Osimertinib or EGFR-TKIs/chemotherapy in patients with EGFR-mutated advanced nonsmall cell lung cancer: A
Lei Huang1, Hao Huang1, Xiao-Ping Zhou2
1Department of Clinical Laboratory, The Affiliated Tumor Hospital of Guangxi Medical University.
Background:
The aim of this meta-analysis is to investigate the impact of Osimertinib on treatment efficacy in advanced nonsmall cell lung cancer (NSCLC).
Methods:
Trials comparing Osimertinib against epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs)/chemotherapy in patients with NSCLC with an epidermal growth factor receptor (EGFR) mutation were included, and the pooled data for progression-free survival (PFS), overall survival (OS), overall response rate (ORR), disease control rate (DCR), and adverse events (AEs) were analyzed.
Results:
Analysis results based on 6 eligible trials showed that Osimertinib significantly improved the overall PFS (hazard ratio [HR] = 0.38, 95% confidence interval [CI] = 0.29-0.50), improved the OS (HR = 0.66, 95% CI = 0.48-0.89), increased the ORR (odds ratio [OR] = 1.76, 95% CI = 1.14-2.72), increased the overall DCR (OR = 1.18, 95% CI = 1.02-1.37), and reduced the grade 3 or greater AEs (relative ratio [RR] = 0.50, 95% CI = 0.33-0.75) in all subgroups except in the ORR in the Exon 19 deletion (Ex19del) and/or L858R subgroup. Compared to patients with Ex19del and/or L858R mutation, patients with the T790M mutation had the benefits of a greater PFS (41.7%), a greater ORR (80.0%), a greater DCR (71.2%), and fewer grade 3 or greater AEs (70.7%) (each P < .05). Race, sex, age, EGFR mutation, and smoking history may significantly predict additional benefits from Osimertinib, but there were no significant differences between subgroups stratified by these clinical characteristics.
Conclusions:
Osimertinib showed greater treatment benefit for patients with NSCLC with EGFR mutation than EGFR-TKIs/chemotherapy, especially for T790M mutation-positive patients.
Insights
Osimertinib significantly improves outcomes for advanced non-small cell lung cancer (NSCLC) patients with EGFR mutations. This targeted therapy offers better progression-free survival, overall survival, and response rates, with fewer severe adverse events, particularly for T790M mutation-positive cases.
Area of Science:
- Oncology
- Pharmacology
- Clinical Trials
Background:
- Advanced non-small cell lung cancer (NSCLC) poses significant treatment challenges.
- Epidermal growth factor receptor (EGFR) mutations are key drivers in a subset of NSCLC.
- Targeted therapies like Osimertinib aim to improve efficacy in EGFR-mutated NSCLC.
Purpose of the Study:
- To conduct a meta-analysis evaluating Osimertinib's impact on treatment efficacy in advanced NSCLC.
- To compare Osimertinib with existing epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) or chemotherapy.
- To analyze key efficacy endpoints and safety profiles.
Main Methods:
- Systematic review and meta-analysis of 6 eligible clinical trials.
- Inclusion criteria: NSCLC patients with EGFR mutations comparing Osimertinib to EGFR-TKIs/chemotherapy.
- Pooled analysis of progression-free survival (PFS), overall survival (OS), overall response rate (ORR), disease control rate (DCR), and adverse events (AEs).
Main Results:
- Osimertinib demonstrated significant improvements in PFS (HR=0.38) and OS (HR=0.66) compared to control groups.
- Higher ORR (OR=1.76) and DCR (OR=1.18) were observed with Osimertinib.
- Reduced incidence of grade 3 or greater AEs (RR=0.50) was noted, particularly in T790M mutation-positive patients.
- Subgroup analyses indicated potential predictive value of race, sex, age, EGFR mutation type, and smoking history, though not statistically significant across all strata.
Conclusions:
- Osimertinib offers superior treatment benefits over traditional EGFR-TKIs/chemotherapy for NSCLC patients with EGFR mutations.
- The efficacy advantage is particularly pronounced in patients with the T790M mutation.
- Osimertinib represents a valuable therapeutic option, improving survival and response rates while enhancing safety in this patient population.
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