GALLE, P. R., M. KUDO, J. M. LLOVET, R. S. FINN, M. KARWAL, D. PEZET, T. Y. KIM, T. S. YANG, S. LONARDI, Jiří TOMÁŠEK, J. M. PHELIP, Y. TOUCHEFEU, S. J. KOH, G. STIRNIMANN, K. LIANG, K. D. OGBURN, C. X. WANG, P. ABADA, R. C. WIDAU a A. X. ZHU. Ramucirumab in patients with previously treated advanced hepatocellular carcinoma: Impact of liver disease aetiology. Liver International. Hoboken: John Viley & Sons, 2021, roč. 41, č. 11, s. 2759-2767. ISSN 1478-3223. Dostupné z: https://dx.doi.org/10.1111/liv.14994.
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Základní údaje
Originální název Ramucirumab in patients with previously treated advanced hepatocellular carcinoma: Impact of liver disease aetiology
Autoři GALLE, P. R. (garant), M. KUDO, J. M. LLOVET, R. S. FINN, M. KARWAL, D. PEZET, T. Y. KIM, T. S. YANG, S. LONARDI, Jiří TOMÁŠEK (203 Česká republika, domácí), J. M. PHELIP, Y. TOUCHEFEU, S. J. KOH, G. STIRNIMANN, K. LIANG, K. D. OGBURN, C. X. WANG, P. ABADA, R. C. WIDAU a A. X. ZHU.
Vydání Liver International, Hoboken, John Viley & Sons, 2021, 1478-3223.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30219 Gastroenterology and hepatology
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 8.754
Kód RIV RIV/00216224:14110/21:00122114
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1111/liv.14994
UT WoS 000682738200001
Klíčová slova anglicky hepatitis B; hepatitis C; hepatocellular carcinoma; ramucirumab
Štítky 14110811, rivok
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 7. 12. 2021 13:05.
Anotace
Background & Aims Hepatocellular carcinoma (HCC) is a common complication of chronic liver disease with diverse underlying aetiologies. REACH/REACH-2 were global phase III studies investigating ramucirumab in advanced HCC (aHCC) following sorafenib treatment. We performed an exploratory analysis of outcomes by liver disease aetiology and baseline serum viral load. Methods Meta-analysis was conducted in patients with aHCC and alpha-fetoprotein (AFP) >= 400 ng/mL (N = 542) from REACH/REACH-2 trials. Individual patient-level data were pooled with results reported by aetiology subgroup (hepatitis B [HBV] or C [HCV] and Other). Pre-treatment serum HBV DNA and HCV RNA were quantified using Roche COBAS AmpliPrep/COBAS TaqMan. Overall survival (OS) and progression-free survival (PFS) were evaluated using the Kaplan-Meier method and Cox proportional hazard model (stratified by study). Results Baseline characteristics were generally balanced between arms in each subgroup (HBV: N = 225, HCV: N = 127, Other: N = 190). No significant difference in treatment effect by aetiology subgroup was detected (OS interaction P-value = .23). Median OS (ramucirumab vs placebo) in months was 7.7 versus 4.5 (HR 0.74, 95% CI 0.55-0.99) for HBV, 8.2 versus 5.5 (HR 0.82, 95% CI 0.55-1.23) for HCV and 8.5 versus 5.4 (HR 0.56, 95% CI 0.40-0.79) for Other. Ramucirumab showed similar overall safety profiles across subgroups. Worst outcomes were noted in patients with a detectable HBV load. Use of HBV antiviral therapy, irrespective of viral load, was beneficial for survival, liver function and liver-specific adverse events. Conclusions Ramucirumab improved survival across aetiology subgroups with a tolerable safety profile, supporting its use in patients with aHCC and elevated AFP.
VytisknoutZobrazeno: 18. 7. 2024 15:38