Literature DB >> 22318199

Stroke With Transfusions Changing to Hydroxyurea (SWiTCH).

Russell E Ware1, Ronald W Helms.   

Abstract

Stroke is a devastating complication of sickle cell anemia (SCA) with high recurrence if untreated. Chronic transfusions reduce recurrent strokes but have associated morbidities including iron overload. Stroke With Transfusions Changing to Hydroxyurea (SWiTCH) was a multicenter phase 3 randomized trial comparing standard treatment (transfusions/chelation) to alternative treatment (hydroxyurea/phlebotomy) for children with SCA, stroke, and iron overload. SWiTCH was a noninferiority trial with a composite primary end point, allowing an increased stroke risk but requiring superiority for removing iron. Subjects on standard treatment received monthly transfusions plus daily deferasirox iron chelation. Subjects on alternative treatment received hydroxyurea plus overlap transfusions during dose escalation to maximum tolerated dose (MTD), followed by monthly phlebotomy. Subjects on standard treatment (N = 66) maintained 30% sickle hemoglobin (HbS) and tolerated deferasirox at 28.2 ± 6.0 mg/kg/d. Subjects on alternative treatment (N = 67) initiated hydroxyurea and 60 (90%) reached MTD at 26.2 ± 4.9 mg/kg/d with 29.1% ± 6.7% fetal hemoglobin (HbF). Adjudication documented no strokes on transfusions/chelation but 7 (10%) on hydroxyurea/phlebotomy, still within the noninferiority stroke margin. The National Heart, Lung, and Blood Institute closed SWiTCH after interim analysis revealed equivalent liver iron content, indicating futility for the composite primary end point. Transfusions and chelation remain a better way to manage children with SCA, stroke, and iron overload.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22318199      PMCID: PMC3350359          DOI: 10.1182/blood-2011-11-392340

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


  33 in total

1.  Noninvasive measurement and imaging of liver iron concentrations using proton magnetic resonance.

Authors:  Timothy G St Pierre; Paul R Clark; Wanida Chua-anusorn; Adam J Fleming; Gary P Jeffrey; John K Olynyk; Pensri Pootrakul; Erin Robins; Robert Lindeman
Journal:  Blood       Date:  2004-07-15       Impact factor: 22.113

2.  Hydroxyurea: an alternative to transfusion therapy for stroke in sickle cell anemia.

Authors:  R E Ware; M H Steinberg; T R Kinney
Journal:  Am J Hematol       Date:  1995-10       Impact factor: 10.047

3.  Phlebotomy to reduce iron overload in patients cured of thalassemia by bone marrow transplantation. Italian Cooperative Group for Phlebotomy Treatment of Transplanted Thalassemia Patients.

Authors:  E Angelucci; P Muretto; G Lucarelli; M Ripalti; D Baronciani; B Erer; M Galimberti; C Giardini; D Gaziev; P Polchi
Journal:  Blood       Date:  1997-08-01       Impact factor: 22.113

4.  Discontinuing prophylactic transfusions used to prevent stroke in sickle cell disease.

Authors:  Robert J Adams; Donald Brambilla
Journal:  N Engl J Med       Date:  2005-12-29       Impact factor: 91.245

5.  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

Review 6.  Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease.

Authors:  Sophie Lanzkron; John J Strouse; Renee Wilson; Mary Catherine Beach; Carlton Haywood; HaeSong Park; Catherine Witkop; Eric B Bass; Jodi B Segal
Journal:  Ann Intern Med       Date:  2008-05-05       Impact factor: 25.391

Review 7.  Hydroxyurea for children with sickle cell disease.

Authors:  Matthew M Heeney; Russell E Ware
Journal:  Pediatr Clin North Am       Date:  2008-04       Impact factor: 3.278

Review 8.  Hydroxyurea for sickle cell disease: a systematic review for efficacy and toxicity in children.

Authors:  John J Strouse; Sophie Lanzkron; Mary Catherine Beach; Carlton Haywood; Haeseong Park; Catherine Witkop; Renee F Wilson; Eric B Bass; Jodi B Segal
Journal:  Pediatrics       Date:  2008-12       Impact factor: 7.124

9.  R2* magnetic resonance imaging of the liver in patients with iron overload.

Authors:  Jane S Hankins; M Beth McCarville; Ralf B Loeffler; Matthew P Smeltzer; Mihaela Onciu; Fredric A Hoffer; Chin-Shang Li; Winfred C Wang; Russell E Ware; Claudia M Hillenbrand
Journal:  Blood       Date:  2009-03-04       Impact factor: 22.113

10.  Longitudinal analysis of heart and liver iron in thalassemia major.

Authors:  Leila J Noetzli; Susan M Carson; Anne S Nord; Thomas D Coates; John C Wood
Journal:  Blood       Date:  2008-07-23       Impact factor: 22.113

View more
  94 in total

1.  Frequent red cell transfusions reduced vascular endothelial activation and thrombogenicity in children with sickle cell anemia and high stroke risk.

Authors:  Hyacinth I Hyacinth; Robert J Adams; Jenifer H Voeks; Jacqueline M Hibbert; Beatrice E Gee
Journal:  Am J Hematol       Date:  2013-11-28       Impact factor: 10.047

2.  Heart disease and stroke statistics--2014 update: a report from the American Heart Association.

Authors:  Alan S Go; Dariush Mozaffarian; Véronique L Roger; Emelia J Benjamin; Jarett D Berry; Michael J Blaha; Shifan Dai; Earl S Ford; Caroline S Fox; Sheila Franco; Heather J Fullerton; Cathleen Gillespie; Susan M Hailpern; John A Heit; Virginia J Howard; Mark D Huffman; Suzanne E Judd; Brett M Kissela; Steven J Kittner; Daniel T Lackland; Judith H Lichtman; Lynda D Lisabeth; Rachel H Mackey; David J Magid; Gregory M Marcus; Ariane Marelli; David B Matchar; Darren K McGuire; Emile R Mohler; Claudia S Moy; Michael E Mussolino; Robert W Neumar; Graham Nichol; Dilip K Pandey; Nina P Paynter; Matthew J Reeves; Paul D Sorlie; Joel Stein; Amytis Towfighi; Tanya N Turan; Salim S Virani; Nathan D Wong; Daniel Woo; Melanie B Turner
Journal:  Circulation       Date:  2013-12-18       Impact factor: 29.690

3.  Beneficial Effect of Low Fixed Dose of Hydroxyurea in Vaso-occlusive Crisis and Transfusion Requirements in Adult HbSS Patients: A Prospective Study in a Tertiary Care Center.

Authors:  Sudha Sethy; Tribikram Panda; Rabindra Kumar Jena
Journal:  Indian J Hematol Blood Transfus       Date:  2017-09-04       Impact factor: 0.900

4.  Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemia.

Authors:  Patrick T McGann; Omar Niss; Min Dong; Anu Marahatta; Thad A Howard; Tomoyuki Mizuno; Adam Lane; Theodosia A Kalfa; Punam Malik; Charles T Quinn; Russell E Ware; Alexander A Vinks
Journal:  Am J Hematol       Date:  2019-06-12       Impact factor: 10.047

5.  Contribution of Sickle Cell Disease to the Pediatric Stroke Burden Among Hospital Discharges of African-Americans-United States, 1997-2012.

Authors:  Charlotte Baker; Althea M Grant; Mary G George; Scott D Grosse; Thomas V Adamkiewicz
Journal:  Pediatr Blood Cancer       Date:  2015-07-14       Impact factor: 3.167

6.  Brain venular pattern by 7T MRI correlates with memory and haemoglobin in sickle cell anaemia.

Authors:  Enrico M Novelli; C Elizabeth Sarles; Howard Jay Aizenstein; Tamer S Ibrahim; Meryl A Butters; Anne Connelly Ritter; Kirk I Erickson; Caterina Rosano
Journal:  Psychiatry Res       Date:  2015-04-25       Impact factor: 3.222

Review 7.  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 8.  Sickle cell disease: when and how to transfuse.

Authors:  Jo Howard
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2016-12-02

Review 9.  Advances in Understanding Ischemic Stroke Physiology and the Impact of Vasculopathy in Children With Sickle Cell Disease.

Authors:  Kristin P Guilliams; Melanie E Fields; Michael M Dowling
Journal:  Stroke       Date:  2019-02       Impact factor: 7.914

10.  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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.