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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Long-term outcome with dasatinib after imatinib failure in chronic-phase chronic myeloid leukemia: follow-up of a phase 3 study
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Long-term outcome with dasatinib after imatinib failure in chronic-phase chronic myeloid leukemia: follow-up of a phase 3 study

机译:在慢性相慢性骨髓白血病中的伊马替尼失效后与Dasatinib的长期结果:第3期研究的后续行动

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We present long-term follow-up of a dasatinib phase 3 study of patients with imatinib-resistant/-intolerant chronic myeloid leukemia (CML). In the CA180-034 study, 670 patients with imatinib-resistant/-intolerant CML in chronic phase (CML-CP) received dasatinib 100 mg once daily, 50 mg twice daily, 140 mg once daily, or 70 mg twice daily. At 6 years, 188 (28%) of 670 patients remained on study treatment. Estimated 6-year protocol-defined progression-free survival (PFS) rates were 49%, 51%, 40%, and 47%, respectively, and estimated 6-year overall survival (OS) rates were 71%, 74%, 77%, and 70%, respectively (intent-to-treat population, including protocol-defined progression or death after discontinuation). Estimated 6-year rates of survival without transformation on study treatment were 76%, 80%, 83%, and 74%, respectively. Major molecular response was achieved in 43% (100 mg once daily) and 40% (all other arms) of patients by 6 years. Molecular and cytogenetic responses at 3 and 6 months were highly predictive of PFS and OS. Notably, estimated 6-year PFS rates based on <= 1%, >1% to 10%, and >10% BCR-ABL transcripts at 3 months were 68%, 58%, and 26%, respectively. Most adverse events occurred by 2 years. Imatinib-resistant/-intolerant patients with CML-CP can experience long-term benefit with dasatinib therapy, particularly if achieving BCR-ABL <= 10% at 3 months. This study was registered at ClinicalTrials.gov: NCT00123474.
机译:我们呈现达斯替尼阶段的长期随访3阶段的含有伊马替尼抗性/ - 耐温性慢性髓性白血病(CML)的研究。在CA180-034研究中,670例慢性期耐药性/ - CMM的CML患者(CML-CP)每日一次,每日每天两次,每日两次,每日140毫克,每天两次,每天都有50毫克,每天两次。在6岁时,188名(28%)670名患者仍然是研究治疗。估计6年的方案定义的无进展生存期(PFS)率分别为49%,51%,40%和47%,估计6年总体生存率(OS)率为71%,74%,77分别为%,70%(意图对治疗群体,包括在停止后的议定定义的进展或死亡)。估计的6年生存率不转化的研究治疗分别为76%,80%,83%和74%。主要的分子反应在6年内以43%(每日100毫克每日一次)和40%(所有其他武器)实现。在3和6个月的分子和细胞遗传学反应高度预测PFS和OS。值得注意的是,基于<= 1%,> 1%至10%的估计为6年的PFS速率,3个月,> 10%BCR-ABL转录物分别为68%,58%和26%。大多数不良事件发生在2年。含有CML-CP的耐药性/ - 耐药患者可以使用达斯替尼治疗经历长期益处,特别是如果在3个月内实现BCR-ABL <= 10%。该研究在Clinicaltrials.gov注册:NCT00123474。

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