Center for Health Outcomes and Pharmacoeconomic Research & Arizona Cancer Center, University of Arizona, Tucson, AZ, USA.
Matrix45, Tucson, AZ, USA.
Leuk Res. 2021 Dec;111:106734. doi: 10.1016/j.leukres.2021.106734. Epub 2021 Oct 21.
Although adherence to imatinib is critical for attaining treatment responses in chronic myeloid leukemia, there is evidence of varying adherence among patients. Our aim was to model and determine the margin of tolerance, if any, required to ensure treatment responses among patients prescribed imatinib before treatment response is at risk.
We performed post hoc analyses of the ADAGIO study conducted in Belgium on 169 evaluable patients (Blood 2009). Applying Kaplan-Meier methods using adherence instead of the conventional time variable, we modeled the likelihood of complete cytogenetic (CCyR), complete hematological (CHR), major molecular (MMR) and optimal (OR) response as a function of 90-day pill count adherence.
Analyses showed that ∼100 % adherence of prescribed dose is associated with probabilities of 0.84 for CHR, 0.83 for CCyR, 0.82 for OR, and 0.77 for MMR; compared to, 0.37 (CHR and CCyR), 0.35 (OR), and 0.39 (MMR) at 90 % adherence. Increasing intake of imatinib from 90 % to 100 % of the prescribed dose increased the likelihood of the various treatment responses by 1.95-2.35-fold.
There is virtually no margin for nonadherence, if the objective is to optimize the likelihood of treatment response, and a minimal margin to avoid impaired treatment response.
尽管在慢性髓性白血病中,坚持使用伊马替尼对于获得治疗反应至关重要,但患者的依从性存在差异。我们的目的是建立模型并确定在治疗反应面临风险之前,确保规定伊马替尼的患者获得治疗反应所需的可接受范围(如果有的话)。
我们对在比利时进行的 ADAGIO 研究中的 169 例可评估患者(Blood 2009)进行了事后分析。应用 Kaplan-Meier 方法,用依从性代替传统的时间变量,我们构建了 90 天内药物计数依从性与完全细胞遗传学缓解(CCyR)、完全血液学缓解(CHR)、主要分子缓解(MMR)和最佳缓解(OR)的可能性之间的关系。
分析表明,规定剂量的 100%依从性与 CHR 的概率为 0.84、CCyR 的概率为 0.83、OR 的概率为 0.82、MMR 的概率为 0.77 相关;相比之下,90%依从性时,CHR 和 CCyR 的概率为 0.37、OR 的概率为 0.35、MMR 的概率为 0.39。从 90%增加到 100%的伊马替尼摄入量使各种治疗反应的可能性增加了 1.95-2.35 倍。
如果目标是优化治疗反应的可能性,那么几乎没有不依从的余地,如果要避免治疗反应受损,则需要有最小的余地。