转移性前列腺癌中基于数字病理学的人工智能生物标志物验证。

IF 8.3 1区 医学 Q1 ONCOLOGY European urology oncology Pub Date : 2024-12-10 DOI:10.1016/j.euo.2024.11.009
Mark C Markowski, Yi Ren, Meghan Tierney, Trevor J Royce, Rikiya Yamashita, Danielle Croucher, Huei-Chung Huang, Tamara Todorovic, Emmalyn Chen, Timothy N Showalter, Michael A Carducci, Yu-Hui Chen, Glenn Liu, Charles T A Parker, Andre Esteva, Felix Y Feng, Gerhardt Attard, Christopher J Sweeney
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引用次数: 0

摘要

背景和目的:由于转移性激素敏感性前列腺癌(mHSPC)治疗选择的扩大,以及对预后和治疗反应差异的临床亚组的认识,在这种情况下需要预后和预测性生物标志物来个性化护理。我们的目的是评估mHSPC的多模态人工智能(MMAI)生物标志物的预后能力。方法:我们使用的数据来自3期charted试验;456/790例mHSPC患者具有可评估的数字组织病理学图像和必要的临床变量,以生成MMAI评分以纳入我们的分析。我们通过单变量Cox比例风险和Fine-Gray模型评估了MMAI评分与总生存期(OS)、临床进展(CP)和去势抵抗性PC (CRPC)的关系。主要发现和局限性:在分析队列中,370例(81.1%)患者被划分为mmai高风险,86例(18.9%)患者被划分为mmai中/低风险。MMAI高组的5年OS估计为39%,MMAI中组为58%,MMAI低组为83% (log-rank p)。结论和临床意义:我们的研究结果表明,无论临床亚组或接受的治疗如何,MMAI生物标志物都是mHSPC患者OS、CP和CRPC的预后指标。MMAI生物标志物在晚期PC中的进一步研究是有必要的。患者总结:我们研究了人工智能(AI)工具的性能,该工具可以解释一组癌症已经扩散到前列腺以外的男性前列腺癌组织样本的图像。人工智能工具能够识别出预后较差的高风险患者。这些结果表明,人工智能工具在帮助患者及其医疗团队做出治疗决策方面具有潜在的好处。
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Digital Pathology-based Artificial Intelligence Biomarker Validation in Metastatic Prostate Cancer.

Background and objective: Owing to the expansion of treatment options for metastatic hormone-sensitive prostate cancer (mHSPC) and an appreciation of clinical subgroups with differential prognosis and treatment responses, prognostic and predictive biomarkers are needed to personalize care in this setting. Our aim was to evaluate a multimodal artificial intelligence (MMAI) biomarker for prognostic ability in mHSPC.

Methods: We used data from the phase 3 CHAARTED trial; 456/790 patients with mHSPC had evaluable digital histopathology images and requisite clinical variables to generate MMAI scores for inclusion in our analysis. We assessed the association of MMAI score with overall survival (OS), clinical progression (CP), and castration-resistant PC (CRPC) via univariable Cox proportional-hazards and Fine-Gray models.

Key findings and limitations: In the analysis cohort, 370 patients (81.1%) were classified as MMAI-high and 86 (18.9%) as MMAI-intermediate/low risk. Estimated 5-yr OS was 39% for the MMAI-high, 58% for the MMAI-intermediate, and 83% for the MMAI-low groups (log-rank p < 0.001). The MMAI score was associated with OS (hazard ratio [HR] 1.51, 95% confidence interval [CI] 1.33-1.73; p < 0.001), CP (subdistribution HR 1.54, 95% CI 1.36-1.74; p < 0.001), and CRPC (subdistribution HR 1.63, 95% CI 1.45-1.83; p < 0.001). The proportion of MMAI-high cases was 50.0%, 83.7%, 66.7%, and 92.1% in the subgroups with low-volume metachronous (n = 74), low-volume synchronous (n = 80), high-volume metachronous (n = 48), and high-volume synchronous (n = 254) mHSPC, respectively. The MMAI biomarker remained prognostic after adjustment for treatment, volume status, and diagnosis stage.

Conclusions and clinical implications: Our findings show that the MMAI biomarker is prognostic for OS, CP, and CRPC among patients with mHSPC, regardless of clinical subgroup or treatment received. Further investigations of MMAI biomarkers in advanced PC are warranted.

Patient summary: We looked at the performance of an artificial intelligence (AI) tool that interprets images of samples of prostate cancer tissue in a group of men whose cancer had spread beyond the prostate. The AI tool was able to identify patients at higher risk of worse outcomes. These results show the potential benefit of AI tools in helping patients and their health care team in making treatment decisions.

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来源期刊
CiteScore
15.50
自引率
2.40%
发文量
128
审稿时长
20 days
期刊介绍: Journal Name: European Urology Oncology Affiliation: Official Journal of the European Association of Urology Focus: First official publication of the EAU fully devoted to the study of genitourinary malignancies Aims to deliver high-quality research Content: Includes original articles, opinion piece editorials, and invited reviews Covers clinical, basic, and translational research Publication Frequency: Six times a year in electronic format
期刊最新文献
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