Literature DB >> 19959100

New agents for AML and MDS.

Steven Grant1.   

Abstract

The heterogeneity of acute myeloid leukaemia (AML) and myelodysplastic syndromes (MDS) has led to a multiplicity of treatments, from cytotoxic agents to signal transduction modulators, cell-cycle inhibitors and epigenetic therapies. While some have shown promising initial results, the outlook for AML patients, particularly older and relapsed patients, as well as patients whose cells exhibit certain adverse chromosomal abnormalities or mutant oncoproteins, continues to be grim. Combination chemotherapy using new agents that act at a number of different levels may provide the greatest potential for successful future therapies. A select number of new agents, approaches and combinations are reviewed here.

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Year:  2009        PMID: 19959100      PMCID: PMC2793080          DOI: 10.1016/j.beha.2009.08.003

Source DB:  PubMed          Journal:  Best Pract Res Clin Haematol        ISSN: 1521-6926            Impact factor:   3.020


  31 in total

1.  A limited number of 5-azacitidine cycles can be effective treatment in MDS.

Authors:  Catharina Müller-Thomas; Tibor Schuster; Christian Peschel; Katharina S Götze
Journal:  Ann Hematol       Date:  2008-08-12       Impact factor: 3.673

2.  Efficacy of azacitidine compared with that of conventional care regimens in the treatment of higher-risk myelodysplastic syndromes: a randomised, open-label, phase III study.

Authors:  Pierre Fenaux; Ghulam J Mufti; Eva Hellstrom-Lindberg; Valeria Santini; Carlo Finelli; Aristoteles Giagounidis; Robert Schoch; Norbert Gattermann; Guillermo Sanz; Alan List; Steven D Gore; John F Seymour; John M Bennett; John Byrd; Jay Backstrom; Linda Zimmerman; David McKenzie; Cl Beach; Lewis R Silverman
Journal:  Lancet Oncol       Date:  2009-02-21       Impact factor: 41.316

3.  A randomized study of clofarabine versus clofarabine plus low-dose cytarabine as front-line therapy for patients aged 60 years and older with acute myeloid leukemia and high-risk myelodysplastic syndrome.

Authors:  Stefan Faderl; Farhad Ravandi; Xuelin Huang; Guillermo Garcia-Manero; Alessandra Ferrajoli; Zeev Estrov; Gautam Borthakur; Srdan Verstovsek; Deborah A Thomas; Monica Kwari; Hagop M Kantarjian
Journal:  Blood       Date:  2008-06-18       Impact factor: 22.113

4.  The novel nuclear factor-kappaB inhibitor LC-1 is equipotent in poor prognostic subsets of chronic lymphocytic leukemia and shows strong synergy with fludarabine.

Authors:  Saman Hewamana; Thet Thet Lin; Chris Jenkins; Alan K Burnett; Craig T Jordan; Chris Fegan; Paul Brennan; Clare Rowntree; Chris Pepper
Journal:  Clin Cancer Res       Date:  2008-12-15       Impact factor: 12.531

5.  Rapamycin reverses NPM-ALK-induced glucocorticoid resistance in lymphoid tumor cells by inhibiting mTOR signaling pathway, enhancing G1 cell cycle arrest and apoptosis.

Authors:  L Gu; J Gao; Q Li; Y P Zhu; C S Jia; R Y Fu; Y Chen; Q K Liao; Z Ma
Journal:  Leukemia       Date:  2008-08-07       Impact factor: 11.528

6.  FMS-like tyrosine kinase 3-internal tandem duplication tyrosine kinase inhibitors display a nonoverlapping profile of resistance mutations in vitro.

Authors:  Nikolas von Bubnoff; Richard A Engh; Espen Aberg; Jana Sänger; Christian Peschel; Justus Duyster
Journal:  Cancer Res       Date:  2009-03-24       Impact factor: 12.701

7.  Transient potent BCR-ABL inhibition is sufficient to commit chronic myeloid leukemia cells irreversibly to apoptosis.

Authors:  Neil P Shah; Corynn Kasap; Christopher Weier; Minna Balbas; John M Nicoll; Eric Bleickardt; Claude Nicaise; Charles L Sawyers
Journal:  Cancer Cell       Date:  2008-12-09       Impact factor: 31.743

Review 8.  Cotargeting survival signaling pathways in cancer.

Authors:  Steven Grant
Journal:  J Clin Invest       Date:  2008-09       Impact factor: 14.808

9.  Patients with acute myeloid leukemia and RAS mutations benefit most from postremission high-dose cytarabine: a Cancer and Leukemia Group B study.

Authors:  Andreas Neubauer; Kati Maharry; Krzysztof Mrózek; Christian Thiede; Guido Marcucci; Peter Paschka; Robert J Mayer; Richard A Larson; Edison T Liu; Clara D Bloomfield
Journal:  J Clin Oncol       Date:  2008-06-16       Impact factor: 44.544

10.  A pharmacodynamic study of the FLT3 inhibitor KW-2449 yields insight into the basis for clinical response.

Authors:  Keith W Pratz; Jorge Cortes; Gail J Roboz; Niranjan Rao; Omotayo Arowojolu; Adam Stine; Yukimasa Shiotsu; Aiko Shudo; Shiro Akinaga; Donald Small; Judith E Karp; Mark Levis
Journal:  Blood       Date:  2008-11-24       Impact factor: 22.113

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  2 in total

Review 1.  Inhibition of bromodomain and extra-terminal proteins (BET) as a potential therapeutic approach in haematological malignancies: emerging preclinical and clinical evidence.

Authors:  Aristeidis Chaidos; Valentina Caputo; Anastasios Karadimitris
Journal:  Ther Adv Hematol       Date:  2015-06

Review 2.  Epigenetic therapies in MDS and AML.

Authors:  Elizabeth A Griffiths; Steven D Gore
Journal:  Adv Exp Med Biol       Date:  2013       Impact factor: 2.622

  2 in total

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