Chang Jose, Couture Felix, Young Scott, McWatters Kara-Lee, Lau Catherine Y
Durham Regional Cancer Centre, Oshawa, Canada.
J Clin Oncol. 2005 Apr 20;23(12):2597-605. doi: 10.1200/JCO.2004.12.027. Epub 2004 Sep 27.
Epoetin alfa administered at 40,000 U once weekly (qw) to anemic cancer patients receiving chemotherapy increases hemoglobin levels, improves quality of life (QOL), and reduces transfusions. The benefit of epoetin alfa in maintaining hemoglobin levels in cancer patients with hemoglobin less than 12 g/dL has not been evaluated.
Breast cancer patients (N = 354) receiving chemotherapy were randomly assigned in 1:1 ratio to epoetin alfa (40,000 U qw) or standard of care (SOC). QOL was assessed at baseline and week 12. Hemoglobin responses, transfusion requirements, and prognostic factors for responses were measured.
At week 12, Functional Assessment of Cancer Therapy-Anemia (FACT-An; mean, 2.16 +/- 12.84 for epoetin alfa v -4.43 +/- 13.42 for SOC) and FACT-An fatigue (mean, 1.85 +/- 10.52 for epoetin alfa v -3.55 +/- 11.14 for SOC) change scores were significantly higher in the epoetin alfa group (P < .0001). Hemoglobin responses defined as mean hemoglobin > or = 12 g/dL or a > or = 2 g/dL increase compared with baseline were significantly higher in the epoetin alfa group versus SOC: 52.0% v 5.1% and 65.7% v 6.3%, respectively (P < .0001 for both comparisons). Percentage transfused was significantly lower in the epoetin alfa group compared with SOC (8.6% v 22.9%). More than 90% of patients did not require a dose increase and 28.7% had a dose reduction.
Epoetin alfa administered at 40,000 U qw is effective in improving QOL, maintaining hemoglobin level, and reducing transfusion requirements in breast cancer patients. The high effectiveness observed could be attributed in part to early treatment with epoetin alfa.
对于接受化疗的贫血癌症患者,每周一次给予40000单位的促红细胞生成素α可提高血红蛋白水平、改善生活质量(QOL)并减少输血需求。促红细胞生成素α在维持血红蛋白水平低于12g/dL的癌症患者血红蛋白水平方面的益处尚未得到评估。
将接受化疗的乳腺癌患者(N = 354)按1:1比例随机分配至促红细胞生成素α组(40000单位/周)或标准治疗组(SOC)。在基线和第12周评估生活质量。测量血红蛋白反应、输血需求及反应的预后因素。
在第12周时,促红细胞生成素α组癌症治疗贫血功能评估(FACT - An;促红细胞生成素α组均值为2.16±12.84,标准治疗组为 - 4.43±13.42)和FACT - An疲劳变化评分(促红细胞生成素α组均值为1.85±10.52,标准治疗组为 - 3.55±11.14)显著更高(P <.0001)。与基线相比,血红蛋白反应定义为平均血红蛋白≥12g/dL或升高≥2g/dL,促红细胞生成素α组显著高于标准治疗组:分别为52.0%对5.1%和65.7%对6.3%(两组比较P均<.0001)。促红细胞生成素α组输血百分比显著低于标准治疗组(8.6%对22.9%)。超过90%的患者不需要增加剂量,28.7%的患者需要减少剂量。
每周一次给予40000单位促红细胞生成素α可有效改善乳腺癌患者的生活质量、维持血红蛋白水平并减少输血需求。观察到的高有效性部分可归因于促红细胞生成素α的早期治疗。