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Pathways towards indolent B-cell lymphoma - Etiology and therapeutic strategies.
van den Brand, Michiel; Scheijen, Blanca; Hess, Corine J; van Krieken, J Han Jm; Groenen, Patricia J T A.
Afiliação
  • van den Brand M; Department of Pathology, Radboud university medical center, Geert Grooteplein Zuid 10, 6525GA Nijmegen, The Netherlands; Pathology-DNA, location Rijnstate, Wagnerlaan 55, 6815AD Arnhem, The Netherlands. Electronic address: Michiel.vandenBrand@radboudumc.nl.
  • Scheijen B; Department of Pathology, Radboud university medical center, Geert Grooteplein Zuid 10, 6525GA Nijmegen, The Netherlands. Electronic address: Blanca.Scheijen@radboudumc.nl.
  • Hess CJ; Department of Hematology, Radboud university medical center, Geert Grooteplein Zuid 10, 6525GA Nijmegen, The Netherlands. Electronic address: Corine.Hess@radboudumc.nl.
  • van Krieken JHJ; Department of Pathology, Radboud university medical center, Geert Grooteplein Zuid 10, 6525GA Nijmegen, The Netherlands. Electronic address: Han.vanKrieken@radboudumc.nl.
  • Groenen PJTA; Department of Pathology, Radboud university medical center, Geert Grooteplein Zuid 10, 6525GA Nijmegen, The Netherlands. Electronic address: Patricia.Groenen@radboudumc.nl.
Blood Rev ; 31(6): 426-435, 2017 11.
Article em En | MEDLINE | ID: mdl-28802906
Although patients with indolent B-cell lymphomas have a relatively good survival rate, conventional chemotherapy is not curative. Disease courses are typically characterized by multiple relapses and progressively shorter response duration with subsequent lines of therapy. There has been an explosion of innovative targeted agents in the past years. This review discusses current knowledge on the etiology of indolent B-cell lymphomas with respect to the role of micro-organisms, auto-immune diseases, and deregulated pathways caused by mutations. In particular, knowledge on the mutational landscape of indolent B-cell lymphomas has strongly increased in recent years and harbors great promise for more accurate decision making in the current wide range of therapeutic options. Despite this promise, only in chronic lymphocytic leukemia the detection of TP53 mutations and/or del17p currently have a direct effect on treatment decisions. Nevertheless, it is expected that in the near future the role of genetic testing will increase for prediction of response to targeted treatment as well as for more accurate prediction of prognosis in indolent B-cell lymphomas.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma de Células B Tipo de estudo: Etiology_studies Limite: Animals / Humans Idioma: En Revista: Blood Rev Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma de Células B Tipo de estudo: Etiology_studies Limite: Animals / Humans Idioma: En Revista: Blood Rev Ano de publicação: 2017 Tipo de documento: Article