Evidence map›Paper›PMID 41383350›Full record

ArticleMolecular and clinical oncology2026

TTF-1 expression is associated with survival in patients with non-squamous non-small cell lung cancer treated with immune checkpoint inhibitor therapy.

Nozomu Murayama, Minehiko Inomata, Daisuke Furukawa, Moe Hashizume, Naoki Takata, Zenta Seto, Kotaro Tokui, Seisuke Okazawa, Shingo Imanishi, Toshiro Miwa and 3 more

Abstract read
In one paragraph

Article in Molecular and clinical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
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

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

13 authors.

Nozomu MurayamaFirst Department of Internal Medicine, Toyama University Hospital, Toyama 930-0194, Japan.
Minehiko InomataFirst Department of Internal Medicine, Toyama University Hospital, Toyama 930-0194, Japan.
Daisuke FurukawaFirst Department of Internal Medicine, Toyama University Hospital, Toyama 930-0194, Japan.
Moe HashizumeFirst Department of Internal Medicine, Toyama University Hospital, Toyama 930-0194, Japan.
Naoki TakataFirst Department of Internal Medicine, Toyama University Hospital, Toyama 930-0194, Japan.
Zenta SetoFirst Department of Internal Medicine, Toyama University Hospital, Toyama 930-0194, Japan.
Kotaro TokuiFirst Department of Internal Medicine, Toyama University Hospital, Toyama 930-0194, Japan.
Seisuke OkazawaFirst Department of Internal Medicine, Toyama University Hospital, Toyama 930-0194, Japan.
Shingo ImanishiFirst Department of Internal Medicine, Toyama University Hospital, Toyama 930-0194, Japan.
Toshiro MiwaFirst Department of Internal Medicine, Toyama University Hospital, Toyama 930-0194, Japan.
Ryuji HayashiDepartment of Medical Oncology and Palliative Medicine, Toyama University Hospital, Toyama 930-0194, Japan.
Kohji TakagiDepartment of Diagnostic Pathology, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama 930-0194, Japan.
Kenichi HirabayashiDepartment of Diagnostic Pathology, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama 930-0194, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thyroid transcription factor-1 (TTF-1) expression has been associated with the prognosis of patients with non-small cell lung cancer treated with immune checkpoint inhibitor (ICI) therapy; however, it has also been suggested that there is no such link. The present study analyzed the association of TTF-1 expression, evaluated using a cocktail antibody (TTF-1/napsin A; clone, SPT24/TMU-Ad02), with survival after the initiation of ICI therapy in patients with EGFR/ALK wild-type non-squamous non-small cell lung cancer receiving first-line treatment with ICI monotherapy or chemoimmunotherapy. A total of 49 patients were enrolled to the present study. Multivariate analysis using the Cox proportional hazard model showed that TTF-1 expression was associated with progression-free survival (PFS) after the initiation of treatment with ICI monotherapy or chemoimmunotherapy (hazard ratio: 0.18, 95% confidence interval: 0.06-0.54). Subset analysis showed that the TTF-1-positive group exhibited significantly longer PFS than the negative group in both the ICI monotherapy (median PFS, 17.6 months vs. 2.9 months, P<0.001, log-rank test) and chemoimmunotherapy (median PFS, 10.4 months vs. 5.2 months, P=0.021, log-rank test) groups. In conclusion, the current study observed an association between TTF-1 expression evaluated using a cocktail antibody and the effectiveness of treatment with ICI monotherapy or chemoimmunotherapy.

Indexed as

immune checkpoint inhibitorlung cancernapsin Aprognosisthyroid transcription factor-1

Identifiers

PMID41383350
PMCPMC12690345

What OpenQuestion holds

Textmetadata
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.