Abdel-Razeq Hikmat, Abbasi Salah, Saadi Iyad, Jaber Rana, Abdelelah Hazem
Department of Internal Medicine, King Hussein Cancer Center, Amman, Jordan.
Drug Des Devel Ther. 2013 Aug 30;7:939-44. doi: 10.2147/DDDT.S45674. eCollection 2013.
Anemia in patients with cancer who are undergoing active therapy is commonly encountered and may worsen quality of life in these patients. The effect of blood transfusion is often temporary and may be associated with serious adverse events. Erythropoiesis-stimulating agents are not effective in 30%-50% of patients and may have a negative effect on overall survival.
To assess the efficacy and feasibility of intravenous iron therapy in patients with cancer who have non-iron-deficiency anemia and who are undergoing treatment with chemotherapy without the use of erythropoiesis-stimulating agents.
Adult patients with solid cancers and non-iron-deficiency anemia were included. Ferric sucrose at a dose of 200 mg was given in short intravenous infusions weekly for a total of 12 weeks. Hemoglobin level was measured at baseline, every 3 weeks, and 2 weeks after the last iron infusion (week 14). Adverse events related to intravenous iron were prospectively reported.
Of 25 patients included, 19 (76.0%) completed at least three iron infusions and 14 (56.0%) finished the planned 12 weeks of therapy. The mean hemoglobin level of the 25 patients at baseline was 9.6 g/dL (median, 9.9 g/dL; range, 6.9 g/dL 10.9 g/dL). The mean change in hemoglobin level for the 15 patients who completed at least 9 treatments was 1.7 g/dL (median, 1.1 g/dL; range, -1.9 g/dL to 3.2 g/dL); it reached 2.1 g/dL (median, 1.3 g/dL; range, -0.2 g/dL to 4.6 g/dL; P = 0.0007) for the 14 patients who completed all 12 weekly treatments. Five (20.0%) patients were transfused and considered as treatment failures. No treatment-related adverse events were reported.
Intravenous iron treatment alone is safe and may reduce blood transfusion requirements and improve hemoglobin level in patients with cancer who are undergoing anticancer therapy. Further randomized studies are needed to confirm these findings.
正在接受积极治疗的癌症患者中贫血情况常见,这可能会使这些患者的生活质量恶化。输血的效果往往是暂时的,且可能与严重不良事件相关。促红细胞生成素在30%-50%的患者中无效,并且可能对总生存期产生负面影响。
评估静脉铁剂治疗在患有非缺铁性贫血且正在接受化疗且未使用促红细胞生成素的癌症患者中的疗效和可行性。
纳入患有实体癌和非缺铁性贫血的成年患者。每周通过短时间静脉输注给予200mg蔗糖铁,共12周。在基线、每3周以及最后一次铁剂输注后2周(第14周)测量血红蛋白水平。前瞻性报告与静脉铁剂相关的不良事件。
纳入的25例患者中,19例(76.0%)完成了至少3次铁剂输注,14例(56.0%)完成了计划的12周治疗。25例患者基线时的平均血红蛋白水平为9.6g/dL(中位数,9.9g/dL;范围,6.9g/dL至10.9g/dL)。完成至少9次治疗的15例患者血红蛋白水平的平均变化为1.7g/dL(中位数,1.1g/dL;范围,-1.9g/dL至3.2g/dL);完成全部12周每周治疗的14例患者血红蛋白水平达到2.1g/dL(中位数,1.3g/dL;范围,-0.2g/dL至4.6g/dL;P = 0.0007)。5例(20.0%)患者接受了输血并被视为治疗失败。未报告与治疗相关的不良事件。
单独静脉铁剂治疗是安全的,并且可能减少正在接受抗癌治疗的癌症患者的输血需求并提高血红蛋白水平。需要进一步的随机研究来证实这些发现。