Skip to content

Clinicopathological Profiles and Prognosis of Postoperative HER2-Mutant Non-Small Cell Lung Cancer: A Real-World Analysis.

Aug 2026 · Current Cancer Drug Targets · 0 citations
Medicine

Abstract

BACKGROUND/INTRODUCTION Patients with non-small cell lung cancer (NSCLC) harboring HER2 mutations remain at high risk of recurrence, even following radical resection for early-stage disease. Currently, there is a paucity of research investigating the clinicopathological characteristics and disease-free survival (DFS) outcomes of this specific postoperative population.

Methods

This retrospective study investigated the clinicopathological and molecular characteristics of 77 patients with surgically resected HER2-mutant NSCLC. HER2 mutation status was identified via next-generation sequencing (NGS).

Results

HER2 exon 20 insertions were the most prevalent variant in this cohort. Overall, 76.6% of patients exhibited invasive adenocarcinoma phenotypes. Histopathological examination revealed highly invasive papillary and micropapillary components in 51.9% and 45.5% of patients, respectively. The median DFS was 17.0 months (95% CI, 11.4-22.5), with significant variation across disease stages (P = 0.004). The cumulative number of high-risk recurrence factors (0, 1-3, >3) was significantly associated with DFS (median, 29.3 vs. 14.2 vs. 7.1 months; P = 0.045). However, PD-L1 expression status, TP53 alterations, and histological phenotypes demonstrated no significant impact on DFS. Among the entire cohort, 80.5% of patients experienced postoperative recurrence, with the lung being the most frequent site of metastasis.

Conclusion

HER2-mutant NSCLC constitutes a distinct subtype characterized by unique clinicopathological and molecular features. For postoperative patients presenting with advanced disease or an increased burden of high-risk recurrence factors, more aggressive therapeutic strategies should be considered.

View source

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.