HILLMEN, Peter, Barbara EICHHORST, Jennifer R BROWN, Nicole LAMANNA, Susan M BRIEN, Constantine S TAM, Lugui QIU, Maciej KAZMIERCZAK, Keshu ZHOU, Martin SIMKOVIC, Jiří MAYER, Amanda GILLESPIE-TWARDY, Mazyar SHADMAN, Alessandra FERRAJOLI, Peter S GANLY, Robert WEINKOVE, Sebastian GROSICKI, Andrzej MITAL, Tadeusz ROBAK, Anders OSTERBORG, Habte A YIMER, Tommi SALMI, Meng JI, Jessica YECIES, Adam IDOINE, Kenneth WU, Jane HUANG a Wojciech JURCZAK. Zanubrutinib Versus Ibrutinib in Relapsed/Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma: Interim Analysis of a Randomized Phase III Trial. Journal of clinical oncology. United States: LIPPINCOTT WILLIAMS & WILKINS, 2023, roč. 41, č. 5, s. "1035"-"+", 12 s. ISSN 0732-183X. Dostupné z: https://dx.doi.org/10.1200/JCO.22.00510.
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Základní údaje
Originální název Zanubrutinib Versus Ibrutinib in Relapsed/Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma: Interim Analysis of a Randomized Phase III Trial
Autoři HILLMEN, Peter (garant), Barbara EICHHORST, Jennifer R BROWN, Nicole LAMANNA, Susan M BRIEN, Constantine S TAM, Lugui QIU, Maciej KAZMIERCZAK, Keshu ZHOU, Martin SIMKOVIC, Jiří MAYER (203 Česká republika, domácí), Amanda GILLESPIE-TWARDY, Mazyar SHADMAN, Alessandra FERRAJOLI, Peter S GANLY, Robert WEINKOVE, Sebastian GROSICKI, Andrzej MITAL, Tadeusz ROBAK, Anders OSTERBORG, Habte A YIMER, Tommi SALMI, Meng JI, Jessica YECIES, Adam IDOINE, Kenneth WU, Jane HUANG a Wojciech JURCZAK.
Vydání Journal of clinical oncology, United States, LIPPINCOTT WILLIAMS & WILKINS, 2023, 0732-183X.
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: 45.300 v roce 2022
Kód RIV RIV/00216224:14110/23:00130697
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1200/JCO.22.00510
UT WoS 000946950600015
Klíčová slova anglicky Zanubrutinib; Ibrutinib; Relapsed/Refractory Chronic Lymphocytic Leukemia; Small Lymphocytic Lymphoma
Štítky 14110212, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 2. 5. 2023 10:30.
Anotace
PURPOSE Zanubrutinib is a potent, irreversible next-generation Bruton tyrosine kinase (BTK) inhibitor designed to maximize BTK occupancy and minimize off-target kinase inhibition. We hypothesized that complete/sustained BTK occupancy may improve efficacy outcomes and increased BTK specificity may minimize off-target inhibition-related toxicities.PATIENTS AND METHODS ALPINE (ClinicalTrials.gov identifier: ) is a global, randomized, open-label phase III study of zanubrutinib versus ibrutinib in patients with relapsed/refractory chronic lymphocytic leukemia. The primary end point was investigator-assessed overall response rate (ORR). The preplanned interim analysis was scheduled approximately 12 months after the first 415 patients were enrolled.RESULTS Between November 1, 2018, and December 14, 2020, 652 patients were enrolled. We present the interim analysis of the first 415 enrolled patients randomly assigned to receive zanubrutinib (n = 207) or ibrutinib (n = 208). At 15 months of median follow-up, ORR (partial or complete response) was significantly higher with zanubrutinib (78.3%; 95% CI, 72.0 to 83.7) versus ibrutinib (62.5%; 95% CI, 55.5 to 69.1; two-sided P < .001). ORR was higher with zanubrutinib versus ibrutinib in subgroups with del(17p)/TP53 mutations (80.5% v 50.0%) and del(11q) (83.6% v 69.1%); 12-month progression-free survival in all patients was higher with zanubrutinib (94.9%) versus ibrutinib (84.0%; hazard ratio, 0.40; 95% CI, 0.23 to 0.69). Atrial fibrillation rate was significantly lower with zanubrutinib versus ibrutinib (2.5% v 10.1%; two-sided P = .001). Rates of cardiac events, major hemorrhages, and adverse events leading to treatment discontinuation/death were lower with zanubrutinib.CONCLUSION Zanubrutinib had a significantly higher ORR, lower atrial fibrillation rate, and improved progression-free survival and overall cardiac safety profile versus ibrutinib. These data support improved efficacy/safety outcomes with selective BTK inhibition.
VytisknoutZobrazeno: 1. 8. 2024 02:20