| Literature DB >> 31365177 |
Massimo Iavarone1, Federica Invernizzi1, Carolin Czauderna2, Marco Sanduzzi-Zamparelli3, Sherrie Bhoori4, Giuliana Amaddeo5, Matteo A Manini6, Miguel F López7, Margarita Anders8, Matthias Pinter9, Maria J B Rodríguez10, Mario R Cristóbal11, Gabriel A Soteras12, Federico Piñero13, Gerda E Villadsen14, Arndt Weinmann2, Gonzalo Crespo15, Vincenzo Mazzaferro16, Helene Regnault5, Massimo De Giorgio6, Maria L González-Diéguez7, Maria F Donato1, Maria Varela7, Marcus-Alexander Wörns2, Jordi Bruix3, Pietro Lampertico1, Maria Reig3.
Abstract
Regorafenib is one option for second-line treatment of hepatocellular carcinoma (HCC), improving overall survival (OS) of sorafenib-tolerant patients who develop progression. We aim to evaluate the safety and outcomes of regorafenib as second-line treatment for HCC recurrence after liver transplantation (LT). This is a retrospective, multicenter, international study including regorafenib-treated LT patients (2015-2018), with analysis of baseline characteristics and evolutionary events during sorafenib/regorafenib treatment. Twenty-eight LT patients (57 years, 7% cirrhotics, 54% performance status 1) were included. Median time from LT to regorafenib initiation was 3.9 (1.1-18.5) years; median time on sorafenib was 11.3 (0.7-76.4) months and 14 (1-591) days from sorafenib discontinuation to regorafenib. During regorafenib (6.3 months), all patients had at least one adverse event (AE), the most common grade 3/4 AEs were fatigue (n = 7) and dermatological reaction (n = 5). While no liver rejection was observed, plasma levels of immunosuppressive drugs increased in five. Twenty-four patients developed progression (38% extrahepatic growth, 33% new extrahepatic lesions/vascular invasion). Median OS from regorafenib initiation was 12.9 (95% CI, 6.7-19.1) and 38.4 months (95% CI, 18.5-58.4) for the sorafenib initiation. This is the first study showing safety of regorafenib after LT, thus providing the rational of considering regorafenib in the clinical decision-making in sorafenib-tolerant patients with HCC recurrence after LT.Entities:
Keywords: cancer/malignancy/neoplasia; chemotherapy; clinical research/practice; drug interaction; liver transplantation/hepatology; pharmacology; side effects
Year: 2019 PMID: 31365177 DOI: 10.1111/ajt.15551
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086