Evidence map›Paper›PMID 40205178›Full record

ArticleCancer immunology, immunotherapy : CII2025

Expression of costimulatory molecule CD70 is prognostic in small cell lung cancer.

David Dora, Zsolt Megyesfalvi, Imre Vörös, Ágnes Paál, Peter Takacs, Daniela Dobos, Bence Lőrincz, Syeda Mahak Zahra Bokhari, Kenan Aloss, Gergely Pallag and 7 more

Abstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

17 authors.

David DoraDepartment of Anatomy, Histology, and Embryology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Zsolt MegyesfalviDepartment of Tumor Biology, National Koranyi Institute of Pulmonology, Budapest, Hungary.
Imre VörösCardiometabolic and HUN-REN-SU System Pharmacology Research Group, Department of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Ágnes PaálCardiometabolic and HUN-REN-SU System Pharmacology Research Group, Department of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Peter TakacsDepartment of Anatomy, Histology, and Embryology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Daniela DobosDepartment of Anatomy, Histology, and Embryology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Bence LőrinczDepartment of Anatomy, Histology, and Embryology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Syeda Mahak Zahra BokhariTranslational Medicine Institute, Semmelweis University, Tűzoltó Utca 37-47, 1094, Budapest, Hungary.
Kenan AlossTranslational Medicine Institute, Semmelweis University, Tűzoltó Utca 37-47, 1094, Budapest, Hungary.
Gergely PallagDepartment of Anatomy, Histology, and Embryology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Christopher RivardDivision of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, USA.
Hui YuDivision of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, USA.
Fred R HirschDivision of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, USA.
Anikó GörbeCardiometabolic and HUN-REN-SU System Pharmacology Research Group, Department of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Zoltán V VargaCenter for Pharmacology and Drug Research and Development, Semmelweis University, Budapest, Hungary.
Zoltan LohinaiTranslational Medicine Institute, Semmelweis University, Tűzoltó Utca 37-47, 1094, Budapest, Hungary. lohinai.zoltan@semmelweis.hu.
Balazs DomeDepartment of Tumor Biology, National Koranyi Institute of Pulmonology, Budapest, Hungary. balazs.dome@meduniwien.ac.at.

Funding

Austrian Science Fund FWF I3522, FWF I3977, and I4677EU HORIZON-MSCA 2022-SE-01 "BIOSMALL"Hungarian National Research, Development and Innovation Office OTKA-PD, #142287Hungarian National Research, Development, and Innovation Office 2020-1.1.6-JÖVŐ, TKP2021-EGA-33, FK-143751 and FK-147045Hungarian National Research, Development, and Innovation Office OTKA-FK, #146775Magyar Tudományos Akadémia Bolyai Research FellowshipMagyar Tudományos Akadémia Momentum Research Grant Momentum Research Grant LP- 2021-14
6 · The paper itself

Abstract

introductionSmall cell lung cancer (SCLC) is a highly aggressive malignancy with poor survival outcomes. The CD70-CD27 axis has been implicated in immune regulation and tumor progression across cancers, but its role in SCLC has not yet been elucidated. This research explores the expression patterns and prognostic significance of CD70 and CD27 in early-stage SCLC.

methodsIn this retrospective study, we analyzed 190 surgically resected SCLC tumor samples using immunohistochemistry (IHC) for CD70 and CD27 expression and RNAscope for CD70 RNA detection. Immune infiltration was assessed using CD45, CD8, and CD20 staining. Quantification of RNAscope signals was performed using QPath software. Kaplan-Meier survival analysis and multivariate Cox regression were used to assess the prognostic impact of CD70, CD27, and immune cell infiltrates on overall survival (OS).

resultsCD70 was expressed in 46% of tumors, primarily within tumor nests, with lower expression in stromal areas. High CD70 expression correlated with significantly decreased OS (p = 0.0078, HR: 1.795) without any correlation with CD45 + , CD8 + or CD20 + immune cell infiltrates. CD27 expression was mainly confined to the stroma, and it did not show a significant association with OS (p = 0.582). Importantly, high CD27 expression was linked to reduced CD45 + and CD8 + cell densities in the stroma. Both CD70 and CD27 were expressed on CD68 + macrophages, CD27 was expressed on CAFs, and both molecules exhibited a partial coexpression with CD3. Furthermore, patients with high CD20 + B-cell densities or the presence of tertiary lymphoid structures (TLS) had significantly improved OS (p = 0.0017, HR: 0.491), suggesting the importance of B-cell-related immune responses in SCLC prognosis.

conclusionCD70, B-cell density and the presence of TLSs, but not CD27, emerged as a significant prognostic biomarker for OS in surgically treated SCLC, suggesting its potential as a therapeutic target.

Indexed as

Biomarkers, TumorCD27 LigandLung NeoplasmsSmall Cell Lung CarcinomaTumor Necrosis Factor Receptor Superfamily, Member 7AdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesBiomarkers, TumorCD27 LigandCD70 protein, humanTumor Necrosis Factor Receptor Superfamily, Member 7B-cellCD27CD70Small-cell lung cancerTLSTumor microenvironment

Identifiers

PMID40205178
PMCPMC11981989

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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.