A multi-center open-labeled study of recombinant erythropoietin-β in the treatment of anemic patients with multiple myeloma, low-grade non-Hodgkin’s lymphoma, or chronic lymphocytic leukemia in Chinese population
The purpose of this study is to investigate the efficacy and safety of recombinant erythropoietin-β in the treatment of anemic patients with multiple myeloma (MM), low-grade non-Hodgkin’s lymphoma (NHL), and chronic lymphocytic leukemia (CLL). From December 2005 to November 2006, the patients with M...
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Published in | International journal of hematology Vol. 88; no. 2; pp. 139 - 144 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Tokyo
Springer Japan
01.09.2008
Springer |
Subjects | |
Online Access | Get full text |
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Summary: | The purpose of this study is to investigate the efficacy and safety of recombinant erythropoietin-β in the treatment of anemic patients with multiple myeloma (MM), low-grade non-Hodgkin’s lymphoma (NHL), and chronic lymphocytic leukemia (CLL). From December 2005 to November 2006, the patients with MM, low-grade NHL, and CLL were enrolled in this study, male or female, aged ≥18 years, transfusion-dependant, and receiving anti-neoplasia chemotherapy. Recombinant human erythropoietin-β was used in this study with the dose initiated at 150 IU/kg, thrice a week, subcutaneously. The total treatment duration was 12 weeks. The primary endpoint of the study is response rate (RR), which is defined as hemoglobin increasing ≥2 g/dL comparing to baseline level, or returning to normal range, without any transfusion within 6 weeks of evaluation. Fifty out of 82 (64.6%) patients enrolled in this study responded to the treatment and 29 patients had no response. Hypertension (12.2%) is the most common adverse effect; however, all the adverse events were mild, categorized in NCI grade I or II. We conclude that recombinant erythropoietin-β was effective in the treatment of anemia of the patients with MM, NHL, and CLL, as well as it is well-tolerated. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0925-5710 1865-3774 |
DOI: | 10.1007/s12185-008-0130-3 |