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开发一种与胰腺癌辅助吉西他滨治疗结果相关的人工智能衍生组织学特征。

Development of an artificial intelligence-derived histologic signature associated with adjuvant gemcitabine treatment outcomes in pancreatic cancer.

机构信息

Valar Labs, Inc., Palo Alto, CA, USA.

Valar Labs, Inc., Palo Alto, CA, USA.

出版信息

Cell Rep Med. 2023 Apr 18;4(4):101013. doi: 10.1016/j.xcrm.2023.101013. Epub 2023 Apr 11.

Abstract

Pancreatic ductal adenocarcinoma (PDAC) has been left behind in the evolution of personalized medicine. Predictive markers of response to therapy are lacking in PDAC despite various histological and transcriptional classification schemes. We report an artificial intelligence (AI) approach to histologic feature examination that extracts a signature predictive of disease-specific survival (DSS) in patients with PDAC receiving adjuvant gemcitabine. We demonstrate that this AI-generated histologic signature is associated with outcomes following adjuvant gemcitabine, while three previously developed transcriptomic classification systems are not (n = 47). We externally validate this signature in an independent cohort of patients treated with adjuvant gemcitabine (n = 46). Finally, we demonstrate that the signature does not stratify survival outcomes in a third cohort of untreated patients (n = 161), suggesting that the signature is specifically predictive of treatment-related outcomes but is not generally prognostic. This imaging analysis pipeline has promise in the development of actionable markers in other clinical settings where few biomarkers currently exist.

摘要

胰腺导管腺癌 (PDAC) 在个性化医学的发展中落后了。尽管有各种组织学和转录分类方案,但 PDAC 缺乏对治疗反应的预测标志物。我们报告了一种人工智能 (AI) 方法来检查组织学特征,该方法提取了一个预测 PDAC 患者接受辅助吉西他滨治疗时疾病特异性生存 (DSS) 的特征。我们证明,这种 AI 生成的组织学特征与接受辅助吉西他滨治疗后的结果相关,而之前开发的三种转录组分类系统则没有 (n=47)。我们在接受辅助吉西他滨治疗的另一组独立患者中对该特征进行了外部验证 (n=46)。最后,我们证明该特征不能分层未治疗患者的生存结果 (n=161),这表明该特征专门预测与治疗相关的结果,但并非普遍预后。这种成像分析流程有望在其他目前很少有生物标志物的临床环境中开发出可操作的标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cc4/10140610/03d9d9976098/fx1.jpg

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