TMA secondary to SLE: rituximab improves overall but not renal survival

Clin Rheumatol. 2018 Jan;37(1):213-218. doi: 10.1007/s10067-017-3793-4. Epub 2017 Aug 30.

Abstract

Thrombotic microangiopathy (TMA) includes a series of life-threatening disorders. Systemic lupus erythematosus (SLE) is one of the most common acquired causes. To identify predictors of prognosis in patients with TMA secondary to SLE, we conducted a single-center historical study. From January 2013 to June 2016, of 2182 SLE hospitalized patients in the Ren Ji Hospital, a total of 21 consecutive patients with TMA secondary to SLE were identified. The 90-day short-term mortality was 33.3%. The kidney involvement (66.7%) was associated with poor prognosis, while the administration of rituximab (n = 13) was an independent protective factor according to logistic regression analysis. Compared to conventional treatment, i.e., plasma exchange, high-dose glucocorticoids, and intravenous immunoglobulin, the overall survival is significantly higher among patients receiving rituximab add-on (92.2 vs 33.3%, p = 0.0173); however, five out of seven patients with renal involvement in the rituximab group were eventually hemodialysis dependent. Our data indicated that add-on rituximab in the background of conventional therapy may improve the overall but not the renal survival in SLE-TMA patients.

Keywords: Rituximab; Systemic lupus erythematosus; Thrombotic microangiopathy; Thrombotic thrombocytopenic purpura.

MeSH terms

  • Adult
  • Female
  • Humans
  • Immunologic Factors / therapeutic use*
  • Kidney / physiopathology*
  • Lupus Erythematosus, Systemic / complications
  • Lupus Erythematosus, Systemic / drug therapy*
  • Lupus Erythematosus, Systemic / mortality
  • Lupus Erythematosus, Systemic / physiopathology
  • Male
  • Middle Aged
  • Prognosis
  • Rituximab / therapeutic use*
  • Survival Rate
  • Thrombotic Microangiopathies / drug therapy*
  • Thrombotic Microangiopathies / etiology
  • Thrombotic Microangiopathies / mortality
  • Thrombotic Microangiopathies / physiopathology
  • Treatment Outcome
  • Young Adult

Substances

  • Immunologic Factors
  • Rituximab