Mafodda Antonino, Giuffrida D, Prestifilippo A, Azzarello D, Giannicola R, Mare M, Maisano R
Department of Oncology, A.O. Bianchi-Melacrino-Morelli, Via Melacrino Giuseppe, 21, 89124, Reggio Calabria, (RC), Italy.
Istituto Oncologico del Mediterraneo, Via Penninazzo, 7 - 95029, Viagrande, (Catania), Italy.
Support Care Cancer. 2017 Sep;25(9):2779-2786. doi: 10.1007/s00520-017-3690-z. Epub 2017 Apr 9.
Erythropoiesis-stimulating agents (ESAs) are often used in treatment of patients with chemotherapy-induced anemia. Many studies have demonstrated an improved hemoglobin (Hb) response when ESA is combined with intravenous iron supplementation and a higher effectiveness of intravenous iron over traditional oral iron formulations. A new formulation of oral sucrosomial iron featuring an increased bioavailability compared to traditional oral formulations has recently become available and could provide a valid alternative to those by intravenous (IV) route. Our study evaluated the performance of sucrosomial iron versus intravenous iron in increasing hemoglobin in anemic cancer patients receiving chemotherapy and darbepoetin alfa, as well as safety, need of transfusion, and quality of life (QoL).
The present study considered a cohort of 64 patients with chemotherapy-related anemia (Hb >8 g/dL <10 g/dL) and no absolute or functional iron deficiency, scheduled to receive chemotherapy and darbepoetin. All patients received darbepoetin alfa 500 mcg once every 3 weeks and were randomly assigned to receive 8 weeks of IV ferric gluconate 125 mg weekly or oral sucrosomial iron 30 mg daily. The primary endpoint was to demonstrate the performance of oral sucrosomial iron in improving Hb response, compared to intravenous iron. The Hb response was defined as the Hb increase ≥2 g/dL from baseline or the attainment Hb ≥ 12 g/dL.
There was no difference in the Hb response rate between the two treatment arms. Seventy one percent of patients treated with IV iron achieved an erythropoietic response, compared to 70% of patients treated with oral iron. By conventional criteria, this difference is considered to be not statistically significant. There were also no differences in the proportion of patients requiring red blood cell transfusions and changes in QoL. Sucrosomial oral iron was better tolerated.
In cancer patients with chemotherapy-related anemia receiving darbepoetin alfa, sucrosomial oral iron provides similar increase in Hb levels and Hb response, with higher tolerability without the risks or side effects of IV iron.
促红细胞生成素常用于治疗化疗所致贫血患者。许多研究表明,促红细胞生成素与静脉补铁联合使用时,血红蛋白(Hb)反应有所改善,且静脉补铁比传统口服铁剂制剂效果更佳。一种新型口服蔗糖铁制剂,与传统口服制剂相比生物利用度有所提高,最近已上市,可为静脉(IV)途径的铁剂提供有效的替代方案。我们的研究评估了蔗糖铁与静脉铁剂在提高接受化疗和达贝泊汀α治疗的贫血癌症患者血红蛋白水平方面的表现,以及安全性、输血需求和生活质量(QoL)。
本研究纳入了64例化疗相关性贫血(Hb>8 g/dL<10 g/dL)且无绝对或功能性缺铁的患者,这些患者计划接受化疗和达贝泊汀治疗。所有患者每3周接受一次500 mcg的达贝泊汀α,并随机分配接受为期8周的每周一次125 mg静脉葡萄糖酸铁或每日一次30 mg口服蔗糖铁治疗。主要终点是证明与静脉铁剂相比,口服蔗糖铁在改善Hb反应方面的表现。Hb反应定义为Hb较基线增加≥2 g/dL或达到Hb≥12 g/dL。
两个治疗组的Hb反应率无差异。接受静脉铁剂治疗的患者中有71%达到了促红细胞生成反应,而接受口服铁剂治疗的患者中这一比例为70%。按照传统标准,这种差异被认为无统计学意义。在需要红细胞输血的患者比例和生活质量变化方面也无差异。口服蔗糖铁的耐受性更好。
在接受达贝泊汀α治疗的化疗相关性贫血癌症患者中,口服蔗糖铁能使Hb水平和Hb反应有类似的升高,耐受性更高,且无静脉铁剂的风险或副作用。