Outpatient subcutaneous alemtuzumab is feasible and safe for aplastic anemia and is associated with high response rates.

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Tác giả: Louise Arnold, Celso Arrais-Rodrigues, Vinicius Campos de Molla, Ana Rita da Fonseca, Thales Dalessandro, Morag Griffin, Anita Hill, Caio Cesar Justino, Richard Kelly, Austin Kulasekararaj, Talha Munir, Iara Baldim Rabelo, Antonio M Risitano, Phillip Scheinberg, Elvira Velloso, Patricia Eiko Yamakawa

Ngôn ngữ: eng

Ký hiệu phân loại: 346.04344 Private law

Thông tin xuất bản: United States : Blood advances , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 175963

 Immunosuppressive therapy using horse antithymocyte globulin (ATG
  h-ATG) combined with cyclosporine (CsA) and eltrombopag is the standard care for aplastic anemia (AA) in patients without a suitable matched donor. However, in many countries, h-ATG use has been discontinued, leaving rabbit ATG (r-ATG), which has a lower response rates and poorer survival, as the only alternative. In previous studies, alemtuzumab (ALZ), a humanized monoclonal antibody targeting CD52, combined with CsA, resulted in an adequate overall response rate (ORR) in patients with AA. This study describes a multicenter, international retrospective analysis of ALZ for treating AA.We analyzed a series of patients who received subcutaneous ALZ for AA in 4 centers in Brazil and the United Kingdom from March 2009 to January 2024. We analyzed 64 ALZ treatments in 61 adult patients with AA, 76% with severe AA (SAA) or very SAA. The ORR was 59.4% at 12 months (complete, 21.9%
  partial, 37.5%). Cumulative incidence (CI) of response was 54.7% at 6 months and 59.4% at 12 months. Younger patients (age <
 65 years) had higher CI of response (67% vs 31%
  P = .03), as did patients treated with a total dose of 103 mg (70% vs 38%
  P = .02). Overall survival was 86% at 1 year, 78% at 2 years, and 70% at 4 years, significantly higher in responders (90% vs 44%
  P <
  .0001). Adverse events were of low grade, and infectious events were infrequent. Subcutaneous ALZ is a feasible, effective, and safe alternative to r-ATG for patients with AA requiring immunosuppressive treatment when h-ATG access is limited.
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