Clonal evolution leading to ibrutinib resistance in chronic lymphocytic leukemia

Inhye E. Ahn(Cancer Institute (WIA)), Chingiz Underbayev(National Institutes of Health), Adam Albitar(NeoGenomics (United States)), Sarah E. M. Herman(National Institutes of Health), Xin Tian(National Heart Lung and Blood Institute), Irina Marić(Center for Clinical Research (United States)), Diane C. Arthur(National Institutes of Health), Laura Wake(National Institutes of Health), Stefania Pittaluga(National Institutes of Health), Constance M. Yuan(National Institutes of Health), Maryalice Stetler‐Stevenson(National Institutes of Health), Susan Soto(National Institutes of Health), Janet Valdez(National Institutes of Health), Pia Nierman(National Institutes of Health), Jennifer Lotter(National Institutes of Health), Liqiang Xi(National Institutes of Health), Mark Raffeld(National Institutes of Health), Mohammed Farooqui(National Institutes of Health), Maher Albitar(NeoGenomics (United States)), Adrian Wiestner(National Institutes of Health)
Blood
January 3, 2017
Cited by 340Open Access
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Abstract

(within the autoinhibitory domain) were found in 9 patients (10.7%), in 8 of 10 patients with progressive CLL, and in 1 patient with prolymphocytic transformation. Applying high-sensitivity testing (detection limit ∼1 in 1000 cells) to stored samples, we detected mutations up to 15 months before manifestation of clinical progression (range, 2.9-15.4 months). In 5 patients (6.0%), multiple subclones carrying different mutations arose independently, leading to subclonal heterogeneity of resistant disease. For a seamless transition to alternative targeted agents, patients progressing with CLL were continued on ibrutinib for up to 3 months, with 19.8 months median survival from the time of progression. This trial was registered at www.clinicaltrials.gov as #NCT01500733.


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