Evidence map›Paper›PMID 41912779›Full record

ArticleCommunications medicine2026

Machine learning survival model for personalised prevention of catheter-related thrombosis in tumour patients.

Hewei Ge, Qiao Liu, Junying Xie, Jianan Pang, Bin Li, Jie Xue, Lina Xu, Nana Yang, Haifeng Cai, Jian Wang and 17 more

Abstract read
In one paragraph

Article in Communications medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Hewei Ge *Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.ORCID http://orcid.org/0000-0002-9852-2733
Qiao Liu *Department of Radiation and Medical Oncology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Junying XieManagement Centre, Beijing Chaoyang Huanxing Cancer Hospital, Beijing, China.
Jianan PangCancer Center, The First Hospital of Jilin University, Jilin, China.
Bin LiManagement Centre, Beijing Chaoyang Huanxing Cancer Hospital, Beijing, China.
Jie XueManagement Centre, Beijing Chaoyang Huanxing Cancer Hospital, Beijing, China.
Lina XuManagement Centre, Beijing Chaoyang Huanxing Cancer Hospital, Beijing, China.
Nana YangManagement Centre, Beijing Chaoyang Huanxing Cancer Hospital, Beijing, China.
Haifeng CaiDepartment of Oncology Surgery, Tangshan People's Hospital, Tangshan, China.
Jian WangDepartment of Gastrointestinal Surgery, Tangshan People's Hospital, Tangshan, China.
Yalong QiDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Yuhan WeiDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.ORCID http://orcid.org/0000-0002-8238-4663
Hongnan MoDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.ORCID http://orcid.org/0000-0002-2887-7985
Sidan LiDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Lili ZhangCancer Center, The First Hospital of Jilin University, Jilin, China.
Ziming LiuCancer Center, The First Hospital of Jilin University, Jilin, China.
Hongyi WangCancer Center, The First Hospital of Jilin University, Jilin, China.
Zehao LiCancer Center, The First Hospital of Jilin University, Jilin, China.
Xinqiao ChenCancer Center, The First Hospital of Jilin University, Jilin, China.
Xiaoxue GaoCancer Center, The First Hospital of Jilin University, Jilin, China.
Fangqi LiCancer Center, The First Hospital of Jilin University, Jilin, China.
Weiwei XingCancer Center, The First Hospital of Jilin University, Jilin, China.
Xiaoying SunDepartment of Medical Oncology, Beijing Chaoyang Huanxing Cancer Hospital, Beijing, China.
Yufeng LiThe Cancer Institute, Hebei Key Laboratory of Molecular Oncology, Tangshan People's Hospital, Tangshan, China.
Haili QianState Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.ORCID http://orcid.org/0000-0003-0652-4801
Jiuwei CuiCancer Center, The First Hospital of Jilin University, Jilin, China. cuijw@jlu.edu.cn.ORCID http://orcid.org/0000-0001-6496-7550
Fei MaDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. drmafei@126.com.ORCID http://orcid.org/0000-0001-9432-1902

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82230058National Natural Science Foundation of China (National Science Foundation of China) 82273191National Natural Science Foundation of China (National Science Foundation of China) 92459304
6 · The paper itself

Abstract

backgroundCentral venous catheters for drug delivery introduce catheter-related thrombosis (CRT) and influence the survival of cancer patients. The key unmet needs to personalise CRT prevention include identifying high-risk patients and optimising extubation time. In this study, we aimed to develop a survival model to facilitate personalised CRT prevention strategies.

methodsWe prospectively collected tumour patient catheterization data across 4 centres. The SM-CRT survival model, which provides both continuous risk ranking (crank) predictions and the survival distribution (distr) predictions was constructed.

resultsHere we include a total of 30,947 patients. The SM-CRT model exhibits robust performance in identifying high-risk patients, with c-indexes of 0.714 in the prospective test dataset and 0.678 and 0.779 in 2 external test datasets based on crank predictions. Femorally inserted central catheter (FICC), peripherally inserted central catheter (PICC), tumours in the thoracic cavity, and alkylating agents are identified as high-risk factors. Patients are subsequently divided into high-risk, low-risk, and long-term period groups on the basis of their distr predictions. The predicted low-risk and long-term groups present significantly fewer CRT events per day than the high-risk group in both the training dataset (odds ratio [OR] = 0.54, 95% CI [0.38-0.91], adjusted p-value [p

conclusionsThe high c-indexes based on crank predictions demonstrated the ability of the SM-CRT model to identify high-risk patients for thromboprophylaxis. Additionally, the SM-CRT model can guide extubation time by identifying high-risk periods through distr predictions.

Identifiers

PMID41912779
PMCPMC13199492

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