Evidence map›Paper›PMID 39369769›Full record

ReviewCancer letters2024

Therapeutic potential of tumor-infiltrating lymphocytes in non-small cell lung cancer.

Daniel R Plaugher, Avery R Childress, Christian M Gosser, Dave-Preston Esoe, Kassandra J Naughton, Zhonglin Hao, Christine F Brainson

Abstract readReview
In one paragraph

Review in Cancer letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
–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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  11. Clinicopathological and Genomic Analysis ofCancer management and research · 2026
    Article
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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

7 authors.

Daniel R PlaugherDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA. Electronic address: plaugher_dr@uky.edu.
Avery R ChildressDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA.
Christian M GosserDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA.
Dave-Preston EsoeDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA.
Kassandra J NaughtonDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA.
Zhonglin HaoDepartment of Internal Medicine - Medical Oncology, University of Kentucky, Lexington, KY, 40536, USA; Markey Cancer Center, University of Kentucky, Lexington, KY, 40536, USA.
Christine F BrainsonDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA; Markey Cancer Center, University of Kentucky, Lexington, KY, 40536, USA. Electronic address: cfbrainson@uky.edu.

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers · 2013 to 2026
$38.3M
University of Kentucky Center for Cancer MetabolismP20GM121327 · NIGMS · UNIVERSITY OF KENTUCKY · PI Jianhang Jia · 2017 to 2026
$25.0M
Interdisciplinary Research Training in Cancer BiologyT32CA165990 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers, KATHLEEN L. O'CONNOR · 2013 to 2026
$3.2M
Aberrant Glycogen in Lung Adenocarcinoma TumorigenesisR01CA266004 · NCI · UNIVERSITY OF KENTUCKY · PI Matthew S. Gentry, Ramon C. Sun · 2022 to 2026
$2.6M
Targeting Lung Fibrosis Using Epigenetic TherapyR01HL170193 · NHLBI · UNIVERSITY OF KENTUCKY · PI Christine Fillmore Brainson · 2024 to 2026
$2.1M
Targeting Epigenetic Heterogeneity to Improve Lung Cancer Immunotherapy ResponseR01CA237643 · NCI · UNIVERSITY OF KENTUCKY · PI BRAINSON, CHRISTINE FILLMORE · 2019 to 2023
$1.9M
Targeting Glycogen Metabolism in Ewing's Sarcoma: Diagnostic, Prognostic, and Therapeutic ApplicationsR01CA288696 · NCI · UNIVERSITY OF FLORIDA · PI Matthew S. Gentry, Ramon C. Sun · 2024 to 2026
$1.8M
NCI NIH HHS P30 CA177558NCI NIH HHS R01 CA237643NCI NIH HHS R01 CA266004NCI NIH HHS R01 CA288696NCI NIH HHS T32 CA165990NHLBI NIH HHS R01 HL170193NIGMS NIH HHS P20 GM121327
6 · The paper itself

Abstract

Lung cancer is the leading cause of cancer-related death worldwide, with poor outcomes even for those diagnosed at early stages. Current standard-of-care for most non-small cell lung cancer (NSCLC) patients involves an array of chemotherapy, radiotherapy, immunotherapy, targeted therapy, and surgical resection depending on the stage and location of the cancer. While patient outcomes have certainly improved, advances in highly personalized care remain limited. However, there is growing excitement around harnessing the power of tumor-infiltrating lymphocytes (TILs) through the use of adoptive cell transfer (ACT) therapy. These TILs are naturally occurring, may already recognize tumor-specific antigens, and can have direct anti-cancer effect. In this review, we highlight comparisons of various ACTs, including a brief TIL history, show current advances and successes of TIL therapy in NSCLC, discuss the potential roles for epigenetics in T cell expansion, and highlight challenges and future directions of the field to combat NSCLC in a personalized manner.

Indexed as

Carcinoma, Non-Small-Cell LungImmunotherapy, AdoptiveLung NeoplasmsLymphocytes, Tumor-InfiltratingEpigenesis, GeneticHumansAdoptive cell transferNon-small cell lung cancerTumor-infiltrating lymphocytes

Identifiers

PMID39369769
PMCPMC11560632

What OpenQuestion holds

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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.