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Ramucirumab in elderly patients with hepatocellular carcinoma and elevated alpha-fetoprotein after sorafenib in REACH and REACH-2.
Kudo, Masatoshi; Galle, Peter R; Llovet, Josep M; Finn, Richard S; Vogel, Arndt; Motomura, Kenta; Assenat, Eric; Merle, Philippe; Brandi, Giovanni; Daniele, Bruno; Okusaka, Takuji; Tomásek, Jirí; Borg, Christophe; Dadduzio, Vincenzo; Morimoto, Manabu; Pracht, Marc; Jen, Min-Hua; Drove Ubreva, Nora; Widau, Ryan C; Shinozaki, Kenta; Yoshikawa, Reigetsu; Zhu, Andrew X.
  • Kudo M; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka, Japan.
  • Galle PR; Department of Internal Medicine, Mainz University Medical Center, Mainz, Germany.
  • Llovet JM; Translational Research in Hepatic Oncology Group, Liver Unit, IDIBAPS, Hospital Clinic Barcelona, University of Barcelona, Barcelona, Catalonia, Spain.
  • Finn RS; Mount Sinai Liver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Vogel A; Department of Medicine, Division of Hematology/Oncology, Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
  • Motomura K; Department of Hepatology, Gastroenterology and Endocrinology, Medizinische Hochschule Hannover, Hannover, Germany.
  • Assenat E; Department of Hepatology, Aso Iizuka Hospital, Fukuoka, Japan.
  • Merle P; Department of Medical Oncology, CHU de Montpellier, Montpellier, France.
  • Brandi G; Hepatology and Gastroenterology Unit, Croix-Rousse Hospital, Northern Lyon Hospital Group, Lyon, France.
  • Daniele B; Department of Experimental, Diagnostic and Speciality Medicicne, University Hospital S.Orsola-Malpighi, Bologna, Italy.
  • Okusaka T; Department of Oncology, Azienda Ospedaliera Gaetano Rummo, Benevento, Italy.
  • Tomásek J; Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Borg C; Department of Complex Oncology Care, Masaryk Memorial Cancer Institute, Masaryk University, Brno, Czech Republic.
  • Dadduzio V; Department of Medical Oncology, University Hospital of Besançon, Besançon, France.
  • Morimoto M; Department of Clinical and Experimental Oncology, Medical Oncology Unit-1, Veneto Institute of Oncology (IOV) - IRCCS, Padua, Italy.
  • Pracht M; Department of Hepatobiliary and Pancreatic Oncology, Kanagawa Cancer Center, Yokohama, Japan.
  • Jen MH; Department of Medical Oncology, Centre Eugène Marquis, Rennes, France.
  • Drove Ubreva N; Global Statistical Sciences, Eli Lilly and Company, Surrey, UK.
  • Widau RC; Medicines Development Unit Japan, Eli Lilly Japan K.K, Kobe, Japan.
  • Shinozaki K; Oncology, Eli Lilly and Company, Indianapolis, IN, USA.
  • Yoshikawa R; Medicines Development Unit Japan, Eli Lilly Japan K.K, Kobe, Japan.
  • Zhu AX; Medicines Development Unit Japan, Eli Lilly Japan K.K, Kobe, Japan.
Liver Int ; 40(8): 2008-2020, 2020 08.
Article en En | MEDLINE | ID: mdl-32279446
ABSTRACT
BACKGROUND &

AIMS:

Limited data on treatment of elderly patients with hepatocellular carcinoma (HCC) increase the unmet need. REACH and REACH-2 were global phase III studies of ramucirumab in patients with HCC after prior sorafenib, where patients with alpha-fetoprotein (AFP) ≥400 ng/mL showed an overall ssurvival (OS) benefit for ramucirumab. These post-hoc analyses examined efficacy and safety of ramucirumab in patients with HCC and baseline AFP ≥ 400 ng/mL by three prespecified age subgroups (<65, ≥65 to <75 and ≥75 years).

METHODS:

Individual patient data were pooled from REACH (baseline AFP ≥400 ng/mL) and REACH-2. Kaplan-Meier and Cox proportional hazards regression methods (stratified by study) assessed OS, progression-free survival (PFS), time to progression (TTP) and patient-reported outcomes (Functional Hepatobiliary System Index-8 [FHSI-8] score).

RESULTS:

A total of 542 patients (<65 years n = 302; ≥65 to <75 years n = 160; ≥75 years n = 80) showed similar baseline characteristics between ramucirumab and placebo. Older subgroups had higher hepatitis C and steatohepatitis incidences, and lower AFP levels, than the <65 years subgroup. Ramucirumab prolonged OS in patients <65 years (hazard ratio [HR], 0.753; 95% CI 0.581-0.975), ≥65 to <75 years (0.602; 0.419-0.866) and ≥75 years (0.709; 0.420-1.199), PFS and TTP irrespective of age. Ramucirumab showed similar overall safety profiles across subgroups, with a consistent median relative dose intensity ≥97.8%. A trend towards a delay in symptom deterioration in FHSI-8 with ramucirumab was observed in all subgroups.

CONCLUSIONS:

In this post-hoc analysis, ramucirumab showed a survival benefit across age subgroups with a tolerable safety profile, supporting its use in advanced HCC with elevated AFP, irrespective of age, including ≥75 years.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Neoplasias Hepáticas Tipo de estudio: Clinical_trials Límite: Aged / Humans Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Neoplasias Hepáticas Tipo de estudio: Clinical_trials Límite: Aged / Humans Idioma: En Año: 2020 Tipo del documento: Article