Literature DB >> 20693115

[Therapeutic alternatives to native L-asparaginase in the treatment of adult acute lymphoblastic leukemia].

X Thomas1, G Cannas, Y Chelghoum, A Gougounon.   

Abstract

L-asparaginase is an effective antineoplastic agent, which is an integral part of combination chemotherapy protocols for adult acute lymphoblastic leukemia. Its antitumor effect results from the depletion of asparagine, an amino acid essential to leukemia cells, and subsequent inhibition of protein synthesis leading to cytotoxicity. However, its use has been limited by a high rate of hypersensitivity reactions and development of neutrolizing anti-asparaginase antibodies, and by the need of frequent administration. To overcome these limitations modified versions of L-asparaginase (such as asparaginase from other sources, pegylated formulations, and asparaginase loaded into erythrocytes) have been recently proposed. Advantages of these therapeutic alternatives to native L-asparaginase and their results as part of preliminary clinical trials in adults have been outlined in this review.

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Year:  2010        PMID: 20693115     DOI: 10.1684/bdc.2010.1168

Source DB:  PubMed          Journal:  Bull Cancer        ISSN: 0007-4551            Impact factor:   1.276


  3 in total

Review 1.  Erythrocyte encapsulated l-asparaginase (GRASPA) in acute leukemia.

Authors:  Xavier Thomas; Caroline Le Jeune
Journal:  Int J Hematol Oncol       Date:  2016-05-05

2.  Optimization of Culture Conditions for Production of the Anti-Leukemic Glutaminase Free L-Asparaginase by Newly Isolated Streptomyces olivaceus NEAE-119 Using Response Surface Methodology.

Authors:  Noura El-Ahmady El-Naggar; Hassan Moawad; Nancy M El-Shweihy; Sara M El-Ewasy
Journal:  Biomed Res Int       Date:  2015-06-09       Impact factor: 3.411

3.  A retrospective comparison of Escherichia coli and polyethylene glycol-conjugated asparaginase for the treatment of adolescents and adults with newly diagnosed acute lymphoblastic leukemia.

Authors:  Jiabao Liang; Pengcheng Shi; Xutao Guo; Jie Li; Lingli He; Yan Wang; Qi Wei; Fen Huang; Zhiping Fan; Bing Xu
Journal:  Oncol Lett       Date:  2017-10-26       Impact factor: 2.967

  3 in total

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