Evidence map›Paper›PMID 41418101›Full record

ArticleCancer research2026

Distinct Tumor-Immune Ecologies in Patients with Lung Cancer Predict Progression and Define a Clinical Biomarker of Therapy Response.

Sandhya Prabhakaran, Chandler D Gatenbee, Mark Robertson-Tessi, Zarifa Gahramanli Ozturk, Theresa A Boyle, Jhanelle E Gray, Scott J Antonia, Robert A Gatenby, Amer A Beg, Alexander R A Anderson

Registry-linked trialAbstract read
In one paragraph

Article in Cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02638090 (A Phase I/II Study of Pembrolizumab and Vorinostat in Patients With Immune Therapy Naïve and Immune Therapy Pretreated Stage IV NSCLC), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

NCT02638090 phase1 / phase2active not recruitingnot on this map

A Phase I/II Study of Pembrolizumab and Vorinostat in Patients With Immune Therapy Naïve and Immune Therapy Pretreated Stage IV NSCLC

TypeinterventionalSponsorH. Lee Moffitt Cancer Center and Research InstituteRan2016 to 2026Enrolled120ConditionsLung Cancer, Non-small Cell Lung CancerArmsVorinostat, Pembrolizumab
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Applications and development of in situ nucleic acid visualization techniques.Frontiers in bioengineering and biotechnology · 2026
    Review
  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

10 authors.

Sandhya PrabhakaranDepartment of Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.ORCID 0000-0002-9537-507X
Chandler D GatenbeeDepartment of Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.ORCID 0000-0002-9730-5964
Mark Robertson-TessiDepartment of Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.ORCID 0000-0003-0143-9587
Zarifa Gahramanli OzturkDepartment of Thoracic Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.ORCID 0000-0002-9353-1542
Theresa A BoyleDepartment of Pathology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.ORCID 0000-0001-5950-3970
Jhanelle E GrayDepartment of Thoracic Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.ORCID 0000-0003-1304-7062
Scott J AntoniaDepartment of Medicine, Duke University School of Medicine, Durham, North Carolina.ORCID 0000-0002-0029-9685
Robert A GatenbyDepartment of Radiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.ORCID 0000-0002-1621-1510
Amer A BegDepartment of Thoracic Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.ORCID 0000-0003-3834-774X
Alexander R A AndersonDepartment of Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.ORCID 0000-0002-2536-4383

Funding

The Delta Ecology of NSCLC TreatmentU54CA274507 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI Joel Brown · 2023 to 2026
$9.4M
Eco-Evolutionary dynamics of NSCLC to immunotherapy: Response and ResistanceU01CA232382 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI ANDERSON, ALEXANDER ROBERTSON ALLAN, ANTONIA, SCOTT J. · 2018 to 2022
$3.3M
Moffitt Cancer Center (MCC) Moffit Lung Cancer Center of ExcellenceMoffitt Cancer Center (MCC) Moffitt Center of Excellence for Evolutionary TherapyNational Cancer Institute (NCI) U01CA232382National Cancer Institute (NCI) U54CA274507NCI NIH HHS U01 CA232382NCI NIH HHS U54 CA274507
6 · The paper itself

Abstract

Multiplexed imaging of tissues is an approach that holds promise for improving early detection, diagnosis, and treatment of cancer. In this study, we investigated multiplexed histologic images of paired pretreatment and on-treatment samples from nine patients with immunotherapy-refractory non-small cell lung cancer (NSCLC) treated with an oral histone deacetylase inhibitor (vorinostat) combined with a PD-1 inhibitor (pembrolizumab). Patient responses were comprised of either stable disease (SD) or progressive disease (PD). An extensive multiplexed image analysis pipeline involving both cell segmentation and quadrats, coupled with spatial statistics, machine learning, and deep learning, was built to analyze the spatial and temporal features that predict disease progression and identify potential clinical biomarkers. Distinct spatial immune ecologies existed between SD and PD patients, and tumors from PD patients were already characterized by an immunosuppressive environment prior to treatment. Finally, the learned spatial ecologies predicted disease progression better than PD-L1 status alone, suggesting that these ecologies could be used as potential companion biomarkers with PD-L1 in NSCLC. These findings will be investigated in a larger cohort study generated from an ongoing clinical trial (NCT02638090) that includes a wider range of responses, including complete and partial responders. Together, this study developed a computational infrastructure for analyzing multiplex imaging to predict immunotherapy response in NSCLC, which can potentially be generalized to any type of cancer. SIGNIFICANCE: Integration of multiplexed imaging, spatial statistics, and machine learning identifies distinct tumor-immune ecologies that differentiate immunotherapy responders from nonresponders, improving the prediction of progression to guide precision therapy. This article is part of a special series: Driving Cancer Discoveries with Computational Research, Data Science, and Machine Learning/AI .

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungLung NeoplasmsTumor MicroenvironmentAgedAntineoplastic Combined Chemotherapy ProtocolsDisease ProgressionFemaleHumansImmune Checkpoint InhibitorsMachine LearningMaleMiddle AgedPrognosisBiomarkers, TumorImmune Checkpoint Inhibitors

Identifiers

PMID41418101
PMCPMC12871056

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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.