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缺氧与侵袭性肿瘤表型:对治疗和预后的影响。

Hypoxia and aggressive tumor phenotype: implications for therapy and prognosis.

作者信息

Vaupel Peter

机构信息

Institute of Physiology and Pathophysiology, University of Mainz, Duesbergweg 6, 55099 Mainz, Germany.

出版信息

Oncologist. 2008;13 Suppl 3:21-6. doi: 10.1634/theoncologist.13-S3-21.

Abstract

Tumor hypoxia, mostly resulting from poor perfusion and anemia, is one of the key factors in inducing the development of cell clones with an aggressive and treatment-resistant phenotype that leads to rapid progression and poor prognosis. Studies in patients with solid tumors suggest that there is a range of hemoglobin (Hb) concentrations that is optimum for tumor oxygenation. When used to achieve an Hb level within this range, erythropoiesis-stimulating agents (ESAs) can be expected to increase tumor oxygenation, and this may favorably influence sensitivity to treatment as well as quality of life. There is no robust evidence that ESAs, when used as indicated, have a negative effect on survival in patients with solid tumors. When used outside the indications recommended, the rise in Hb level that results may reduce tumor blood flow and tissue oxygenation because of a raised viscosity within the abnormal tumor microvasculature. In the current situation, it remains important to use ESAs within the approved indications and according to treatment guidelines such as those developed by the European Organization for Research and Treatment of Cancer.

摘要

肿瘤缺氧主要由灌注不良和贫血引起,是诱导具有侵袭性和抗治疗表型的细胞克隆发展的关键因素之一,这会导致肿瘤快速进展和预后不良。对实体瘤患者的研究表明,存在一系列对肿瘤氧合最为适宜的血红蛋白(Hb)浓度。当用于使Hb水平达到该范围内时,促红细胞生成素(ESAs)有望增加肿瘤氧合,这可能会对治疗敏感性以及生活质量产生有利影响。没有确凿证据表明按适应证使用ESAs会对实体瘤患者的生存产生负面影响。当超出推荐适应证使用时,由于异常肿瘤微血管内粘度升高,导致的Hb水平升高可能会减少肿瘤血流和组织氧合。在当前情况下,按照欧洲癌症研究与治疗组织制定的治疗指南等批准的适应证使用ESAs仍然很重要。

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