Evidence map›Paper›PMID 38310164›Full record

ArticleNPJ precision oncology2024

Deep representation learning of tissue metabolome and computed tomography annotates NSCLC classification and prognosis.

Marc Boubnovski Martell, Kristofer Linton-Reid, Sumeet Hindocha, Mitchell Chen, Paula Moreno, Marina Álvarez-Benito, Ángel Salvatierra, Richard Lee, Joram M Posma, Marco A Calzado and 1 more

Open access · goldAbstract read
In one paragraph

Article in NPJ precision oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

11 authors at 3 institutions in 2 countries.

Marc Boubnovski MartellImperial College London Hammersmith Campus, London, SW7 2AZ, UK.
Kristofer Linton-ReidImperial College London Hammersmith Campus, London, SW7 2AZ, UK.
Sumeet HindochaEarly Diagnosis and Detection Centre, National Institute for Health and Care Research Biomedical Research Centre at the Royal Marsden and Institute of Cancer Research, London, SW3 6JJ, UK.
Mitchell ChenImperial College London Hammersmith Campus, London, SW7 2AZ, UK.ORCID http://orcid.org/0000-0002-3779-5615
Paula MorenoInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, 14004, Spain.
Marina Álvarez-BenitoInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, 14004, Spain.
Ángel SalvatierraInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, 14004, Spain.
Richard LeeEarly Diagnosis and Detection Centre, National Institute for Health and Care Research Biomedical Research Centre at the Royal Marsden and Institute of Cancer Research, London, SW3 6JJ, UK.ORCID http://orcid.org/0000-0001-8368-3406
Joram M PosmaImperial College London Hammersmith Campus, London, SW7 2AZ, UK.ORCID http://orcid.org/0000-0002-4971-9003
Marco A CalzadoInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, 14004, Spain. bq2cacam@uco.es.
Eric O AboagyeImperial College London Hammersmith Campus, London, SW7 2AZ, UK. eric.aboagye@imperial.ac.uk.ORCID http://orcid.org/0000-0003-2276-6771
Hammersmith Hospital · GBInstituto Maimónides de Investigación Biomédica de Córdoba · ESInstitute of Cancer Research · GB

Funding

Medical Research Council MR/M015858/1
6 · The paper itself

Abstract

The rich chemical information from tissue metabolomics provides a powerful means to elaborate tissue physiology or tumor characteristics at cellular and tumor microenvironment levels. However, the process of obtaining such information requires invasive biopsies, is costly, and can delay clinical patient management. Conversely, computed tomography (CT) is a clinical standard of care but does not intuitively harbor histological or prognostic information. Furthermore, the ability to embed metabolome information into CT to subsequently use the learned representation for classification or prognosis has yet to be described. This study develops a deep learning-based framework -- tissue-metabolomic-radiomic-CT (TMR-CT) by combining 48 paired CT images and tumor/normal tissue metabolite intensities to generate ten image embeddings to infer metabolite-derived representation from CT alone. In clinical NSCLC settings, we ascertain whether TMR-CT results in an enhanced feature generation model solving histology classification/prognosis tasks in an unseen international CT dataset of 742 patients. TMR-CT non-invasively determines histological classes - adenocarcinoma/squamous cell carcinoma with an F1-score = 0.78 and further asserts patients' prognosis with a c-index = 0.72, surpassing the performance of radiomics models and deep learning on single modality CT feature extraction. Additionally, our work shows the potential to generate informative biology-inspired CT-led features to explore connections between hard-to-obtain tissue metabolic profiles and routine lesion-derived image data.

Identifiers

PMID38310164
PMCPMC10838282
OpenAlexW4391514686

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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.