Sundsvall Hospital, Sundsvall, Sweden.
Leuk Lymphoma. 2012 Nov;53(11):2151-8. doi: 10.3109/10428194.2012.684347. Epub 2012 May 22.
Erythropoiesis-stimulating agents (ESAs) are approved to treat anemia in patients with non-myeloid malignancies receiving myelosuppressive chemotherapy. ESAs reduce transfusion rates, but some clinical studies suggest that ESAs may reduce survival or increase disease progression. This study-level meta-analysis examined the effects of darbepoetin alfa, epoetin alfa or epoetin beta on mortality, disease progression and transfusion incidence in patients with lymphoproliferative malignancies, using randomized, controlled trials of patients receiving chemotherapy and ESAs or standard of care. The odds ratio (OR) for mortality was 1.04 (95% confidence interval [CI], 0.81-1.34, random-effects model, 10 studies); the risk difference was - 0.01 (95% CI, - 0.03-0.02). The OR for disease progression was 1.02 (95% CI 0.81-1.30, random-effects model, five studies). A lower proportion of ESA-treated patients than controls received transfusions (seven studies). In this meta-analysis, ESAs reduced transfusions with no clear effect on mortality or disease progression in patients with lymphoproliferative malignancies receiving chemotherapy.
红细胞生成刺激剂 (ESAs) 被批准用于治疗接受骨髓抑制化疗的非髓性恶性肿瘤患者的贫血。ESAs 可降低输血率,但一些临床研究表明,ESAs 可能会降低生存率或增加疾病进展。本研究水平的荟萃分析使用接受化疗和 ESA 或标准治疗的患者的随机对照试验,检查达贝泊汀、促红细胞生成素 α 或促红细胞生成素 β 对接受化疗的淋巴瘤患者的死亡率、疾病进展和输血发生率的影响。死亡率的比值比 (OR) 为 1.04(95%置信区间 [CI],0.81-1.34,随机效应模型,10 项研究);风险差为-0.01(95% CI,-0.03-0.02)。疾病进展的 OR 为 1.02(95% CI 0.81-1.30,随机效应模型,五项研究)。与对照组相比,接受 ESA 治疗的患者输血比例较低(七项研究)。在这项荟萃分析中,ESAs 减少了输血,而对接受化疗的淋巴瘤患者的死亡率或疾病进展没有明显影响。