First-Generation and Second-Generation Bruton Tyrosine Kinase Inhibitors in Waldenström Macroglobulinemia
Author:
Publisher
Elsevier BV
Subject
Oncology,Hematology
Reference64 articles.
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2. The genomic landscape of Waldenstrom macroglobulinemia is characterized by highly recurring MYD88 and WHIM-like CXCR4 mutations, and small somatic deletions associated with B-cell lymphomagenesis;Hunter;Blood,2014
3. C1013G/CXCR4 acts as a driver mutation of tumor progression and modulator of drug resistance in lymphoplasmacytic lymphoma;Roccaro;Blood,2014
4. Genome wide SNP array identified multiple mechanisms of genetic changes in Waldenstrom macroglobulinemia;Poulain;Am J Hematol,2013
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2. Case report: Circulating tumor DNA technology displays temporal and spatial heterogeneity in Waldenström macroglobulinemia during treatment with BTK inhibitors;Pathology and Oncology Research;2023-04-19
3. Waldenström´s macroglobulinemia, overview of clinical symptoms, and therapy and our experience with ibrutinib therapy;Onkologie;2022-10-14
4. The Use of Bruton Tyrosine Kinase Inhibitors in Waldenström’s Macroglobulinemia;Clinical Hematology International;2022-05-23
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