KUTER, D. J., M. EFRAIM, Jiří MAYER, Marek TRNĚNÝ, V. MCDONALD, R. BIRD, T. REGENBOGEN, M. GARG, Z. KAPLAN, N. TZVETKOV, P. Y. CHOI, A. J. G. JANSEN, Milan KOSTAL, R. BAKER, Jaromir GUMULEC, E. J. LEE, I. CUNNINGHAM, I. GONCALVES, M. WARNER, R. BOCCIA, T. GERNSHEIMER, W. GHANIMA, O. BANDMAN, R. BURNS, A. NEALE, D. THOMAS, P. ARORA, B. ZHENG a Cooper N. RILZABRUTINIB. Rilzabrutinib, an Oral BTK Inhibitor, in Immune Thrombocytopenia. New England Journal of Medicine. Waltham: Massachussetts Medical Society, 2022, roč. 386, č. 15, s. 1421-1431. ISSN 0028-4793. Dostupné z: https://dx.doi.org/10.1056/NEJMoa2110297.
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Základní údaje
Originální název Rilzabrutinib, an Oral BTK Inhibitor, in Immune Thrombocytopenia
Autoři KUTER, D. J., M. EFRAIM, Jiří MAYER (203 Česká republika, domácí), Marek TRNĚNÝ (203 Česká republika), V. MCDONALD, R. BIRD, T. REGENBOGEN, M. GARG, Z. KAPLAN, N. TZVETKOV, P. Y. CHOI, A. J. G. JANSEN, Milan KOSTAL (203 Česká republika), R. BAKER, Jaromir GUMULEC (203 Česká republika), E. J. LEE, I. CUNNINGHAM, I. GONCALVES, M. WARNER, R. BOCCIA, T. GERNSHEIMER, W. GHANIMA, O. BANDMAN, R. BURNS, A. NEALE, D. THOMAS, P. ARORA, B. ZHENG a Cooper N. RILZABRUTINIB.
Vydání New England Journal of Medicine, Waltham, Massachussetts Medical Society, 2022, 0028-4793.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30218 General and internal medicine
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 158.500
Kód RIV RIV/00216224:14110/22:00126144
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1056/NEJMoa2110297
UT WoS 000798829500005
Klíčová slova anglicky Rilzabrutinib; Oral BTK Inhibito; Immune Thrombocytopenia
Štítky 14110212, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 28. 6. 2022 09:07.
Anotace
BACKGROUND & nbsp;Rilzabrutinib, an oral, reversible covalent inhibitor of Bruton's tyrosine kinase, may increase platelet counts in patients with immune thrombocytopenia by means of dual mechanisms of action: decreased macrophage (Fc gamma receptor)-mediated platelet destruction and reduced production of pathogenic autoantibodies.& nbsp;METHODS & nbsp;In an international, adaptive, open-label, dose-finding, phase 1-2 clinical trial, we evaluated rilzabrutinib therapy in previously treated patients with immune thrombocytopenia. We used intrapatient dose escalation of oral rilzabrutinib over a period of 24 weeks; the lowest starting dose was 200 mg once daily, with higher starting doses of 400 mg once daily, 300 mg twice daily, and 400 mg twice daily. The primary end points were safety and platelet response (defined as at least two consecutive platelet counts of >= 50x10(3) per cubic millimeter and an increase from baseline of >= 20x10(3) per cubic millimeter without the use of rescue medication).& nbsp;RESULTS & nbsp;Sixty patients were enrolled. At baseline, the median platelet count was 15x10(3) per cubic millimeter, the median duration of disease was 6.3 years, and patients had received a median of four different immune thrombocytopenia therapies previously. All the treatment-related adverse events were of grade 1 or 2 and transient. There were no treatment-related bleeding or thrombotic events of grade 2 or higher. At a median of 167.5 days (range, 4 to 293) of treatment, 24 of 60 patients (40%) overall and 18 of the 45 patients (40%) who had started rilzabrutinib treatment at the highest dose met the primary end point of platelet response. The median time to the first platelet count of at least 50x10(3) per cubic millimeter was 11.5 days. Among patients with a primary platelet response, the mean percentage of weeks with a platelet count of at least 50x10(3) per cubic millimeter was 65%.& nbsp;CONCLUSIONS & nbsp;Rilzabrutinib was active and associated with only low-level toxic effects at all dose levels. The dose of 400 mg twice daily was identified as the dose for further testing. Overall, rilzabrutinib showed a rapid and durable clinical activity that improved with length of treatment.
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