Ibrutinib as Initial Therapy for Patients with Chronic Lymphocytic Leukemia

Jan A. Burger(The University of Texas MD Anderson Cancer Center), Alessandra Tedeschi(Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda), Paul M. Barr(University of Rochester), Tadeusz Robak(Copernicus Memorial Hospital), Carolyn Owen, Paolo Ghia(Vita-Salute San Raffaele University), Osnat Bairey(Tel Aviv University), Peter Hillmen, Nancy L. Bartlett(Washington University in St. Louis), Jianyong Li(Jiangsu Province Hospital), David Simpson(North Shore Hospital), Sebastian Grosicki(Medical University of Silesia), Stephen Devereux(King's College - North Carolina), Helen O. McCarthy(Royal Bournemouth Hospital), Steven Coutré(Stanford University), Hang Quach(The University of Melbourne), Gianluca Gaïdano(Università degli Studi del Piemonte Orientale “Amedeo Avogadro”), Zvenyslava Maslyak(Institute of Blood Pathology and Transfusion Medicine of the National Academy of Medical Sciences of Ukraine), Don A. Stevens(Norton Healthcare), Ann Janssens, Fritz Offner(Ghent University Hospital), Jiřı́ Mayer(University Hospital Brno), Michael O’Dwyer(University Hospital Galway), Andrzej Hellmann(Gdańsk Medical University), Anna Schuh(University of Oxford), Tanya Siddiqi(City Of Hope National Medical Center), Aaron Polliack(Hadassah Medical Center), Constantine S. Tam(Peter MacCallum Cancer Centre), Deepali Suri(Pharmacyclics (United States)), Mei Cheng(Pharmacyclics (United States)), Fong Clow(Pharmacyclics (United States)), Lori Styles(Pharmacyclics (United States)), Danelle F. James(Pharmacyclics (United States)), Thomas J. Kipps(University of California San Diego)
New England Journal of Medicine
December 6, 2015
Cited by 1,553Open Access
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Abstract

BACKGROUND: Chronic lymphocytic leukemia (CLL) primarily affects older persons who often have coexisting conditions in addition to disease-related immunosuppression and myelosuppression. We conducted an international, open-label, randomized phase 3 trial to compare two oral agents, ibrutinib and chlorambucil, in previously untreated older patients with CLL or small lymphocytic lymphoma. METHODS: We randomly assigned 269 previously untreated patients who were 65 years of age or older and had CLL or small lymphocytic lymphoma to receive ibrutinib or chlorambucil. The primary end point was progression-free survival as assessed by an independent review committee. RESULTS: The median age of the patients was 73 years. During a median follow-up period of 18.4 months, ibrutinib resulted in significantly longer progression-free survival than did chlorambucil (median, not reached vs. 18.9 months), with a risk of progression or death that was 84% lower with ibrutinib than that with chlorambucil (hazard ratio, 0.16; P<0.001). Ibrutinib significantly prolonged overall survival; the estimated survival rate at 24 months was 98% with ibrutinib versus 85% with chlorambucil, with a relative risk of death that was 84% lower in the ibrutinib group than in the chlorambucil group (hazard ratio, 0.16; P=0.001). The overall response rate was higher with ibrutinib than with chlorambucil (86% vs. 35%, P<0.001). The rates of sustained increases from baseline values in the hemoglobin and platelet levels were higher with ibrutinib. Adverse events of any grade that occurred in at least 20% of the patients receiving ibrutinib included diarrhea, fatigue, cough, and nausea; adverse events occurring in at least 20% of those receiving chlorambucil included nausea, fatigue, neutropenia, anemia, and vomiting. In the ibrutinib group, four patients had a grade 3 hemorrhage and one had a grade 4 hemorrhage. A total of 87% of the patients in the ibrutinib group are continuing to take ibrutinib. CONCLUSIONS: Ibrutinib was superior to chlorambucil in previously untreated patients with CLL or small lymphocytic lymphoma, as assessed by progression-free survival, overall survival, response rate, and improvement in hematologic variables. (Funded by Pharmacyclics and others; RESONATE-2 ClinicalTrials.gov number, NCT01722487.).


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