Tuminello Stephanie, Turner Wiley M, Untalan Matthew, Ivic-Pavlicic Tara, Flores Raja, Taioli Emanuela
Institute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Thoracic Surgery, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
J Natl Cancer Inst. 2025 Jan 1;117(1):112-119. doi: 10.1093/jnci/djae225.
Precision therapies, such as targeted and immunotherapies, have substantially changed the landscape of late-stage non-small cell lung cancer (NSCLC). Yet, utilization of these therapies is disproportionate across strata defined by race and socioeconomic status, possibly because of disparities in molecular diagnostic testing (or biomarker testing), which is a prerequisite to treatment.
We extracted a cohort of NSCLC patients from the Surveillance, Epidemiology, and End Results-Medicare linked data. The primary outcome was receipt of a molecular diagnostic test, based on claims data. The primary predictors were race and socioeconomic status. Likelihood of receiving a molecular diagnostic test and overall survival were investigated using logistic and Cox proportional hazards regression, adjusted for sex, age, residence, histology, marital status, and comorbidity.
Of the 28 511 NSCLC patients, 11 209 (39.3%) received molecular diagnostic testing. Compared with White patients, fewer Black patients received a molecular diagnostic test (40.4% vs 27.9%; P < .001). After adjustment, Black patients (adjusted odds ratio [OR] = 0.64, 95% confidence interval [CI] = 0.58 to 0.71) and those living in areas with greater poverty (adjusted OR = 0.85, 95% CI = 0.80 to 0.89) had statistically significant decreased likelihood of molecular diagnostic testing. Patients who did receive testing had a statistically significant decreased risk of death (adjusted hazard ratio [HR] = 0.74, 95% CI = 0.72 to 0.76). These results held in the stratified analysis of stage IV NSCLC patients.
Disparities exist in comprehensive molecular diagnostics, which is critical for clinical decision making. Addressing barriers to molecular testing could help close gaps in cancer care and improve patient outcomes.
精准治疗,如靶向治疗和免疫治疗,已极大地改变了晚期非小细胞肺癌(NSCLC)的治疗格局。然而,这些治疗方法在按种族和社会经济地位划分的各阶层中的使用情况并不均衡,这可能是由于分子诊断检测(或生物标志物检测)存在差异,而分子诊断检测是治疗的前提条件。
我们从监测、流行病学和最终结果 - 医疗保险关联数据中提取了一组NSCLC患者。主要结局是基于索赔数据的分子诊断检测情况。主要预测因素是种族和社会经济地位。使用逻辑回归和Cox比例风险回归研究接受分子诊断检测的可能性和总生存期,并对性别、年龄、居住地、组织学、婚姻状况和合并症进行了调整。
在28511例NSCLC患者中,11209例(39.3%)接受了分子诊断检测。与白人患者相比,接受分子诊断检测的黑人患者较少(40.4%对27.9%;P <.001)。调整后,黑人患者(调整后的优势比[OR] = 0.64,95%置信区间[CI] = 0.58至0.71)和生活在贫困程度较高地区的患者(调整后的OR = 0.85,95% CI = 0.80至0.89)接受分子诊断检测的可能性在统计学上显著降低。接受检测的患者死亡风险在统计学上显著降低(调整后的风险比[HR] = 0.74,95% CI = 0.72至0.76)。这些结果在IV期NSCLC患者的分层分析中依然成立。
全面分子诊断存在差异,这对临床决策至关重要。消除分子检测障碍有助于缩小癌症治疗差距并改善患者预后。