Evidence map›Paper›PMID 37264091›Full record

ArticleNPJ precision oncology2023

Deep computational image analysis of immune cell niches reveals treatment-specific outcome associations in lung cancer.

Cristian Barrera, Germán Corredor, Vidya Sankar Viswanathan, Ruiwen Ding, Paula Toro, Pingfu Fu, Christina Buzzy, Cheng Lu, Priya Velu, Philipp Zens and 11 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in NPJ precision oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01673867 (An Open-Label Randomized Phase III Trial of BMS-936558), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
8.7field-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.

NCT01673867 phase3completednot on this map

An Open-Label Randomized Phase III Trial of BMS-936558 (Nivolumab) Versus Docetaxel in Previously Treated Metastatic Non-squamous Non-small Cell Lung Cancer (NSCLC)

TypeinterventionalSponsorBristol-Myers SquibbRan2012 to 2021Enrolled582ConditionsNon-Squamous Cell Non-small Cell Lung CancerArmsNivolumab, Docetaxel
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  4. Advancements and future trends in machine learning for lung cancer: a comprehensive bibliometric analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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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

21 authors at 11 institutions in 4 countries.

Cristian BarreraDepartment of Biomedical Engineering, School of Medicine, Emory University, Atlanta, GA, USA.
Germán CorredorDepartment of Biomedical Engineering, School of Medicine, Emory University, Atlanta, GA, USA.ORCID http://orcid.org/0000-0003-3002-0937
Vidya Sankar ViswanathanDepartment of Biomedical Engineering, School of Medicine, Emory University, Atlanta, GA, USA.
Ruiwen DingCase Western Reserve University, School of Engineering, Cleveland, OH, USA.
Paula ToroCleveland Clinic, Cleveland, OH, USA.
Pingfu FuDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, OH, USA.ORCID http://orcid.org/0000-0002-2334-5218
Christina BuzzyCase Western Reserve University, School of Engineering, Cleveland, OH, USA.
Cheng LuDepartment of Biomedical Engineering, School of Medicine, Emory University, Atlanta, GA, USA.
Priya VeluWeill Cornell Medical College, New York, NY, USA.
Philipp ZensInstitute of Pathology, University of Bern, Bern, Switzerland.
Sabina BerezowskaInstitute of Pathology, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0001-5442-9791
Merzu BeleteBristol Myers Squibb, New York, NY, USA.
David BalliBristol Myers Squibb, New York, NY, USA.
Han ChangBristol Myers Squibb, New York, NY, USA.
Vipul BaxiBristol Myers Squibb, New York, NY, USA.
Konstantinos SyrigosSchool of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
David L RimmSchool of Medicine, Yale University, New Haven, CT, USA.ORCID http://orcid.org/0000-0001-5820-4397
Vamsidhar VelchetiNew York University, New York, NY, USA.
Kurt SchalperSchool of Medicine, Yale University, New Haven, CT, USA.
Eduardo RomeroUniversidad Nacional de Colombia, Facultad de Medicina, Bogotá, Colombia.
Anant MadabhushiDepartment of Biomedical Engineering, School of Medicine, Emory University, Atlanta, GA, USA. anantm@emory.edu.ORCID http://orcid.org/0000-0002-5741-0399
Emory University · USBristol-Myers Squibb (United States) · USUniversity of Bern · CHUniversity School · USYale University · USCase Western Reserve University · USCleveland Clinic · USCornell University · USNational and Kapodistrian University of Athens · GRNew York University · USUniversidad Nacional de Colombia · CO

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
GALANIN IN ALZHEIMER'S DISEASER01AG010668 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI MUFSON, ELLIOTT JAY · 1991 to 2011
$4.1M
BIOMEDICAL ENGINEERING RESEARCH FACILITIESC06RR012463 · NCRR · CASE WESTERN RESERVE UNIVERSITY · PI KUTINA, KENNETH L · 1997 to 1997
–
NCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

The tumor immune composition influences prognosis and treatment sensitivity in lung cancer. The presence of effective adaptive immune responses is associated with increased clinical benefit after immune checkpoint blockers. Conversely, immunotherapy resistance can occur as a consequence of local T-cell exhaustion/dysfunction and upregulation of immunosuppressive signals and regulatory cells. Consequently, merely measuring the amount of tumor-infiltrating lymphocytes (TILs) may not accurately reflect the complexity of tumor-immune interactions and T-cell functional states and may not be valuable as a treatment-specific biomarker. In this work, we investigate an immune-related biomarker (PhenoTIL) and its value in associating with treatment-specific outcomes in non-small cell lung cancer (NSCLC). PhenoTIL is a novel computational pathology approach that uses machine learning to capture spatial interplay and infer functional features of immune cell niches associated with tumor rejection and patient outcomes. PhenoTIL's advantage is the computational characterization of the tumor immune microenvironment extracted from H&E-stained preparations. Association with clinical outcome and major non-small cell lung cancer (NSCLC) histology variants was studied in baseline tumor specimens from 1,774 lung cancer patients treated with immunotherapy and/or chemotherapy, including the clinical trial Checkmate 057 (NCT01673867).

Identifiers

PMID37264091
PMCPMC10235089
OpenAlexW4379052971

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.