Literature DB >> 21826782

Stroke With Transfusions Changing to Hydroxyurea (SWiTCH): a phase III randomized clinical trial for treatment of children with sickle cell anemia, stroke, and iron overload.

Russell E Ware1, William H Schultz, Nancy Yovetich, Nicole A Mortier, Ofelia Alvarez, Lee Hilliard, Rathi V Iyer, Scott T Miller, Zora R Rogers, J Paul Scott, Myron Waclawiw, Ronald W Helms.   

Abstract

BACKGROUND: Stroke occurs in 5-10% of children with sickle cell anemia (SCA) and has a high (>50%) risk of recurrence without therapy. Chronic monthly erythrocyte transfusions effectively prevent recurrent stroke, but their long-term use is limited by serious side effects, including iron overload. An alternative to transfusion for secondary stroke prevention in SCA is needed, especially one that also improves the management of iron overload.
METHODS: Stroke With Transfusions Changing to Hydroxyurea (SWiTCH) is an NHLBI-sponsored Phase III multicenter randomized controlled clinical trial for children with SCA, stroke, and iron overload (NCT00122980). The primary goal of SWiTCH is to compare 30 months of alternative therapy (hydroxyurea and phlebotomy) with standard therapy (transfusions and chelation) for the prevention of secondary stroke and reduction of transfusional iron overload. DISCUSSION: SWiTCH has several distinctive study features including novel methodological and design components: (1) composite primary endpoint including both stroke recurrence rate and iron burden; (2) non-inferiority design with an "acceptable" increased stroke risk; (3) transfusion goals based on current academic community practices; (4) special oversight for the enrollment and randomization process; (5) overlap treatment period within the alternative treatment arm; (6) masking of the overall trial Principal Investigator to treatment results; (7) inclusive independent stroke adjudication process for all suspected new neurological events; and (8) periodic therapeutic phlebotomy program to alleviate iron overload.
CONCLUSION: Investigation of alternative treatments in SWiTCH could lead to changes in the management of cerebrovascular disease for selected patients with SCA, stroke, and iron overload.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21826782      PMCID: PMC3171640          DOI: 10.1002/pbc.23145

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  26 in total

Review 1.  Current risk for transfusion transmitted infections.

Authors:  Roger Y Dodd
Journal:  Curr Opin Hematol       Date:  2007-11       Impact factor: 3.284

Review 2.  Hydroxyurea for the treatment of sickle cell anemia.

Authors:  Orah S Platt
Journal:  N Engl J Med       Date:  2008-03-27       Impact factor: 91.245

3.  Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell disease.

Authors:  S K Ballas
Journal:  Semin Hematol       Date:  2001-01       Impact factor: 3.851

4.  Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease.

Authors:  R E Ware; S A Zimmerman; W H Schultz
Journal:  Blood       Date:  1999-11-01       Impact factor: 22.113

5.  Cerebrovascular accidents in sickle cell disease: rates and risk factors.

Authors:  K Ohene-Frempong; S J Weiner; L A Sleeper; S T Miller; S Embury; J W Moohr; D L Wethers; C H Pegelow; F M Gill
Journal:  Blood       Date:  1998-01-01       Impact factor: 22.113

6.  Severity of iron overload in patients with sickle cell disease receiving chronic red blood cell transfusion therapy.

Authors:  P Harmatz; E Butensky; K Quirolo; R Williams; L Ferrell; T Moyer; D Golden; L Neumayr; E Vichinsky
Journal:  Blood       Date:  2000-07-01       Impact factor: 22.113

7.  Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group.

Authors:  T R Kinney; R W Helms; E E O'Branski; K Ohene-Frempong; W Wang; C Daeschner; E Vichinsky; R Redding-Lallinger; B Gee; O S Platt; R E Ware
Journal:  Blood       Date:  1999-09-01       Impact factor: 22.113

8.  Barriers to adherence of deferoxamine usage in sickle cell disease.

Authors:  Marsha J Treadwell; Amy W Law; Jennifer Sung; Ekua Hackney-Stephens; Keith Quirolo; Eileen Murray; G Alastair Glendenning; Elliott Vichinsky
Journal:  Pediatr Blood Cancer       Date:  2005-05       Impact factor: 3.167

9.  Erythrocyte autoantibodies in paediatric patients with sickle cell disease receiving transfusion therapy: frequency, characteristics and significance.

Authors:  S M Castellino; M R Combs; S A Zimmerman; P D Issitt; R E Ware
Journal:  Br J Haematol       Date:  1999-01       Impact factor: 6.998

10.  Chronic transfusion practice for children with sickle cell anaemia and stroke.

Authors:  Banu Aygun; Marsha A McMurray; William H Schultz; Janet L Kwiatkowski; Lee Hilliard; Ofelia Alvarez; Matthew Heeney; Karen Kalinyak; Margaret T Lee; Scott Miller; Ronald W Helms; Russell E Ware
Journal:  Br J Haematol       Date:  2008-03-13       Impact factor: 6.998

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  29 in total

1.  Discontinuing prophylactic transfusions increases the risk of silent brain infarction in children with sickle cell disease: data from STOP II.

Authors:  Miguel R Abboud; Eunsil Yim; Khaled M Musallam; Robert J Adams
Journal:  Blood       Date:  2011-06-01       Impact factor: 22.113

Review 2.  The epidemiology, evaluation and treatment of stroke in adults with sickle cell disease.

Authors:  John J Strouse; Sophie Lanzkron; Victor Urrutia
Journal:  Expert Rev Hematol       Date:  2011-12       Impact factor: 2.929

3.  Stroke With Transfusions Changing to Hydroxyurea (SWiTCH).

Authors:  Russell E Ware; Ronald W Helms
Journal:  Blood       Date:  2012-02-07       Impact factor: 22.113

Review 4.  Interventions for preventing silent cerebral infarcts in people with sickle cell disease.

Authors:  Lise J Estcourt; Patricia M Fortin; Sally Hopewell; Marialena Trivella; Carolyn Doree; Miguel R Abboud
Journal:  Cochrane Database Syst Rev       Date:  2017-05-13

Review 5.  Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease.

Authors:  Lise J Estcourt; Patricia M Fortin; Sally Hopewell; Marialena Trivella; Winfred C Wang
Journal:  Cochrane Database Syst Rev       Date:  2017-01-17

6.  Intravenous magnesium for pediatric sickle cell vaso-occlusive crisis: methodological issues of a randomized controlled trial.

Authors:  Oluwakemi Badaki-Makun; J Paul Scott; Julie A Panepinto; T Charles Casper; Cheryl A Hillery; J Michael Dean; David C Brousseau
Journal:  Pediatr Blood Cancer       Date:  2014-01-17       Impact factor: 3.167

7.  Hemoglobinopathies and stroke: strategies for prevention and treatment.

Authors:  Noorjahan Ali; Rothtida Srey; Steven Pavlakis
Journal:  Curr Treat Options Cardiovasc Med       Date:  2012-06

8.  Exploring barriers and facilitators to clinical trial enrollment in the context of sickle cell anemia and hydroxyurea.

Authors:  Jeffrey D Lebensburger; Robert F Sidonio; Michael R Debaun; Monika M Safford; Thomas H Howard; Isabel C Scarinci
Journal:  Pediatr Blood Cancer       Date:  2013-02-15       Impact factor: 3.167

9.  Genetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemia.

Authors:  Jonathan M Flanagan; Vivien Sheehan; Heidi Linder; Thad A Howard; Yong-Dong Wang; Carolyn C Hoppe; Banu Aygun; Robert J Adams; Geoffrey A Neale; Russell E Ware
Journal:  Blood       Date:  2013-02-19       Impact factor: 22.113

10.  Pain and other non-neurological adverse events in children with sickle cell anemia and previous stroke who received hydroxyurea and phlebotomy or chronic transfusions and chelation: results from the SWiTCH clinical trial.

Authors:  Ofelia Alvarez; Nancy A Yovetich; J Paul Scott; William Owen; Scott T Miller; William Schultz; Alexandre Lockhart; Banu Aygun; Jonathan Flanagan; Melanie Bonner; Brigitta U Mueller; Russell E Ware
Journal:  Am J Hematol       Date:  2013-08-30       Impact factor: 10.047

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