AUTHOR=Chen Fei , Chen Naifei , Yu Yu , Cui Jiuwei 

TITLE=Efficacy and Safety of Epidermal Growth Factor Receptor (EGFR) Inhibitors Plus Antiangiogenic Agents as First-Line Treatments for Patients With Advanced EGFR-Mutated Non-small Cell Lung Cancer: A Meta-Analysis

JOURNAL=Frontiers in Oncology

VOLUME=10

YEAR=2020

URL=https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2020.00904

DOI=10.3389/fonc.2020.00904

ISSN=2234-943X

ABSTRACT=<p><bold>Background:</bold> Tyrosine kinase inhibitors (TKIs) are standard treatment options for non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (<italic>EGFR</italic>) mutations. Increasing clinical investigations have explored the value of EGFR-TKIs plus antiangiogenic drugs as the first-line treatment for <italic>EGFR</italic>-mutated NSCLC.</p><p><bold>Methods:</bold> We systematically searched PubMed, Cochrane Library, and EMBASE for randomized controlled trials (RCTs) investigating EGFR-TKIs administered with or without antiangiogenic agents for advanced <italic>EGFR</italic>-mutated NSCLC. The latest RCT that was presented orally at the 2019 European Society for Medical Oncology Congress was obtained online. The endpoints included progression-free survival (PFS), overall survival (OS), objective response rate (ORR), disease control rates (DCRs), and grade 3 or higher adverse events (AEs).</p><p><bold>Results:</bold> We included seven articles on five trials with 1,226 patients. The interventions for the experimental group were the first-generation EGFR-TKI erlotinib combined with bevacizumab (four studies) or ramucirumab (one study), and erlotinib monotherapy (four studies) or erlotinib plus placebo (one study) for the control group. All studies reached their primary study endpoints (i.e., PFS). Compared to erlotinib monotherapy, erlotinib plus antiangiogenic agents remarkably prolonged PFS [hazard ratio (HR) = 0.59, 95% confidence interval (CI) = 0.51–0.69, <italic>P</italic> = 0.000]; however, ORR, DCR, and OS were similar between the two groups. The overall grade 3–5 AEs increased in combination group (OR = 5.772, 95% CI = 2.38–13.94, <italic>P</italic> = 0.000), particularly the incidence of diarrhea (OR = 2.51, 95% CI = 1.21–5.23, <italic>P</italic> = 0.014), acneiform (OR = 1.815, 95% CI = 1.084–3.037, <italic>P</italic> = 0.023), hypertension (OR = 6.77, 95% CI = 3.62–12.66, <italic>P</italic> = 0.000), and proteinuria (OR = 13.48, 95% CI = 4.11–44.22, <italic>P</italic> = 0.000). Additionally, subgroup analysis demonstrated that Asian patients could significantly benefit from combination therapy (HR = 0.59, 95% CI = 0.50–0.69, <italic>P</italic> = 0.000). Patients with <italic>exon 19</italic> deletions (HR = 0.61, 95% CI = 0.49–0.75, <italic>P</italic> = 0.000) and <italic>21 Leu858Arg</italic> mutations (HR = 0.59, 95% CI = 0.47–0.73, <italic>P</italic> = 0.000) had almost equivalent PFS benefits when treated with double-blocking therapy. Patients with brain metastases at baseline in the combination group had a trend toward better PFS (HR = 0.55, 95% CI = 0.30–1.01, <italic>P</italic> = 0.001).</p><p><bold>Conclusions:</bold> Erlotinib plus bevacizumab or ramucirumab in EFGR-mutated NSCLC first-line setting yielded remarkable PFS benefits; however, this was accompanied by higher AEs. Epidermal growth factor receptor–TKI plus antiangiogenic agent therapy may be considered a new option for advanced <italic>EGFR</italic>-mutated NSCLC patients.</p>