Literature DB >> 22272702

Rasburicase for the treatment of tumor lysis in hematological malignancies.

Giulia Malaguarnera1, Maria Giordano, Mariano Malaguarnera.   

Abstract

Tumor lysis syndrome (TLS) is a common oncologic emergency in patients with hematological malignancies sensitive to cytotoxic treatment that present a high proliferative rate. High proliferative cancer rate, high sensitivity of cytotoxic treatment and renal failure represent risk factors for development of TLS. TLS is also responsible for several electrolytic alterations, such as hyperuricemia, hyperkalemia, hyperphosphatemia and hypocalcemia. There are different established therapeutic options for the treatment of TLS such as hydration, allopurinol and rasburicase. Rasburicase reduces uric acid levels within 4 h, both in pediatric and adult patients, catalyzing the oxidation of uric acid into allantoin, rapidly excreted by the kidneys. Rasburicase is well tolerated and was approved in the EU and in the USA for the management of acute hyperuricemia.

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Year:  2012        PMID: 22272702     DOI: 10.1586/ehm.11.73

Source DB:  PubMed          Journal:  Expert Rev Hematol        ISSN: 1747-4094            Impact factor:   2.929


  3 in total

Review 1.  Rasburicase in the management of tumor lysis: an evidence-based review of its place in therapy.

Authors:  Jennifer Dinnel; Bonny L Moore; Brent M Skiver; Prithviraj Bose
Journal:  Core Evid       Date:  2015-01-13

2.  Spontaneous Tumor Lysis Syndrome: A Case Report and Critical Evaluation of Current Diagnostic Criteria and Optimal Treatment Regimens.

Authors:  Alicia C Weeks; Michelle E Kimple
Journal:  J Investig Med High Impact Case Rep       Date:  2015-08-25

Review 3.  Tumor lysis syndrome in an extraskeletal osteosarcoma: a case report and review of the literature.

Authors:  Vito Emanuele Catania; Michele Vecchio; Michele Malaguarnera; Roberto Madeddu; Giulia Malaguarnera; Saverio Latteri
Journal:  J Med Case Rep       Date:  2017-03-24
  3 in total

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