IL-2/LAK therapy for refractory acute monoblastic leukemia relapsing after unrelated allogeneic bone marrow transplantation

Bone Marrow Transplant. 1999 Jan;23(2):183-5. doi: 10.1038/sj.bmt.1701550.

Abstract

Leukemia relapse is a major cause of treatment failure after allogeneic bone marrow transplantation. We administered recombinant interleukin-2 (rIL-2) to a patient who relapsed after unrelated allogeneic bone marrow transplantation (uBMT). While the number of peripheral blood monoblastic leukemia cells increased after administration of rIL-2, the patient achieved durable remission for 5 months after low-dose chemotherapy followed by adoptive transfer of engrafted graft-derived lymphokine-activated killer (LAK) cells. Following the disappearance of the blast cells, however, both cutaneous and liver GVHD were exacerbated. Administration of rIL-2 and adoptive transfer of graft-derived LAK cells are considered to be possible choices for the treatment of acute leukemia relapsing after uBMT when donor leukocyte transfusion is not available.

MeSH terms

  • Adjuvants, Immunologic / therapeutic use*
  • Adult
  • Bone Marrow Transplantation*
  • Female
  • Humans
  • Interleukin-2 / therapeutic use*
  • Leukemia, Monocytic, Acute / therapy*
  • Peptides / therapeutic use*

Substances

  • Adjuvants, Immunologic
  • Interleukin-2
  • Peptides
  • poly(lysyl-(leucyl-poly-alanine))