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Management of chronic myeloid leukaemia in clinical practice in France: Results of the French subset of patients from the UNIC studyCML management in France

机译:法国临床实践中慢性骨髓白血病的管理:法国法国法国患者患者的结果

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Objective: To assess real-life treatment practices with imatinib for chronic-phase chronic myeloid leukaemia (CP-CML) in France. Research design and methods: In the observational Unmet Needs in CML (UNIC) study of CML management in Europe, case report forms were completed retrospectively for eligible patients (≥18 years of age, currently treated for CML) during enrolment (September 2006March 2007). Results from the subset of patients from France are presented. Main outcome measures: Primary objectives were to estimate from the collected data the proportions of patients ever treated with imatinib and those experiencing imatinib resistance and/or intolerance as determined by physicians diagnoses of resistance/intolerance leading to a change in imatinib use. Collected data were analysed descriptively. Secondary descriptive measures included imatinib dose modifications and methods for treatment response monitoring. Results: Of the 654 French CP-CML patients, 95.9 had received imatinib. Of these, 15 were judged by physicians as imatinib-resistant and 31 as imatinib-intolerant (not mutually exclusive) during treatment, 44 required dose modification and 23 discontinued imatinib. In the 12 months preceding the last observation, 65 had a cytogenetic features analysis and 93 had a polymerase chain reaction (PCR) assessment of molecular response. Importantly, and contrasting with European recommendations, 46 of imatinib-resistant patients had never been assessed for BCR-ABL mutations. Limitations: The observational study design limits data collection and interpretation. The findings are specific to the French healthcare system and may not apply to other countries. Conclusion: This observational study of CP-CML management in France confirmed that most patients are treated with imatinib, a treatment widely recognised as efficacious. The study highlights opportunities for optimising CML management, as a proportion of patients may require alternative treatment strategies due to imatinib resistance/intolerance. Response monitoring rates differ from recommendations, representing another opportunity for improving care for CP-CML patients through early identification of patients failing current therapy.
机译:目的:评估法国慢性阶段慢性骨髓白血病(CP-CML)的伊马替尼对伊马替尼进行的现实寿命治疗实践。研究设计和方法:在CML(UNIC)研究中的观察未满足需求,在欧洲CML管理的研究中,案例报告表格为符合条件的患者(≥18岁,目前为CML的年龄)进行了回顾性(2006年9月2007年9月) 。提出了法国患者子集的结果。主要观察措施:主要目标是从收集的数据中估计,患有伊马替尼治疗的患者的比例和那些经受医生诊断抵抗/不耐受的伊马替尼阻力和/或不容忍的患者导致伊马替尼的变化。描述了收集的数据。二次描述措施包括伊马替尼剂量修饰和治疗反应监测方法。结果:654例法国CP-CML患者,95.9均收到伊马替尼。其中,15由医生判断为伊马替尼抗性,并且在治疗过程中作为伊马替尼 - 不宽容(不相互排斥),44个所需剂量改性和23个停止的伊马替尼。在上次观察之前的12个月内,65具有细胞遗传学特征分析,93具有聚合酶链反应(PCR)分子反应的评估。重要的是,与欧洲建议的对比,伊马替尼抗性患者的46名从未评估了BCR-ABL突变。局限性:观察研究设计限制了数据收集和解释。调查结果特定于法国医疗保健系统,可能不适用于其他国家。结论:该法国CP-CML管理的观察研究证实,大多数患者用伊马替尼治疗,一种良好地认为是潜力的含量。该研究突出了优化CML管理的机会,因为患者的比例可能需要由于伊马替尼电阻/不耐受而需要替代治疗策略。响应监测率不同于建议,代表通过早期鉴定失败的患者改善CP-CML患者的其他机会。

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