Evidence map›Paper›PMID 40568160›Full record

ArticlebioRxiv : the preprint server for biology2025

Path2Omics: Enhanced transcriptomic and methylation prediction accuracy from tumor histopathology.

Danh-Tai Hoang, Eldad D Shulman, Saugato Rahman Dhruba, Nishanth Ulhas Nair, Ranjan K Barman, H Lalchungnunga, Omkar Singh, MacLean P Nasrallah, Eric A Stone, Kenneth Aldape and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Danh-Tai HoangCancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0003-2640-4196
Eldad D ShulmanCancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0002-1859-8819
Saugato Rahman DhrubaCancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Nishanth Ulhas NairCancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Ranjan K BarmanCancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
H LalchungnungaLaboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Omkar SinghLaboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
MacLean P NasrallahDivision of Neuropathology, Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Eric A StoneBiological Data Science Institute, College of Science, Australian National University, Canberra, ACT, Australia.
Kenneth AldapeLaboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Eytan RuppinCancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0002-7862-3940

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precision oncology is becoming increasingly integral to clinical practice, demonstrating notable improvements in treatment outcomes. While molecular data provide comprehensive insights, obtaining such data remains costly and time-consuming. To address this challenge, we developed Path2Omics, a deep learning model that predicts gene expression and methylation from histopathology for 23 cancer types. Path2Omics was trained on 20,497 slides (9,456 formalin-fixed and paraffin-embedded (FFPE) and 11,041 fresh frozen (FF)) from 8,007 patients across 23 The Cancer Genome Atlas cohorts. When tested on FFPE slides, the most readily available format in clinical pathology practice, the integrated model outperformed its individual FF and FFPE components, robustly predicting nearly 5,000 genes on average, approximately five times more than our recently published DeepPT model. Externally evaluated on seven independent cohorts, Path2Omics robustly predicted the expression of approximately 4,400 genes, yielding a 30% increase over the FFPE model alone. Finally, we demonstrate that the inferred gene expression is nearly as effective as the actual values in predicting patient survival and treatment response. These results lay the basis for using Path2Omics to advance precision oncology from histopathology slides in a speedy and cost-effective manner.

Identifiers

PMID40568160
PMCPMC12190742

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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.