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   <subfield code="a">Sorafenib for non-selected patient population with advanced hepatocellular carcinoma: efficacy and safety data according to liver function</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Jon Zugazagoitia, Aránzazu Manzano, Javier Sastre, Jose Ladero, Javier Puente, Eduardo Díaz-Rubio]</subfield>
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   <subfield code="a">Objective: Sorafenib is the standard treatment of patients with advanced hepatocellular carcinoma, regardless of the liver functional reserve. We present a single institutional series of Child-Pugh A and Child-Pugh B patients treated with sorafenib with the aim to establish the efficacy and safety of sorafenib in patients of daily clinical conditions and to compare these results between Child-Pugh A and Child-Pugh B patients. Materials and methods: A total of 51 patients were treated with sorafenib 400mg/12h until disease progression or unacceptable toxicity. Results: The median progression-free survival and overall survival for the overall population were 3.5 and 8.2months, respectively, with a 1-year survival rate of 27%. Overall survival was significantly longer for patients Child-Pugh A compared with those with Child-Pugh B liver function (8.7 vs. 4.7months, respectively). The most common adverse events were fatigue (62.7%), diarrhea (58%), hypertension (31.3%), and hand-foot syndrome (31.3%), and in most cases grade 1 or 2 according to the NCI-CTC 3.0. Grade 4 liver-related events occurred mainly in Child-Pugh B patients with decompensated cirrhosis at the time of sorafenib initiation (54.5% of that group). Discussion: The benefit of sorafenib in Child-Pugh B patients, if exist, may be limited by frequent liver-related events, especially in decompensated patients, and then, toxicity and impact in quality of life should be carefully monitored.</subfield>
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   <subfield code="a">Federación de Sociedades Españolas de Oncología (FESEO), 2012</subfield>
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   <subfield code="a">Child-Pugh score</subfield>
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   <subfield code="a">Hepatocellular carcinoma</subfield>
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   <subfield code="a">Zugazagoitia</subfield>
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   <subfield code="u">Oncology Department, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), c/Martin Lagos s/n, 28040, Madrid, Spain</subfield>
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   <subfield code="a">Manzano</subfield>
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   <subfield code="a">Sastre</subfield>
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   <subfield code="t">Clinical and Translational Oncology</subfield>
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