Neutropenia in glycogen storage disease Ib: outcomes for patients treated with granulocyte colony-stimulating factor.


Journal

Current opinion in hematology
ISSN: 1531-7048
Titre abrégé: Curr Opin Hematol
Pays: United States
ID NLM: 9430802

Informations de publication

Date de publication:
01 2019
Historique:
pubmed: 20 11 2018
medline: 7 2 2020
entrez: 20 11 2018
Statut: ppublish

Résumé

Glycogen storage disease Ib (GSD Ib) is characterized by hepatomegaly, hypoglycemia, neutropenia, enterocolitis and recurrent bacterial infections. It is attributable to mutations in G6PT1, the gene for the glucose-6-phosphate transporter responsible for transport of glucose into the endoplasmic reticulum. Neutropenia in GSD Ib is now frequently treated with granulocyte colony-stimulating factor (G-CSF). We formed a cooperative group to review outcomes of the long-term treatment of GSD Ib patients treated with G-CSF. The study enrolled 103 patients (48 men and 55 women), including 47 currently adult patients. All of these patients were treated with G-CSF, starting at a median age of 3.8 years (range 0.04-33.9 years) with a median dose of 3.0 mcg/kg/day (range 0.01-93.1 mcg/kg/day) for a median of 10.3 years (range 0.01-29.3 years). Neutrophils increased in response to G-CSF in all patients (median values before G-CSF 0.2 × 10/l, on G-CSF 1.20 x 10/l). Treatment increased spleen size (before G-CSF, 47%, on treatment on G-CSF 76%), and splenomegaly was the dose-limiting adverse effect of treatment (pain and early satiety). Clinical observations and records attest to reduce frequency of infectious events and the severity of inflammatory bowel symptoms, but fever and recurrent infections remain a significant problem. In the cohort of patients followed carefully through the Severe Chronic Neutropenia International Registry, four patients have developed myelodysplasia or acute myeloid leukemia and we are aware of four other cases, (altogether seven on G-CSF, one never treated with G-CSF). Liver transplantation in five patients did not correct neutropenia. Four patients had hematopoietic stem cell transplantation; two adults and two children were transplanted; one adult and one child survived. GSD Ib is a complex disorder of glucose metabolism causing severe chronic neutropenia. G-CSF is effective to raise blood neutrophil counts and reduce fevers and infections in most patients. In conjunction with other therapies (salicylates, mesalamine sulfasalazine and prednisone), G-CSF ameliorates inflammatory bowel symptoms, but doses must be limited because it increases spleen size associated with abdominal pain.

Identifiants

pubmed: 30451720
doi: 10.1097/MOH.0000000000000474
pmc: PMC7000169
mid: NIHMS1548665
doi:

Substances chimiques

Granulocyte Colony-Stimulating Factor 143011-72-7

Types de publication

Clinical Trial Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

16-21

Subventions

Organisme : NIAID NIH HHS
ID : R24 AI049393
Pays : United States

Références

Curr Opin Hematol. 2015 Jan;22(1):3-11
pubmed: 25427142
J Med Case Rep. 2008 Sep 30;2:319
pubmed: 18826620
Mol Genet Metab. 2001 Jun;73(2):117-25
pubmed: 11386847
J Clin Invest. 1991 Feb;87(2):704-10
pubmed: 1704019
Biochem Biophys Res Commun. 2017 Jan 22;482(4):569-574
pubmed: 27864142
Blood. 1996 Jul 1;88(1):335-40
pubmed: 8704192
Blood. 2018 Jan 25;131(4):408-416
pubmed: 29092827
Eur J Pediatr. 2005 Aug;164(8):501-8
pubmed: 15906092
Pediatr Hematol Oncol. 2018 Feb;35(1):45-51
pubmed: 29652549
Obstet Gynecol. 2015 Jan;125(1):197-203
pubmed: 25560125
Br J Haematol. 2010 Jul;150(2):196-9
pubmed: 20456363
Curr Opin Hematol. 2017 Jan;24(1):46-53
pubmed: 27841775
Blood. 1996 Dec 15;88(12):4435-44
pubmed: 8977235
J Inherit Metab Dis. 2018 Nov;41(6):1007-1014
pubmed: 29663270
Inflamm Bowel Dis. 2001 May;7(2):128-32
pubmed: 11383585
J Immunol. 2016 Sep 1;197(5):1989-99
pubmed: 27481851
Blood. 2001 Jan 15;97(2):376-82
pubmed: 11154211
N Engl J Med. 1992 Jun 18;326(25):1666-9
pubmed: 1375344
Eur J Pediatr. 2002 Oct;161 Suppl 1:S88-92
pubmed: 12373579
Genet Med. 2014 Nov;16(11):e1
pubmed: 25356975
Blood. 2014 May 1;123(18):2843-53
pubmed: 24565827
Haematologica. 2014 Aug;99(8):1395-402
pubmed: 24997149
Ann Intern Med. 1994 Feb 1;120(3):218-26
pubmed: 8273986
Eur J Pediatr. 2002 Oct;161 Suppl 1:S10-9
pubmed: 12373566
J Pediatr Hematol Oncol. 2002 Dec;24(9):756-8
pubmed: 12468919
J Pediatr. 1984 Sep;105(3):428-31
pubmed: 6590826
Eur J Pediatr. 2002 Oct;161 Suppl 1:S83-7
pubmed: 12373578
Orphanet J Rare Dis. 2013 Jun 13;8:84
pubmed: 23758768
Eur J Pediatr. 2002 Oct;161 Suppl 1:S120-3
pubmed: 12373585
N Engl J Med. 2017 Dec 7;377(23):2290-2292
pubmed: 29211670

Auteurs

David C Dale (DC)

Division of GIM, Department of Medicine, University of Washington.

Audrey Anna Bolyard (AA)

Department of Medicine, University of Washington, Severe Chronic Neutropenia International Registry, Seattle, Washington.

Tracy Marrero (T)

Department of Medicine, University of Washington, Severe Chronic Neutropenia International Registry, Seattle, Washington.

Merideth L Kelley (ML)

Division of GIM, Department of Medicine, University of Washington.

Vahagn Makaryan (V)

Division of GIM, Department of Medicine, University of Washington.

Emily Tran (E)

Department of Medicine, University of Washington, Severe Chronic Neutropenia International Registry, Seattle, Washington.

Jamie Leung (J)

Department of Medicine, University of Washington, Severe Chronic Neutropenia International Registry, Seattle, Washington.

Laurence A Boxer (LA)

Pediatric Hematology Oncology, University of Michigan, Ann Arbor, Michigan.

Priya S Kishnani (PS)

Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina.

Stephanie Austin (S)

Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina.

Corbinian Wanner (C)

Department of Pediatrics, Glycogen Storage Disease Program, Connecticut Children's Medical Center, Hartford, Connecticut, USA.

Iris A Ferrecchia (IA)

Department of Pediatrics, Glycogen Storage Disease Program, Connecticut Children's Medical Center, Hartford, Connecticut, USA.

Dina Khalaf (D)

Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.

Dawn Maze (D)

Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.

Joanne Kurtzberg (J)

Department of Pediatrics/Pediatric Blood and Marrow Transplantation/Department of Pathology, Duke University Medical Center, Durham, North Carolina, USA.

Cornelia Zeidler (C)

Department of Molecular Hematopoiesis, Medizinische Hochschule Hannover, Hannover.

Karl Welte (K)

Division of Hematology/Oncology, Department of Molecular Hematopoiesis, University Children's Hospital of Tuebingen, Tuebingen, Germany.

David A Weinstein (DA)

Department of Pediatrics, Glycogen Storage Disease Program, Connecticut Children's Medical Center, Hartford, Connecticut, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH