A prospective observational study of the effectiveness, safety, and effect on fatigue of darbepoetin alfa for the treatment of chemotherapy-induced anaemia

被引:0
|
作者
Mel, J. R. [2 ]
Salar, A. [3 ]
Rodriguez, C. A. [4 ]
Alegre, A. [5 ]
Gonzalez, A. [6 ]
Cassinello, J. [7 ]
Montesinos, J.
Gasquet, J. A. [8 ]
Sanchez, J. [8 ]
Saigi, E. [1 ]
机构
[1] Corp Sanit Parc Tauli, Dept Med Oncol, Sabadell 08208, Spain
[2] Complexo Hosp Xeral Calde, Lugo 27004, Spain
[3] Hosp Nuestra Senora Mar, Barcelona 08003, Spain
[4] Hosp Clin Univ Salamanca, Salamanca 37007, Spain
[5] Hosp La Princesa, Madrid 28006, Spain
[6] CO Galicia JA Quiroga Pineiro, La Coruna 15006, Spain
[7] Hosp Univ Guadalajara, Guadalajara 19002, Spain
[8] Amgen SA, World Trade Ctr Barcelona, Barcelona 08039, Spain
关键词
Anaemia; Darbepoetin alfa; Fatigue; Multi-cycle chemotherapy;
D O I
10.1185/03007990802381323
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Anaemia is common in cancer patients treated with chemotherapy. Darbepoetin alfa (DA) is the only erythropoiesis-stimulating protein approved for administration at weekly and every-three-week intervals in cancer patients receiving chemotherapy. This article investigates the effectiveness, tolerability and effect on fatigue of DA. Methods: Prospective, observational study performed in 30 Spanish centres. Eligible patients were >= 18 years of age, anaemic (haemoglobin [Hb] <= 11 g/dL), with non-myeloid malignancies, receiving chemotherapy. DA (150 mu g) was administered weekly for a maximum of 16 weeks (dosage doubled if Hb increased < 1 g/dL after 4 weeks). Main outcome measures: Haematopoietic response (Hb increase >= 2 g/dL or Hb >= 12 g/dL in the absence of transfusions in the previous 28 days), transfusion required between Weeks 5 and 16 and fatigue measured by the Fatigue subscale of the Functional Assessment of Cancer Therapy. Results: 293 adults were recruited (56.4% women), with lymphoproliferative malignancies (44.3%) or solid tumours (55.7%). Baseline Hb was 9-11 g/dL in 83.7% of patients. Sixty-four per cent (95% CI: 58.1-69.4%) had a haematopoietic response and 12% required transfusions. After adjusting for performance status, concomitant diseases and chemotherapy type, an increase in Hb level was significantly associated with an improvement in Fatigue subscale (+1.9 points per 1 g/dL). Only 2% of patients had treatment-related adverse events: thromboembolic pulmonary disease (0.3%); hypersensitivity reaction (0.3%); local pain following DA administration (0.3%); insomnia (0.3%); thrombocytosis (0.3%) and deep vein thrombosis (0.3%). Conclusions: Fixed-dose DA administered once weekly seems to be an effective, well-tolerated treatment for chemotherapy-induced anaemia in patients with non-myeloid malignancies, and there is an indication of a possible benefit on fatigue in the clinical practice.
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收藏
页码:2931 / 2942
页数:12
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