WASSERBAUER, Martin, Stepan HLAVA, Jiri DRABEK, Jan STOVICEK, Petra MINARIKOVA, Lenka NEDBALOVA, Tomas DRASAR, Zdena ZADOROVA, Jiří DOLINA, Štefan KONEČNÝ, Vladimír KOJECKY, Jana KOZELUHOVA, Pavlina CERNIKOVA, Dita PICHLEROVA, Barbora KUCEROVA, Stepan COUFAL a Radan KEIL. Adalimumab biosimilars in the therapy of Crohn´s disease and ulcerative colitis: Prospective multicentric clinical monitoring. PLOS One. SAN FRANCISCO: PUBLIC LIBRARY SCIENCE, 2022, roč. 17, č. 8, s. 1-13. ISSN 1932-6203. Dostupné z: https://dx.doi.org/10.1371/journal.pone.0271299.
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Základní údaje
Originální název Adalimumab biosimilars in the therapy of Crohn´s disease and ulcerative colitis: Prospective multicentric clinical monitoring
Autoři WASSERBAUER, Martin (203 Česká republika), Stepan HLAVA (203 Česká republika, garant), Jiri DRABEK (203 Česká republika), Jan STOVICEK (203 Česká republika), Petra MINARIKOVA (203 Česká republika), Lenka NEDBALOVA (203 Česká republika), Tomas DRASAR (203 Česká republika), Zdena ZADOROVA (203 Česká republika), Jiří DOLINA (203 Česká republika, domácí), Štefan KONEČNÝ (703 Slovensko, domácí), Vladimír KOJECKY (203 Česká republika), Jana KOZELUHOVA (203 Česká republika), Pavlina CERNIKOVA (203 Česká republika), Dita PICHLEROVA (203 Česká republika), Barbora KUCEROVA (203 Česká republika), Stepan COUFAL (203 Česká republika) a Radan KEIL (203 Česká republika).
Vydání PLOS One, SAN FRANCISCO, PUBLIC LIBRARY SCIENCE, 2022, 1932-6203.
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: 3.700
Kód RIV RIV/00216224:14110/22:00128066
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1371/journal.pone.0271299
UT WoS 000922632200001
Klíčová slova anglicky adalimumab biosimilars; Crohn´s disease; ulcerative colitis
Štítky 14110213, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 24. 2. 2023 07:55.
Anotace
Objective The adalimumab biosimilars FKB327 and GP2017 were approved for the therapy of patients with inflammatory bowel disease (IBD). Relatively few prospective studies with biosimilar adalimumab in patients with IBD have been published. The aim of this prospective observational study was to evaluate the effectiveness and safety of the biosimilar adalimumab. Material and methods Adalimumab biosimilars FKB327 (Hulio®) and GP2017 (Hyrimoz®) were indicated to 50 naive patients in terms of biological therapy with Crohn’s disease (CD) or ulcerative colitis (UC). Effectiveness of therapy was evaluated via the Crohn’s Disease Activity Index [CDAI] or the Mayo Scoring System [MSS] in patients with CD or UC, respectively, before and after 12 weeks. Additional goals were to evaluate weight changes, laboratory tests and complications or adverse events of this therapy. Results In CD patients, remission (CDAI <150) was achieved in 73.5% of cases, partial response (≥70-point decrease in CDAI score from baseline) in 11.8%, no response in 11.8% and 2.9% patients discontinued therapy. In UC patients, remission (total score on partial Mayo index ≤2 points) was achieved only in 18.8% of cases, partial response (≥2-point decrease in partial Mayo score from baseline) in 43.8%, no response in 25.0% and 12.5% patients discontinued therapy. There were statistically significant improvements in CDAI, MSS, haemoglobin, fecal calprotectin, albumin and CRP serum levels after 12 weeks of therapy. Seven adverse events were identified, three of which resulted in therapy being discontinued. Conclusions This prospective observational study proved the effectiveness of the adalimumab biosimilars FKB327 and GP2017 in IBD.
VytisknoutZobrazeno: 9. 5. 2024 09:31