[急性早幼粒细胞白血病基因检测的意义]。

Yumiko Satoh, Akiko Masuda, Yutaka Yatomi
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引用次数: 0

摘要

大多数急性早幼粒细胞白血病(APL)患者存在t (15;17) (q22;q12)易位,导致PML-RARA mRNA表达。全反式维甲酸(ATRA)是针对PML-RARA的具有代表性的分子靶向药物。因此,PML-RARA mRNA的检测对于APL的诊断和治疗政策的制定是必不可少的。一旦通过基因检测确诊,就可以开始基于atra的诱导治疗。这也适用于非典型情况,如M3变种。此外,在以atra为基础的诱导治疗后,通过定量PCR分析评估疗效。因此,基因检测在APL患者的随访中具有重要意义。(审查)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The Significance of Genetic Testing for Acute Promyelocytic Leukemia].

The majority of patients with acute promyelocytic leukemia (APL) harbor the t (15;17) (q22;q12) transloca- tion, which results in the expression of PML-RARA mRNA. All-trans retinoic acid (ATRA) is a representa- tive molecular-targeted drug and is directed against PML-RARA. Therefore, the detection of PML-RARA mRNA has become indispensable for the diagnosis of APL and the decision regarding the treatment policy. Once the diagnosis is confirmed by genetic testing, ATRA-based induction therapy can be initiated. This is also applicable in atypical cases such as the M3 variant. Furthermore, after ATRA-based induction therapy, the curative effect is evaluated by quantitative PCR analysis. Thus, genetic testing is important in the follow-up of patients with APL. [Review].

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