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Antithymocyte globulin has limited efficacy and substantial toxicity in unselected anemic patients with myelodysplastic syndrome.

Abstract
Antithymocyte globulin (ATG) has recently been popularized as an effective treatment in myelodysplastic syndrome (MDS). We treated 8 anemic MDS patients (refractory anemia [RA] and refractory anemia with excess blasts [RAEB-1]) with ATG (40 mg/kg/d for 4 days) and prednisone in a phase 2 trial. The study was stopped early according to a preset termination rule because of lack of efficacy. There were no salutary responses. Toxicities included serum sickness (in all patients), transient neutropenia and thrombocytopenia, diarrhea, vomiting, and syncope with a generalized seizure. At least 3 patients had the HLA-DR15 (DR2) allele. We conclude that the risk-benefit ratio of ATG in an unselected population of MDS patients may be unfavorable, and more work is needed to define the subset of patients who will respond to ATG before its widespread use can be recommended.
AuthorsDavid P Steensma, Angela Dispenzieri, S Breanndan Moore, Georgene Schroeder, Ayalew Tefferi
JournalBlood (Blood) Vol. 101 Issue 6 Pg. 2156-8 (Mar 15 2003) ISSN: 0006-4971 [Print] United States
PMID12411290 (Publication Type: Clinical Trial, Clinical Trial, Phase II, Journal Article)
Chemical References
  • Antilymphocyte Serum
  • HLA-DR Antigens
  • HLA-DR Serological Subtypes
  • HLA-DR15 antigen
Topics
  • Aged
  • Anemia (complications, immunology, therapy)
  • Anemia, Refractory (complications, therapy)
  • Anemia, Refractory, with Excess of Blasts (complications, therapy)
  • Antilymphocyte Serum (adverse effects, therapeutic use)
  • Female
  • HLA-DR Antigens (analysis, genetics)
  • HLA-DR Serological Subtypes
  • Histocompatibility Testing
  • Humans
  • Male
  • Middle Aged
  • Myelodysplastic Syndromes (complications, immunology, therapy)

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