Evidence map›Paper›PMID 37285559›Full record

ArticleJCO precision oncology2023

Distinguishing Renal Cell Carcinoma From Normal Kidney Tissue Using Mass Spectrometry Imaging Combined With Machine Learning.

Vishnu Shankar, Kanchustambham Vijayalakshmi, Rosalie Nolley, Geoffrey A Sonn, Chia-Sui Kao, Hongjuan Zhao, Ru Wen, Livia S Eberlin, Robert Tibshirani, Richard N Zare and 1 more

Open access · greenAbstract read
In one paragraph

Article in JCO precision oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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 2 institutions in 1 country.

Vishnu ShankarProgram in Immunology, Stanford University School of Medicine, Stanford, CA.ORCID 0000-0001-9323-9034
Kanchustambham VijayalakshmiDepartment of Chemistry, Stanford University, Stanford, CA.ORCID 0000-0002-2927-1045
Rosalie NolleyDepartment of Urology, Stanford University School of Medicine, Stanford, CA.
Geoffrey A SonnDepartment of Urology, Stanford University School of Medicine, Stanford, CA.ORCID 0000-0002-0850-1956
Chia-Sui KaoDepartment of Pathology, Stanford University School of Medicine, Stanford, CA.
Hongjuan ZhaoDepartment of Urology, Stanford University School of Medicine, Stanford, CA.
Ru WenDepartment of Urology, Stanford University School of Medicine, Stanford, CA.
Livia S EberlinDepartment of Surgery, Baylor College of Medicine, Houston, TX.
Robert TibshiraniDepartment of Biomedical Data Science, and Statistics, Stanford University, Stanford, CA.
Richard N ZareDepartment of Chemistry, Stanford University, Stanford, CA.ORCID 0000-0001-5266-4253
James D BrooksDepartment of Urology, Stanford University School of Medicine, Stanford, CA.ORCID 0000-0003-4521-7505
Stanford University · USBaylor College of Medicine · US

Funding

DESI-MS detection of positive margins in kidney cancerR21CA229933 · NCI · STANFORD UNIVERSITY · PI BROOKS, JAMES D., ZARE, RICHARD N · 2018 to 2019
$369k
NCI NIH HHS R21 CA229933
6 · The paper itself

Abstract

purposeAccurately distinguishing renal cell carcinoma (RCC) from normal kidney tissue is critical for identifying positive surgical margins (PSMs) during partial and radical nephrectomy, which remains the primary intervention for localized RCC. Techniques that detect PSM with higher accuracy and faster turnaround time than intraoperative frozen section (IFS) analysis can help decrease reoperation rates, relieve patient anxiety and costs, and potentially improve patient outcomes. MATERIALS AND

methodsHere, we extended our combined desorption electrospray ionization mass spectrometry imaging (DESI-MSI) and machine learning methodology to identify metabolite and lipid species from tissue surfaces that can distinguish normal tissues from clear cell RCC (ccRCC), papillary RCC (pRCC), and chromophobe RCC (chRCC) tissues.

resultsFrom 24 normal and 40 renal cancer (23 ccRCC, 13 pRCC, and 4 chRCC) tissues, we developed a multinomial lasso classifier that selects 281 total analytes from over 27,000 detected molecular species that distinguishes all histological subtypes of RCC from normal kidney tissues with 84.5% accuracy. On the basis of independent test data reflecting distinct patient populations, the classifier achieves 85.4% and 91.2% accuracy on a Stanford test set (20 normal and 28 RCC) and a Baylor-UT Austin test set (16 normal and 41 RCC), respectively. The majority of the model's selected features show consistent trends across data sets affirming its stable performance, where the suppression of arachidonic acid metabolism is identified as a shared molecular feature of ccRCC and pRCC.

conclusionTogether, these results indicate that signatures derived from DESI-MSI combined with machine learning may be used to rapidly determine surgical margin status with accuracies that meet or exceed those reported for IFS.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsHumansKidneyMachine LearningMass Spectrometry

Identifiers

PMID37285559
PMCPMC10309512
OpenAlexW4379742970

What OpenQuestion holds

Textmetadata
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.