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TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, randomised controlled trial
BACKGROUND: For children with sickle cell anaemia and elevated transcranial Doppler (TCD) flow velocities, regular blood transfusions effectively prevent primary stroke, but must be continued indefinitely. The efficacy of hydroxyurea in this setting is unknown. METHODS: TWiTCH was a multicentre Phas...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724392/ https://www.ncbi.nlm.nih.gov/pubmed/26670617 http://dx.doi.org/10.1016/S0140-6736(15)01041-7 |
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author | Ware, Russell E. Davis, Barry R. Schultz, William H. Brown, R. Clark Aygun, Banu Sarnaik, Sharada Odame, Isaac Fuh, Beng George, Alex Owen, William Luchtman-Jones, Lori Rogers, Zora R. Hilliard, Lee Gauger, Cynthia Piccone, Connie Lee, Margaret T. Kwiatkowski, Janet L. Jackson, Sherron Miller, Scott T. Roberts, Carla Heeney, Matthew M. Kalfa, Theodosia A. Nelson, Stephen Imran, Hamayun Nottage, Kerri Alvarez, Ofelia Rhodes, Melissa Thompson, Alexis A. Rothman, Jennifer A. Helton, Kathleen J. Roberts, Donna Coleman, Jamie Bonner, Melanie J. Kutlar, Abdullah Patel, Niren Wood, John Piller, Linda Wei, Peng Luden, Judy Mortier, Nicole A. Stuber, Susan E. Luban, Naomi L. C. Cohen, Alan R. Pressel, Sara Adams, Robert J. |
author_facet | Ware, Russell E. Davis, Barry R. Schultz, William H. Brown, R. Clark Aygun, Banu Sarnaik, Sharada Odame, Isaac Fuh, Beng George, Alex Owen, William Luchtman-Jones, Lori Rogers, Zora R. Hilliard, Lee Gauger, Cynthia Piccone, Connie Lee, Margaret T. Kwiatkowski, Janet L. Jackson, Sherron Miller, Scott T. Roberts, Carla Heeney, Matthew M. Kalfa, Theodosia A. Nelson, Stephen Imran, Hamayun Nottage, Kerri Alvarez, Ofelia Rhodes, Melissa Thompson, Alexis A. Rothman, Jennifer A. Helton, Kathleen J. Roberts, Donna Coleman, Jamie Bonner, Melanie J. Kutlar, Abdullah Patel, Niren Wood, John Piller, Linda Wei, Peng Luden, Judy Mortier, Nicole A. Stuber, Susan E. Luban, Naomi L. C. Cohen, Alan R. Pressel, Sara Adams, Robert J. |
author_sort | Ware, Russell E. |
collection | PubMed |
description | BACKGROUND: For children with sickle cell anaemia and elevated transcranial Doppler (TCD) flow velocities, regular blood transfusions effectively prevent primary stroke, but must be continued indefinitely. The efficacy of hydroxyurea in this setting is unknown. METHODS: TWiTCH was a multicentre Phase III randomised open label, non-inferiority trial comparing standard treatment (transfusions) to alternative treatment (hydroxyurea) in children with abnormal TCD velocities but no severe vasculopathy. Iron overload was managed with chelation (Standard Arm) and serial phlebotomy (Alternative Arm). The primary study endpoint was the 24-month TCD velocity calculated from a general linear mixed model, with non-inferiority margin = 15 cm/sec. FINDINGS: Among 121 randomised participants (61 transfusions, 60 hydroxyurea), children on transfusions maintained <30% sickle haemoglobin, while those taking hydroxyurea (mean 27 mg/kg/day) averaged 25% fetal haemoglobin. The first scheduled interim analysis demonstrated non-inferiority, and the sponsor terminated the study. Final model-based TCD velocities (mean ± standard error) on Standard versus Alternative Arm were 143 ± 1.6 and 138 ± 1.6 cm/sec, respectively, with difference (95% CI) = 4.54 (0.10, 8.98), non-inferiority p=8.82 × 10(−16) and post-hoc superiority p=0.023. Among 29 new neurological events adjudicated centrally by masked reviewers, no strokes occurred but there were 3 transient ischaemic attacks per arm. Exit brain MRI/MRA revealed no new cerebral infarcts in either arm, but worse vasculopathy in one participant (Standard Arm). Iron burden decreased more in the Alternative Arm, with ferritin difference −1047 ng/mL (−1524, −570), p<0.001 and liver iron difference −4.3 mg Fe/gm dry weight (−6.1, −2.5), p=0.001. INTERPRETATION: For high-risk children with sickle cell anaemia and abnormal TCD velocities, after four years of transfusions and without severe MRA vasculopathy, hydroxyurea therapy can substitute for chronic transfusions to maintain TCD velocities and help prevent primary stroke. |
format | Online Article Text |
id | pubmed-5724392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-57243922017-12-11 TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, randomised controlled trial Ware, Russell E. Davis, Barry R. Schultz, William H. Brown, R. Clark Aygun, Banu Sarnaik, Sharada Odame, Isaac Fuh, Beng George, Alex Owen, William Luchtman-Jones, Lori Rogers, Zora R. Hilliard, Lee Gauger, Cynthia Piccone, Connie Lee, Margaret T. Kwiatkowski, Janet L. Jackson, Sherron Miller, Scott T. Roberts, Carla Heeney, Matthew M. Kalfa, Theodosia A. Nelson, Stephen Imran, Hamayun Nottage, Kerri Alvarez, Ofelia Rhodes, Melissa Thompson, Alexis A. Rothman, Jennifer A. Helton, Kathleen J. Roberts, Donna Coleman, Jamie Bonner, Melanie J. Kutlar, Abdullah Patel, Niren Wood, John Piller, Linda Wei, Peng Luden, Judy Mortier, Nicole A. Stuber, Susan E. Luban, Naomi L. C. Cohen, Alan R. Pressel, Sara Adams, Robert J. Lancet Article BACKGROUND: For children with sickle cell anaemia and elevated transcranial Doppler (TCD) flow velocities, regular blood transfusions effectively prevent primary stroke, but must be continued indefinitely. The efficacy of hydroxyurea in this setting is unknown. METHODS: TWiTCH was a multicentre Phase III randomised open label, non-inferiority trial comparing standard treatment (transfusions) to alternative treatment (hydroxyurea) in children with abnormal TCD velocities but no severe vasculopathy. Iron overload was managed with chelation (Standard Arm) and serial phlebotomy (Alternative Arm). The primary study endpoint was the 24-month TCD velocity calculated from a general linear mixed model, with non-inferiority margin = 15 cm/sec. FINDINGS: Among 121 randomised participants (61 transfusions, 60 hydroxyurea), children on transfusions maintained <30% sickle haemoglobin, while those taking hydroxyurea (mean 27 mg/kg/day) averaged 25% fetal haemoglobin. The first scheduled interim analysis demonstrated non-inferiority, and the sponsor terminated the study. Final model-based TCD velocities (mean ± standard error) on Standard versus Alternative Arm were 143 ± 1.6 and 138 ± 1.6 cm/sec, respectively, with difference (95% CI) = 4.54 (0.10, 8.98), non-inferiority p=8.82 × 10(−16) and post-hoc superiority p=0.023. Among 29 new neurological events adjudicated centrally by masked reviewers, no strokes occurred but there were 3 transient ischaemic attacks per arm. Exit brain MRI/MRA revealed no new cerebral infarcts in either arm, but worse vasculopathy in one participant (Standard Arm). Iron burden decreased more in the Alternative Arm, with ferritin difference −1047 ng/mL (−1524, −570), p<0.001 and liver iron difference −4.3 mg Fe/gm dry weight (−6.1, −2.5), p=0.001. INTERPRETATION: For high-risk children with sickle cell anaemia and abnormal TCD velocities, after four years of transfusions and without severe MRA vasculopathy, hydroxyurea therapy can substitute for chronic transfusions to maintain TCD velocities and help prevent primary stroke. 2015-12-06 2016-02-13 /pmc/articles/PMC5724392/ /pubmed/26670617 http://dx.doi.org/10.1016/S0140-6736(15)01041-7 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This manuscript version is made available under the CC BY-NC-ND 4.0 license. |
spellingShingle | Article Ware, Russell E. Davis, Barry R. Schultz, William H. Brown, R. Clark Aygun, Banu Sarnaik, Sharada Odame, Isaac Fuh, Beng George, Alex Owen, William Luchtman-Jones, Lori Rogers, Zora R. Hilliard, Lee Gauger, Cynthia Piccone, Connie Lee, Margaret T. Kwiatkowski, Janet L. Jackson, Sherron Miller, Scott T. Roberts, Carla Heeney, Matthew M. Kalfa, Theodosia A. Nelson, Stephen Imran, Hamayun Nottage, Kerri Alvarez, Ofelia Rhodes, Melissa Thompson, Alexis A. Rothman, Jennifer A. Helton, Kathleen J. Roberts, Donna Coleman, Jamie Bonner, Melanie J. Kutlar, Abdullah Patel, Niren Wood, John Piller, Linda Wei, Peng Luden, Judy Mortier, Nicole A. Stuber, Susan E. Luban, Naomi L. C. Cohen, Alan R. Pressel, Sara Adams, Robert J. TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, randomised controlled trial |
title | TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, randomised controlled trial |
title_full | TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, randomised controlled trial |
title_fullStr | TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, randomised controlled trial |
title_full_unstemmed | TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, randomised controlled trial |
title_short | TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, randomised controlled trial |
title_sort | tcd with transfusions changing to hydroxyurea (twitch): a multicentre, randomised controlled trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724392/ https://www.ncbi.nlm.nih.gov/pubmed/26670617 http://dx.doi.org/10.1016/S0140-6736(15)01041-7 |
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