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首页> 外文期刊>Leukemia and lymphoma >Long-term follow-up of patients with chronic myeloid leukemia in chronic phase developing sudden blast phase on imatinib therapy
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Long-term follow-up of patients with chronic myeloid leukemia in chronic phase developing sudden blast phase on imatinib therapy

机译:伊马替尼治疗慢性粒细胞白血病慢性期发展为急变期的长期随访

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Sudden blast phase (SBP) is a rare event that occurs in an unpredictable fashion amongst patients with chronic myeloid leukemia (CML) who otherwise appear to be responding satisfactorily to imatinib (IM) treatment. We investigated the incidence, clinical characteristics, treatment outcome and long-term follow-up of 213 patients with chronic phase CML treated with IM according to the European LeukemiaNet guidelines. Nine patients, eight of whom received IM as first-line therapy, developed SBP (4.2% of the total). They tended to have low or intermediate risk Sokal scores at diagnosis, a predominance of the lymphoid phenotype and a short interval from "optimal" response to the development of BP. Five of the nine patients with SBP are alive in complete molecular remission; however, all of them underwent allogeneic hematopoietic stem cell transplant. The cumulative incidence of SBP for the patients who received IM as first-line therapy was 5.9% and the 2-year overall survival of the nine patients who developed SBP was 56%. Despite the improved outcome for patients with SBP receiving tyrosine kinase inhibitors (TKIs) and transplant, many of these patients are not salvaged with these therapies. This illustrates the need to develop predictive models to identify patients early whose response to TKI therapy will not be durable and hopefully prevent the transformation to advanced disease.
机译:在患有慢性粒细胞白血病(CML)的患者中,突然爆炸阶段(SBP)以不可预测的方式发生,否则他们似乎对伊马替尼(IM)的治疗满意。我们根据欧洲LeukemiaNet指南调查了用IM治疗的213例慢性期CML患者的发病率,临床特征,治疗结果和长期随访。 9名患者(其中8名接受IM作为一线治疗)发展为SBP(占总数的4.2%)。他们倾向于在诊断时具有较低或中等风险的Sokal评分,主要表现为淋巴表型,并且距对BP发生的“最佳”反应间隔很短。 9例SBP患者中有5例完全分子缓解。然而,他们都进行了异基因造血干细胞移植。接受IM作为一线治疗的患者的SBP累积发生率为5.9%,而9名发生SBP的患者的2年总生存率为56%。尽管接受酪氨酸激酶抑制剂(TKIs)和移植的SBP患者的预后得到改善,但其中许多患者并未获得这些疗法的救助。这说明需要开发预测模型以及早识别对TKI治疗的反应不会持久的患者,并有希望阻止其发展为晚期疾病。

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