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The EUTOS CML score aims to support clinical decision-making

机译:EUTOS CML分数旨在支持临床决策

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Marin et al recently have praised the Sokal score and expressed reluctance in being the first when new ways are tried. Unfortunately, the data they presented do not support their message. The data of 2060 patients in the European Treatment and Outcome Study (EUTOS) for CML were used to develop and validate the EUTOS score. The objective of the EUTOS score is to support clinical decision-making within the first 18 months after the initiation of treatment with Imatinib. The timeline of 18 months was chosen as our data showed convincingly that patients who did not achieve complete cytogenetic response (CCyR) up to this time point were less likely to achieve a CCyR during the further course of therapy and suffered a considerable risk of progressive disease. Thus, our work was focused on prognosticating as precise and efficient as possible the chance to be in CCyR after 18 months of therapy with Imatinib. Using the percentage of basophiles and the size of the spleen at diagnosis, the score divides the patients into a high-risk and a low-risk group with respect to a failure in meeting the therapeutic target of CCyR at 18 months.
机译:Marin等人最近赞扬了Sokal分数,并表示不愿意尝试新方法。不幸的是,他们提供的数据不支持他们的信息。欧洲CML的治疗和结果研究(EUTOS)中的2060名患者的数据用于制定和验证EUTOS评分。 EUTOS评分的目的是在伊马替尼治疗开始后的前18个月内支持临床决策。选择18个月的时间表是因为我们的数据令人信服地表明,在此时间点之前尚未达到完全细胞遗传学应答(CCyR)的患者在进一步的治疗过程中获得CCyR的可能性较小,并且患有进行性疾病的相当大的风险。因此,我们的工作集中在尽可能准确和有效地预测伊马替尼治疗18个月后进入CCyR的机会。使用在诊断时嗜碱性粒细胞的百分比和脾脏的大小,就在18个月内未能达到CCyR的治疗目标而言,该评分将患者分为高危组和低危组。

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