Evidence map›Paper›PMID 37790315›Full record

ArticleResearch square2023

Prediction of cancer treatment response from histopathology images through imputed transcriptomics.

Danh-Tai Hoang, Gal Dinstag, Leandro C Hermida, Doreen S Ben-Zvi, Efrat Elis, Katherine Caley, Stephen-John Sammut, Sanju Sinha, Neelam Sinha, Christopher H Dampier and 20 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors at 11 institutions in 8 countries.

Danh-Tai HoangBiological Data Science Institute, College of Science, Australian National University, Canberra, ACT, Australia.
Gal DinstagPangea Biomed Ltd., Tel Aviv, Israel.
Leandro C HermidaDepartment of Immunology, University of Pittsburgh, Pittsburgh, PA, USA.
Doreen S Ben-ZviPangea Biomed Ltd., Tel Aviv, Israel.ORCID 0000-0002-8609-1286
Efrat ElisPangea Biomed Ltd., Tel Aviv, Israel.
Katherine CaleyBiological Data Science Institute, College of Science, Australian National University, Canberra, ACT, Australia.ORCID 0000-0002-8459-6168
Stephen-John SammutBreast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, United Kingdom.
Sanju SinhaCancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0002-2688-0603
Neelam SinhaCancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Christopher H DampierLaboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0003-3099-6462
Chani StosselOncology Institute, Sheba Medical Center at Tel-Hashomer, Tel Aviv University, Tel Aviv, Israel.
Tejas PatilDivision of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Arun RajanThoracic and GI Malignancies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0003-2776-3385
Wiem LassouedCenter for Immuno-Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Julius StraussCenter for Immuno-Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Shania BaileyCenter for Immuno-Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Clint AllenSurgical Oncology Program, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0001-6586-5804
Jason RedmanCenter for Immuno-Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Tuvik BekerPangea Biomed Ltd., Tel Aviv, Israel.
Peng JiangCancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0002-7828-5486
Talia GolanOncology Institute, Sheba Medical Center at Tel-Hashomer, Tel Aviv University, Tel Aviv, Israel.
Scott WilkinsonLaboratory of Genitourinary Cancer Pathogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0002-2613-8425
Adam G SowalskyLaboratory of Genitourinary Cancer Pathogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0003-2760-1853
Sharon R PineDivision of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.ORCID 0000-0001-5318-0277
Carlos CaldasCancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, Cambridge, UK.ORCID 0000-0003-3547-1489
James L GulleyGenitourinary Malignancy Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0002-6569-2912
Kenneth AldapeLaboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0001-5119-7550
Ranit AharonovPangea Biomed Ltd., Tel Aviv, Israel.
Eric A StoneBiological Data Science Institute, College of Science, Australian National University, Canberra, ACT, Australia.
Eytan RuppinCancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.ORCID 0000-0002-7862-3940
National Cancer Institute · USPan-European University · SKCancer Institute (WIA) · INNational Institutes of Health · USAustralian National University · AUTel Aviv University · ILUniversity of Colorado Anschutz Medical Campus · USInstitut de Recherche Vaccinale · FRInstitute of Cancer Research · GBUniversity of Cambridge · GBUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in artificial intelligence have paved the way for leveraging hematoxylin and eosin (H&E)-stained tumor slides for precision oncology. We present ENLIGHT-DeepPT, an approach for predicting response to multiple targeted and immunotherapies from H&E-slides. In difference from existing approaches that aim to predict treatment response directly from the slides, ENLIGHT-DeepPT is an indirect two-step approach consisting of (1) DeepPT, a new deep-learning framework that predicts genome-wide tumor mRNA expression from slides, and (2) ENLIGHT, which predicts response based on the DeepPT inferred expression values. DeepPT successfully predicts transcriptomics in all 16 TCGA cohorts tested and generalizes well to two independent datasets. Our key contribution is showing that ENLIGHT-DeepPT successfully predicts true responders in five independent patients' cohorts involving four different treatments spanning six cancer types with an overall odds ratio of 2.44, increasing the baseline response rate by 43.47% among predicted responders, without the need for any treatment data for training. Furthermore, its prediction accuracy on these datasets is comparable to a supervised approach predicting the response directly from the images, which needs to be trained and tested on the same cohort. ENLIGHT-DeepPT future application could provide clinicians with rapid treatment recommendations to an array of different therapies and importantly, may contribute to advancing precision oncology in developing countries.

Identifiers

PMID37790315
PMCPMC10543028
OpenAlexW4386763722

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.