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Title
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Darbepoetin alfa for treating chemotherapy-induced anemia in patients with a baseline hemoglobin level < 10 g/dL versus : an exploratory analysis from a randomized, double-blind, active-controlled trial
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Author
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Abstract
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| Background Several studies have shown that darbepoetin alfa, an erythropoiesis-stimulating agent (ESA), can reduce transfusions and increase hemoglobin (Hb) levels in patients with chemotherapy-induced anemia (CIA). Recent safety concerns, however, have prompted changes to ESA product information. In the European Union and United States, ESA therapy initiation for CIA is now recommended at a Hb level ¡Ü10 g/dL. The present exploratory analysis examined how ESA initiation at this Hb level may impact patient care. Methods Data from a phase 3 randomized trial were retrospectively reanalyzed. CIA patients with nonmyeloid malignancies were randomized 1:1 to 500 mcg darbepoetin alfa every three weeks (Q3W) or 2.25 mcg/kg darbepoetin alfa weekly (QW) for 15 weeks. A previously published report from this trial showed Q3W dosing was non-inferior to QW dosing for reducing transfusions from week 5 to end-of-the-treatment period (EOTP). In the present analysis, outcomes were reanalyzed by baseline Hb <10 g/dL and ¡Ý10 g/dL. Endpoints included transfusion rates, Hb outcomes, and safety profiles. Results This study reanalyzed 351 and 354 patients who initiated ESA therapy at a baseline Hb of <10 g/dL or ¡Ý10 g/dL, respectively. From week 5 to EOTP, the estimated Kaplan-Meier transfusion incidence (Q3W vs QW) was lower in the ¡Ý10 g/dL baseline-Hb group (14% vs 21%) compared with the <10 g/dL baseline-Hb group (36% vs 41%). By week 5, the ¡Ý10 g/dL baseline-Hb group, but not the <10 g/dL baseline-Hb group, achieved a mean Hb ¡Ý11 g/dL. The Kaplan-Meier estimate of percentage of patients (Q3W vs QW) who achieved Hb ¡Ý11 g/dL from week 1 to EOTP was 90% vs 85% in the ¡Ý10 g/dL baseline-Hb group and 54% vs 57% in the <10 g/dL baseline-Hb group. Both baseline-Hb groups maintained mean Hb levels <12 g/dL and had similar safety profiles, though more patients in the ¡Ý10 g/dL baseline-Hb group reached the threshold Hb of ¡Ý13 g/dL. Conclusion In this exploratory analysis, darbepoetin alfa Q3W and QW raised Hb levels and maintained mean Hb at <12 g/dL in both baseline-Hb groups. The ¡Ý10 g/dL baseline-Hb group had fewer transfusions and faster anemia correction. Additional studies should prospectively evaluate the relationship between Hb levels at ESA initiation and outcomes. |
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Language
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English
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Source (journal)
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BMC cancer. - London
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Publication
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London
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2009
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ISSN
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1471-2407
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DOI
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10.1186/1471-2407-9-311
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Volume/pages
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9
(2009)
, p. 311,1-311,12
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ISI
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000270309300002
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Full text (Publisher's DOI)
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Full text (open access)
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