| Literature DB >> 28864640 |
Aparna Lakshmanan1, John C Byrd1.
Abstract
<b/> In this issue Grommes and colleagues elegantly show that the irreversible inhibitor of Bruton tyrosine kinase, ibrutinib, promotes a high proportion of durable responses in primary central nervous system lymphoma, a type of diffuse large B-cell lymphoma (DLBCL), and also in secondary DLBCL relapsing to the central nervous system. Mutations in the B-cell antigen receptor-associated protein CD79B with upregulation of the MTOR pathway were associated with diminished response, but preclinical combination of PIK3CA and PIK3CD inhibitors synergized with ibrutinib to overcome this resistance mechanism, providing opportunity for further targeted therapy of this difficult-to-treat disease. Cancer Discov; 7(9); 940-2. ©2017 AACRSee related article by Grommes et al., p. 1018. ©2017 American Association for Cancer Research.Entities:
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Year: 2017 PMID: 28864640 DOI: 10.1158/2159-8290.CD-17-0714
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397