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肺癌化疗期间血清促红细胞生成素、血清铁及不饱和铁结合力水平的变化

Changes in levels of serum erythropoietin, serum iron and unsaturated iron binding capacity during chemotherapy for lung cancer.

作者信息

Sawabe Y, Takiguchi Y, Kikuno K, Iseki T, Ito J, Iida S, Kuriyama T, Yonemitsu H

机构信息

Division of Laboratory Medicine, Chiba University Hospital, Japan.

出版信息

Jpn J Clin Oncol. 1998 Mar;28(3):182-6. doi: 10.1093/jjco/28.3.182.

Abstract

BACKGROUND

The serum erythropoietin level increases markedly during chemotherapy for leukemia. A number of hypotheses have been built for the mechanism, none of them satisfactory. Difficulty in evaluating bone marrow activity hampers the elucidation. Therefore, we focused on patients who had non-hematological cancer and no evidence of bone marrow suppression.

METHODS

Twelve patients, who had lung cancer (four with small cell cancer and eight with non-small cell cancer) and who had not undergone any chemotherapy, were studied. During chemotherapy, we measured serum erythropoietin, serum iron, unsaturated iron binding capacity and hemoglobin concentration in these patients.

RESULTS

The serum erythropoietin level before chemotherapy (10.8 +/- 7.4 mU/ml) was within the normal range but the peak values after the first treatment (73.4 +/- 90.4 mU/ml) increased in all patients. In the patients with small cell cancer, a transient but marked increase in erythropoietin value (204.6 +/- 167.3 mU/ml) was observed after each session of chemotherapy while hemoglobin concentration decreased gradually. Throughout treatments, elevation of the serum iron concentration and concomitant reduction of unsaturated iron binding capacity were observed after each session of chemotherapy. They regained their original values whilst the serum erythropoietin level decreased after each chemotherapy session was completed.

CONCLUSIONS

It is suggested that the suppression of erythroid marrow by chemotherapeutic agents causes the changes in serum erythropoietin level during chemotherapy in patients with lung cancer.

摘要

背景

白血病化疗期间血清促红细胞生成素水平显著升高。针对其机制已提出多种假说,但均不尽人意。评估骨髓活性存在困难,这阻碍了对其机制的阐明。因此,我们将重点放在患有非血液系统癌症且无骨髓抑制证据的患者身上。

方法

研究了12例未接受过任何化疗的肺癌患者(4例小细胞癌患者和8例非小细胞癌患者)。在化疗期间,我们测量了这些患者的血清促红细胞生成素、血清铁、不饱和铁结合能力和血红蛋白浓度。

结果

化疗前血清促红细胞生成素水平(10.8±7.4 mU/ml)在正常范围内,但所有患者首次治疗后的峰值(73.4±90.4 mU/ml)均升高。在小细胞癌患者中,每次化疗后促红细胞生成素值出现短暂但显著的升高(204.6±167.3 mU/ml),而血红蛋白浓度逐渐下降。在整个治疗过程中,每次化疗后均观察到血清铁浓度升高以及不饱和铁结合能力相应降低。在每次化疗疗程结束后血清促红细胞生成素水平下降时,它们恢复到原始值。

结论

提示化疗药物对红系骨髓的抑制导致肺癌患者化疗期间血清促红细胞生成素水平发生变化。

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