Dismal response to high-dose methylprednisolone after failure to respond to standard dose in patients with acute GVHD

Corticosteroids such as methylprednisolone (MP) remain the primary therapy for acute GVHD (aGVHD). Patients who are refractory to standard treatment (MP 2 mg/kg/day) may be treated with high-dose MP. This study evaluated the response to high-dose MP in children with aGVHD refractory to standard dose...

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Veröffentlicht in:Bone marrow transplantation (Basingstoke) 2010-12, Vol.45 (12), p.1749-1753
Hauptverfasser: Schechter, T, Macartney, C, Finkelstein, Y, Gassas, A, Husain, M, Doyle, J, Dupuis, L L
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container_end_page 1753
container_issue 12
container_start_page 1749
container_title Bone marrow transplantation (Basingstoke)
container_volume 45
creator Schechter, T
Macartney, C
Finkelstein, Y
Gassas, A
Husain, M
Doyle, J
Dupuis, L L
description Corticosteroids such as methylprednisolone (MP) remain the primary therapy for acute GVHD (aGVHD). Patients who are refractory to standard treatment (MP 2 mg/kg/day) may be treated with high-dose MP. This study evaluated the response to high-dose MP in children with aGVHD refractory to standard dose MP. Children who underwent hematopoietic SCT (HSCT) at our hospital between 1 June 2002 and 31 July 2006 and were treated with high-dose MP upon developing steroid-refractory aGVHD were included. Response to aGVHD therapy, adverse effects attributed to MP and overall outcomes were documented. Ten children received high-dose MP (⩾20 mg/kg/day) on 3–5 consecutive days followed by a tapering dose for steroid-refractory aGVHD, at a median of 12 days after starting standard treatment. Nine patients had ⩾grade III aGVHD. Only one patient with grade III aGVHD had a complete response. Two patients had a partial response but flared when MP was tapered. Complications included hypertension (100%), hyperglycemia requiring insulin therapy (33%) and four documented severe infections. Five children (50%) died (median follow-up: 5.9 years). Salvage therapy other than high-dose MP should be considered in children who fail to respond to MP 2 mg/kg/day.
doi_str_mv 10.1038/bmt.2010.47
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ispartof Bone marrow transplantation (Basingstoke), 2010-12, Vol.45 (12), p.1749-1753
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subjects 631/92/436/108
692/699/249/1529
Acute Disease
Adolescent
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Bone marrow
Bone marrow, stem cells transplantation. Graft versus host reaction
Care and treatment
Cell Biology
Child
Child, Preschool
Children
Complications
Complications and side effects
Corticoids
Corticosteroids
Development and progression
Dosage and administration
Dose-Response Relationship, Drug
Female
Glucocorticoids - administration & dosage
Graft versus host reaction
Graft vs Host Disease - drug therapy
Health aspects
Hematology
Hematopoietic Stem Cell Transplantation - adverse effects
Humans
Hyperglycemia
Hypertension
Infant
Infant, Newborn
Insulin
Internal Medicine
Male
Medical sciences
Medicine
Medicine & Public Health
Methylprednisolone
Methylprednisolone - administration & dosage
original-article
Patient outcomes
Patients
Political aspects
Public Health
Risk factors
Stem cell transplantation
Stem Cells
Steroids
Tapering
Therapy
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
title Dismal response to high-dose methylprednisolone after failure to respond to standard dose in patients with acute GVHD
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