Evidence map›Paper›PMID 38886156›Full record

ArticleThe oncologist2024

Investigating risk factors and treatment options for severe, partially steroid responsive, and steroid-refractory checkpoint inhibitor pneumonitis.

Meghana Moodabagil, Robert Easterling, Jing Peng, Hamzah Abu-Sbeih, Alexa Meara, Edwin Donnelly, Dwight H Owen, Kevin Ho

Abstract read
In one paragraph

Article in The oncologist, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

8 authors.

Meghana MoodabagilDepartment of Internal Medicine, The Ohio State Wexner Medical Center, Columbus, OH 43210, United States.
Robert EasterlingDepartment of Pulmonary, Critical Care, and Sleep Medicine, Medical University of South Carolina, Charlestown, SC 29425, United States.
Jing PengCenter for Biostatistics, The Ohio State University, James Comprehensive Cancer Center, Columbus, OH 43210, United States.
Hamzah Abu-SbeihDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University, James Comprehensive Cancer Center, Columbus, OH 43210, United States.ORCID 0000-0003-3577-6741
Alexa MearaDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University, James Comprehensive Cancer Center, Columbus, OH 43210, United States.ORCID 0000-0002-8406-3556
Edwin DonnellyDivision of Radiology, The Ohio State Wexner Medical Center, Columbus, OH 43210, United States.ORCID 0000-0003-0740-3075
Dwight H OwenDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University, James Comprehensive Cancer Center, Columbus, OH 43210, United States.ORCID 0000-0002-6598-4886
Kevin HoDivision of Pulmonary, Critical Care, and Sleep Medicine, The Ohio State Wexner Medical Center, Columbus, OH 43210, United States.ORCID 0000-0002-9803-4465

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) have revolutionized cancer care with incredible reductions in mortality. One of the most devastating complications of treatment is ICI-related pneumonitis (ICI-p). Despite this, little is known regarding risk factors for severe pneumonitis and treatment effectiveness of various therapeutic options for steroid-refractory disease. To address this, we conducted a retrospective study on patients with cancer who developed ICI-p.

methodsWe examined consecutive patients who received ICIs and developed ICI-p. Risk factors of interest for severe disease and steroid-refractory ICI-p, including pre-treatment pulmonary function tests (PFTs) and chest imaging, were compared between patients with severe (grades 3-5) and mild (grades 1-2) pneumonitis. The clinical and treatment courses for patients with steroid-refractory ICI-p were recorded.

resultsA total of 132 patients developed ICI-p, with 60 patients having mild and 72 with severe disease. We found that lower forced vital capacity percent predicted (66.24 vs 85.05, P = .05), lower total lung capacity percent predicted (85.23 vs 99.71, P = .13), and specific radiographic patterns on pre-treatment chest imaging were predictors of severe disease. Initial corticosteroid dose of less than 1 milligram per kilogram prednisone equivalent (P = .14) was correlated with partially steroid-responsive or steroid-refractory ICI-p. Ten patients had steroid refractory ICI-p, and those who received IVIG alone as the immune suppressant beyond corticosteroids had improved survival (P = 05).

conclusionsWe are the first to identify pre-treatment PFTs and chest imaging abnormalities as risk factors for severe ICI-p. We also found that lower corticosteroid doses were associated with partially steroid-responsive and steroid-refractory ICI-p. Larger, prospective studies are needed to validate our results.

Indexed as

Immune Checkpoint InhibitorsPneumoniaAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedNeoplasmsRetrospective StudiesRisk FactorsSteroidsImmune Checkpoint InhibitorsSteroidscheckpoint inhibitor pneumonitisimmune checkpoint inhibitorsimmune-related adverse eventssteroid refractory pneumonitis

Identifiers

PMID38886156
PMCPMC11546723

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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.