KUTER, D. J., D. M. ARNOLD, F. RODEGHIERO, A. JANSSENS, D. SELLESLAG, R. BIRD, A. NEWLAND, Jiří MAYER, K. J. WANG a R. OLIE. Safety and efficacy of self-administered romiplostim in patients with immune thrombocytopenia: Results of an integrated database of five clinical trials. American Journal of Hematology. Hoboken: John Wiley & Sons, 2020, roč. 95, č. 6, s. 643-651. ISSN 0361-8609. Dostupné z: https://dx.doi.org/10.1002/ajh.25776.
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Základní údaje
Originální název Safety and efficacy of self-administered romiplostim in patients with immune thrombocytopenia: Results of an integrated database of five clinical trials
Autoři KUTER, D. J. (840 Spojené státy, garant), D. M. ARNOLD (124 Kanada), F. RODEGHIERO (56 Belgie), A. JANSSENS (56 Belgie), D. SELLESLAG (56 Belgie), R. BIRD (36 Austrálie), A. NEWLAND (826 Velká Británie a Severní Irsko), Jiří MAYER (203 Česká republika, domácí), K. J. WANG (840 Spojené státy) a R. OLIE (756 Švýcarsko).
Vydání American Journal of Hematology, Hoboken, John Wiley & Sons, 2020, 0361-8609.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30205 Hematology
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 10.047
Kód RIV RIV/00216224:14110/20:00116538
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1002/ajh.25776
UT WoS 000522675000001
Klíčová slova anglicky immune thrombocytopenia; romiplostim
Štítky 14110212, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 30. 9. 2020 14:03.
Anotace
Romiplostim self-administration by patients or caregivers may offer time/cost savings to healthcare professionals (HCPs) and convenience for patients who avoid weekly clinic visits. We performed an integrated analysis of five clinical trials to evaluate the efficacy and safety of romiplostim self-administration. Data were analyzed from adults with immune thrombocytopenia (ITP) who received weekly romiplostim via self-administration or from an HCP. Patients who achieved a stable romiplostim dose for >= 3 weeks (HCP group >= 5 weeks to provide an appropriate index date to enable comparisons with the self-administration group) with platelet counts >= 50 x 10(9)/L were eligible. In the self-administration (n = 621) vs HCP (n = 133) groups, respectively, median age was 53 vs 58 years, median time since primary ITP diagnosis was 3.7 vs 2.5 years, and median baseline platelet count at ITP diagnosis was 19.0 vs 20.0 x 10(9)/L. In the self-administration and HCP-dosed groups, median romiplostim treatment duration was 89 vs 52 weeks and median total number of doses was 81 vs 50, respectively. In the self-administration and HCP groups, respectively: 95.0% and 100.0% of patients achieved >= 1 platelet response (defined as weekly platelet count >= 50 x 10(9)/L without rescue medication in previous 4 weeks); the median percentage of weeks with a response was 94.5% and 95.9%; and rescue medication was used in 36.7% and 39.8% of patients. Self-administration did not adversely affect safety; duration-adjusted rates for all treatment-emergent adverse events (TEAEs) and bleeding TEAEs were numerically lower with self-administration. Romiplostim self-administration appears effective and well tolerated in eligible patients with ITP.
VytisknoutZobrazeno: 26. 4. 2024 22:10