Diagnosis and Grading of Prostate Cancer by Relaxation Maps From Synthetic MRI

前列腺癌 接收机工作特性 磁共振成像 核医学 磁共振弥散成像 有效扩散系数 前列腺 放射科 医学 曼惠特尼U检验 分级(工程) 增生 多参数磁共振成像 病理 癌症 内科学 生物 生态学
作者
Yadong Cui,Siyuan Han,Ming Liu,Pu‐Yeh Wu,Wei Zhang,Jintao Zhang,Chunmei Li,Min Chen
出处
期刊:Journal of Magnetic Resonance Imaging [Wiley]
卷期号:52 (2): 552-564 被引量:69
标识
DOI:10.1002/jmri.27075
摘要

Background The interpretation system for prostate MRI is largely based on qualitative image contrast of different tissue types. Therefore, a fast, standardized, and robust quantitative technique is necessary. Synthetic MRI is capable of quantifying multiple relaxation parameters, which might have potential applications in prostate cancer (PCa). Purpose To investigate the use of quantitative relaxation maps derived from synthetic MRI for the diagnosis and grading of PCa. Study Type Prospective. Subjects In all, 94 men with pathologically confirmed PCa or benign pathological changes. Field Strength/Sequence T 1 ‐weighted imaging, T 2 ‐weighted imaging, diffusion‐weighted imaging, and synthetic MRI at 3.0T. Assessment Four kinds of tissue types were identified on pathology, including PCa, stromal hyperplasia (SH), glandular hyperplasia (GH), and noncancerous peripheral zone (PZ). PCa foci were grouped as low‐grade (LG, Gleason score ≤6) and intermediate/high‐grade (HG, Gleason score ≥7). Regions of interest were manually drawn by two radiologists in consensus on parametric maps according to the pathological results. Statistical Tests Independent sample t ‐test, Mann–Whitney U ‐test, and receiver operating characteristic curve analysis. Results T 1 and T 2 values of PCa were significantly lower than SH ( P = 0.015 and 0.002). The differences of T 1 and T 2 values between PCa and noncancerous PZ were also significant ( P ≤ 0.006). The area under the curve (AUC) of the apparent diffusion coefficient (ADC) value was significantly higher than T 1 , T 2 , and proton density (PD) values in discriminating PCa from SH and noncancerous PZ ( P ≤ 0.025). T 2 , PD, and ADC values demonstrated similar diagnostic performance in discriminating LG from HG PCa (AUC = 0.806 [0.640–0.918], 0.717 [0.542–0.854], and 0.817 [0.652–0.925], respectively; P ≥ 0.535). Data Conclusion Relaxation maps derived from synthetic MRI were helpful for discriminating PCa from other benign pathologies. But the overall diagnostic performance was inferior to the ADC values. T 2 , PD, and ADC values performed similarly in discriminating LG from HG PCa lesions. Level of Evidence: 2 Technical Efficacy Stage: 2 J. Magn. Reson. Imaging 2020;52:552–564.
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
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
jkq发布了新的文献求助10
1秒前
qpzn完成签到 ,获得积分10
3秒前
天天快乐应助WangY1263采纳,获得10
3秒前
1223发布了新的文献求助10
3秒前
HJBF666完成签到 ,获得积分10
6秒前
饱满的大碗完成签到 ,获得积分10
8秒前
于艳辉完成签到,获得积分10
9秒前
如烈火如止水完成签到,获得积分10
10秒前
12秒前
慕容雅柏完成签到 ,获得积分10
13秒前
imica完成签到 ,获得积分10
14秒前
16秒前
20秒前
anitachiu1104发布了新的文献求助10
21秒前
凤里完成签到 ,获得积分10
24秒前
maclogos发布了新的文献求助10
25秒前
joker完成签到 ,获得积分10
25秒前
海上众川归完成签到 ,获得积分10
27秒前
111完成签到 ,获得积分10
33秒前
潇湘完成签到 ,获得积分10
35秒前
37秒前
hky完成签到 ,获得积分10
38秒前
qqqqq完成签到,获得积分10
41秒前
秋水完成签到 ,获得积分10
42秒前
42秒前
mawenting完成签到 ,获得积分10
43秒前
你喜欢什么样子的我演给你看完成签到 ,获得积分10
46秒前
Zhusy完成签到 ,获得积分20
55秒前
莫小烦完成签到,获得积分10
56秒前
茶茶发布了新的文献求助10
56秒前
雨柏完成签到 ,获得积分10
59秒前
wad1314完成签到,获得积分10
1分钟前
投必快业必毕完成签到,获得积分10
1分钟前
shizaibide1314完成签到,获得积分10
1分钟前
cdercder应助科研通管家采纳,获得10
1分钟前
cdercder应助科研通管家采纳,获得10
1分钟前
cis2014完成签到,获得积分10
1分钟前
斯文败类应助科研通管家采纳,获得10
1分钟前
JTHe应助科研通管家采纳,获得10
1分钟前
我是老大应助科研通管家采纳,获得10
1分钟前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 3000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Maneuvering of a Damaged Navy Combatant 650
Mindfulness and Character Strengths: A Practitioner's Guide to MBSP 380
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3776051
求助须知:如何正确求助?哪些是违规求助? 3321626
关于积分的说明 10206478
捐赠科研通 3036712
什么是DOI,文献DOI怎么找? 1666435
邀请新用户注册赠送积分活动 797439
科研通“疑难数据库(出版商)”最低求助积分说明 757841