Miranda-Galvis Marisol, Tjioe Kellen C, Sharara Muhannad, Maloney McKenzie, Keruakous Amany R, Jillella Anand, Kota Vamsi, Guha Avirup, Cortes Jorge E
Georgia Cancer Center, Augusta University, Augusta, GA, USA.
Medical College of Georgia, Augusta University, Augusta, GA, USA.
Leukemia. 2025 Sep 11. doi: 10.1038/s41375-025-02763-8.
Despite advances in tyrosine kinase inhibitor (TKI) therapy, outcomes in chronic myeloid leukemia remain (CML) highly variable, underscoring the need to explore determinants beyond conventional clinical indicators. This study examined the relationship between allostatic load (AL), a biomarker-based index of cumulative chronic stress, social determinants of health (SDH), and treatment outcomes. In a retrospective cohort of 194 patients, AL was calculated using 23 biomarkers spanning cardiovascular, metabolic, hematologic, renal, and hepatic systems. Higher AL was associated with adverse SDH and behavioral factors, including greater extreme poverty (p = 0.02), limited transportation access (p = 0.02), reliance on public health coverage (p = 0.03), and physical inactivity (p = 0.05). Each unit increase in AL reduced the odds of achieving optimal molecular response by 18% (p = 0.02). All 11 disease progressions to advanced CML and all 9 deaths occurred in the high AL group, who also had higher rates of composite adverse events, including loss of molecular response, TKI failure, disease progression, and mortality (p = 0.03). These findings position AL as a promising integrative biomarker to identify high-risk patients facing combined physiological stress burden and social disadvantage, enabling oncology practices to refine risk stratification and implement personalized, multidisciplinary interventions.
尽管酪氨酸激酶抑制剂(TKI)疗法取得了进展,但慢性髓性白血病(CML)的治疗结果仍存在很大差异,这突出表明需要探索传统临床指标以外的决定因素。本研究考察了基于生物标志物的累积慢性应激指标——应变负荷(AL)、健康的社会决定因素(SDH)与治疗结果之间的关系。在一项对194例患者的回顾性队列研究中,使用涵盖心血管、代谢、血液、肾脏和肝脏系统的23种生物标志物计算AL。较高的AL与不良的SDH和行为因素相关,包括更高程度的极端贫困(p = 0.02)、交通不便(p = 0.02)、依赖公共医疗保险(p = 0.03)和身体活动不足(p = 0.05)。AL每增加一个单位会使实现最佳分子反应的几率降低18%(p = 0.02)。所有11例进展为晚期CML的病例和所有9例死亡均发生在高AL组中,该组的复合不良事件发生率也更高(包括分子反应丧失、TKI治疗失败、疾病进展和死亡)(p = 0.03)。这些发现表明,AL是一种很有前景的综合生物标志物,可用于识别面临生理应激负担和社会劣势双重影响的高危患者,使肿瘤学实践能够优化风险分层并实施个性化的多学科干预措施。