Background: Sorafenib has shown survival benefits in patients with advanced hepatocellular carcinoma (HCC) and Child-Pugh (CP) class A liver function. There are few prospective data on sorafenib in patients with HCC and CP class B. Patients and methods: A consecutive prospective series of 300 patients with CP class A or B HCC were enrolled in a dual-phase trial to determine survival and safety data according to liver function (class A or B) in patients receiving oral sorafenib 800 mg daily. [Results of this study were presented in part at the ASCO 2012 Gastrointestinal Cancers Symposium, 19-21 January 2012. J Clin Oncol 2012; 30 (Suppl 4): abstract 306.]. Results: Overall progression-free survival (PFS), time to progression (TTP) and overall survival (OS) were 3.9, 4.1 and 9.1 months, respectively. For patients with CP class A versus B status, PFS was 4.3 versus 2.1 months, TTP was 4.2 versus 3.8 months and OS was 10.0 versus 3. 8 months. Extrahepatic spread was associated with worse outcomes but taken together with CP class, liver function played a greater role in reducing survival. Adverse events for the two CP groups were similar. Conclusion: Although patients with HCC and CP class B liver function have poorer outcomes than those with CP class A function, data suggest that patients with CP class B liver function can tolerate treatment and may still benefit from sorafenib. © The Author 2012. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved.

Sorafenib in patients with Child-Pugh class A and B advanced hepatocellular carcinoma: a prospective feasibility analysis / T., Pressiani; C., Boni; L., Rimassa; R., Labianca; S., Fagiuoli; S., Salvagni; D., Ferrari; Cortesi, Enrico; C., Porta; C., Mucciarini; L., Latini; C., Carnaghi; M., Banzi; S., Fanello; M., De Giorgio; F. R., Lutman; G., Torzilli; M. A., Tommasini; R., Ceriani; G., Covini; M. C., Tronconi; L., Giordano; N., Locopo; S., Naimo; A., Santoro. - In: ANNALS OF ONCOLOGY. - ISSN 0923-7534. - 24:2(2013), pp. 406-411. [10.1093/annonc/mds343]

Sorafenib in patients with Child-Pugh class A and B advanced hepatocellular carcinoma: a prospective feasibility analysis.

CORTESI, Enrico;
2013

Abstract

Background: Sorafenib has shown survival benefits in patients with advanced hepatocellular carcinoma (HCC) and Child-Pugh (CP) class A liver function. There are few prospective data on sorafenib in patients with HCC and CP class B. Patients and methods: A consecutive prospective series of 300 patients with CP class A or B HCC were enrolled in a dual-phase trial to determine survival and safety data according to liver function (class A or B) in patients receiving oral sorafenib 800 mg daily. [Results of this study were presented in part at the ASCO 2012 Gastrointestinal Cancers Symposium, 19-21 January 2012. J Clin Oncol 2012; 30 (Suppl 4): abstract 306.]. Results: Overall progression-free survival (PFS), time to progression (TTP) and overall survival (OS) were 3.9, 4.1 and 9.1 months, respectively. For patients with CP class A versus B status, PFS was 4.3 versus 2.1 months, TTP was 4.2 versus 3.8 months and OS was 10.0 versus 3. 8 months. Extrahepatic spread was associated with worse outcomes but taken together with CP class, liver function played a greater role in reducing survival. Adverse events for the two CP groups were similar. Conclusion: Although patients with HCC and CP class B liver function have poorer outcomes than those with CP class A function, data suggest that patients with CP class B liver function can tolerate treatment and may still benefit from sorafenib. © The Author 2012. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved.
2013
sorafenib; hepatocellular; child-pugh class; cirrhosis; carcinoma
01 Pubblicazione su rivista::01a Articolo in rivista
Sorafenib in patients with Child-Pugh class A and B advanced hepatocellular carcinoma: a prospective feasibility analysis / T., Pressiani; C., Boni; L., Rimassa; R., Labianca; S., Fagiuoli; S., Salvagni; D., Ferrari; Cortesi, Enrico; C., Porta; C., Mucciarini; L., Latini; C., Carnaghi; M., Banzi; S., Fanello; M., De Giorgio; F. R., Lutman; G., Torzilli; M. A., Tommasini; R., Ceriani; G., Covini; M. C., Tronconi; L., Giordano; N., Locopo; S., Naimo; A., Santoro. - In: ANNALS OF ONCOLOGY. - ISSN 0923-7534. - 24:2(2013), pp. 406-411. [10.1093/annonc/mds343]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/502030
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