Evidence map›Paper›PMID 40596693›Full record

ArticleScientific reports2025

Validation of an AI-enabled exome/transcriptome liquid biopsy platform for early detection, MRD, disease monitoring, and therapy selection for solid tumors.

J Abraham, V Domenyuk, N Perdigones, S Klimov, S Antani, T Yoshino, E I Heath, E Lou, S V Liu, J L Marshall and 19 more

Abstract readValidation Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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

  1. [Liquid Biopsy Revolutionizes the Precise Management of Tumors Across the Entire Course: Current Situation and Future Prospects].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2026
    Pooled it
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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.

J Abraham *Caris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
V Domenyuk *Caris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
N PerdigonesCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
S KlimovCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
S AntaniCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
T YoshinoNational Cancer Center Hospital East, Chiba, Japan.
E I HeathKarmanos Cancer Institute, Wayne State University, Detroit, MI, USA.
E LouUniversity of Minnesota, Minneapolis, MN, USA.
S V LiuLombardi Comprehensive Cancer Center, Washington, D.C., DC, United States.
J L MarshallLombardi Comprehensive Cancer Center, Washington, D.C., DC, United States.
W S El-DeiryBrown University, Providence, RI, USA.
A F ShieldsKarmanos Cancer Institute, Wayne State University, Detroit, MI, USA.
M F DietrichOncology Network, Orlando, FL, US.
Y NakamuraNational Cancer Center Hospital East, Chiba, Japan.
T FujisawaNational Cancer Center Hospital East, Chiba, Japan.
G D DemetriDana-Farber Cancer Institute and Ludwig Center, Harvard Medical School, Boston, MA, United States.
A BarkerArizona State University, Phoenix, AZ, USA.
J XiuCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
D A SacchettiCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
S StahlCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
R Hahn-LowryCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
A StarkCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
J SwensenCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
G PosteArizona State University, Phoenix, AZ, USA.
D D HalbertCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
M OberleyCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
M RadovichCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
G W SledgeCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA.
David B SpetzlerCaris Life Sciences, 350 W. Washington St, Irving, TX, 85281, USA. dspetzler@carisls.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective clinical management of patients with cancer requires highly accurate diagnosis, precise therapy selection, and highly sensitive monitoring of disease burden. Caris Assure is a multifunctional blood-based assay that couples whole exome and whole transcriptome sequencing on plasma and leukocytes with advanced machine learning techniques to satisfy all three clinical testing needs on one platform. Caris Assure for therapy selection was CLIA validated using 1,910 samples. 376,197 tissue profiles along with 7,061 paired blood and tissue profiles were used to engineer features for three machine learning models. The MCED model was trained on 1,013 patients and validated on an independent set of 2,675 patients. The tissue of origin for MCED model was trained on 1,166 samples and validated using 5-fold cross validation. The MRD & Monitoring model was trained on 3,439 patients and validated on two independent sets of 86 patients for MRD and 101 patients for monitoring. For early detection, sensitivities for stages I-IV cancers (n = 284, 129, 90, 23 respectively) were 83.1%, 86.0%, 84.4%, and 95.7%, all at 99.6% specificity (n = 2149). The diagnostic first-line procedure for tissue of origin was determined for 8 categories with a top-3 accuracy of 85% for stage I and II cancers. Detection of driver mutations for therapy selection from blood collected within 30 days of matched tumor tissue, demonstrated high concordance (PPA of 93.8%, PPV of 96.8%) using CHIP subtraction. For MRD and recurrence monitoring, the disease-free survival of patients whose cancers were predicted to have an event was significantly shorter than those predicted not to have an event using a tumor naïve approach (HR = 33.4, p < 0.005, HR = 4.39, p = 0.008, respectively). The data presented here demonstrate a unified liquid biopsy platform that uses blood-based whole-exome and transcriptome sequencing coupled with artificial intelligence to address the important clinical needs in multi-cancer early detection, monitoring of MRD and recurrent cancers, and precision selection of molecularly targeted therapies.

Indexed as

Artificial IntelligenceEarly Detection of CancerExomeNeoplasm, ResidualNeoplasmsTranscriptomeAdultExome SequencingFemaleGene Expression ProfilingHumansLiquid BiopsyMachine LearningMaleMiddle AgedAILiquid biopsyMCEDMRDWhole exomeWhole transcriptome

Identifiers

PMID40596693
PMCPMC12214926

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.