Ozguroglu M, Arun B, Demir G, Demirelli F, Mandel N M, Buyukunal E, Serdengecti S, Berkarda B
Istanbul University, Cerrahpasa School of Medicine, Department of Internal Medicine, Section of Medical Oncology, Istanbul, Turkey.
Med Oncol. 2000 Feb;17(1):29-34. doi: 10.1007/BF02826213.
Anemia is a frequent complication of cancer and its treatment. A defect in erythropoietin production has been advocated as being the main cause of anemia in cancer patients. We studied serum erythropoietin levels in 74 patients with solid tumors and in a control group consisting of 20 otherwise healthy individuals without any malignancy, who have only iron deficiency anemia. Serum erythropoietin levels were measured by enzyme immunoassay in cancer patients without anemia (n=34), and in anemic cancer patients (n=40); either receiving chemotherapy (n=21) or not (n=19). Anemic cancer patients were found to have decreased response of erythropoietin for a given hemoglobin level (mean, 40.1+/-34.7 u/ml), compared with the patients having only iron deficiency anemia (mean, 69.7+/-68.6 u/ml) (P<0.05). In patients with iron deficiency anemia having no malignancy, erythropoietin response was remarkably high and inversely correlated with the level of hemoglobin (r=-0.69; P=0. 05). Although there was no correlation between hemoglobin and erythropoietin response in cancer anemia (r=-0.07), serum levels of erythropoietin were found to be higher in anemic cancer patients (mean, 40.1+/-34.7 u/ml), compared with cancer patients with normal hemoglobin values (mean, 19.96+/-18.4 u/ml). There was not any statistically significant difference between erythropoietin levels in anemic cancer patients with or without chemotherapy (mean, 43. 7+/-37.7 u/ml and 41.9+/-30.08 u/ml respectively; P>0.05). No difference in serum erythropoietin levels were noted in patients treated with cisplatin or non-cisplatin containing regimens (mean, 48.36+/-33.12 u/ml and 38.55+/-43.52 u/ml, respectively; P>0.05). In this study, we demonstrated that anemia in cancer patients was caused by blunted erythropoietin response, rather than its quantitative deficiency. Serial measurements, however, should be considered in patients receiving chemotherapy.
贫血是癌症及其治疗常见的并发症。促红细胞生成素产生缺陷被认为是癌症患者贫血的主要原因。我们研究了74例实体瘤患者以及由20名无任何恶性肿瘤、仅有缺铁性贫血的健康个体组成的对照组的血清促红细胞生成素水平。采用酶免疫测定法测量了无贫血的癌症患者(n = 34)、贫血癌症患者(n = 40)的血清促红细胞生成素水平,后者中接受化疗的患者(n = 21)和未接受化疗的患者(n = 19)。结果发现,与仅有缺铁性贫血的患者(平均69.7±68.6 u/ml)相比,贫血癌症患者在给定血红蛋白水平下促红细胞生成素反应降低(平均40.1±34.7 u/ml)(P<0.05)。在无恶性肿瘤的缺铁性贫血患者中,促红细胞生成素反应显著升高,且与血红蛋白水平呈负相关(r = -0.69;P = 0.05)。虽然癌症贫血患者的血红蛋白与促红细胞生成素反应之间无相关性(r = -0.07),但贫血癌症患者的血清促红细胞生成素水平(平均40.1±34.7 u/ml)高于血红蛋白值正常的癌症患者(平均19.96±18.4 u/ml)。接受化疗和未接受化疗的贫血癌症患者促红细胞生成素水平之间无统计学显著差异(分别为平均43.7±37.7 u/ml和41.9±30.08 u/ml;P>0.05)。接受顺铂或不含顺铂方案治疗的患者血清促红细胞生成素水平无差异(分别为平均48.36±33.12 u/ml和38.55±43.52 u/ml;P>0.05)。在本研究中,我们证明癌症患者的贫血是由促红细胞生成素反应减弱而非其数量缺乏引起的。然而,对于接受化疗的患者应考虑进行连续测量。