Giannini Valentina, Defeudis Arianna, Rosati Samanta, Cappello Giovanni, Mazzetti Simone, Panic Jovana, Regge Daniele, Balestra Gabriella
Annu Int Conf IEEE Eng Med Biol Soc. 2020 Jul;2020:1339-1342. doi: 10.1109/EMBC44109.2020.9176627.
Liver metastases (mts) from colorectal cancer (CRC) can have different responses to chemotherapy in the same patient. The aim of this study is to develop and validate a machine learning algorithm to predict response of individual liver mts. 22 radiomic features (RF) were computed on pretreatment portal CT scans following a manual segmentation of mts. RFs were extracted from 7x7 Region of Interests (ROIs) that moved across the image by step of 2 pixels. Liver mts were classified as non-responder (R-) if their largest diameter increased more than 3 mm after 3 months of treatment and responder (R+), otherwise. Features selection (FS) was performed by a genetic algorithm and classification by a Support Vector Machine (SVM) classifier. Sensitivity, specificity, negative (NPV) and positive (PPV) predictive values were evaluated for all lesions in the training and validation sets, separately. On the training set, we obtained sensitivity of 86%, specificity of 67%, PPV of 89% and NPV of 61%, while, on the validation set, we reached a sensitivity of 73%, specificity of 47%, PPV of 64% and NPV of 57%. Specificity was biased by the low number of R- lesions on the validation set. The promising results obtained in the validation dataset should be extended to a larger cohort of patient to further validate our method.Clinical Relevance- to personalize treatment of patients with metastastic colorectal cancer, based on the likelihood of response to chemotherapy of each liver metastasis.
结直肠癌(CRC)的肝转移(mts)在同一患者中对化疗可能有不同反应。本研究的目的是开发并验证一种机器学习算法,以预测单个肝转移灶的反应。在对转移灶进行手动分割后,根据治疗前的门静脉CT扫描计算22个放射组学特征(RF)。RF从以2像素步长在图像上移动的7x7感兴趣区域(ROI)中提取。如果肝转移灶在治疗3个月后最大直径增加超过3mm,则分类为无反应者(R-),否则为反应者(R+)。通过遗传算法进行特征选择(FS),并通过支持向量机(SVM)分类器进行分类。分别对训练集和验证集中的所有病灶评估敏感性、特异性、阴性(NPV)和阳性(PPV)预测值。在训练集上,我们获得了86%的敏感性、67%的特异性、89%的PPV和61%的NPV,而在验证集上,我们达到了73%的敏感性、47%的特异性、64%的PPV和57%的NPV。验证集上R-病灶数量少导致特异性存在偏差。在验证数据集中获得的有前景的结果应扩展到更大的患者队列,以进一步验证我们的方法。临床相关性——基于每个肝转移灶对化疗反应的可能性,对转移性结直肠癌患者进行个性化治疗。