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Efficacy of imatinib mesylate in the treatment of refractory sclerodermatous chronic GVHD
- Source :
- Bone Marrow Transplantation. 42:757-760
- Publication Year :
- 2008
- Publisher :
- Springer Science and Business Media LLC, 2008.
-
Abstract
- Treatment of sclerodermatous chronic GVHD (cGVHD) remains disappointing. Imatinib mesylate enables selective, dual inhibition of the transforming growth factor beta (TGFbeta) and PDGF pathways. Recently, the drug's effects on fibroblasts have been reported in both in vitro and in vivo studies. The inhibition of fibroblast growth and decreased collagen production in dermal fibroblasts is thus a logical therapeutic approach. Two patients who developed refractory sclerodermatous cGVHD following allo-SCT received imatinib mesylate at the dose of 400 mg/day. In both patients, the scleroderma symptoms disappeared within 3 months of initiation of the treatment. At the time of this report, the two patients were both alive and had a very good skin response. This report shows that imatinib is effective in patients with refractory sclerodermatous cGVHD. Considering its well-documented clinical profile in other diseases, imatinib is a promising candidate for the treatment of sclerodermatous cGVHD.
- Subjects :
- Adult
Male
Oncology
medicine.medical_specialty
Graft vs Host Disease
Antineoplastic Agents
Pharmacology
Piperazines
Scleroderma
Refractory
Transforming Growth Factor beta
immune system diseases
In vivo
hemic and lymphatic diseases
Internal medicine
medicine
Humans
Transplantation, Homologous
Bone Marrow Transplantation
Transplantation
Scleroderma, Systemic
biology
business.industry
Imatinib
Hematology
Transforming growth factor beta
Fibroblasts
Middle Aged
medicine.disease
Pyrimidines
Treatment Outcome
Imatinib mesylate
Benzamides
Imatinib Mesylate
biology.protein
Female
business
Platelet-derived growth factor receptor
medicine.drug
Subjects
Details
- ISSN :
- 14765365 and 02683369
- Volume :
- 42
- Database :
- OpenAIRE
- Journal :
- Bone Marrow Transplantation
- Accession number :
- edsair.doi.dedup.....ab820a34ca8e6d21072bbb00f94b2c23
- Full Text :
- https://doi.org/10.1038/bmt.2008.252