Correlation between synthetic MRI relaxometry and apparent diffusion coefficient in breast cancer subtypes with different neoadjuvant therapy response

医学 有效扩散系数 乳腺癌 磁共振弥散成像 乳房磁振造影 相关性 新辅助治疗 神经组阅片室 松弛法 放射科 磁共振成像 肿瘤科 癌症 乳腺摄影术 内科学 神经学 几何学 数学 自旋回波 精神科
作者
Wenhong Jiang,Siyao Du,Si Gao,Lizhi Xie,Zichuan Xie,Mengfan Wang,Can Peng,Jing Shi,Lina Zhang
出处
期刊:Insights Into Imaging [Springer Nature]
卷期号:14 (1) 被引量:1
标识
DOI:10.1186/s13244-023-01492-9
摘要

Abstract Background To evaluate the correlation between synthetic MRI (syMRI) relaxometry and apparent diffusion coefficient (ADC) maps in different breast cancer subtypes and treatment response subgroups. Methods Two hundred sixty-three neoadjuvant therapy (NAT)-treated breast cancer patients with baseline MRI were enrolled. Tumor annotations were obtained by drawing regions of interest (ROIs) along the lesion on T1/T2/PD and ADC maps respectively. Histogram features from T1/T2/PD and ADC maps were respectively calculated, and the correlation between each pair of identical features was analyzed. Meanwhile, features between different NAT treatment response groups were compared, and their discriminatory power was evaluated. Results Among all patients, 20 out of 27 pairs of features weakly correlated ( r = – 0.13–0.30). For triple-negative breast cancer (TNBC), features from PD map in the pathological complete response (pCR) group ( r = 0.60–0.86) showed higher correlation with ADC than that of the non-pCR group ( r = 0.30–0.43), and the mean from the ADC and PD maps in the pCR group strongly correlated ( r = 0.86). For HER2-positive, few correlations were found both in the pCR and non-pCR groups. For luminal HER2-negative, T2 map correlated more with ADC than T1 and PD maps. Significant differences were seen in T2 low percentiles and median in the luminal-HER2 negative subtype, yielding moderate AUCs (0.68/0.72/0.71). Conclusions The relationship between ADC and PD maps in TNBC may indicate different NAT responses. The no-to-weak correlation between the ADC and syMRI suggests their complementary roles in tumor microenvironment evaluation. Critical relevance statement The relationship between ADC and PD maps in TNBC may indicate different NAT responses, and the no-to-weak correlation between the ADC and syMRI suggests their complementary roles in tumor microenvironment evaluation. Key points • The relationship between ADC and PD in TNBC indicates different NAT responses. • The no-to-weak correlations between ADC and syMRI complementarily evaluate tumor microenvironment. • T2 low percentiles and median predict NAT response in luminal-HER2-negative subtype. Graphical Abstract

科研通智能强力驱动
Strongly Powered by AbleSci AI
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
JamesPei应助xiaobai123456采纳,获得10
刚刚
刚刚
衢夭完成签到,获得积分10
1秒前
byby完成签到,获得积分10
2秒前
shitzu完成签到 ,获得积分10
3秒前
量子星尘发布了新的文献求助10
4秒前
小一完成签到,获得积分10
4秒前
gzmejiji完成签到,获得积分10
6秒前
fxy完成签到 ,获得积分10
7秒前
等待的白容完成签到,获得积分10
8秒前
诸葛烤鸭完成签到,获得积分10
8秒前
严xixi完成签到 ,获得积分10
8秒前
1762120完成签到,获得积分10
9秒前
典雅的纸飞机完成签到 ,获得积分10
9秒前
keaitiancaiben完成签到,获得积分20
9秒前
free完成签到,获得积分10
10秒前
LLddww完成签到,获得积分10
10秒前
天神完成签到,获得积分10
10秒前
衔尾蛇发布了新的文献求助10
10秒前
完美世界应助等待的白容采纳,获得10
12秒前
12秒前
轻松豁完成签到 ,获得积分10
12秒前
xin发布了新的文献求助10
13秒前
fdpb完成签到,获得积分10
13秒前
wwwcom12完成签到 ,获得积分10
15秒前
泠漓完成签到 ,获得积分10
15秒前
量子星尘发布了新的文献求助10
16秒前
luming完成签到 ,获得积分10
16秒前
研友_Z60ObL完成签到,获得积分10
17秒前
yier完成签到,获得积分10
18秒前
yoyo完成签到 ,获得积分10
19秒前
璃月品茶钟离完成签到,获得积分10
20秒前
炙热的笑翠完成签到,获得积分10
22秒前
wensri完成签到,获得积分10
22秒前
眼睛大的芹菜完成签到 ,获得积分10
22秒前
邢邢完成签到,获得积分10
22秒前
多边棱发布了新的文献求助10
23秒前
超级的冷菱完成签到 ,获得积分10
24秒前
zhong完成签到,获得积分10
25秒前
march完成签到,获得积分10
25秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Aerospace Standards Index - 2026 ASIN2026 3000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
Research Methods for Business: A Skill Building Approach, 9th Edition 500
Social Work and Social Welfare: An Invitation(7th Edition) 410
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6051406
求助须知:如何正确求助?哪些是违规求助? 7860047
关于积分的说明 16267875
捐赠科研通 5196415
什么是DOI,文献DOI怎么找? 2780623
邀请新用户注册赠送积分活动 1763572
关于科研通互助平台的介绍 1645613