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Benefits and risks of ponatinib versus bosutinib following treatment failure of two prior tyrosine kinase inhibitors in patients with chronic phase chronic myeloid leukemia: a matching-adjusted indirect comparison

机译:Ponatinib对慢性相位慢性骨髓白血病患者治疗失败后Ponatinib对Bosutinib的影响:匹配调整的间接比较

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Objective: Comparing the benefit-risk profiles of ponatinib vs. bosutinib in third-line (3L) treatment of chronic phase chronic myeloid leukemia (CP-CML) is challenging because their pivotal trials lacked comparator arms. To characterize the overall benefit-risk profile in 3L CP-CML patients treated with bosutinib vs. ponatinib, a matching-adjusted indirect comparison (MAIC) was performed to compare efficacy outcomes and treatment duration after adjusting for trial subjects' baseline characteristics, and tolerability was assessed with an unadjusted comparison of study-drug discontinuation. Methods: The MAIC was performed using published data from the pivotal bosutinib trial and the most recent individual-patient-level data on file from the pivotal ponatinib trial. Results: Responses were more frequent and durable with ponatinib (n = 70 MAIC-adjusted) than with bosutinib (n = 119) - complete cytogenetic response (CCyR): 61% vs. 26%; Kaplan-Meier estimate of maintaining CCyR at 4 years: 89% vs. 54%. Median treatment duration was longer with ponatinib than with bosutinib: 38.4 vs. 8.6 months. Only 9% of ponatinib patients (n = 97 unadjusted) vs. 42% of bosutinib patients discontinued due to death, disease progression or unsatisfactory response; 19% vs. 24% discontinued due to adverse events. Conclusions: Based on these surrogate measures of patient benefit-risk profiles, ponatinib appears to provide a net overall benefit vs. bosutinib in 3L CP-CML.
机译:目的:比较Ponatinib与Bosutinib在第三线(3L)治疗中的益处风险概况慢性相慢性骨髓性白血病(CP-CML)是挑战性的,因为它们的关键试验缺乏比较器臂。为了表征用Bosutinib与Ponatinib处理的3L CP-CML患者的整体益处风险概况,进行匹配调整的间接比较(MAIC)以在调整试验受试者的基线特征和耐受性后比较疗效结果和治疗持续时间被评估了不受调查的研究 - 药物中断的比较。方法:MAIC使用Pivotal Bosutinib试验的已发布数据和来自POVOTALINIB试验的文件中的最新个人患者级数据进行。结果:对Ponatinib(n = 70麦克风调整)的反应比培斯替尼(n = 119) - 完全细胞遗传学反应(CCYR):61%与26%; Kaplan-Meier在4年内维持CCYR的估计:89%与54%。 Ponatinib的中位数治疗持续时间比与Bosutinib的更长:38.4与8.6个月。只有9%的Ponatinib患者(n = 97不调整)与死亡,疾病进展或不令人满意的患者停产的42%;由于不良事件,19%与24%停产。结论:基于这些患者受益风险型材的替代措施,Ponatinib似乎在3L CP-CML中提供了净整体益处与Bosutinib。

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