Evidence map›Paper›PMID 41309620›Full record

ArticleNature communications2025

A noninvasive machine learning model using a complete blood count for screening of primary vitreoretinal lymphoma.

Shengjie Li, Jiazhen Cao, Danhui Li, Jun Ren, Jianing Wu, Yingzhu Li, Mengyu Zhang, Henggui Hu, Yunxiao Song, Jie Cheng and 2 more

Abstract readMulticenter Study
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
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

12 authors.

Shengjie Li *Department of Clinical Laboratory, Eye & ENT Hospital, Fudan University, Shanghai, China. lishengjie6363020@163.com.ORCID http://orcid.org/0000-0002-6443-740X
Jiazhen Cao *Department of Laboratory Medicine, Huashan Hospital, Fudan University, Shanghai, China.
Danhui Li *Department of Pathology, RenJi Hospital, School of Medicine, Shanghai JiaoTong University, Shanghai, China.
Jun RenDepartment of Clinical Laboratory, Eye & ENT Hospital, Fudan University, Shanghai, China.
Jianing WuDepartment of Clinical Laboratory, Eye & ENT Hospital, Fudan University, Shanghai, China.
Yingzhu LiDepartment of Clinical Laboratory, Eye & ENT Hospital, Fudan University, Shanghai, China.
Mengyu ZhangDepartment of Clinical Laboratory, Anhui Wanbei Electricity Group General Hospital, Suzhou, China.
Henggui HuDepartment of Clinical Laboratory, Anhui Wanbei Electricity Group General Hospital, Suzhou, China.
Yunxiao SongDepartment of Clinical Laboratory, Shanghai Xuhui Central Hospital, Fudan University, Shanghai, China.
Jie ChengDepartment of General Practice, Shanghai Xuhui Central Hospital, Fudan University, Shanghai, China. alex13818908753@126.com.ORCID http://orcid.org/0000-0001-6983-5389
Ming GuanDepartment of Laboratory Medicine, Huashan Hospital, Fudan University, Shanghai, China. guanming88@yahoo.com.ORCID http://orcid.org/0000-0002-8796-2653
Wenjun CaoDepartment of Clinical Laboratory, Eye & ENT Hospital, Fudan University, Shanghai, China. wgkjyk@aliyun.com.ORCID http://orcid.org/0000-0001-6383-9012

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary vitreoretinal lymphoma (PVRL) is a rare and aggressive intraocular malignancy that is frequently misdiagnosed because of its nonspecific early manifestations and the lack of effective screening tools. We conduct a multicentre case-control study including 255 PVRL patients and 292 controls to develop a machine learning-based screening model using complete blood count data. A six-feature random forest model demonstrates high diagnostic accuracy in the discovery cohort (area under the curve [AUC] = 0.85) and validates across all cohorts (AUC = 0.80-0.83), outperforming intraocular biomarkers such as the interleukin-10/interleukin-6 ratio (AUC = 0.65-0.78). Model performance further validates in a hospital-based prospective cohort (n = 100,526), where 38 PVRLs are identified among 66 individuals classified as high risk, and 2 additional cases are identified among 83,610 individuals classified as low risk, yielding a sensitivity of 95.0%, specificity of 99.97%, positive predictive value (PPV) of 57.6%, and negative predictive value of 99.99%. In the community cohort (n = 515,326), 22 individuals are flagged as high risk, 13 of whom are confirmed as having PVRL (PPV = 59.1%). This study presents the noninvasive and scalable blood-based screening strategy for detection of PVRL, with a web application enabling timely triage and population-level risk stratification.

Indexed as

LymphomaMachine LearningRetinal NeoplasmsAdultAgedBiomarkers, TumorBlood Cell CountCase-Control StudiesEarly Detection of CancerFemaleHumansInterleukin-6MaleMiddle AgedProspective StudiesSensitivity and SpecificityBiomarkers, TumorInterleukin-6

Identifiers

PMID41309620
PMCPMC12660402

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.