Risk–benefit of dexrazoxane for preventing anthracycline-related cardiotoxicity: re-evaluating the European labeling

Author:

Reichardt Peter1,Tabone Marie-Dominique2,Mora Jaume3,Morland Bruce4,Jones Robin L5

Affiliation:

1. Department of Oncology, Helios Klinikum Berlin-Buch, Berlin, Germany

2. Department of Paediatric Onco-Haematology, Trousseau Hospital, Paris, France

3. Department of Pediatric Hematology & Oncology, Hospital Sant Joan de Déu, Barcelona, Spain

4. Oncology Department, Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK

5. Division of Clinical Studies, Institute of Cancer Research & Sarcoma Unit of the Royal Marsden NHS Foundation Trust, London, UK

Abstract

Dexrazoxane can prevent anthracycline-associated cardiotoxicity. However, in 2011, its use in children was contraindicated by the EMA over concerns of increased risk of infection, myelosuppression and second primary malignancies, and because its efficacy in children had not then been established. We review here the evidence published since 2011, which confirms that dexrazoxane is an effective cardioprotectant in children and adolescents, is not associated with an increased risk of second primary malignancies or excess early or late mortality and does not impair chemotherapy efficacy. Based on this evidence, the contraindication for children and adolescents requiring high doses of anthracyclines and at risk for cardiotoxicity was removed from the European labeling for dexrazoxane.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

Reference51 articles.

1. EMA. European Medicines Agency. Assessment report. Dexrazoxane-containing medicinal products (EMEA/H/A-31/1275) (2011). www.ema.europa.eu/docs/en_GB/document_library/Referrals_document/Dexrazoxane_31/WC500120340.pdf.

2. CARDIOXANE SmPC. CARDIOXANE SmPC (2015). www.medicines.org.uk/emc/medicine/28199.

3. EMA. European Medicines Agency. Questions and answers on Cardioxane (dexrazoxane: powder for solution for injection: 500 mg). Outcome of a procedure under Article 13 of Regulation (EC) No 1234/2008 (2017).www.ema.europa.eu/docs/en_GB/document_library/Referrals_document/Cardioxane_13/WC500228103.pdf.

4. European Commission. Commission Implementing Decision of 19.7.2017 concerning: in the framework of Article 13 of Commission Regulation (EC) No 1234/2008: the marketing authorisations for medicinal products for human use ‘Cardioxane’: which contain the active substance ‘dexrazoxane’. C(2017) 5248 final (2017). ec.europa.eu/health/documents/community-register/2017/20170719138252/dec_138252_en.pdf.

5. Dexrazoxane use in pediatric patients with acute lymphoblastic or myeloid leukemia from 1999 and 2009: Analysis of a national cohort of patients in the pediatric health information systems database

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