Zanubrutinib Versus Ibrutinib in Relapsed/Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma: Interim Analysis of a Randomized Phase III Trial
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu klinické zkoušky, fáze III, randomizované kontrolované studie, časopisecké články, práce podpořená grantem
PubMed
36395435
PubMed Central
PMC9928683
DOI
10.1200/jco.22.00510
Knihovny.cz E-zdroje
- MeSH
- adenin terapeutické užití MeSH
- B-buněčný lymfom * farmakoterapie MeSH
- chronická lymfatická leukemie * farmakoterapie MeSH
- fibrilace síní * MeSH
- inhibitory proteinkinas terapeutické užití MeSH
- lidé MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- adenin MeSH
- ibrutinib MeSH Prohlížeč
- inhibitory proteinkinas MeSH
- zanubrutinib MeSH Prohlížeč
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: NCT03734016) 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.
4th Department of Internal Medicine Hematology University Hospital Hradec Kralove Czech Republic
Affiliated Cancer Hospital of Zhengzhou University Henan Cancer Hospital Zhengzhou China
Blue Ridge Cancer Care Roanoke VA
Cancer Immunotherapy Programme Malaghan Institute of Medical Research Wellington New Zealand
Chao Family Comprehensive Cancer Center University of California Irvine CA
Department of Haematology Christchurch Hospital Christchurch New Zealand
Department of Hematology and Transplantology Medical University of Gdańsk Gdańsk Poland
Department of Hematology Karolinska University Hospital Stockholm Sweden
Department of Leukemia The University of Texas MD Anderson Cancer Center Houston TX
Department of Medical Oncology Dana Farber Cancer Institute Boston MA
Department of Medicine University of Washington Seattle WA
Department of Oncology Pathology Karolinska Institutet Stockholm Sweden
Faculty of Medicine Charles University Prague Czech Republic
Fred Hutchinson Cancer Research Center Seattle WA
Herbert Irving Comprehensive Cancer Center Columbia University New York NY
Maria Sklodowska Curie National Research Institute of Oncology Krakow Poland
Medical University of Lodz Lodz Poland
Peter MacCallum Cancer Centre Melbourne Victoria Australia
Royal Melbourne Hospital Parkville Victoria Australia
St James's University Hospital Leeds United Kingdom
St Vincent's Hospital Melbourne Fitzroy Victoria Australia
Texas Oncology Tyler US Oncology Research Tyler TX
University of Melbourne Parkville Victoria Australia
Wellington Blood and Cancer Centre Capital and Coast District Health Board Wellington New Zealand
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EHA-EU MCL network guidelines for diagnosis and treatment of mantle cell lymphoma
Bruton's Tyrosine Kinase: A Potential Novel Target for Neurological Disorders
ClinicalTrials.gov
NCT03734016