumor, res, cheng, privacy, cookies, function, information, search, oncology, review, keating, unresectable, therapy,

Topics {✒️}

targets raf/mek/erk pathway month download article/chapter /html/products/pi/nexavar_pi raf/mek/erk pathway abou-alfa gk hand-foot skin reactions tyrosine kinases vegfr/pdgfr open-label study major kinase-independent target ketoconazole-mediated cyp3a inhibition sorafenib relieves cell-intrinsic pro-apoptotic sorafenib signaling di costanzo related subjects llovet jm full article pdf open-label privacy choices/manage cookies augment antitumor immunity asia-pacific region phase iii study dual-action inhibitor intermediate stage hcc phase iii trial field-practice study phase iii failure liver function assessment cheng a cell-extrinsic inhibitions phase ii study sorafenib asia-pacific randomized clinical trial cell death dis european economic area international observational study patient surveillance study phase iv study murine hepatocytes depends european patient subset advanced hepatocellular carcinoma phase iii randomised randomized controlled trial sunitinib versus sorafenib brivanib versus sorafenib linifanib versus sorafenib doxorubicin versus sorafenib advanced hepatocellular cancer systemic agent approved manage adverse effects bayer healthcare pharmaceuticals

Questions {❓}

Learning from 7 years of experience with sorafenib in advanced HCC: sorafenib better than sorafenib?

Schema {🗺️}

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         description:Sorafenib (Nexavar®) is currently the only systemic agent approved for use in hepatocellular carcinoma (HCC). Its approval was based on the results of the pivotal SHARP and Sorafenib Asia-Pacific (AP) trials in Child-Pugh (CP) class A patients with advanced HCC, which showed significantly longer median overall survival (OS) and time to radiological progression (TTP) with sorafenib 400 mg twice daily than with placebo, with no significant between-group difference in the median time to symptomatic progression (TTSP). Subsequent results from real-world studies such as GIDEON also support the use of sorafenib in HCC, including in carefully selected CP class B patients, although the median OS achieved in these patients appears relatively short. Sorafenib has a well characterized tolerability and safety profile, with strategies available to prevent and manage adverse effects such as hand-foot skin reactions. In conclusion, sorafenib remains an important option for the treatment of HCC.
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         Tace
         Median Overall Survival
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