Real-Life Use of First-Generation EGFR-TKI with Chemotherapy in
EGFR-sensitive Mutations in Non-Small-Cell Lung Cancer: A Single-Center
Analysis and Meta-Analysis
Abstract
Background: Recently,epidermal growth factor receptor (EGFR) -targeting
drugs have benefited thousands of patients with EGFR mutation-positive
(EGFR MUT+) non-small-cell lung cancer (NSCLC). Nevertheless, nearly all
patients with NSCLC who were sensitive to first- or second-generation
EGFR-tyrosine kinase inhibitors (EGFR-TKIs), finally developed
resistance. Therefore, numerous clinicians have focused on improving the
clinical effect of first-generation EGFR-TKIs (1st-gen EGFR-TKIs).
Methods: To analyze the therapeutic outcomes of individuals with
progressive NSCLC, a retroactive assessment was performed on 86 patients
who were medicated with only icotinib or combined with pemetrexed and
platinum-based chemotherapy at The First Affiliated Hospital of Henan
University of Science and Technology (HAUST). Results: Eighty-six
patients with NSCLC-bearing EGFR-sensitive mutations were retroactively
analyzed. The results showed statistical significance in PFS (P = 0.049)
and disease control rate DCR (P = 0.031) between icotinib + chemotherapy
and icotinib alone, especially in the brain metastases (P = 0.021) and
L-858R mutation subgroups (P = 0.05). According to the findings of the
multivariate analysis, treatment (P = 0.033) and EGFR mutation status (P
= 0.019) were significant predictive variables. The OS comparison
between icotinib + chemotherapy and icotinib alone were not
significantly different. The study included a total of 1242 patients, of
which 648 obtained combined treatment and 594 obtained first-generation
EGFR-TKI monotherapy. Analyzing the relevant data from multiple studies,
the results showed significant improvements in ORR (RR: 0.63, 95% CI:
0.49–0.82, P = 0.0006), PFS (RR: 0.61, 95% CI: 0.47–0.79, P =
0.0002), and OS (RR: 0.67, 95% CI: 0.51–0.88, P = 0.004) for those on
combination therapy. However, there was also an increase in
treatment-emergent AEs among these patients. Conclusion: In summary,
administering first-generation EGFR-TKI concurrently with chemotherapy
provides an edge in the therapeutic management of locally or severely
advanced NSCLC that is EGFR-positive. Therefore, EGFR mutation-positive
NSCLC (EGFR MUT+ NSCLC) patients in this condition may find it
advantageous to consider using 1st-gen EGFR-TKIs in conjunction with
chemotherapy (1st-gen EGFR-TKIs + Chemo).