Feasibility of low-dose interleukin-2 therapy following T-cell-depleted nonmyeloablative allogeneic hematopoietic stem cell transplantation from HLA-matched or -mismatched family member donors

Cancer Invest. 2011 Jan;29(1):56-61. doi: 10.3109/07357907.2010.535055.

Abstract

Introduction: High relapse rates and infections remain primary causes of failure in nonmyeloablative transplantation. Interleukin-2 (IL-2) may stimulate the immune system and improve outcomes. The primary objective of this pilot study was to evaluate the feasibility of administering IL-2 following a T-cell-depleted nonmyeloablative hematopoietic stem cell transplant.

Methods: Patients received T-cell-depleted nonmyeloablative transplant from a matched or mismatched related donor. Those with allogeneic engraftment, <grade 2 acute GVHD at time of study entry, and no severe end organ damage were eligible and received IL-2 starting 6 weeks after the first day of stem cell infusion. Patients received 1 mu/m2 daily for 5 days each week for 4 weeks followed by a 2-week rest period for a 6-week cycle to continue for up to 1 year.

Results: Eight patients aged 28-69 years were treated. Significant toxicities were limited to GVHD of the skin ≤grade 2 in 3 patients and severe fatigue in 4 patients, limiting the duration of therapy. Two of the 8 patients died of relapsed disease and 1 from CMV. With a median overall duration of follow-up of survivors of 48 months, 5 patients (63%) remain alive and in continuous complete remission.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / adverse effects
  • Chemotherapy, Adjuvant
  • Drug Administration Schedule
  • Family
  • Fatigue / etiology
  • Feasibility Studies
  • Graft vs Host Disease / immunology
  • HLA Antigens / immunology*
  • Hematopoietic Stem Cell Transplantation* / adverse effects
  • Histocompatibility*
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Interleukin-2 / administration & dosage*
  • Interleukin-2 / adverse effects
  • Middle Aged
  • Myelodysplastic Syndromes / immunology
  • Myelodysplastic Syndromes / therapy*
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • North Carolina
  • Pilot Projects
  • Time Factors
  • Tissue Donors*
  • Transplantation Conditioning
  • Transplantation, Homologous
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • HLA Antigens
  • Immunosuppressive Agents
  • Interleukin-2