Montano-Campos J Felipe, Hahn Erin, Haupt Eric, Radich Jerald, Bansal Aasthaa
CHOICE Institute, School of Pharmacy, University of Washington, Seattle, WA.
Department of Health Systems Sciences, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, CA.
JCO Clin Cancer Inform. 2025 Jul;9:e2500003. doi: 10.1200/CCI-25-00003. Epub 2025 Jul 7.
There is little guidance for decision making in chronic myeloid leukemia (CML) after patients achieve molecular remission. Our study addresses this gap by developing a risk prediction model for molecular relapse using early longitudinal factors, such as BCR::ABL1 biomarker-level changes and treatment adherence.
We analyzed electronic health record data of patients with CML diagnosed between 2007 and 2019 from an integrated health system. We used a time-to-event modeling framework using a Cox proportional hazards approach where we evaluated time from molecular remission to molecular relapse. The main predictors were early changes in BCR::ABL1 levels from treatment initiation to the first follow-up measurement (typically around 3 months) and treatment adherence in the first 6 months, categorized as perfect (≥0.98) or less-than-perfect (<0.98). Model performance was assessed through five-fold cross-validation combined with 100 Monte Carlo bootstrapping iterations to ensure robustness and minimize bias.
Patients with early improvement in BCR::ABL1 levels had a 70% lower risk relapse (hazard ratio [HR], 0.30 [95% CI, 0.15 to 0.59]) compared with those without early molecular response. Perfect adherence during this critical early phase of treatment was associated with a 56% lower relapse risk (HR, 0.44 [95% CI, 0.22 to 0.85]). Predictive accuracy was high at 6 months (AUC, 0.90; 95% CI, 0.87 to 0.95) and 1-year postremission (AUC, 0.78; 95% CI, 0.74 to 0.81). Relapse risk was significantly higher among Black, Asian, and Hispanic patients compared with non-Hispanic White patients.
Early biomarker trends and adherence after treatment initiation are critical for accurately predicting relapse among patients who achieve molecular remission. The proposed model addresses a gap in guidance after molecular remission and has the potential to enable personalized monitoring and optimize surveillance strategies, offering transformative potential for CML care.
慢性粒细胞白血病(CML)患者实现分子缓解后,在决策方面几乎没有指导。我们的研究通过使用早期纵向因素(如BCR::ABL1生物标志物水平变化和治疗依从性)开发分子复发风险预测模型,填补了这一空白。
我们分析了2007年至2019年间在一个综合医疗系统中诊断为CML的患者的电子健康记录数据。我们使用了一种事件发生时间建模框架,采用Cox比例风险方法,评估从分子缓解到分子复发的时间。主要预测因素是从治疗开始到首次随访测量(通常约3个月)时BCR::ABL1水平的早期变化,以及前6个月的治疗依从性,分为完美(≥0.98)或不完美(<0.98)。通过五折交叉验证结合100次蒙特卡洛自助抽样迭代评估模型性能,以确保稳健性并最小化偏差。
与没有早期分子反应的患者相比,BCR::ABL1水平早期改善的患者复发风险降低70%(风险比[HR],0.30[95%CI,0.15至0.59])。在治疗的关键早期阶段完美依从与复发风险降低56%相关(HR,0.44[95%CI,0.22至0.85])。在缓解后6个月(AUC,0.90;95%CI,0.87至0.95)和1年时(AUC,0.78;95%CI,0.74至0.81)预测准确性较高。与非西班牙裔白人患者相比,黑人、亚洲人和西班牙裔患者的复发风险显著更高。
治疗开始后的早期生物标志物趋势和依从性对于准确预测实现分子缓解的患者的复发至关重要。所提出的模型填补了分子缓解后指导方面的空白,有可能实现个性化监测并优化监测策略,为CML护理带来变革潜力。