Evidence map›Paper›PMID 42176153›Full record

ArticleGeneral thoracic and cardiovascular surgery2026

Clinical predictors of pathological response after immunotherapy in salvage surgery for non-small cell lung cancer: a supplementary analysis of the CReGYT-05 immune checkpoint inhibitor-salvage study.

Satoshi Takamori, Shinya Tane, Megumi Nishikubo, Takuya Watanabe, Kotaro Nomura, Akira Hamada, Shinkichi Takamori, Shinya Katsumata, Satoshi Shiono

Abstract readMulticenter Study
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In one paragraph

Article in General thoracic and cardiovascular surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Satoshi TakamoriDepartment of Thoracic Surgery, Yamagata Prefectural Central Hospital, Yamagata, Japan. s-takamori@med.id.yamagata-u.ac.jp.
Shinya TaneDivision of Thoracic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Megumi NishikuboDepartment of Chest Surgery, Hyogo Cancer Center, Akashi, Japan.
Takuya WatanabeDivision of Thoracic Surgery, Respiratory Disease Center, Seirei Mikatahara General Hospital, Hamamatsu, Japan.
Kotaro NomuraDepartment of Thoracic Surgery, National Cancer Center Hospital East, Kashiwa, Japan.
Akira HamadaDivision of Thoracic Surgery, Department of Surgery, Faculty of Medicine, Kindai University, Osaka-Sayama, Japan.
Shinkichi TakamoriDepartment of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Shinya KatsumataDivision of Thoracic Surgery, Shizuoka Cancer Center, Shunto-Gun, Japan.
Satoshi ShionoDepartment of Surgery II, Faculty of Medicine, Yamagata University, 2-2-2 Iida-Nishi, Yamagata, 990-9585, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesRadiological responses based on tumor size reduction are often unreliable after immune checkpoint inhibitor (ICI) therapy for non-small cell lung cancer (NSCLC), particularly in salvage surgery. The aim of this study was to evaluate the association between MPR and prognosis, and to determine whether changes in metabolic response on positron emission tomography/computed tomography (PET/CT) and tumor marker levels can identify patients who achieve a major pathological response (MPR) despite residual disease.

methodsThis multicenter retrospective study (CReGYT-05 ICI-Salvage study) included patients with NSCLC who underwent salvage lung resection after ICI therapy at 14 institutions in Japan. Metabolic response was evaluated by changes in maximum standardized uptake value (SUVmax). Pathological response was classified as MPR (≦10% viable tumor cells). Associations among metabolic response, tumor markers, pathological response, and survival were analyzed.

resultsAmong 31 evaluable patients, 11 (35%) achieved MPR. Patients with MPR had improved 5-year overall survival compared with those without MPR (100% vs. 40.3%; p = 0.017). In univariate analysis, serum CEA decreased (odds ratio [OR], 16.000; 95% confidence interval [CI], 2.105-343.167; p = 0.005), SUVmax decreased ≧60% (OR, 25.000; 95% CI, 2.441-661.493; p = 0.005), and cStage IV (OR, 0.125; 95% CI, 0.020-0.608; p = 0.009) were suggested to be associated with MPR.

conclusionsRadiologic response alone is insufficient to identify major pathological responders after ICI therapy. PET/CT metabolic response combined with tumor marker changes provides clinically meaningful information for selecting candidates for salvage surgery.

Indexed as

Carcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsImmunotherapyLung NeoplasmsPneumonectomySalvage TherapyAgedAged, 80 and overBiomarkers, TumorFemaleHumansJapanMaleMiddle AgedPositron Emission Tomography Computed TomographyPredictive Value of TestsBiomarkers, TumorImmune Checkpoint InhibitorsImmune checkpoint inhibitorsNon-small-cell lung cancerPET/CTSalvage surgery

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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.