Evidence map›Paper›PMID 38736491›Full record

ArticleTranslational lung cancer research2024

Clinicopathological characterization of next-generation sequencing detected mutations in lung cancers-a single-center experience.

Julia Walter, Amanda Tufman, Jörg Kumbrink, Jens Neumann, Kathrin Kahnert, Laura Sellmer, Andreas Jung, Jürgen Behr, Diego Kauffmann-Guerrero

Abstract read
In one paragraph

Article in Translational lung cancer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Julia WalterDepartment of Medicine V, University Hospital, LMU Munich, Munich, Germany.
Amanda TufmanDepartment of Medicine V, University Hospital, LMU Munich, Munich, Germany.
Jörg KumbrinkInstitute of Pathology, Faculty of Medicine, Ludwig-Maximilians Universität (LMU) Munich, Munich, Germany.
Jens NeumannInstitute of Pathology, Faculty of Medicine, Ludwig-Maximilians Universität (LMU) Munich, Munich, Germany.
Kathrin KahnertDepartment of Medicine V, University Hospital, LMU Munich, Munich, Germany.
Laura SellmerDepartment of Medicine V, University Hospital, LMU Munich, Munich, Germany.
Andreas JungInstitute of Pathology, Faculty of Medicine, Ludwig-Maximilians Universität (LMU) Munich, Munich, Germany.
Jürgen BehrDepartment of Medicine V, University Hospital, LMU Munich, Munich, Germany.
Diego Kauffmann-GuerreroDepartment of Medicine V, University Hospital, LMU Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Despite many advances in molecular procedures many lung cancer patients do not receive full panel testing. This can limit the comprehensive understanding of their disease and potentially hinder personalized treatment options. Methods: In this retrospective analysis, we used results from next-generation sequencing (NGS) testing of 154 patients with adenocarcinoma (AC) or squamous cell carcinoma (SCC) of the lung treated at the University Hospital, Ludwig-Maximilians Universität (LMU) Munich between 2018 and 2021. We compared different clinicopathological features and patients' baseline characteristics with results of NGS testing. We used Results: NGS testing found mutations in 107 (69.5%) patients; 44 patients (28.6%) had more than one mutation. The majority (79.2%) of patients had AC and 64.9% were metastasized at diagnosis. Patients with detected mutations had significantly higher Conclusions: Mutation profiles differed by histological type and metastases status and were significantly associated with

Indexed as

driver mutationsnext-generation sequencing (NGS)Non-small cell lung cancer (NSCLC)tyrosine kinase inhibitor (TKI)

Identifiers

PMID38736491
PMCPMC11082712

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