Literature DB >> 20974674

American Society of Hematology/American Society of Clinical Oncology clinical practice guideline update on the use of epoetin and darbepoetin in adult patients with cancer.

J Douglas Rizzo1, Melissa Brouwers, Patricia Hurley, Jerome Seidenfeld, Murat O Arcasoy, Jerry L Spivak, Charles L Bennett, Julia Bohlius, Darren Evanchuk, Matthew J Goode, Ann A Jakubowski, David H Regan, Mark R Somerfield.   

Abstract

PURPOSE: To update American Society of Hematology/American Society of Clinical Oncology recommendations for use of erythropoiesis-stimulating agents (ESAs) in patients with cancer.
METHODS: An Update Committee reviewed data published between January 2007 and January 2010. MEDLINE and the Cochrane Library were searched.
RESULTS: The literature search yielded one new individual patient data analysis and four literature-based meta-analyses, two systematic reviews, and 13 publications reporting new results from randomized controlled trials not included in prior or new reviews. RECOMMENDATIONS: For patients undergoing myelosuppressive chemotherapy who have a hemoglobin (Hb) level less than 10 g/dL, the Update Committee recommends that clinicians discuss potential harms (eg, thromboembolism, shorter survival) and benefits (eg, decreased transfusions) of ESAs and compare these with potential harms (eg, serious infections, immune-mediated adverse reactions) and benefits (eg, rapid Hb improvement) of RBC transfusions. Individual preferences for assumed risk should contribute to shared decisions on managing chemotherapy-induced anemia. The Committee cautions against ESA use under other circumstances. If used, ESAs should be administered at the lowest dose possible and should increase Hb to the lowest concentration possible to avoid transfusions. Available evidence does not identify Hb levels ≥ 10 g/dL either as thresholds for initiating treatment or as targets for ESA therapy. Starting doses and dose modifications after response or nonresponse should follow US Food and Drug Administration-approved labeling. ESAs should be discontinued after 6 to 8 weeks in nonresponders. ESAs should be avoided in patients with cancer not receiving concurrent chemotherapy, except for those with lower risk myelodysplastic syndromes. Caution should be exercised when using ESAs with chemotherapeutic agents in diseases associated with increased risk of thromboembolic complications. Table 1 lists detailed recommendations.

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Year:  2010        PMID: 20974674     DOI: 10.1182/blood-2010-08-300541

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  54 in total

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Review 3.  Evaluation and management of anemia in the elderly.

Authors:  Lawrence Tim Goodnough; Stanley L Schrier
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Authors:  J de Castro; P Gascón; A Casas; J Muñoz-Langa; V Alberola; M Cucala; F Barón
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5.  The ESA APPRISE Oncology Program: A History of REMS Requirements, a Review of the Data, And an Approach to Compliance in the Hospital.

Authors:  David J Reeves; Amanda K Quebe; Ranita Patel
Journal:  P T       Date:  2011-07

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Journal:  Blood       Date:  2011-07-05       Impact factor: 22.113

Review 7.  Anaemia of chronic disease.

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Journal:  Clin Med (Lond)       Date:  2013-04       Impact factor: 2.659

8.  Anti-hemojuvelin antibody corrects anemia caused by inappropriately high hepcidin levels.

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9.  Clinical use of ferric carboxymaltose in patients with solid tumours or haematological malignancies in France.

Authors:  Alain Toledano; Elisabeth Luporsi; Jean François Morere; Florian Scotté; Kamel Laribi; Jérôme Barrière; Philippe Huot-Marchand; Ladan Duvillié; Victor Hugo Concas; Roland Bugat
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10.  Management of anemia and iron deficiency in a cancer center in France.

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