Artificial intelligence for assisted HER2 immunohistochemistry evaluation of breast cancer: A systematic review and meta-analysis

荟萃分析 乳腺癌 免疫组织化学 肿瘤科 医学 癌症 内科学
作者
Si Wu,Xiang Li,Jiaxian Miao,Dongyi Xian,Meng Yue,Hong Bo Liu,Shishun Fan,Weiwei Wei,Yueping Liu
出处
期刊:Pathology Research and Practice [Elsevier]
卷期号:260: 155472-155472 被引量:3
标识
DOI:10.1016/j.prp.2024.155472
摘要

Accurate assessment of HER2 expression in tumor tissue is crucial for determining HER2-targeted treatment options. Nevertheless, pathologists' assessments of HER2 status are less objective than automated, computer-based evaluations. Artificial Intelligence (AI) promises enhanced accuracy and reproducibility in HER2 interpretation. This study aimed to systematically evaluate current AI algorithms for HER2 immunohistochemical diagnosis, offering insights to guide the development of more adaptable algorithms in response to evolving HER2 assessment practices. A comprehensive data search of the PubMed, Embase, Cochrane, and Web of Science databases was conducted using a combination of subject terms and free text. A total of 4994 computational pathology articles published from inception to September 2023 identifying HER2 expression in breast cancer were retrieved. After applying predefined inclusion and exclusion criteria, seven studies were selected. These seven studies comprised 6867 HER2 identification tasks, with two studies employing the HER2-CONNECT algorithm, two using the CNN algorithm, one with the multi-class logistic regression algorithm, and two using the HER2 4B5 algorithm. AI's sensitivity and specificity for distinguishing HER2 0/1+ were 0.98 [0.92-0.99] and 0.92 [0.80-0.97] respectively. For distinguishing HER2 2+, the sensitivity and specificity were 0.78 [0.50-0.92] and 0.98 [0.93-0.99], respectively. For HER2 3+ distinction, AI exhibited a sensitivity of 0.99 [0.98-1.00] and specificity of 0.99 [0.97-1.00]. Furthermore, due to the lack of HER2-targeted therapies for HER2-negative patients in the past, pathologists may have neglected to distinguish between HER2 0 and 1+, leaving room for improvement in the performance of artificial intelligence (AI) in this differentiation. AI excels in automating the assessment of HER2 immunohistochemistry, showing promising results despite slight variations in performance across different HER2 status. While incorporating AI algorithms into the pathology workflow for HER2 assessment poses challenges in standardization, application patterns, and ethical considerations, ongoing advancements suggest its potential as a widely effective tool for pathologists in clinical practice in the near future.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
无限平凡发布了新的文献求助10
刚刚
花花完成签到,获得积分10
5秒前
5秒前
Reybor应助务实大神采纳,获得20
5秒前
牧长一完成签到 ,获得积分0
6秒前
大力完成签到,获得积分10
6秒前
6秒前
小苹果发布了新的文献求助10
6秒前
iNk应助rr采纳,获得20
8秒前
++完成签到 ,获得积分10
8秒前
长歌完成签到 ,获得积分10
9秒前
FashionBoy应助CrazyRichard采纳,获得10
9秒前
英俊的铭应助菲莳采纳,获得10
9秒前
9秒前
10秒前
李爱国应助abcc1234采纳,获得10
10秒前
bkagyin应助落寞电灯胆采纳,获得10
10秒前
12秒前
彭于晏应助feixingyuan采纳,获得10
12秒前
NS完成签到,获得积分10
13秒前
qu蛐发布了新的文献求助10
13秒前
1213应助kelly采纳,获得10
14秒前
14秒前
Cao发布了新的文献求助10
15秒前
十七发布了新的文献求助30
15秒前
bin发布了新的文献求助10
15秒前
gg完成签到,获得积分10
15秒前
15秒前
15秒前
15秒前
Yuy完成签到 ,获得积分10
16秒前
独特的紫蓝应助GSQ采纳,获得30
17秒前
17秒前
17秒前
Akim应助Eva采纳,获得10
19秒前
独特的紫蓝应助花花不花采纳,获得30
20秒前
20秒前
槑塞呆呆完成签到 ,获得积分10
20秒前
haokeyan发布了新的文献求助10
20秒前
小蘑菇应助吴谷杂粮采纳,获得10
20秒前
高分求助中
The late Devonian Standard Conodont Zonation 2000
Nickel superalloy market size, share, growth, trends, and forecast 2023-2030 2000
The Lali Section: An Excellent Reference Section for Upper - Devonian in South China 1500
Very-high-order BVD Schemes Using β-variable THINC Method 890
Mantiden: Faszinierende Lauerjäger Faszinierende Lauerjäger 800
PraxisRatgeber: Mantiden: Faszinierende Lauerjäger 800
A new species of Coccus (Homoptera: Coccoidea) from Malawi 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3257985
求助须知:如何正确求助?哪些是违规求助? 2899850
关于积分的说明 8307829
捐赠科研通 2569098
什么是DOI,文献DOI怎么找? 1395469
科研通“疑难数据库(出版商)”最低求助积分说明 653107
邀请新用户注册赠送积分活动 630990