Δημοσίευση

Evaluation of hypochromic erythrocytes in combination with sTfR-F index for predicting response to r-HuEPO in anemic patients with multiple myeloma.

ΤίτλοςEvaluation of hypochromic erythrocytes in combination with sTfR-F index for predicting response to r-HuEPO in anemic patients with multiple myeloma.
Publication TypeJournal Article
Year of Publication2006
AuthorsKatodritou, E., Speletas M., Zervas K., Kapetanos D., Georgiou E., Christoforidou A., Pavlitou A., Sion M., & Christakis J.
JournalLab Hematol
Volume12
Issue1
Pagination47-54
Date Published2006
ISSN1080-2924
Λέξεις κλειδιάAdult, Aged, Aged, 80 and over, Anemia, Hypochromic, Erythrocyte Count, Erythropoietin, Female, Humans, Male, Middle Aged, Monitoring, Physiologic, Multiple Myeloma, Recombinant Proteins
Abstract

The purpose of this study was to evaluate the sTfR-F index and hypochromic erythrocytes (HYPO%) as potential predictors of response to recombinant human erythropoietin (r-HuEPO) of anemic patients with multiple myeloma (MM) before treatment, as well as early in the course of treatment. Twenty-six newly diagnosed anemic MM patients received r-HuEPO 30,000 IU/wk sc, for six weeks. The sTfR-F index and HYPO% were determined at baseline and at weeks 2 and 6. Patients were classified in 1 of 4 categories of a diagnostic plot, according to erythropoietic state (ES I-IV), defined by the combination of sTfR-F index and HYPO%. Sixteen of 20 patients in ES I and II before treatment responded to r-HuEPO, whereas none of the 6 patients in ES III and IV responded (P < .001). At week 2, 44% of patients who responded and 60% of the nonresponders were in functional iron deficiency (FID) and the proportion increased to 69% and 80%, respectively, by week 6. Seven of the patients who did not respond received in addition 200 mg iron sucrose IV weekly, for the next 4 weeks, and 6 of them responded. These results suggest that combination of sTfR-F index and HYPO% in a diagnostic plot can be used as a predictive model to recognize patients who will benefit from r-HuEPO and identify FID requiring iron supplementation, before treatment and early in the course of treatment, contributing thus to optimization of r-HuEPO therapy.

DOI10.1532/LH96.05030
Alternate JournalLab Hematol
PubMed ID16513546

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