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Ph: not bad at all.

机译:Ph:一点也不差。

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摘要

In this issue of Blood, Marzocchi et al (on be-I half of the GIMEMA [Italian Group for He-matologic Malignancies of the Adults] CML Working Party) report for the first time a large systematic analysis of the role of variant Ph translocations in newly diagnosed CML patients in chronic phase. These variant translocations implicate another breakpoint. The mechanisms of generation of the translocations are not fully understood. In addition, the prognostic implication of these cytogenetic abnormalities has been studied by several groups with no uniform and clear conclusions.The analysis by Marzocchi and colleagues included 559 patients all in chronic phase treated with either 400- or 800-mg doses of imatinib. All these patients were included in prospective clinical trials. Patients were followed with real-time quantitative PCR (RQ-PCR) every 3 to 6 months and by cytogenetic and FISH analysis.
机译:在本期《血液》中,Marzocchi等人(在意大利GIMEMA [成人血液系统恶性肿瘤小组] CML工作组的一半左右)中首次报告了对变体Ph易位的作用的大型系统分析在新诊断的慢性期CML患者中。这些变体易位暗示了另一个断点。易位产生的机制尚未完全了解。此外,已经有多个研究小组研究了这些细胞遗传学异常的预后含义,没有统一而明确的结论.Marzocchi及其同事的分析包括559例慢性期患者,均接受400或800 mg伊马替尼治疗。所有这些患者均纳入前瞻性临床试验。每3至6个月对患者进行一次实时定量PCR(RQ-PCR),然后进行细胞遗传学和FISH分析。

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