Modeling absolute lymphocyte counts after treatment of chronic lymphocytic leukemia with ibrutinib

被引:0
|
作者
David D. Smith
Leanne Goldstein
Mei Cheng
Danelle F. James
Lori A. Kunkel
Maria Fardis
Ahmed Hamdy
Raquel Izumi
Joseph J. Buggy
Fong Clow
机构
[1] Division of Biostatistics,
[2] Pharmacyclics Inc.,undefined
[3] Acerta Pharma,undefined
来源
Annals of Hematology | 2015年 / 94卷
关键词
Bruton’s tyrosine kinase; Lymphocytosis; B cell chronic lymphocytic leukemia; Leukemias and lymphomas; Protein tyrosine kinases; Kinase and phosphatase inhibitors; CLL; Chronic lymphocytic leukemia; Ibrutinib; Imbruvica;
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摘要
The objective in this study was to characterize the pattern of the treatment-related lymphocytosis curve in chronic lymphocytic leukemia (CLL) patients treated with ibrutinib, and assess the relationship between the baseline factors and absolute lymphocyte counts (ALC). The PCYC-1102-CA study was a five-arm phase Ib/II open-label, nonrandomized, multicenter study in CLL/SLL. The arms and accruals were 420 and 840 mg/day treatment-naive elderly CLL/SLL (N = 27 and N = 4, respectively), 420 and 840 mg/day relapsed/refractory CLL/SLL (N = 27 and N = 34, respectively), and 420 mg/day high-risk CLL/SLL (N = 24). The results were generated through statistical modeling using data from a clinical trial (PCYC-1102) in five cohorts of treatment-naïve or relapsed/refractory CLL patients treated at 420 and 840 mg daily of ibrutinib. In cases in which the initial increase in ALC doubles by day 28, it takes patients longer to reach their maximum ALC when compared with those with a lower rate of increase. Our models show that all of the cohorts exhibited the same pattern of treatment-related lymphocytosis from ibrutinib, and there are no significant differences between cohorts, including no detectable dose effect. The ALC of the majority of patients return to baseline ALC values by the end of cycle 5.
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页码:249 / 256
页数:7
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