Successful treatment of thrombotic microangiopathy after haematopoietic stem cell transplantation with rituximab

Br J Haematol. 2007 Jun;137(5):475-8. doi: 10.1111/j.1365-2141.2007.06588.x. Epub 2007 Apr 13.

Abstract

Thrombotic microangiopathy (TMA) is a grave complication after haematopoietic stem cell transplantation (HSCT) and effective treatment is undefined. Five patients with postHSCT TMA, which was refractory to at least 1 week of plasma exchange and prednisolone, were treated with rituximab (375 mg/m(2)/week x 4). Remission was achieved in four patients, of whom three remained in remission and one had died of sepsis at a median follow-up of 10 months. ADAMTS13 levels were low in all evaluable patients, and only one patient showed significant anti-ADAMTS13 antibody. The levels of ADAMTS13 and anti-ADAMTS13 antibody did not change significantly with rituximab-induced remission.

MeSH terms

  • ADAM Proteins / immunology
  • ADAMTS13 Protein
  • Adult
  • Antibodies, Monoclonal / therapeutic use*
  • Antibodies, Monoclonal, Murine-Derived
  • Autoantigens / blood
  • Biomarkers / blood
  • Female
  • Glucocorticoids / therapeutic use
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Humans
  • Immunologic Factors / therapeutic use*
  • Infant
  • Male
  • Microcirculation
  • Middle Aged
  • Plasma Exchange
  • Prednisolone / therapeutic use
  • Remission Induction
  • Retrospective Studies
  • Rituximab
  • Thrombosis / drug therapy*
  • Thrombosis / etiology*
  • Thrombosis / therapy
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Autoantigens
  • Biomarkers
  • Glucocorticoids
  • Immunologic Factors
  • Rituximab
  • Prednisolone
  • ADAM Proteins
  • ADAMTS13 Protein
  • ADAMTS13 protein, human