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Automated assessment of necrosis tumor ratio in colorectal cancer using an artificial intelligence-based digital pathology analysis 基于人工智能的数字病理分析对癌症坏死肿瘤比率的自动评估
Pub Date : 2023-03-21 DOI: 10.1002/med4.9
Huifen Ye, Yunrui Ye, Yiting Wang, Tong Tong, Su Yao, Yao Xu, Qingru Hu, Yulin Liu, Changhong Liang, Guangyi Wang, Ke Zhao, Xinjuan Fan, Yanfen Cui, Zaiyi Liu

Background

With the advance in digital pathology and artificial intelligence (AI)-powered approaches, necrosis is proposed as a marker of poor prognosis in colorectal cancer (CRC). However, most previous studies quantified necrosis merely as a tissue type and patch-level segmentation. Thus, it was worth exploring and validating the prognostic and predictive value of necrosis proportion with a pixel-level segmentation in large multicenter cohorts.

Methods

A semantic segmentation model was trained with 12 tissue types labeled by pathologists. Segmentation was performed using the U-net model with a subsequently derived necrosis tumor ratio (NTR). We proposed the NTR score (NTR-low or NTR-high) to evaluate the prognostic and predictive value of necrosis for disease-free survival (DFS) and overall survival (OS) in the development (N = 443) and validation cohorts (N = 333) using 75% as a threshold.

Results

The 2-category NTR was an independent prognostic factor and NTR-low was associated with significant prolonged DFS (unadjusted HR for high vs. low 1.72 [95% CI 1.19–2.49] and 1.98 [1.22–3.23] in the development and validation cohorts). Similar trends were observed for OS. The prognostic value of NTR was maintained in the multivariate analysis for both cohorts. Furthermore, a stratified analysis showed that NTR-high was a high risk with adjuvant chemotherapy for OS in stage II CRC (p = 0.047).

Conclusion

AI-based pixel-level quantified NTR has a stable prognostic value in CRC associated with unfavorable survival. Additionally, adjuvant chemotherapy provided survival benefits for patients with a high NTR score in stage II CRC.

背景随着数字病理学和人工智能(AI)技术的发展,坏死被认为是癌症(CRC)预后不良的标志物。然而,大多数先前的研究仅将坏死量化为组织类型和斑块级别的分割。因此,在大型多中心队列中,像素级分割坏死比例的预后和预测价值值得探索和验证。方法用病理学家标记的12种组织类型训练语义分割模型。使用U-net模型进行分割,随后得出坏死肿瘤比率(NTR)。我们提出了NTR评分(NTR低或NTR高),以75%作为阈值,评估坏死对发展(N=443)和验证队列(N=333)中无病生存率(DFS)和总生存率(OS)的预后和预测价值。结果2类NTR是一个独立的预后因素,NTR低与显著延长的DFS相关(在开发和验证队列中,高与低的未调整HR分别为1.72[95%CI 1.19–2.49]和1.98[1.22–3.23])。OS也出现了类似的趋势。NTR的预后价值在两个队列的多变量分析中都保持不变。此外,分层分析显示,NTR高是II期CRC OS辅助化疗的高风险(p=0.047)。结论基于AI的像素水平量化NTR在与不良生存相关的CRC中具有稳定的预后价值。此外,辅助化疗为II期CRC NTR评分高的患者提供了生存益处。
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引用次数: 0
Should Paxlovid be prescribed for patients with severe COVID-19 in the late course of infection? A case report 感染晚期严重新冠肺炎患者是否应服用奈玛特韦片/利托那韦片组合包装?案例报告
Pub Date : 2023-03-20 DOI: 10.1002/med4.12
Qiang Li, Yibo He, Jin Liu, Xiaozhao Lu, Ziyou Zhou, Yu Kang, Wanying Wu, Jielan Wu, Feng Wang, Yinghao Sun, Wei Wang, Chengyi Hui, Wenting Wei, Miaoyun Wen, Jingjing Chen, Yong Liu

The infection of the coronavirus disease 2019 (COVID-19) is often accompanied by pneumonia with both high incidence and mortality. Paxlovid is commonly prescribed in patients with mild and normal pneumonia within 5 days from the symptom onset. Herein, we report a practically effective use of Paxlovid compensatively in patients with COVID-19 and severe pneumonia after 5 days of infection in a typical case in China. In this case, a 75-year-old man was diagnosed with severe COVID-19 complicated with a pulmonary bacterial infection. After treatment with oxygen inhalation, Cefoperazone-sulbactam and ambroxol, fever and upper respiratory symptoms were alleviated, except for the Oxygenation index (OI) remaining worse, Coronavirus was detected as positive, and levels of interleukin-6 remained high. Paxlovid was prescribed for 5 days subsequently though it was 14 days since symptom onset. Thereafter, the nucleic acid of the patient turned negative in 7 days and the symptoms resolved. This case showed that Paxlovid can be considered in patients with COVID-19 and severe pneumonia even in the later course of infection in clinical practice in China.

2019冠状病毒病(新冠肺炎)的感染通常伴有肺炎,发病率和死亡率都很高。奈玛特韦片/利托那韦片组合包装通常用于症状出现后5天内的轻度和正常肺炎患者。在此,我们报告了奈玛特韦片/利托那韦片组合包装在中国一例典型病例中对新冠肺炎和感染5天后的重症肺炎患者的实际有效补偿使用。在这种情况下,一名75岁的男子被诊断为严重的新冠肺炎合并肺部细菌感染。经吸氧、头孢哌酮舒巴坦和氨溴索治疗后,发烧和上呼吸道症状有所缓解,但氧合指数(OI)仍较低,冠状病毒检测呈阳性,白细胞介素-6水平仍较高。奈玛特韦片/利托那韦片组合包装随后被开了5天的处方,尽管症状出现后14天。此后,患者的核酸在7天内转为阴性,症状消失。该病例表明,在中国临床实践中,即使在感染后期,奈玛特韦片/利托那韦片组合包装也可以用于新冠肺炎和重症肺炎患者。
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