AI Article Synopsis

  • The study aimed to analyze the challenges of using liquid-based cytology (LBC) specimens in next-generation sequencing (NGS) for lung adenocarcinoma and assess the effectiveness of targeted therapies like EGFR-TKIs.
  • A retrospective analysis of 357 advanced lung adenocarcinoma cases revealed similar mutation rates between TKI-naive and TKI-treated groups, but higher EGFR mutation rates in the TKI-treated group, suggesting treatment impacts the genetic makeup of the tumors.
  • Findings emphasized that LBC specimens are valuable for detecting gene mutations in lung cancer, but highlighted the need to evaluate tumor cellularity when using these specimens for molecular testing.

Article Abstract

Background: To explore challenges of liquid-based cytology (LBC) specimens for next-generation sequencing (NGS) in lung adenocarcinoma and evaluate the efficacy of targeted therapy.

Methods: A retrospective analysis was conducted on the NGS test of 357 cases of advanced lung adenocarcinoma LBC specimens and compared with results of histological specimens to assess the consistency. The impact of tumor cellularity on NGS test results was evaluated. The utility of epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) was collected. Clinical efficacy evaluation was performed and survival curve analysis was conducted using the Kaplan-Meier method.

Results: There were 275 TKI-naive and 82 TKI-treated specimens, the mutation rates of cancer-related genes detected in both groups were similar (86.2% vs. 86.6%). The EGFR mutation rate in the TKI treated group was higher than that in the TKI-naive group (69.5% > 54.9%, P = 0.019). There was no significant difference in the EGFR mutation frequency among different tumor cellularity in the TKI-naive group. However, in the TKI treated group, the frequency of EGFR sensitizing mutation and T790M resistance mutation in specimens with < 20% tumor cellularity was significantly lower than that in specimens with ≥ 20% tumor cellularity. Among 22 cases with matched histological specimens, 72.7% (16/22) of LBC specimens were completely consistent with results of histological specimens. Among 92 patients with EGFR-mutant lung adenocarcinoma treated with EGFR-TKIs in the two cohorts, 88 cases experienced progression, and the median progression-free survival (PFS) was 12.1 months.

Conclusions: Cytological specimens are important sources for gene detection of advanced lung adenocarcinoma. When using LBC specimens for molecular testing, it is recommended to fully evaluate the tumor cellularity of the specimens.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11188509PMC
http://dx.doi.org/10.1186/s12885-024-12520-2DOI Listing

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