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 database1. Issue 4 (4th September 2012)
- Record Type:
- Journal Article
- Title:
- 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 database1. Issue 4 (4th September 2012)
- Main Title:
- 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 database1
- Authors:
- Walker, Dana M.
Fisher, Brian T.
Seif, Alix E.
Huang, Yuan‐Shung V.
Torp, Kari
Li, Yimei
Aplenc, Richard - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="abs1-1" sec-type="section"> <title>Background</title> <p>Acute lymphoblastic (ALL) and myeloid leukemia (AML) account for approximately 26% of pediatric cancers. Anthracyclines are widely used to treat these leukemias, but dosing is limited by cardiotoxicity. Data support the efficacy of dexrazoxane as a cardioprotectant in children; however, dexrazoxane use in children is not universally accepted due to concerns about toxicity, impact on the antitumor effect of anthracyclines, and risk of secondary malignant neoplasms (SMN).</p> </sec> <sec id="abs1-2" sec-type="section"> <title>Procedure</title> <p>We conducted a retrospective cohort study to describe patterns of dexrazoxane use in pediatric patients with ALL or AML using the Pediatric Health Information Systems (PHIS) database. Patients identified as having <italic>de novo</italic> ALL and AML at these PHIS hospitals were included.</p> </sec> <sec id="abs1-3" sec-type="section"> <title>Results</title> <p>Of 8, 733 patients with ALL and 2, 556 with AML, 207 (2.4%) and 52 (2.0%) received dexrazoxane, respectively. Dexrazoxane use was greater in older children with ALL and AML and in black patients and males with ALL. Dexrazoxane use varied across time and by region in ALL, but not in AML. Prescribing practices differed across institutions and most patients received the first dose early or late after the start of leukemia treatment.</p> </sec><abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="abs1-1" sec-type="section"> <title>Background</title> <p>Acute lymphoblastic (ALL) and myeloid leukemia (AML) account for approximately 26% of pediatric cancers. Anthracyclines are widely used to treat these leukemias, but dosing is limited by cardiotoxicity. Data support the efficacy of dexrazoxane as a cardioprotectant in children; however, dexrazoxane use in children is not universally accepted due to concerns about toxicity, impact on the antitumor effect of anthracyclines, and risk of secondary malignant neoplasms (SMN).</p> </sec> <sec id="abs1-2" sec-type="section"> <title>Procedure</title> <p>We conducted a retrospective cohort study to describe patterns of dexrazoxane use in pediatric patients with ALL or AML using the Pediatric Health Information Systems (PHIS) database. Patients identified as having <italic>de novo</italic> ALL and AML at these PHIS hospitals were included.</p> </sec> <sec id="abs1-3" sec-type="section"> <title>Results</title> <p>Of 8, 733 patients with ALL and 2, 556 with AML, 207 (2.4%) and 52 (2.0%) received dexrazoxane, respectively. Dexrazoxane use was greater in older children with ALL and AML and in black patients and males with ALL. Dexrazoxane use varied across time and by region in ALL, but not in AML. Prescribing practices differed across institutions and most patients received the first dose early or late after the start of leukemia treatment.</p> </sec> <sec id="abs1-4" sec-type="section"> <title>Conclusions</title> <p>Dexrazoxane administration is limited in patients with ALL and AML and prescribing practices vary across the country. Further work is necessary to understand how dexrazoxane is used in patients at highest risk of developing cardiotoxicity and to define its true effect on the development of SMNs. Pediatr Blood Cancer 2013; 60: 616–620. © 2012 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric blood & cancer. Volume 60:Issue 4(2013:Apr.)
- Journal:
- Pediatric blood & cancer
- Issue:
- Volume 60:Issue 4(2013:Apr.)
- Issue Display:
- Volume 60, Issue 4 (2013)
- Year:
- 2013
- Volume:
- 60
- Issue:
- 4
- Issue Sort Value:
- 2013-0060-0004-0000
- Page Start:
- 616
- Page End:
- 620
- Publication Date:
- 2012-09-04
- Subjects:
- Tumors in children -- Periodicals
Blood -- Diseases -- Periodicals
Cancer in children -- Periodicals
618.92 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1545-5017 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pbc.24270 ↗
- Languages:
- English
- ISSNs:
- 1545-5009
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.533500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3944.xml