Comprehensive machine-learning survival framework develops a consensus model in large-scale multicenter cohorts for pancreatic cancer

医学 肿瘤科 内科学 精密医学 胰腺癌 队列 免疫疗法 生物标志物 阶段(地层学) 癌症 病理 生物 生物化学 古生物学
作者
Libo Wang,Zaoqu Liu,Ruopeng Liang,Weijie Wang,Rongtao Zhu,Jian Li,Zhe Xing,Siyuan Weng,Xinwei Han,Yuling Sun
出处
期刊:eLife [eLife Sciences Publications Ltd]
卷期号:11 被引量:113
标识
DOI:10.7554/elife.80150
摘要

As the most aggressive tumor, the outcome of pancreatic cancer (PACA) has not improved observably over the last decade. Anatomy-based TNM staging does not exactly identify treatment-sensitive patients, and an ideal biomarker is urgently needed for precision medicine. Based on expression files of 1280 patients from 10 multicenter cohorts, we screened 32 consensus prognostic genes. Ten machine-learning algorithms were transformed into 76 combinations, of which we selected the optimal algorithm to construct an artificial intelligence-derived prognostic signature (AIDPS) according to the average C-index in the nine testing cohorts. The results of the training cohort, nine testing cohorts, Meta-Cohort, and three external validation cohorts (290 patients) consistently indicated that AIDPS could accurately predict the prognosis of PACA. After incorporating several vital clinicopathological features and 86 published signatures, AIDPS exhibited robust and dramatically superior predictive capability. Moreover, in other prevalent digestive system tumors, the nine-gene AIDPS could still accurately stratify the prognosis. Of note, our AIDPS had important clinical implications for PACA, and patients with low AIDPS owned a dismal prognosis, higher genomic alterations, and denser immune cell infiltrates as well as were more sensitive to immunotherapy. Meanwhile, the high AIDPS group possessed observably prolonged survival, and panobinostat may be a potential agent for patients with high AIDPS. Overall, our study provides an attractive tool to further guide the clinical management and individualized treatment of PACA.
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
负责天问完成签到,获得积分10
1秒前
1秒前
熊雅完成签到,获得积分10
1秒前
郭小白完成签到 ,获得积分10
1秒前
小陶子完成签到,获得积分10
2秒前
毅然决然必然完成签到,获得积分10
2秒前
2秒前
molihuakai应助风清扬采纳,获得10
2秒前
豆丁小猫完成签到,获得积分10
2秒前
搞怪的小松鼠完成签到,获得积分10
2秒前
yangsheng完成签到 ,获得积分10
2秒前
光亮萤完成签到,获得积分10
4秒前
半颗橙子完成签到 ,获得积分10
6秒前
Bob完成签到 ,获得积分10
6秒前
拼搏的白云完成签到,获得积分0
6秒前
Velarok发布了新的文献求助10
6秒前
max完成签到 ,获得积分10
6秒前
落落完成签到 ,获得积分10
7秒前
小公牛完成签到 ,获得积分10
8秒前
花蝴蝶完成签到 ,获得积分10
8秒前
偏偏海完成签到,获得积分10
9秒前
好好完成签到,获得积分10
9秒前
10秒前
Terry完成签到,获得积分10
10秒前
无与伦比完成签到,获得积分10
11秒前
hy1234完成签到 ,获得积分10
13秒前
Everything发布了新的文献求助10
13秒前
Yy完成签到,获得积分10
14秒前
Triumph完成签到,获得积分10
15秒前
xo80完成签到 ,获得积分10
16秒前
lzc完成签到,获得积分10
17秒前
18秒前
贪玩蓝月3号完成签到,获得积分10
19秒前
bae完成签到 ,获得积分10
19秒前
Hans完成签到,获得积分10
20秒前
611完成签到 ,获得积分10
22秒前
bener完成签到,获得积分10
22秒前
勤恳的隶完成签到,获得积分10
23秒前
欧耶耶完成签到 ,获得积分10
24秒前
pp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
The Cambridge History of China: Volume 4, Sui and T'ang China, 589–906 AD, Part Two 1500
Cowries - A Guide to the Gastropod Family Cypraeidae 1200
Quality by Design - An Indispensable Approach to Accelerate Biopharmaceutical Product Development 800
Pulse width control of a 3-phase inverter with non sinusoidal phase voltages 777
Signals, Systems, and Signal Processing 610
Research Methods for Applied Linguistics: A Practical Guide 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6399520
求助须知:如何正确求助?哪些是违规求助? 8216220
关于积分的说明 17408189
捐赠科研通 5452803
什么是DOI,文献DOI怎么找? 2881941
邀请新用户注册赠送积分活动 1858361
关于科研通互助平台的介绍 1700373