EGFR-mutated mNSCLC: Sharing Clinical Insights and Best Practices - Episode 1
Experts discuss emerging consensus around the value of combination therapy in EGFR-mutated metastatic NSCLC, highlighting practice-changing overall survival data from FLAURA2 and emphasizing how intensified upfront treatment may now redefine the standard of care despite added complexity and toxicity.
At a recent oncology conference, a panel of thoracic oncologists discussed current treatment strategies for patients with EGFR-mutated metastatic non-small cell lung cancer. The conversation opened with an overview of evolving frontline options, including monotherapy with targeted agents and newer combination strategies. The panel emphasized that with increasing complexity in data and treatment choices, the decision between monotherapy and combination therapy is becoming more nuanced. Two key studies—FLAURA2 and MARIPOSA—have provided critical insights into how combining EGFR TKIs with chemotherapy or monoclonal antibodies may improve outcomes compared to monotherapy alone.
The panel highlighted final overall survival data from FLAURA2, presented at the same conference, which showed a median overall survival benefit of 10 months with combination therapy compared to monotherapy. This translated into a hazard ratio of 0.77, signaling a meaningful clinical advantage. Experts noted this was a highly anticipated result and found the magnitude of benefit both surprising and practice-changing. Unlike previous studies, FLAURA2 included significant crossover in the control arm, yet still demonstrated strong overall survival gains. The findings support that intensifying upfront therapy—even beyond the convenience of oral monotherapy—can lead to real survival improvements for patients.
Panelists agreed that these data will likely influence clinical practice moving forward. They underscored that patients were able to stay on the combination therapy for extended periods, with a median duration of targeted therapy exposure reaching 30 months. The benefit was also consistent across key subgroups, reinforcing the broad applicability of the approach. While combination therapy does introduce added toxicity and complexity, the confirmed survival benefit gives clinicians a stronger case for recommending it to appropriate patients. Overall, the discussion reflected growing consensus around the value of combination therapy as a frontline standard for many patients with EGFR-mutant disease.