慢性淋巴细胞白血病:评估预后的新生物标志物。

Simon D Wagner, Kate Cwynarski
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引用次数: 8

摘要

完善的临床分期系统继续构成决定何时开始治疗和分配慢性淋巴细胞白血病预后的基础。然而,这些分期系统并不能识别那些将发展到需要治疗的早期疾病患者。最近的发展提供了多种预后标志物,可以确定预后不良的患者。例如,血清标记物(可溶性CD23)、细胞表面(CD38)和细胞质(ZAP70)蛋白、细胞遗传学和免疫球蛋白基因突变状态都被用于这一目的。为了使患者充分受益于这些发现,需要将它们转化为快速、标准化和具有成本效益的临床实验室检测。讨论了目前预后标记物的范围和测量它们的技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic lymphocytic leukaemia: new biological markers for assessing prognosis.

Well-established clinical staging systems continue to form a basis for deciding when to initiate treatment and assigning prognosis in chronic lymphocytic leukaemia. However, these staging systems do not identify those patients with early-stage disease who will progress to require treatment. Recent developments have provided a variety of prognostic markers, which can determine those patients with poor prognosis disease. For example, serum markers (soluble CD23), cell surface (CD38) and cytoplasmic (ZAP70) proteins, cytogenetics and immunoglobulin gene mutational status have all been utilised for this purpose. In order for patients to benefit fully from these discoveries they need to be translated into rapid, standardised and cost-effective clinical laboratory tests. The current range of prognostic markers, and techniques for measuring them are discussed.

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