Evidence map›Paper›PMID 42502949›Full record

ArticleThoracic cancer2026

Tumor Necrosis on Routine Pretreatment CT as a Potential Prognostic Marker in Advanced NSCLC Treated With Immune Checkpoint Inhibitor Monotherapy: A Two-Center Retrospective Study.

Eiji Takeuchi, Hirokazu Ogino, Kensuke Kondo, Yoshio Okano, Hiroki Takahashi, Kaori Nii, Yugo Matsumura, Takuya Ishida, Seiya Ichihara, Michihiro Kunishige and 8 more

Abstract readMulticenter Study
In one paragraph

Article in Thoracic cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Eiji TakeuchiDepartment of Clinical Investigation, National Hospital Organization Kochi Hospital, Kochi, Japan.ORCID https://orcid.org/0000-0003-1541-9747
Hirokazu OginoDepartment of Respiratory Medicine and Rheumatology, Graduate School of Biomedical Sciences, Tokushima University, Tokushima, Japan.ORCID https://orcid.org/0000-0002-2446-8789
Kensuke KondoDepartment of Respiratory Medicine and Rheumatology, Graduate School of Biomedical Sciences, Tokushima University, Tokushima, Japan.
Yoshio OkanoDepartment of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.
Hiroki TakahashiDepartment of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.
Kaori NiiDepartment of Community Medicine for Respirology, Graduate School of Biomedical Sciences, Tokushima University, Tokushima, Japan.
Yugo MatsumuraDepartment of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.
Takuya IshidaDepartment of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.
Seiya IchiharaDepartment of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.
Michihiro KunishigeDepartment of Respiratory Medicine and Rheumatology, Graduate School of Biomedical Sciences, Tokushima University, Tokushima, Japan.
Naoki KadotaDepartment of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.
Hisanori MachidaDepartment of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.
Nobuo HatakeyamaDepartment of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.
Keishi NaruseDepartment of Pathology, National Hospital Organization Kochi Hospital, Kochi, Japan.
Seidai SatoDepartment of Respiratory Medicine and Rheumatology, Graduate School of Biomedical Sciences, Tokushima University, Tokushima, Japan.
Hiroshi NokiharaDepartment of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, Japan.
Tsutomu ShinoharaDepartment of Community Medicine for Respirology, Graduate School of Biomedical Sciences, Tokushima University, Tokushima, Japan.ORCID https://orcid.org/0000-0002-1562-2043
Yasuhiko NishiokaDepartment of Respiratory Medicine and Rheumatology, Graduate School of Biomedical Sciences, Tokushima University, Tokushima, Japan.ORCID https://orcid.org/0000-0001-6311-1654

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prognostic value of CT-detected tumor necrosis in advanced non-small cell lung cancer (NSCLC) treated with immune checkpoint inhibitor (ICI) monotherapy remains unclear. This two-center retrospective study investigated whether tumor necrosis on pretreatment CT independently predicts overall survival (OS).

methodsA total of 151 advanced NSCLC patients who received ICI monotherapy between March 2016 and August 2021 at two Japanese institutions were retrospectively analyzed. Tumor necrosis was visually assessed and operationally defined as an intratumoral area of low attenuation or cavitary lesion ≥ 5 mm on pretreatment chest CT (contrast-enhanced in 113 patients [75%] and non-contrast in 38 [25%]). Cox regression analyses identified independent prognostic factors for OS, with internal validation using 1000 bootstrap resamples.

resultsAmong 151 patients (mean age 69 years; 90% with ECOG PS 0-1), 121 (80%) had CT-detected necrosis. Median OS was significantly shorter in necrosis-positive patients than in necrosis-negative patients (374 vs. 1035 days; log-rank p = 0.02). A multivariate Cox regression analysis identified tumor necrosis as an independent adverse prognostic factor (HR = 1.84, 95% CI = 1.03-3.30; p = 0.04), along with blood-based biomarkers, tumor size, and PD-L1 expression. The detection rate of necrosis differed between CT modalities (contrast-enhanced 84% vs. non-contrast 68%, p = 0.04).

conclusionThis exploratory two-center retrospective study indicates the potential of CT-detected tumor necrosis as a readily accessible prognostic marker in ICI-treated NSCLC. However, the results obtained require validation in larger, prospective, multicenter studies with standardized CT imaging protocols before clinical implementation.

Indexed as

Carcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsLung NeoplasmsTomography, X-Ray ComputedAgedAged, 80 and overFemaleHumansMaleMiddle AgedNecrosisPrognosisRetrospective StudiesImmune Checkpoint Inhibitorsbiomarkercomputed tomographyimmune checkpoint inhibitorsnon‐small cell lung cancertumor necrosis

Identifiers

PMID42502949
PMCPMC13401793

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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.