Evidence map›Paper›PMID 42706502›Full record

ArticleGenes, chromosomes & cancer2026

Clinicopathologic Features of NRG1 Fusion-Positive Non-Small Cell Lung Cancer.

Bahadır Köylü, Nur İlayda Genç, Mehmet Haluk Yücel, Anıl Yıldız, Esra Aşık, Cevat İlteriş Kıkılı, Fatih Kemik, Nazan Demir, Pınar Bulutay, Ömer Fatih Ölmez and 1 more

Abstract readMulticenter Study
In one paragraph

Article in Genes, chromosomes & 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.

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

11 authors.

Bahadır KöylüDivision of Medical Oncology, Department of Internal Medicine, Koç University School of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0002-4462-6393
Nur İlayda GençDepartment of Internal Medicine, Koç University School of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0002-0260-8568
Mehmet Haluk YücelDivision of Medical Oncology, Department of Internal Medicine, Medipol University School of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0001-6880-7204
Anıl YıldızDepartment of Medical Oncology, Başakşehir Çam and Sakura City Hospital, Istanbul, Türkiye.ORCID https://orcid.org/0000-0002-6402-4445
Esra AşıkDivision of Medical Oncology, Department of Internal Medicine, Karadeniz Technical University Faculty of Medicine, Trabzon, Türkiye.ORCID https://orcid.org/0000-0003-3030-2475
Cevat İlteriş KıkılıDivision of Medical Oncology, Department of Internal Medicine, Koç University School of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0001-8604-9988
Fatih KemikDivision of Medical Oncology, Department of Internal Medicine, Koç University School of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0001-6085-1921
Nazan DemirDivision of Medical Oncology, Department of Internal Medicine, Koç University School of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0009-0000-2988-4450
Pınar BulutayDepartment of Pathology, Koç University School of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0001-5497-1513
Ömer Fatih ÖlmezDepartment of Medical Oncology, Acibadem Maslak Hospital, Istanbul, Türkiye.ORCID https://orcid.org/0000-0001-7934-7039
Fatih SelçukbiricikDivision of Medical Oncology, Department of Internal Medicine, Koç University School of Medicine, Istanbul, Türkiye.ORCID https://orcid.org/0000-0002-1273-1674

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Data on the clinicopathological features of NRG1 fusion-positive non-small cell lung cancer (NSCLC) are limited. We conducted a retrospective, multicenter study and included patients with NRG1 fusion-positive NSCLC diagnosed between January 2018 and February 2025. Six patients were identified; five were female (83.3%), two were never-smokers (33.3%), and four were former smokers (66.7%). Adenocarcinoma was the predominant histology (n = 5), comprising mucinous (n = 2), enteric (n = 2), and not otherwise specified (n = 1) variants, while one patient had squamous cell carcinoma. All were PD-L1-negative, and CD74-NRG1 was the most common fusion (50%). Three patients received afatinib; only one achieved a partial response with a progression-free survival of 8.7 months. Median overall survival was 6.7 months. Our study demonstrates the histologic and molecular heterogeneity of NRG1 fusion-positive NSCLC, encompassing mucinous and enteric variants of adenocarcinoma. Responses to afatinib were variable, underscoring the need for more effective therapies, including zenocutuzumab and emerging agents.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsNeuregulin-1Oncogene Proteins, FusionAfatinibAgedFemaleHumansMaleMiddle AgedRetrospective StudiesAfatinibNeuregulin-1NRG1 protein, humanOncogene Proteins, Fusionafatinibgene fusionlung cancermucinous adenocarcinomaNeuregulin

Identifiers

PMID42706502
PMCPMC13550098

What Socratic 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 Socratic graph.