Evidence map›Paper›PMID 39572521›Full record

ArticleNature communications2024

Deep generative AI models analyzing circulating orphan non-coding RNAs enable detection of early-stage lung cancer.

Mehran Karimzadeh, Amir Momen-Roknabadi, Taylor B Cavazos, Yuqi Fang, Nae-Chyun Chen, Michael Multhaup, Jennifer Yen, Jeremy Ku, Jieyang Wang, Xuan Zhao and 19 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
–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

31 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  9. Current trends and future directions of artificial intelligence in lung cancer diagnosis.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2026
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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

29 authors.

Mehran Karimzadeh *Exai Bio Inc., Palo Alto, CA, US.ORCID 0000-0002-7324-6074
Amir Momen-Roknabadi *Exai Bio Inc., Palo Alto, CA, US.
Taylor B Cavazos *Exai Bio Inc., Palo Alto, CA, US.
Yuqi FangExai Bio Inc., Palo Alto, CA, US.
Nae-Chyun ChenExai Bio Inc., Palo Alto, CA, US.
Michael MulthaupExai Bio Inc., Palo Alto, CA, US.
Jennifer YenExai Bio Inc., Palo Alto, CA, US.
Jeremy KuExai Bio Inc., Palo Alto, CA, US.
Jieyang WangExai Bio Inc., Palo Alto, CA, US.
Xuan ZhaoExai Bio Inc., Palo Alto, CA, US.
Philip MurzynowskiExai Bio Inc., Palo Alto, CA, US.
Kathleen WangExai Bio Inc., Palo Alto, CA, US.
Rose HannaExai Bio Inc., Palo Alto, CA, US.
Alice HuangExai Bio Inc., Palo Alto, CA, US.
Diana CortiExai Bio Inc., Palo Alto, CA, US.
Dang NguyenExai Bio Inc., Palo Alto, CA, US.
Ti LamExai Bio Inc., Palo Alto, CA, US.
Seda KilincExai Bio Inc., Palo Alto, CA, US.
Patrick ArensdorfExai Bio Inc., Palo Alto, CA, US.
Kimberly H ChauExai Bio Inc., Palo Alto, CA, US.
Anna HartwigExai Bio Inc., Palo Alto, CA, US.
Lisa FishExai Bio Inc., Palo Alto, CA, US.
Helen LiExai Bio Inc., Palo Alto, CA, US.ORCID 0000-0002-1145-6527
Babak BehsazExai Bio Inc., Palo Alto, CA, US.
Olivier ElementoWeill Cornell Medicine, New York, NY, US.ORCID 0000-0002-8061-9617
James ZouStanford University, Stanford, CA, US.ORCID 0000-0001-8880-4764
Fereydoun HormozdiariExai Bio Inc., Palo Alto, CA, US. fereydounh@exai.bio.ORCID 0000-0003-2703-9274
Babak AlipanahiExai Bio Inc., Palo Alto, CA, US. babaka@exai.bio.ORCID 0000-0001-8216-7178
Hani GoodarziUniversity of California, San Francisco, CA, US. hani@arcinstitute.org.ORCID 0000-0002-9648-8949

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liquid biopsies have the potential to revolutionize cancer care through non-invasive early detection of tumors. Developing a robust liquid biopsy test requires collecting high-dimensional data from a large number of blood samples across heterogeneous groups of patients. We propose that the generative capability of variational auto-encoders enables learning a robust and generalizable signature of blood-based biomarkers. In this study, we analyze orphan non-coding RNAs (oncRNAs) from serum samples of 1050 individuals diagnosed with non-small cell lung cancer (NSCLC) at various stages, as well as sex-, age-, and BMI-matched controls. We demonstrate that our multi-task generative AI model, Orion, surpasses commonly used methods in both overall performance and generalizability to held-out datasets. Orion achieves an overall sensitivity of 94% (95% CI: 87%-98%) at 87% (95% CI: 81%-93%) specificity for cancer detection across all stages, outperforming the sensitivity of other methods on held-out validation datasets by more than  ~ 30%.

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungEarly Detection of CancerLung NeoplasmsAgedArtificial IntelligenceDeep LearningFemaleHumansLiquid BiopsyMaleMiddle AgedNeoplasm StagingRNA, UntranslatedSensitivity and SpecificityBiomarkers, TumorRNA, Untranslated

Identifiers

PMID39572521
PMCPMC11582319

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.