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Radioimmunotherapy of interleukin-2Rα - Expressing adult T-cell leukemia with yttrium-90 - Labeled anti-Tac

  • T. A. Waldmann(corresponding author)
    ,
  • J. D. White
    ,
  • J. A. Carrasquillo
    ,
  • J. C. Reynolds
    ,
  • C. H. Paik
    ,
  • O. A. Gansow
*Corresponding author for this work
  • National Institutes of Health, Bethesda
    ,
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Adult T-cell leukemia (ATL) is a malignancy of mature lymphocytes caused by the retrovirus human T-cell lymphotropic virus-I. It is an aggressive leukemia with a median survival time of 9 months; no chemotherapy regimen appears successful in inducing long-term disease-free survival. The scientific basis of the present study is that ATL cells express high-affinity interleukin-2 receptors identified by the anti-Tac monoclonal antibody, whereas normal resting cells do not. To exploit this difference, we administered anti-Tac armed with Yttrium-90 (90Y) to 18 patients with ATL initially (first 9 patients) in a phase I dose-escalation trial and subsequently (second group of 9 patients) in a phase II trial involving a uniform 10-mCi dose of 90Y-labeled anti-Tac. Patients undergoing a remission were permitted to receive up to eight additional doses. At the 5- to 15-mCi doses used, 9 of 16 evaluable patients responded to 90Y anti-Tac with a partial (7 patients) or complete (2 patients) remission. The responses observed represent improved efficacy in terms of length of remission when compared with previous results with unmodified anti-Tac. Clinically meaningful (≥grade 3) toxicity was largely limited to the hematopoietic system. In conclusion, radioimmunotherapy with 90Y anti-Tac directed toward the IL-2R expressed on ATL cells may provide a useful approach for treatment of this aggressive malignancy. This is a US government work. There are no restrictions on its use.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 4063-4075 (13 pages)

Journal (Volume, Issue Number)

Blood (Volume 86, Issue 11)

Publication milestones

  • Published - 12/01/1995

Publication status

Published - 12/01/1995

ISSN

0006-4971

Publication IDs

  • Scopus: 0028840870
  • PubMed: 7492762

Publication metrics

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Scopus
citations
Fractional count
1
Fractional count
0.05
Fractional count
18
Fractional count
0.95
Fractional count
1
Fractional count
1

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Citation count
241
Captures
32