Literature DB >> 15079153

Use of fludarabine in the treatment of mantle cell lymphoma, Waldenström's macroglobulinemia and other uncommon B- and T-cell lymphoid malignancies.

Stephen A Johnson1.   

Abstract

After initial efforts using fludarabine as a single agent in the treatment of acute leukemia, its activity at lower and safer doses was demonstrated in chronic lymphocytic leukemia (CLL) patients who were refractory or had relapsed from traditional chemotherapies, representing a highly effective therapy for this condition. Fludarabine was also rapidly shown to be beneficial as first-line therapy in CLL. There is now considerable evidence that fludarabine is an effective agent in non-Hodgkin's lymphoma and in combination therapy for acute myeloid leukemia. Further, good responses are achieved when fludarabine-based approaches are used as conditioning regimens prior to transplantation procedures. The actions of fludarabine are not restricted to these settings and its potential role in the treatment of a range of uncommon T- and B-cell lymphoid malignancies is slowly emerging. This review will focus on the characteristics and treatment options for two B-cell disorders, mantle cell lymphoma and Waldenström's macroglobulinemia, with emphasis on the clinical activity of fludarabine. Additionally, the advantages of using fludarabine-containing regimens for a range of other lymphoproliferative conditions will also be discussed. These include B-cell neoplasms such as the CLL variant prolymphocytic leukemia, hairy cell leukemia and mucosa-associated lymphoid tissue-derived lymphomas; the T-cell disorders cutaneous T-cell lymphoma, angioimmunoblastic lymphadenopathy and other rarer T-cell diseases; and aggressive variants of non-Hodgkin's lymphoma including Richter's syndrome.

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Year:  2004        PMID: 15079153     DOI: 10.1038/sj.thj.6200391

Source DB:  PubMed          Journal:  Hematol J        ISSN: 1466-4860


  4 in total

1.  Long-term results of the treatment of patients with mantle cell lymphoma with cladribine (2-CDA) alone (95-80-53) or 2-CDA and rituximab (N0189) in the North Central Cancer Treatment Group.

Authors:  David J Inwards; Paul A S Fishkin; David W Hillman; David W Brown; Stephen M Ansell; Paul J Kurtin; Rafael Fonseca; Roscoe F Morton; Michael H Veeder; Thomas E Witzig
Journal:  Cancer       Date:  2008-07-01       Impact factor: 6.860

2.  The addition of rituximab to fludarabine and cyclophosphamide chemotherapy results in a significant improvement in overall survival in patients with newly diagnosed mantle cell lymphoma: results of a randomized UK National Cancer Research Institute trial.

Authors:  Simon Rule; Paul Smith; Peter W M Johnson; Simon Bolam; George Follows; Joanne Gambell; Peter Hillmen; Andrew Jack; Stephen Johnson; Amy A Kirkwood; Anton Kruger; Christopher Pocock; John F Seymour; Milena Toncheva; Jan Walewski; David Linch
Journal:  Haematologica       Date:  2015-11-26       Impact factor: 9.941

3.  A phase II study of two dose levels of ofatumumab induction followed by maintenance therapy in symptomatic, previously untreated chronic lymphocytic leukemia.

Authors:  Ian W Flinn; Amy S Ruppert; William Harwin; David Waterhouse; Steven Papish; Jeffrey A Jones; John Hainsworth; John C Byrd
Journal:  Am J Hematol       Date:  2016-07-22       Impact factor: 10.047

4.  Downregulation of deoxycytidine kinase in cytarabine-resistant mantle cell lymphoma cells confers cross-resistance to nucleoside analogs gemcitabine, fludarabine and cladribine, but not to other classes of anti-lymphoma agents.

Authors:  Magdalena Klanova; Lucie Lorkova; Ondrej Vit; Bokang Maswabi; Jan Molinsky; Jana Pospisilova; Petra Vockova; Cory Mavis; Lucie Lateckova; Vojtech Kulvait; Dana Vejmelkova; Radek Jaksa; Francisco Hernandez; Marek Trneny; Martin Vokurka; Jiri Petrak; Pavel Klener
Journal:  Mol Cancer       Date:  2014-06-27       Impact factor: 27.401

  4 in total

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