AI Article Synopsis

  • A phase 1/2 study involved 21 patients with rapidly progressive multiple sclerosis (MS) receiving intense immune suppressive therapy and autologous hematopoietic stem cell (HSC) support, with no deaths recorded in the first year.
  • After treatment, most patients with lower pretransplantation disability scores (EDSS ≤ 6.0) showed no increase in disability, while some with higher scores experienced progressive neurologic deterioration.
  • The findings indicate that this treatment may not be effective for patients with severe disabilities, highlighting a need for further research on its efficacy in less disabled patients with more active inflammatory disease.

Article Abstract

There were 21 patients with rapidly progressive multiple sclerosis (MS) treated on a phase 1/2 study of intense immune suppressive therapy and autologous hematopoietic stem cell (HSC) support with no 1-year mortality. Following transplantation, one patient had a confirmed acute attack of MS. Neurologic progression defined by the expanded disability status scale (EDSS) did not increase in disability by 1.0 or more steps in any of 9 patients with a pretransplantation EDSS of 6.0 or less. In 8 of 12 patients with high pretransplantation disability scores (EDSS > 6.0), progressive neurologic disability as defined by at least a 1-point increase in the EDSS has occurred and was manifested as gradual neurologic deterioration. There were 2 patients with a pretransplantation EDSS of 7.0 and 8.0 who died from complications of progressive disease at 13 and 18 months following treatment. Our experience suggests that intense immune suppression using a total body irradiation (TBI)-based regimen and hematopoietic stem cell transplantation (HSCT) are not effective for patients with progressive disease and high pretransplantation disability scores. Further studies are necessary to determine the role of intense immune suppressive therapy and HSC support in ambulatory patients with less accumulated disability and more inflammatory disease activity. Specifically, more patients and longer follow-up would be required in patients with an EDSS of 6.0 or less before drawing conclusions on this subgroup.

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Source
http://dx.doi.org/10.1182/blood-2003-03-0877DOI Listing

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