Postprogression survival of patients with advanced hepatocellular carcinoma : Rationale for second-line trial design
Reig, María (Hospital Clínic i Provincial de Barcelona)
Rimola, Jordi (Hospital Clínic i Provincial de Barcelona)
Torres, Ferran (Universitat Autònoma de Barcelona. Departament de Pediatria, Obstetrícia i Ginecologia i de Medicina Preventiva i Salut Pública)
Darnell, Anna (Hospital Clínic i Provincial de Barcelona)
Forner, Alejandro (Hospital Clínic i Provincial de Barcelona)
Llarch, Neus (Hospital Clínic i Provincial de Barcelona)
Ríos, José (Universitat Autònoma de Barcelona. Departament de Pediatria, Obstetrícia i Ginecologia i de Medicina Preventiva i Salut Pública)
Ayuso, Carmen (Hospital Clínic i Provincial de Barcelona)
Bruix, Jordi (Hospital Clínic i Provincial de Barcelona)

Date:	2013
Abstract:	Sorafenib improves overall survival (OS) of patients with hepatocellular carcinoma (HCC) in the absence of objective response. Thus, time to tumor progression (TTP) is used to capture benefits of novel molecular agents, but proof of its surrogacy with survival is lacking. Furthermore, survival predictors upon progression are not established and there is a need to characterize postprogression survival (PPS) and assess with time-dependent covariates analysis if it is influenced by progression pattern, and not solely by simultaneous impairment of liver function and performance status. We prospectively followed HCC patients treated with sorafenib. Clinical and biochemical evaluation were done every 4 weeks. Radiologic assessment of progression was done at week 4 and then every 8 weeks using RECIST 1. 1. The progression pattern was divided into: intrahepatic/extrahepatic increase in tumor size, new intrahepatic lesion, and new extrahepatic lesion (NEH). We included 147 patients (hepatitis C virus [HCV] 57. 1%, performance status [PS] 0 83. 6%, Child-Pugh A 82. 3%, and BCLC-C 47. 3%). The median OS was 12. 7 months and its independent predictors (hazard ratio [HR], 95% confidence interval [CI]) were: baseline BCLC 2. 49 [1. 66-3. 73], PS 1. 86 [1. 12-3. 10], registration during follow-up of Child-Pugh B or Child-Pugh C scores (2. 36 [1. 51-3. 69] and 2. 89 [1. 62-5. 15], respectively), definitive sorafenib interruption 2. 48 [1. 54-4. 01], and TTP 3. 39 [1. 89-6. 1]. The presence of NEH 2. 42 [1. 32-4. 44] is also an independent predictor of OS and PPS in patients with radiologic progression. Conclusion: Tumor progression is a surrogate of survival but its impact varies according to progression pattern. Thus, PPS is influenced by progression pattern and this is key in prognostic prediction and second-line trial design and analysis.
Grants:	Ministerio de Ciencia e Innovación PI11/01830 Ministerio de Ciencia e Innovación FI09/00510
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Language:	Anglès
Document:	Article ; recerca ; Versió acceptada per publicar
Published in:	Hepatology, Vol. 58, Num. 6 (December 2013) , p. 2023-2031, ISSN 1527-3350

DOI: 10.1002/hep.26586
PMID: 23787822

Postprint 32 p, 1.7 MB

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