Bispecific T-Cell Engager (BiTE) Antibody Construct Blinatumomab for the Treatment of Patients With Relapsed/Refractory Non-Hodgkin Lymphoma: Final Results From a Phase I Study

Blinatumoab公司 医学 淋巴瘤 加药 内科学 不利影响 药效学 胃肠病学 肿瘤科 耐火材料(行星科学) 药代动力学 白血病 淋巴细胞白血病 天体生物学 物理
作者
Maria-Elisabeth Goebeler,Stefan Knop,Andreas Viardot,Peter Kufer,Max S. Topp,Hermann Einsele,Richard Noppeney,Georg Heß,С. Каллерт,Andréas Mackensen,Kathrin Rupertus,Lothar Kanz,M. Libicher,Dirk Nagorsen,Gerhard Zugmaier,Matthias Klinger,Andreas Wolf,B Dorsch,Beate D. Quednau,Margit Schmidt,J. Scheele,Patrick A. Baeuerle,Eugen Leo,Ralf C. Bargou
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:34 (10): 1104-1111 被引量:383
标识
DOI:10.1200/jco.2014.59.1586
摘要

Blinatumomab is a CD19/CD3 BiTE (bispecific T-cell engager) antibody construct for the treatment of Philadelphia chromosome-negative acute B-lymphoblastic leukemia. We evaluated blinatumomab in relapsed/refractory B-cell non-Hodgkin lymphoma (NHL).This 3 + 3 design, phase I dose-escalation study determined adverse events and the maximum tolerated dose (MTD) of continuous intravenous infusion blinatumomab in patients with relapsed/refractory NHL. Blinatumomab was administered over 4 or 8 weeks at seven different dose levels (0.5 to 90 μg/m(2)/day). End points were incidence of adverse events, pharmacokinetics, pharmacodynamics, and overall response rate.Between 2004 and 2011, 76 heavily pretreated patients with relapsed/refractory NHL, who included 14 with diffuse large B-cell lymphoma, were enrolled; 42 received treatment in the formal dose-escalation phase. Neurologic events were dose limiting, and 60 μg/m(2)/day was established as the MTD. Thirty-four additional patients were recruited to evaluate antilymphoma activity and strategies for mitigating neurologic events at a prespecified MTD. Stepwise dosing (5 to 60 μg/m(2)/day) plus pentosan polysulfate SP54 (n = 3) resulted in no treatment discontinuations; single-step (n = 5) and double-step (n = 24) dosing entailed two and seven treatment discontinuations due to neurologic events, respectively. Grade 3 neurologic events occurred in 22% of patients (no grade 4/5). Among patients treated at 60 μg/m(2)/day (target dose; n = 35), the overall response rate was 69% across NHL subtypes and 55% for diffuse large B-cell lymphoma (n = 11); median response duration was 404 days (95% CI, 207 to 1,129 days).In this phase I study of relapsed/refractory NHL, continuous infusion with CD19-targeted immunotherapy blinatumomab at various doses and schedules was feasible, with an MTD of 60 μg/m(2)/day. Single-agent blinatumomab showed antilymphoma activity.
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