Agarwal Arushi, Pritchard Daryl, Winzeler Alissa, Mohammed Hina, Brown Thomas D, Gustavsen Gary G
Health Advances LLC, San Francisco, CA 94105, USA.
Personalized Medicine Coalition, Washington, DC 20036, USA.
J Pers Med. 2024 Sep 20;14(9):997. doi: 10.3390/jpm14090997.
While adoption of personalized medicine (PM) continues to increase in clinical oncology, there is limited data connecting the level of PM adoption at a given institution to improved clinical outcomes for patients. The purpose of this study was to analyze the correlation between health care providers' scores on a previously described PM integration framework and two outcome measures: the use of targeted therapy and clinical trial enrollment.
This study was conducted using real-world data (RWD) from the Syapse Learning Health Network (LHN). The PM integration score for six community hospital systems in the LHN was calculated and subsequently correlated with the two outcome measures.
Across six institutions, a strong correlation between PM integration score and targeted therapy use was observed in metastatic non-small cell lung cancer (mNSCLC) (R = 0.81), an indication with a significant number of approved targeted agents. Conversely, a strong correlation between PM integration score and clinical trial enrollment was observed in metastatic triple-negative breast cancer (TNBC) (R = 0.63), an indication with fewer marketed targeted therapies but an active targeted therapy pipeline.
The results in these cases suggest that PM integration is a strong indicator of high-quality care practices for both utilization of targeted therapy in more mature PM indications (e.g., mNSCLC) and clinical trial enrollment in more emerging PM indications (e.g., TNBC).
虽然个性化医疗(PM)在临床肿瘤学中的应用持续增加,但在特定机构中,将PM的应用水平与患者改善的临床结局联系起来的数据有限。本研究的目的是分析医疗保健提供者在先前描述的PM整合框架上的得分与两项结局指标之间的相关性:靶向治疗的使用和临床试验入组情况。
本研究使用来自Syapse学习健康网络(LHN)的真实世界数据(RWD)进行。计算了LHN中六个社区医院系统的PM整合得分,并随后将其与两项结局指标相关联。
在六个机构中,在转移性非小细胞肺癌(mNSCLC)中观察到PM整合得分与靶向治疗使用之间存在强相关性(R = 0.81),该适应症有大量已获批的靶向药物。相反,在转移性三阴性乳腺癌(TNBC)中观察到PM整合得分与临床试验入组之间存在强相关性(R = 0.63),该适应症上市的靶向治疗较少,但有活跃的靶向治疗研发管线。
这些案例的结果表明,对于在更成熟的PM适应症(如mNSCLC)中使用靶向治疗以及在更多新兴的PM适应症(如TNBC)中进行临床试验入组而言,PM整合是高质量医疗实践的有力指标。