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Automatic discovery of image-based signatures for ipilimumab response prediction in malignant melanoma

机译:自动发现基于图像的签名用于恶性黑色素瘤患者的ipilimumab反应预测

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In the context of precision medicine with immunotherapies there is an increasing need for companion diagnostic tests to identify potential therapy responders and avoid treatment coming along with severe adverse events for non-responders. Here, we present a retrospective case study to discover image-based signatures for developing a potential companion diagnostic test for ipilimumab (IPI) in malignant melanoma. Signature discovery is based on digital pathology and fully automatic quantitative image analysis using virtual multiplexing as well as machine learning and deep learning on whole-slide images. We systematically correlated the patient outcome data with potentially relevant local image features using a Tissue Phenomics approach with a sound cross validation procedure for reliable performance evaluation. Besides uni-variate models we also studied combinations of signatures in several multi-variate models. The most robust and best performing model was a decision tree model based on relative densities of CD8+ tumor infiltrating lymphocytes in the intra-tumoral infiltration region. Our results are well in agreement with observations described in previously published studies regarding the predictive value of the immune contexture, and thus, provide predictive potential for future development of a companion diagnostic test.
机译:在具有免疫疗法的精密医学的背景下,对伴随诊断测试的需求不断增长,以识别潜在的治疗反应者并避免治疗伴随无反应者的严重不良事件。在这里,我们提出一项回顾性案例研究,以发现基于图像的特征,以开发潜在的伴随诊断性恶性黑色素瘤伊立木单抗(IPI)。签名发现基于数字病理学和使用虚拟多路复用以及对整张幻灯片图像进行机器学习和深度学习的全自动定量图像分析。我们使用组织造物学方法以及可靠的交叉验证程序对患者结果数据与潜在相关的局部图像特征进行系统地关联,以进行可靠的性能评估。除了单变量模型外,我们还研究了几种多变量模型中签名的组合。最健壮和最佳性能的模型是基于肿瘤内浸润区域中CD8 +肿瘤浸润淋巴细胞相对密度的决策树模型。我们的结果与先前发表的关于免疫环境的预测价值的研究中描述的观察结果非常吻合,因此为伴随诊断测试的未来发展提供了预测潜力。

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