Table 6.

The principles and rationale for non-myeloablative stem cell transplantation (NST) in acute myelocytic leukemia (AML) and myelodysplastic syndromes (MDS).

  • Maximal chemoradiotherapy may not be sufficient for eradication of disease in AML/MDS.

  • Host-versus-graft tolerance may be accomplished without myeloablation by a window of immunosuppression allowing engraftment of donor stem cells.

  • Following engraftment, alloreactive donor lymphocytes may be effective against AML and MDS, despite resistance of tumor cells to chemoradiotherapy.

  • Graft-versus-leukemia (GVL) effects may be induced by alloreactive donor T cells in tolerant mixed chimeras; hence, myeloablative conditioning may not be mandatory.

  • Following NST, donor lymphocyte infusion (DLI) may eliminate residual or recurrent leukemia.

  • NST may be applied after failure of earlier myeloablative BMT or subsequent to autologous BMT for optimal tumor debulking.

  • NST may offer an easier, safer and more effective option for inducing GVL effects especially at the stage of minimal disease.

 
  • Maximal chemoradiotherapy may not be sufficient for eradication of disease in AML/MDS.

  • Host-versus-graft tolerance may be accomplished without myeloablation by a window of immunosuppression allowing engraftment of donor stem cells.

  • Following engraftment, alloreactive donor lymphocytes may be effective against AML and MDS, despite resistance of tumor cells to chemoradiotherapy.

  • Graft-versus-leukemia (GVL) effects may be induced by alloreactive donor T cells in tolerant mixed chimeras; hence, myeloablative conditioning may not be mandatory.

  • Following NST, donor lymphocyte infusion (DLI) may eliminate residual or recurrent leukemia.

  • NST may be applied after failure of earlier myeloablative BMT or subsequent to autologous BMT for optimal tumor debulking.

  • NST may offer an easier, safer and more effective option for inducing GVL effects especially at the stage of minimal disease.

 

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