Evidence map›Paper›PMID 40622275›Full record

ArticleCancer research communications2025

Impact of Glucocorticoids on Immune Checkpoint Inhibitor Efficacy and Circulating Biomarkers in Non-Small Cell Lung Cancer Patients.

Lauren Polyakov, Angelina Lim, Alexandra Meyer, Aubree Mades, Joshua Ni, Ryan Cooper, Shirley Ye, Ryutaro Kajihara, Takaaki Oba, Leslie Contreras and 10 more

Abstract read
In one paragraph

Article in Cancer research communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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.

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

13 citing papers in PubMed.

  1. Article
  2. Review
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  5. Article
  6. Article
  7. The management of rheumatic immune related adverse events.Best practice & research. Clinical rheumatology · 2026
    Review
  8. 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

20 authors.

Lauren PolyakovDepartment of Surgery, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0009-0009-9682-9772
Angelina LimDepartment of Surgery, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0000-0001-5508-0392
Alexandra MeyerDepartment of Surgery, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0009-0008-3220-5445
Aubree MadesDepartment of Medicine, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0000-0003-4707-9505
Joshua NiDepartment of Surgery, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0009-0009-8572-9418
Ryan CooperDepartment of Medicine, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0000-0002-5473-2392
Shirley YeDepartment of Medicine, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0009-0002-0126-6962
Ryutaro KajiharaCenter for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0003-0908-2543
Takaaki ObaCenter for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0001-8283-4989
Leslie ContrerasDepartment of Surgery, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0009-0009-4631-2855
Eihab AbdelfatahDepartment of Surgical Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0002-5503-8685
Joy SarkarDepartment of Surgical Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0002-7920-1926
Junko MatsuzakiCenter for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0002-2555-1234
Ming LiDepartment of Population and Public Health Sciences, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0009-0007-4563-6917
Rajeev SharmaDepartment of Medicine, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, The State University of New York, Buffalo, New York.ORCID 0000-0003-1342-7153
Brahm H SegalDepartment of Medicine, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, The State University of New York, Buffalo, New York.ORCID 0000-0001-5043-7380
Robert C HsuDepartment of Medicine, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0000-0003-3957-6106
Hongbin ChenDepartment of Medicine, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, The State University of New York, Buffalo, New York.ORCID 0000-0002-5086-4769
Jorge NievaDepartment of Medicine, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0000-0003-1605-4719
Fumito ItoDepartment of Surgery, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California.ORCID 0000-0002-6866-671X

Funding

USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Fumito Ito · 1985 to 2026
$181.4M
Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
Novel immunological biomarkers ovarian cancer prognosisR01CA188900 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MOYSICH, KIRSTEN B., SEGAL, BRAHM H. · 2015 to 2019
$3.3M
Targeting complement to enhance antitumor immunity and control malignant effusions in patients with recurrent epithelial ovarian cancerR01CA267690 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Brahm H. Segal, Emese Zsiros · 2022 to 2026
$3.3M
Lung Cancer Early Detection and Immunotherapy Response Prediction and Monitoring with an Exo-PROS Liquid Biopsy AssayR01CA272827 · NCI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI DY, GRACE, ITO, FUMITO · 2022 to 2025
$3.1M
In situ radioimmunotherapy to maximize the engagement of conventional type 1 dendritic cells against non-T cell-inflamed tumorsR01CA255240 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ITO, FUMITO · 2021 to 2025
$2.0M
USC/CHLA Summer Oncology Research Fellowship (SORF) Program for Medical StudentsR25CA225513 · NCI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI ANAT ERDREICH-EPSTEIN, WIJBE MARTIN KAST · 2019 to 2026
$1.7M
Adoptive Cell Therapy with Rejuvenated Antigen-Specific T CellsK08CA197966 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ITO, FUMITO · 2015 to 2019
$875k
NCI NIH HHS K08 CA197966NCI NIH HHS P30 CA014089NCI NIH HHS P30 CA016056NCI NIH HHS R01 CA188900NCI NIH HHS R01 CA255240NCI NIH HHS R01 CA267690NCI NIH HHS R01 CA272827NCI NIH HHS R25 CA225513
6 · The paper itself

Abstract

Corticosteroids are frequently prescribed to patients with non-small cell lung cancer (NSCLC) for palliation of cancer-related symptoms; however, the potential impact of baseline steroid use on immune checkpoint inhibitor (ICI) therapy and its underlying mechanisms remain unclear. In this study, we evaluated clinical outcomes of 277 patients with NSCLC treated with ICI therapy at two academic institutions. Twenty-one patients (8%) were taking steroids at the start of ICIs. Patients on baseline steroids had a lower overall response rate with markedly shorter progression-free survival and overall survival compared with those not receiving steroids. In multivariate analysis, steroid use was the only significant independent risk factor for disease progression and mortality in both independent cohorts, Roswell Park Comprehensive Cancer Center (n = 88) and University of Southern California (n = 189). A baseline peripheral blood neutrophil-to-lymphocyte ratio <5 was a strong prognostic indicator; however, the prognostic value of neutrophil-to-lymphocyte ratio was absent in patients receiving steroids. Additionally, the baseline frequency of circulating CX3CR1+CD8+ T cells was substantially lower in patients on steroids. Using a bedside-to-bench approach, we found that concurrent steroid use significantly decreased antitumor efficacy of anti-PD-1 therapy and attenuated the increase of CX3CR1+CD8+ T cells in mice bearing MC38 tumors whereas discontinuation of steroid at the start of treatment did not make a negative impact on survival. Collectively, baseline steroid use was associated with worse outcomes and decreased frequency of circulating differentiated effector T cells in patients with NSCLC. Caution should be taken when interpreting the results from circulating immune-related biomarkers in patients on steroids. SIGNIFICANCE: The impact of corticosteroids, widely prescribed for palliation of cancer-related symptoms, on ICI therapy remains unclear. This study shows that baseline steroid use is a negative independent prognostic factor in patients with NSCLC undergoing ICI therapy and provides insights into the decreased T-cell effector differentiation and utility of predictive blood-based markers by steroids.

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungGlucocorticoidsImmune Checkpoint InhibitorsLung NeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPrognosisBiomarkers, TumorGlucocorticoidsImmune Checkpoint Inhibitors

Identifiers

PMID40622275
PMCPMC12232904

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Registered trials

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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.