Wenric Stephane, Sangli Chithra, Guittar John, Islam Farahnaz, Zander Alia, Won Hyun Seung, Davison James M, Mayhew Gregory M, Beebe Kirk, Beauchamp Kyle, Patel Miral, Brown Kacie, Chen James, Nimeiri Halla, Milburn Michael V, Perou Charles M, Guinney Justin, Taxter Timothy J, Benson Al
Tempus AI, Chicago, IL.
GeneCentric Therapeutics, Durham, NC.
JCO Precis Oncol. 2025 Sep;9:e2500197. doi: 10.1200/PO-25-00197. Epub 2025 Sep 4.
FOLFIRINOX (FFX) and gemcitabine + nab-paclitaxel (GnP) are the most commonly administered first-line (1L) regimens for advanced, nonresectable, pancreatic ductal adenocarcinoma (PDAC). In the absence of biomarkers to predict response, clinical covariates such as age and performance status are often used by clinicians to select optimal treatment regimens. Purity independent subtyping of tumors (PurIST) is a molecular subtyping algorithm that classifies tumors as classical or basal. The current study was designed to validate PurIST as a prognostic biomarker for patients receiving 1L FFX and as a predictive biomarker for patients more likely to benefit from FFX versus GnP.
This is a prospectively designed, retrospective study using a real-world data set of 931 patients with advanced PDAC, treated with either 1L FFX or GnP, and designed to demonstrate associations of PurIST subtypes with clinical outcomes. The primary end point was overall survival (OS) in classical versus basal patients treated with 1L FFX, while the secondary end point was OS in classical patients-with an Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1-to compare 1L FFX versus GnP.
Within the cohort of patients receiving 1L FFX (n = 536), basal subtype patients had a median OS of 7 months compared with classical subtype patients with a median OS of 11.8 months (hazard ratio [HR], 1.86 [95% CI, 1.49 to 2.33]; < .001). In an analysis restricted to patients with classical subtype and ECOG PS of 0 or 1 (n = 311), there was a 33% relative risk reduction of death in patients treated with FFX compared with GnP, adjusting for age and ECOG PS (HR, 0.67 [95% CI, 0.48 to 0.94]; < .009), with no comparable risk reduction in basal patients (subtype-treatment interaction, = .002).
Patients with PDAC of the PurIST classical subtype showed a significant OS benefit when treated with FFX as 1L versus GnP.
FOLFIRINOX(FFX)和吉西他滨+纳米白蛋白结合型紫杉醇(GnP)是晚期、不可切除胰腺导管腺癌(PDAC)最常用的一线(1L)治疗方案。在缺乏预测反应的生物标志物的情况下,临床协变量如年龄和体能状态常被临床医生用于选择最佳治疗方案。肿瘤纯度独立亚型分类法(PurIST)是一种分子亚型分类算法,可将肿瘤分为经典型或基底型。本研究旨在验证PurIST作为接受1L FFX治疗患者的预后生物标志物,以及作为更有可能从FFX与GnP治疗中获益的患者的预测生物标志物。
这是一项前瞻性设计的回顾性研究,使用了931例晚期PDAC患者的真实世界数据集,这些患者接受了1L FFX或GnP治疗,旨在证明PurIST亚型与临床结局之间的关联。主要终点是接受1L FFX治疗的经典型与基底型患者的总生存期(OS),次要终点是东部肿瘤协作组体能状态(ECOG PS)为0或1的经典型患者的OS,以比较1L FFX与GnP。
在接受1L FFX治疗的患者队列(n = 536)中,基底型亚型患者的中位OS为7个月,而经典型亚型患者的中位OS为11.8个月(风险比[HR],1.86[95%CI,1.49至2.33];P <.001)。在一项仅限于经典型亚型且ECOG PS为0或1的患者(n = 311)的分析中,与GnP相比,接受FFX治疗的患者死亡相对风险降低了33%,对年龄和ECOG PS进行校正后(HR,0.67[95%CI,0.48至0.94];P <.009),基底型患者没有类似的风险降低(亚型-治疗交互作用,P =.002)。
PurIST经典型亚型的PDAC患者接受1L FFX治疗时,与GnP相比,总生存期有显著获益。