Evidence map›Paper›PMID 41187938›Full record

ArticleCancer reports (Hoboken, N.J.)2025

TGFβ1 and SMAD3 Expression Are Associated With Survival After the Immune Checkpoint Inhibitor Therapy for Small Cell Lung Cancer.

Zenta Seto, Minehiko Inomata, Akira Noguchi, Tomonobu Kado, Nozomu Murayama, Naoki Takata, Kotaro Tokui, Seisuke Okazawa, Shingo Imanishi, Tosihiro Miwa and 3 more

Abstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2025. 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.

Zenta SetoFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Minehiko InomataFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.ORCID 0000-0002-6846-187X
Akira NoguchiDepartment of Diagnostic Pathology, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan.ORCID 0000-0002-4338-0432
Tomonobu KadoFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.ORCID 0000-0002-7750-3023
Nozomu MurayamaFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Naoki TakataFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Kotaro TokuiFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Seisuke OkazawaFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.ORCID 0000-0002-2592-7131
Shingo ImanishiFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Tosihiro MiwaFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Ryuji HayashiDepartment of Clinical Oncology, Toyama University Hospital, Toyama, Japan.ORCID 0000-0002-4205-9540
Kenichi HirabayashiDepartment of Diagnostic Pathology, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan.ORCID 0000-0002-9516-1792
Kazuyuki TobeFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.ORCID 0000-0003-0015-0255

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumor immunity is involved in the progression of malignant tumors. However, there are few reports on the relationship between the immunological environment and the efficacy of immune checkpoint inhibitors in small cell lung cancer (SCLC). We analyzed the relationship between tumor-infiltrating immune cells and protein expression and survival in patients with SCLC treated with combined therapy with immune checkpoint inhibitors plus chemotherapy.

methodsPatients with SCLC who received combined therapy with immune checkpoint inhibitors plus chemotherapy between 2019 and 2023 were enrolled. Immune cell infiltration levels, including CD4, CD8, FOXP3, CD163-positive cells and expression levels of TGFβ1 and SMAD3 proteins in tumor tissue were evaluated by immunohistochemistry. Progression-free survival (PFS) and overall survival (OS) were evaluated as endpoints.

resultsData from 22 patients were analyzed. The high CD4-positive T lymphocyte (p = 0.008, log-rank test) and the high CD8-positive T lymphocyte infiltration group (p = 0.031, log-rank test) showed statistically significantly longer OS than the low infiltration group. On the other hand, the low TGFβ1 expression group showed significantly longer PFS (p = 0.026, log-rank test) and the low SMAD3 expression group showed significantly longer OS (p = 0.042, log-rank test) than the high expression group.

conclusionIn conclusion, it is suggested that infiltration of T lymphocytes and expression of TGFβ1 and SMAD3 may be related to the efficacy of the combined therapy with immune checkpoint inhibitors plus chemotherapy in patients with SCLC.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsImmune Checkpoint InhibitorsLung NeoplasmsSmad3 ProteinSmall Cell Lung CarcinomaTransforming Growth Factor beta1AdultAgedBiomarkers, TumorFemaleHumansLymphocytes, Tumor-InfiltratingMaleMiddle AgedPrognosisProgression-Free SurvivalBiomarkers, TumorImmune Checkpoint InhibitorsSmad3 ProteinSMAD3 protein, humanTGFB1 protein, humanTransforming Growth Factor beta1immune checkpoint inhibitorSMAD3small cell lung cancerTGFβ

Identifiers

PMID41187938
PMCPMC12585284

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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.