Regorafenib in patients with advanced Child‐Pugh B hepatocellular carcinoma: A multicentre retrospective study

Introduction Regorafenib is an approved agent in patients with advanced hepatocellular carcinoma (HCC) who progressed on sorafenib, but little is known about its clinical outcomes in Child‐Pugh B patients. We aimed to investigate the safety and effectiveness of regorafenib in Child‐Pugh B HCC patien...

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Veröffentlicht in:Liver international 2020-10, Vol.40 (10), p.2544-2552
Hauptverfasser: Kim, Hyung‐Don, Bang, Yeonghak, Lee, Myung Ah, Kim, Jin Won, Kim, Jee Hyun, Chon, Hong Jae, Kang, Beodeul, Kang, Myoung Joo, Kim, Ilhwan, Cheon, Jaekyung, Hwang, Jun‐Eul, Kang, Jung Hun, Byeon, Seonggyu, Hong, Jung Yong, Ryoo, Baek‐Yeol, Lim, Ho Yeong, Yoo, Changhoon
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Sprache:eng
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Zusammenfassung:Introduction Regorafenib is an approved agent in patients with advanced hepatocellular carcinoma (HCC) who progressed on sorafenib, but little is known about its clinical outcomes in Child‐Pugh B patients. We aimed to investigate the safety and effectiveness of regorafenib in Child‐Pugh B HCC patients. Methods This multicentre retrospective study included 59 patients with Child‐Pugh B HCC who received regorafenib. Comparative analyses were performed with an independent cohort of Child‐Pugh class A patients from the same registry (n = 440). Results The median age was 58 years (range, 19‐83). All patients had progression on prior sorafenib. Regorafenib was given as 2nd line, and 3rd‐4th line systemic therapy in 37 (62.7%) and 22 (37.3%) patients respectively. Compared to Child‐Pugh A cohort, grade 3‐4 AEs were more common in the Child‐Pugh B cohort (27.1% vs 14.1%, P = .017). The median progression‐free survival (PFS) and overall survival (OS) were 1.8 and 4.6 months, respectively, and these were significantly poorer than the Child‐Pugh A cohort (P = .008 and P 
ISSN:1478-3223
1478-3231
DOI:10.1111/liv.14573