High-dose immunosuppressive therapy for severe systemic sclerosis: initial outcomes.

Journal Article (Clinical Trial;Journal Article)

Systemic sclerosis (SSc) is a multisystem disease of presumed autoimmune pathogenesis for which no proven effective treatment exists. High-dose immunosuppressive therapy (HDIT) has been proposed as an investigational treatment for severe autoimmune diseases. Nineteen patients with poor-prognosis SSc underwent HDIT. The median age was 40 years (range, 23-61 years), the median modified Rodnan skin score (a measure of dermal sclerosis) was 31, and the median DLCO was 57%. Conditioning therapy involved 800 cGy total body irradiation (TBI) (+/- lung shielding to approximately 200 cGy), 120 mg/kg cyclophosphamide, and 90 mg/kg equine antithymocyte globulin. CD34-selected granulocyte-colony-stimulating factor-mobilized autologous blood stem cells provided hematopoietic rescue. With median follow-up at 14.7 months, the Kaplan-Meier estimated 2-year survival rate was 79%. Three patients died of treatment complications and one of disease progression. Two of the first 8 patients had fatal regimen-related pulmonary injury, a complication not found among 11 subsequent patients who received lung shielding for TBI. Overall, internal organ functions were stable to slightly worse after HDIT, and 4 patients had progressive or nonresponsive disease. As measured by modified Rodnan skin scores and modified health assessment questionnaire disability index (mHAQ-DI) scores, significant disease responses occurred in 12 of 12 patients evaluated at 1 year after HDIT. In conclusion, though important treatment-related toxicities occurred after HDIT for SSc, modifications of initial approaches appear to reduce treatment risks. Responses in skin and mHAQ-DI scores exceed those reported with other therapies, suggesting that HDIT is a promising new therapy for SSc that should be evaluated in prospective randomized studies.

Full Text

Duke Authors

Cited Authors

  • McSweeney, PA; Nash, RA; Sullivan, KM; Storek, J; Crofford, LJ; Dansey, R; Mayes, MD; McDonagh, KT; Nelson, JL; Gooley, TA; Holmberg, LA; Chen, CS; Wener, MH; Ryan, K; Sunderhaus, J; Russell, K; Rambharose, J; Storb, R; Furst, DE

Published Date

  • September 1, 2002

Published In

Volume / Issue

  • 100 / 5

Start / End Page

  • 1602 - 1610

PubMed ID

  • 12176878

Pubmed Central ID

  • PMC2956742

International Standard Serial Number (ISSN)

  • 0006-4971


  • eng

Conference Location

  • United States