Potential drugs for elimination of acute lymphatic leukemia cells from autologous bone marrow

Exp Hematol. 1986 Aug;14(7):683-8.

Abstract

Five drugs, selected because of minimal in vivo myelotoxicity, have been investigated for inhibition of the growth of three acute lymphatic leukemia-derived cell lines. Granulocyte-macrophage colony-forming units (GM-CFU) inhibition with these five drugs after 60-min incubation was first established. Drug concentrations giving up to 90% kill of GM-CFU were then used. Spirogermanium and L-asparaginase did not have an effect on any of the three cell lines under the culture conditions tested, while 4-hydroperoxycyclophosphamide (4-HC) and vincristine inhibited the growth of all three cell lines tested, and bleomycin inhibited the growth of two cell lines. In addition to 4-HC, bleomycin and vincristine should be considered as possible agents in eliminating leukemic cells from autologous marrow grafts. These drugs also deserve further investigation in clonal systems.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antineoplastic Agents / toxicity*
  • Asparaginase / toxicity
  • Bleomycin / toxicity
  • Bone Marrow / drug effects
  • Bone Marrow / pathology
  • Bone Marrow Cells*
  • Cell Division / drug effects
  • Cell Line
  • Cyclophosphamide / analogs & derivatives
  • Cyclophosphamide / toxicity
  • Germanium / toxicity
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / drug effects
  • Humans
  • Kinetics
  • Leukemia, Lymphoid / pathology*
  • Organometallic Compounds*
  • Spiro Compounds / toxicity
  • Vincristine / toxicity

Substances

  • Antineoplastic Agents
  • Organometallic Compounds
  • Spiro Compounds
  • Germanium
  • Bleomycin
  • spirogermanium
  • Vincristine
  • Cyclophosphamide
  • Asparaginase
  • perfosfamide