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
- National Institutes of Health, Bethesda,
Sustainable Development Goals
- 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
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
ISSN
0006-4971Publication IDs
- Scopus: 0028840870
- PubMed: 7492762
