High-dose immunoablation with autologous haematopoietic stem cell transplantation in aggressive multiple sclerosis: a single centre 10-year experience
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
20350962
DOI
10.1177/1352458510364538
PII: 1352458510364538
Knihovny.cz E-zdroje
- MeSH
- cyklofosfamid terapeutické užití MeSH
- cytarabin MeSH
- dospělí MeSH
- etoposid MeSH
- faktor stimulující kolonie granulocytů terapeutické užití MeSH
- imunosupresivní léčba metody MeSH
- Kaplanův-Meierův odhad MeSH
- karmustin MeSH
- kombinovaná terapie MeSH
- lidé MeSH
- melfalan MeSH
- přežití bez známek nemoci MeSH
- protokoly protinádorové kombinované chemoterapie MeSH
- roztroušená skleróza terapie MeSH
- transplantace hematopoetických kmenových buněk MeSH
- věkové faktory MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cyklofosfamid MeSH
- cytarabin MeSH
- etoposid MeSH
- faktor stimulující kolonie granulocytů MeSH
- karmustin MeSH
- melfalan MeSH
There are multiple sclerosis patients who suffer from an aggressive course of the disease with severe relapses and rapid accumulation of disability despite adequate treatment. In such cases high-dose immunoablation with autologous haematopoietic stem cell transplantation (ASCT) may be considered. Our objective was to report our experience with 26 multiple sclerosis patients treated with ASCT within the years 1998-2008. Twenty-six patients (Expanded Disability Status Scale 2.5-7.5 (median 6.0), multiple sclerosis duration 2-19 years (median 7)) with aggressive multiple sclerosis underwent autologous haematopoietic stem cell transplantation. Stem cells were mobilized by high-dose cyclophosphamide and granulocyte colony-stimulating factor, BEAM (carmustine, etoposide, cytarabine, melphalan) was used for immunoablation. Patients were evaluated at baseline and every six months post ASCT for adverse events and clinical outcome. Follow-up period was 11-132 months (median 66). Progression-free survival was calculated using the Kaplan- Meier method. At 3 and 6 years of follow-up 70.8% and 29.2% of patients respectively were free of progression. Patients with relapsing multiple sclerosis course, disease duration <5 years and age <35 years had a more favourable outcome. There was no death within 100 days after ASCT. We conclude that ASCT represents a viable and effective treatment option for aggressive multiple sclerosis.
Citace poskytuje Crossref.org
Long-term Outcomes After Autologous Hematopoietic Stem Cell Transplantation for Multiple Sclerosis