基于碳水化合物抗原19-9动态的综合评分的开发,用于预测新辅助治疗后碳水化合物抗原19-9产生的胰腺导管腺癌患者的生存率。

IF 5.3 2区 医学 Q1 ONCOLOGY JCO precision oncology Pub Date : 2024-10-01 Epub Date: 2024-11-20 DOI:10.1200/PO.24.00193
Ingmar F Rompen, Elisabetta Sereni, Joseph R Habib, Jonathan Garnier, Veronica Galimberti, Lucas R Perez Rivera, Deepa Vatti, Kelly J Lafaro, D Brock Hewitt, Greg D Sacks, William R Burns, Steven Cohen, Brian Kaplan, Richard A Burkhart, Olivier Turrini, Christopher L Wolfgang, Jin He, Ammar A Javed
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引用次数: 0

摘要

目的:在对胰腺导管腺癌(PDAC)患者进行新辅助化疗(NAT)期间和化疗后,碳水化合物抗原 19-9 (CA19-9) 的动态变化经常为治疗决策提供依据。然而,关于特定 CA19-9 阈值和动态的临床相关性仍存在相当大的争议。因此,我们旨在定义 CA19-9 值的最佳阈值,并创建一个生化驱动的综合评分来预测 NAT 后 CA19-9 生成的 PDAC 患者的生存率:方法: 从三个高容量中心回顾性地识别了2012年至2022年期间接受NAT和手术切除的PDAC患者。排除了CA19-9不产生者、90天死亡率和大体切除不完全的患者。根据 CA19-9 的相对变化以及新定义的新辅助治疗前后总生存(OS)最佳阈值,利用两个中心的患者创建了一个综合评分,并利用第三个中心的数据进行了验证:共有 492 名患者符合研究队列的纳入标准。预测OS差异的最佳CA19-9临界值为:新辅助治疗前202 U/mL,新辅助治疗后78 U/mL。此外,新辅助治疗期间CA19-9的升高与较差的OS有关(中位OS,17.5个月对26.0个月;P = .008)。与获得 2-3 分的患者相比,未超过任何或仅超过其中一个阈值(综合评分为 0-1)的患者的 OS 有所改善(中位 OS 为 29.9 个月对 15.8 个月;P < .001)。主要血清学反应(CA19-9下降90%)的阳性预测值为32%,阴性预测值为88%:由诊断时、新辅助治疗后的 CA19-9 水平及其动态变化组成的综合评分显示了低分和高分之间的预后鉴别力。然而,还需要更好的预测性生物标志物来帮助新辅助治疗期间的治疗决策。
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Development of a Composite Score Based on Carbohydrate Antigen 19-9 Dynamics to Predict Survival in Carbohydrate Antigen 19-9-Producing Patients With Pancreatic Ductal Adenocarcinoma After Neoadjuvant Treatment.

Purpose: Dynamics of carbohydrate antigen 19-9 (CA19-9) often inform treatment decisions during and after neoadjuvant chemotherapy (NAT) of patients with pancreatic ductal adenocarcinoma (PDAC). However, considerable dispute persists regarding the clinical relevance of specific CA19-9 thresholds and dynamics. Therefore, we aimed to define optimal thresholds for CA19-9 values and create a biochemically driven composite score to predict survival in CA19-9-producing patients with PDAC after NAT.

Methods: Patients with PDAC who underwent NAT and surgical resection from 2012 to 2022 were retrospectively identified from three high-volume centers. CA19-9 nonproducers and patients with 90-day mortality, and macroscopically incomplete resections were excluded. A composite score was created on the basis of relative CA19-9 change and newly defined optimal thresholds of pre- and postneoadjuvant values for overall survival (OS) using patients from two centers and validated using data from the third center.

Results: A total of 492 patients met inclusion criteria in the development cohort. Optimal CA19-9 cutoff values for predicting a difference in OS were 202 U/mL for preneoadjuvant and 78 U/mL for postneoadjuvant levels. Furthermore, increase in CA19-9 during neoadjuvant treatment was associated with worse OS (median-OS, 17.5 months v 26.0 months; P = .008). Not surpassing any or only one of these thresholds (composite score of 0-1) was associated with improved OS compared with patients with 2-3 points (median-OS, 29.9 months v 15.8 months; P < .001). Major serological response (90% decrease of CA19-9) had a positive and negative predictive value of 32% and 88%, respectively.

Conclusion: The composite score consisting of CA19-9 levels at diagnosis, after neoadjuvant treatment, and its dynamics demonstrates prognostic discrimination between low and high scores. However, better predictive biomarkers are needed to facilitate treatment decisions during neoadjuvant treatment.

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