Off-label oral cabozantinib 60 mg daily was added to oral osimertinib 80 mg daily in an effort to target these MET mutations (Table 1). Although he achieved stable disease (Fig. 1), he developed considerable fatigue, gastrointestinal toxicity, and cytopenias on dual-inhibitor therapy, thus requiring cessation of cabozantinib. A repeat liquid biopsy revealed the original truncal EGFR mutation, MET amplification, and the known MET-D1228X mutations (Fig. 1). He was continued on osimertinib but died after 3 months.