Evidence map›Paper›PMID 40205411›Full record

ArticleBMC cancer2025

Molecular characterization of early-stage lung adenocarcinoma presenting as subsolid nodules in a real-life European cohort.

Riccardo Tajè, Filippo Tommaso Gallina, Mauro Caterino, Daniele Forcella, Alexandro Patirelis, Gabriele Alessandrini, Simonetta Buglioni, Fabiana Letizia Cecere, Francesca Fusco, Federico Cappelli and 5 more

Abstract read
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Prognostic value of baselineFrontiers in nuclear medicine · 2026
    Article
  4. Article
  5. 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

15 authors.

Riccardo TajèDoctoral School of Microbiology, Immunology, Infectious Diseases and Transplants, MIMIT, University of Rome "Tor Vergata", Rome, Italy.
Filippo Tommaso GallinaThoracic Surgery Unit, IRCCS "Regina Elena" National Cancer Institute, Via Elio Chianesi 53, Rome, 00144, Italy. filippogallina92@gmail.com.
Mauro CaterinoDepartment of Radiology, IRCCS "Regina Elena" National Cancer Institute, Rome, Italy.
Daniele ForcellaThoracic Surgery Unit, IRCCS "Regina Elena" National Cancer Institute, Via Elio Chianesi 53, Rome, 00144, Italy.
Alexandro PatirelisDoctoral School of Microbiology, Immunology, Infectious Diseases and Transplants, MIMIT, University of Rome "Tor Vergata", Rome, Italy.
Gabriele AlessandriniThoracic Surgery Unit, IRCCS "Regina Elena" National Cancer Institute, Via Elio Chianesi 53, Rome, 00144, Italy.
Simonetta BuglioniDepartment of Pathology, IRCCS "Regina Elena" National Cancer Institute, Rome, Italy.
Fabiana Letizia CecereMedical Oncology 2, IRCCS "Regina Elena" National Cancer Institute, Rome, Italy.
Francesca FuscoMedical Oncology 2, IRCCS "Regina Elena" National Cancer Institute, Rome, Italy.
Federico CappelliDepartment of Radiology, IRCCS "Regina Elena" National Cancer Institute, Rome, Italy.
Enrico MelisThoracic Surgery Unit, IRCCS "Regina Elena" National Cancer Institute, Via Elio Chianesi 53, Rome, 00144, Italy.
Paolo ViscaDepartment of Pathology, IRCCS "Regina Elena" National Cancer Institute, Rome, Italy.
Federico CappuzzoMedical Oncology 2, IRCCS "Regina Elena" National Cancer Institute, Rome, Italy.
Vincenzo AmbrogiDepartment of Thoracic Surgery, Tor Vergata University, Rome, Italy.
Antonello VidiriDepartment of Radiology, IRCCS "Regina Elena" National Cancer Institute, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSubsolid nodules emerged as frequent radiological variants of lung adenocarcinoma. Radiological features including solid-component prevalence and larger tumour dimensions prompt tumoral invasiveness guiding prognosis and management. Thus, we aimed to clarify the molecular grounds that dictate these radiological appearances and clinical behaviour in a real-life European-cohort. Additionally, following the growing interest toward targeted-therapies in early-stage diseases, we aimed to present real-life epidemiological data of actionable mutations in these patients.

methodsIn this retrospective single-centre study, targeted next-generation sequencing was performed continuatively in all the resected subsolid lung adenocarcinomas in the period between May 2016 and December 2023. Clinico-radiological data were collected. The genetic landscape of our real-life European subsolid adenocarcinoma population is defined. Common and actionable mutations (frequency > 5%) relation to key clinico-radiological features are evaluated.

resultsOverall, 156 subsolid adenocarcinomas were analysed. KRAS-mutations, mostly KRAS p.G12C, were the most prevalent followed by EGFR, including 25% uncommon EGFR-mutations, TP53 and MET mutations. Amongst the clinico-radiological variables, KRAS-mutations and KRAS p.G12C-mutation were associated to smoking history (≥ 20 pack/years), aggressive histologic subtype and higher consolidation-to-tumor ratio (CTR). Moreover, KRAS-mutated nodules had faster tumour-doubling-time. Conversely, EGFR-mutations were associated to female sex and lower CTR. The latter not being confirmed in common EGFR-mutations. Additionally, in common EGFR-mutated nodules, aggressive histological components were rarer.

conclusionOur study presents the molecular profile of subsolid lung adenocarcinoma in a real-life European-cohort. KRAS-mutations were the most prevalent, and were related to smoking history, higher CTR and faster growth. Conversely, common EGFR-mutations were rarer than expected and unrelated to smoking history and radiological features.

Indexed as

Adenocarcinoma of LungLung NeoplasmsAgedAged, 80 and overErbB ReceptorsEuropeFemaleHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMutationNeoplasm StagingProto-Oncogene Proteins p21(ras)Retrospective StudiesTumor Suppressor Protein p53EGFR protein, humanErbB ReceptorsKRAS protein, humanProto-Oncogene Proteins p21(ras)TP53 protein, humanTumor Suppressor Protein p53Early stage lung cancerGround glassLung cancerMolecular characterizationNext generation sequencingPulmonary nodulesSubsolid nodules

Identifiers

PMID40205411
PMCPMC11983824

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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.