# Molecular Profiling in Non-Small-Cell Lung Cancer: A Single-Center Study on Prevalence and Prognosis

**Authors:** Mustafa Özgür Arıcı, Bora Demirkan, Ebru Taştekin, Derya Kıvrak Salim

PMC · DOI: 10.3390/curroncol32050274 · Current Oncology · 2025-05-09

## TL;DR

This study shows that molecular profiling helps identify treatable genetic changes in lung cancer patients, leading to better survival outcomes when targeted therapies are used.

## Contribution

The study provides new evidence on the survival benefits of targeted therapies based on molecular profiling in metastatic non-small-cell lung cancer.

## Key findings

- 80% of patients had at least one molecular alteration, with TP53 being the most common.
- Patients who received matched targeted therapy had significantly longer overall survival.
- Targetable alterations in first-line treatment improved progression-free survival.

## Abstract

The aim of this study is to evaluate the prognostic value of molecular profiling in patients with metastatic non-small-cell lung cancer (NSCLC). This single-center study included patients diagnosed and treated between July 2020 and April 2024. The molecular profiles of patients detected by either next-generation sequencing or conventional methods were reviewed retrospectively. Survival analyses were conducted based on the targetable alterations and treatments received. Seventy patients were included, with a median age of 65 years and a median overall survival (OS) of 13 months. Of all patients, 56 (80%) had at least one molecular alteration, and the most frequent alteration was TP53 (52.9%), followed by KRAS (20%) and EGFR (8.6%). Eighteen patients (25.7%) had an alteration amenable to targeted therapy. Patients who could reach a matched targeted therapy at any treatment line exhibited a longer median OS compared to those who could not (not reached vs. 6.9 months, p = 0.042). Patients with a targetable alteration for first-line treatment demonstrated a longer progression-free survival compared to those without a targetable alteration (not reached vs. 4.9 months, p = 0.006). According to current guidelines, conducting molecular testing to identify all potential targetable alterations in NSCLC is the cornerstone of the treatment decision process. The survival analysis in this study emphasized the impact of the use of targeted therapies on the survival outcomes.

## Linked entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157], KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845], EGFR (epidermal growth factor receptor) [NCBI Gene 1956]
- **Diseases:** non-small-cell lung cancer (MONDO:0005233)

## Full-text entities

- **Genes:** KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** NSCLC (MESH:D002289)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12109736/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12109736/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12109736/full.md

---
Source: https://tomesphere.com/paper/PMC12109736