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促红细胞生成素受体和促红细胞生成素刺激剂对癌症疾病进展的影响。

Effects of erythropoietin receptors and erythropoiesis-stimulating agents on disease progression in cancer.

机构信息

Institut Multidisciplinaire d' Oncologie, Clinique de Genolier, Route du Muids 3, PO Box 100, Genolier CH-1272, Switzerland.

出版信息

Br J Cancer. 2012 Mar 27;106(7):1249-58. doi: 10.1038/bjc.2012.42. Epub 2012 Mar 6.


DOI:10.1038/bjc.2012.42
PMID:22395661
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3314780/
Abstract

Erythropoiesis-stimulating agents (ESAs) increase red blood cell (RBC) production in bone marrow by activating the erythropoietin receptor (EpoR) on erythrocytic-progenitor cells. Erythropoiesis-stimulating agents are approved in the United States and Europe for treating anaemia in cancer patients receiving chemotherapy based on randomised, placebo-controlled trials showing that ESAs reduce RBC transfusions. Erythropoiesis-stimulating agent-safety issues include thromboembolic events and concerns regarding whether ESAs increase disease progression and/or mortality in cancer patients. Several trials have reported an association between ESA use and increased disease progression and/or mortality, whereas other trials in the same tumour types have not provided similar findings. This review thoroughly examines available evidence regarding whether ESAs affect disease progression. Both clinical-trial data on ESAs and disease progression, and preclinical data on how ESAs could affect tumour growth are summarised. Preclinical topics include (i) whether tumour cells express EpoR and could be directly stimulated to grow by ESA exposure and (ii) whether endothelial cells express EpoR and could be stimulated by ESA exposure to undergo angiogenesis and indirectly promote tumour growth. Although assessment and definition of disease progression vary across studies, the current clinical data suggest that ESAs may have little effect on disease progression in chemotherapy patients, and preclinical data indicate a direct or indirect effect of ESAs on tumour growth is not strongly supported.

摘要

促红细胞生成素刺激剂(ESAs)通过激活红细胞生成素受体(EpoR)在骨髓中增加红细胞(RBC)的产生。促红细胞生成素刺激剂在美国和欧洲被批准用于治疗接受基于随机、安慰剂对照试验的化疗的癌症患者的贫血,这些试验表明 ESAs 可减少 RBC 输血。促红细胞生成素刺激剂的安全性问题包括血栓栓塞事件,以及对 ESAs 是否会增加癌症患者的疾病进展和/或死亡率的担忧。几项试验报告了 ESA 使用与疾病进展和/或死亡率增加之间的关联,而同一肿瘤类型的其他试验则没有提供类似的发现。这篇综述彻底检查了关于 ESAs 是否影响疾病进展的现有证据。总结了关于 ESAs 和疾病进展的临床试验数据,以及关于 ESAs 如何影响肿瘤生长的临床前数据。临床前主题包括:(i)肿瘤细胞是否表达 EpoR,并且可以通过 ESA 暴露直接刺激生长,以及(ii)内皮细胞是否表达 EpoR,并且可以通过 ESA 暴露刺激发生血管生成并间接促进肿瘤生长。尽管疾病进展的评估和定义在研究中有所不同,但目前的临床数据表明,ESAs 对化疗患者的疾病进展可能影响不大,临床前数据表明 ESA 对肿瘤生长的直接或间接影响并没有得到强有力的支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e72/3314780/8c3889dc5651/bjc201242f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e72/3314780/8c3889dc5651/bjc201242f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e72/3314780/8c3889dc5651/bjc201242f1.jpg

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本文引用的文献

[1]
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