Evidence map›Paper›PMID 36927889›Full record

ArticleScientific reports2023

Predicting EGFR mutational status from pathology images using a real-world dataset.

James J Pao, Mikayla Biggs, Daniel Duncan, Douglas I Lin, Richard Davis, Richard S P Huang, Donna Ferguson, Tyler Janovitz, Matthew C Hiemenz, Nathanial R Eddy and 5 more

Open access · goldFull text read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
7.3field-weighted citation impact, top 2% of its field
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

23 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Genomic Characterization of Lung Cancer in Never-Smokers Using Deep Learning.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2026
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  19. Using Vision Transformer for high robustness and generalization in predicting EGFR mutation status in lung adenocarcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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  20. Review
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

15 authors at 1 institution.

James J PaoFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Mikayla BiggsFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Daniel DuncanFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Douglas I LinFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Richard DavisFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Richard S P HuangFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Donna FergusonFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Tyler JanovitzFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Matthew C HiemenzFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Nathanial R EddyFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Erik LehnertFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Moran N CabiliFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Garrett M FramptonFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Priti S HegdeFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA.
Lee A AlbackerFoundation Medicine Inc., 150 Second Street, Cambridge, MA, USA. lalbacker@foundationmedicine.com.
Foundation Medicine (United States)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment of non-small cell lung cancer is increasingly biomarker driven with multiple genomic alterations, including those in the epidermal growth factor receptor (EGFR) gene, that benefit from targeted therapies. We developed a set of algorithms to assess EGFR status and morphology using a real-world advanced lung adenocarcinoma cohort of 2099 patients with hematoxylin and eosin (H&E) images exhibiting high morphological diversity and low tumor content relative to public datasets. The best performing EGFR algorithm was attention-based and achieved an area under the curve (AUC) of 0.870, a negative predictive value (NPV) of 0.954 and a positive predictive value (PPV) of 0.410 in a validation cohort reflecting the 15% prevalence of EGFR mutations in lung adenocarcinoma. The attention model outperformed a heuristic-based model focused exclusively on tumor regions, and we show that although the attention model also extracts signal primarily from tumor morphology, it extracts additional signal from non-tumor tissue regions. Further analysis of high-attention regions by pathologists showed associations of predicted EGFR negativity with solid growth patterns and higher peritumoral immune presence. This algorithm highlights the potential of deep learning tools to provide instantaneous rule-out screening for biomarker alterations and may help prioritize the use of scarce tissue for biomarker testing.

Indexed as

Adenocarcinoma of LungCarcinoma, Non-Small-Cell LungLung NeoplasmsErbB ReceptorsHumansMutationRetrospective StudiesEGFR protein, humanErbB Receptors

Identifiers

PMID36927889
PMCPMC10020556
OpenAlexW4327568832

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read23
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.