Annals of Hematology

, Volume 70, Issue 6, pp 313–318 | Cite as

Long-term therapy with recombinant human erythropoietin (rHu-EPO) in progressing multiple myeloma

  • F. Silvestris
  • A. Romito
  • P. Fanelli
  • A. Vacca
  • F. Dammacco
Original Article


Recombinant human erythropoietin (rHu-EPO) is an effective growth factor for erythroid progenitor cells in anemia provoked by several conditions, including bone marrow tumors such as multiple myeloma (MM). We studied a group of 54 patients with MM undergoing second-induction chemotherapy. Thirty of them were randomly assigned to receive rHu-EPO at an initial dosage of 150 units/kg body weight three times a week, increased to 300 units/kg from the sixth week to the end of the 24-week study. Hemoglobin (Hb) levels increased in 77.7% of these patients by the eighth week. In addition, five transfusion-dependent patients in treatment with the VMCP protocol completed the trial without requiring blood supplement after the third month, whereas seven control patients required frequent supplements. Monthly assessment of hematologic parameters demonstrated the ability of rHu-EPO to increase reticulocyte counts, whereas five patients became resistant to the second-induction chemotherapy in apparent concurrence with their rHu-EPO therapy. The response to rHu-EPO in four of the five MM patients receiving cytotoxic protocols combined with α-interferon (α-IFN) included an increase of serum IgM after the third month. This effect was not demonstrable in any other group, including three rHu-EPO-untreated patients undergoing α-IFN + VMCP combined therapy, as well as rHu-EPO-treated patients not receiving a-IFN. Our data suggest that α-IFN plus rHu-EPO treatment in MM patients is effective in restoring normal B cell function. These results may reflect in vivo the modulation of normal human B cells and lymphoblasts by rHu-EPO observed in vitro.

Key words

Anemia α-Interferon Chemotherapy Multiple myeloma rHu-EPO 


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Copyright information

© Springer-Verlag 1995

Authors and Affiliations

  • F. Silvestris
    • 1
  • A. Romito
    • 1
  • P. Fanelli
    • 1
  • A. Vacca
    • 1
  • F. Dammacco
    • 1
  1. 1.Department of Biomedical Sciences and Human Oncology Section of Internal Medicine and Clinical OncologyUniversity of BariBariItaly

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