Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment. Issue 11 (14th July 2015)
- Record Type:
- Journal Article
- Title:
- Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment. Issue 11 (14th July 2015)
- Main Title:
- Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment
- Authors:
- Lê, Phu Quoc
Gulbis, Béatrice
Dedeken, Laurence
Dupont, Sophie
Vanderfaeillie, Anna
Heijmans, Catherine
Huybrechts, Sophie
Devalck, Christine
Efira, André
Dresse, Marie‐Françoise
Rozen, Laurence
Benghiat, Fleur Samantha
Ferster, Alina - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25608-sec-0001" sec-type="section"> <title>Objective</title> <p>To evaluate the survival of patients with sickle cell disease (SCD) recorded in the Belgian SCD Registry and to assess the impact of disease‐modifying treatments (DMT).</p> </sec> <sec id="pbc25608-sec-0002" sec-type="section"> <title>Method</title> <p>The Registry created in 2008 included patients of eight centers. All available data in 2008 were retrospectively encoded in the database. After 2008 and until 2012, all data were recorded prospectively for already registered patients as well as newly diagnosed subjects. Data were registered from neonatal screening or from diagnosis (first contact) until last follow‐up or death. Data included diagnosis, demography, and outcome data.</p> </sec> <sec id="pbc25608-sec-0003" sec-type="section"> <title>Results</title> <p>We collected data from 469 patients over a 5, 110 patient years (PY) follow‐up period. The global mortality rate was low (0.25/100 PY), although 13 patients died (2.8%) and was similar between children, adolescents (10–18 years), and young adults (<italic>P </italic>= 0.76). Out of the cohort, 185 patients received hydroxyurea at last follow‐up (median duration of treatment: 10.3 years), 90 underwent hematopoietic stem cell transplantation (HSCT), 24 were chronically transfused, and 170 had never had any DMT. Hydroxyurea showed significant<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25608-sec-0001" sec-type="section"> <title>Objective</title> <p>To evaluate the survival of patients with sickle cell disease (SCD) recorded in the Belgian SCD Registry and to assess the impact of disease‐modifying treatments (DMT).</p> </sec> <sec id="pbc25608-sec-0002" sec-type="section"> <title>Method</title> <p>The Registry created in 2008 included patients of eight centers. All available data in 2008 were retrospectively encoded in the database. After 2008 and until 2012, all data were recorded prospectively for already registered patients as well as newly diagnosed subjects. Data were registered from neonatal screening or from diagnosis (first contact) until last follow‐up or death. Data included diagnosis, demography, and outcome data.</p> </sec> <sec id="pbc25608-sec-0003" sec-type="section"> <title>Results</title> <p>We collected data from 469 patients over a 5, 110 patient years (PY) follow‐up period. The global mortality rate was low (0.25/100 PY), although 13 patients died (2.8%) and was similar between children, adolescents (10–18 years), and young adults (<italic>P </italic>= 0.76). Out of the cohort, 185 patients received hydroxyurea at last follow‐up (median duration of treatment: 10.3 years), 90 underwent hematopoietic stem cell transplantation (HSCT), 24 were chronically transfused, and 170 had never had any DMT. Hydroxyurea showed significant benefit on patients outcome as reflected by a lower mortality rate compared to transplanted individuals or people without DMT (0.14, 0.36, and 0.38 per 100 PY, respectively) and by higher Kaplan–Meier estimates of 15 year survival (99.4%) compared to HSCT (93.8%; <italic>P </italic>= 0.01) or no DMT groups (95.4%; <italic>P</italic> = 0.04).</p> </sec> <sec id="pbc25608-sec-0004" sec-type="section"> <title>Conclusion</title> <p>SCD mortality in Belgium is low with no increase observed in young adults. Patients treated with hydroxyurea demonstrate a significant benefit in survival when compared to those without DMT or transplanted. Pediatr Blood Cancer © 2015 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric blood & cancer. Volume 62:Issue 11(2015:Nov.)
- Journal:
- Pediatric blood & cancer
- Issue:
- Volume 62:Issue 11(2015:Nov.)
- Issue Display:
- Volume 62, Issue 11 (2015)
- Year:
- 2015
- Volume:
- 62
- Issue:
- 11
- Issue Sort Value:
- 2015-0062-0011-0000
- Page Start:
- 1956
- Page End:
- 1961
- Publication Date:
- 2015-07-14
- 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.25608 ↗
- 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:
- 3555.xml