Department of Pathology, The University of Rochester Medical Center, Rochester, NY, USA.
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
J Pathol. 2022 Jan;256(1):4-14. doi: 10.1002/path.5795. Epub 2021 Oct 25.
Artificial intelligence-based tools designed to assist in the diagnosis of lymphoid neoplasms remain limited. The development of such tools can add value as a diagnostic aid in the evaluation of tissue samples involved by lymphoma. A common diagnostic question is the determination of chronic lymphocytic leukemia (CLL) progression to accelerated CLL (aCLL) or transformation to diffuse large B-cell lymphoma (Richter transformation; RT) in patients who develop progressive disease. The morphologic assessment of CLL, aCLL, and RT can be diagnostically challenging. Using established diagnostic criteria of CLL progression/transformation, we designed four artificial intelligence-constructed biomarkers based on cytologic (nuclear size and nuclear intensity) and architectural (cellular density and cell to nearest-neighbor distance) features. We analyzed the predictive value of implementing these biomarkers individually and then in an iterative sequential manner to distinguish tissue samples with CLL, aCLL, and RT. Our model, based on these four morphologic biomarker attributes, achieved a robust analytic accuracy. This study suggests that biomarkers identified using artificial intelligence-based tools can be used to assist in the diagnostic evaluation of tissue samples from patients with CLL who develop aggressive disease features. © 2021 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
基于人工智能的工具旨在协助诊断淋巴肿瘤,但仍存在局限性。此类工具的开发可以作为诊断辅助手段,用于评估淋巴瘤累及的组织样本。在进展性疾病患者中,常见的诊断问题是确定慢性淋巴细胞白血病(CLL)是否进展为加速型 CLL(aCLL)或转化为弥漫性大 B 细胞淋巴瘤(Richter 转化;RT)。CLL、aCLL 和 RT 的形态学评估具有诊断挑战性。我们使用 CLL 进展/转化的既定诊断标准,基于细胞学(核大小和核强度)和结构(细胞密度和细胞到最近邻居的距离)特征设计了四个人工智能构建的生物标志物。我们分析了单独实施这些生物标志物的预测值,然后以迭代顺序方式区分具有 CLL、aCLL 和 RT 的组织样本。我们的模型基于这四个形态学生物标志物属性,实现了强大的分析准确性。这项研究表明,使用基于人工智能的工具识别的生物标志物可用于辅助诊断评估发生侵袭性疾病特征的 CLL 患者的组织样本。