Table 3. Summary of the clinical trials on third-generation EGFR-TKIs combined with SBRT.
Clinical trial | Setting | Cases | Condition | Treatment | Measures | Study completion |
---|---|---|---|---|---|---|
NCT04908956 | Phase II | 60 | Oligo-metastatic EGFR-mutant NSCLC | Risk-adapted SBRT × up to 5 fractions, osimertinib 80 mg once daily | Pneumonia grade ≥2, PFS, RECIST v. 1.1 | 2023/3/26 |
NCT05167851 | Phase II | 68 | Oligometastatic EGFR-mutant NSCLC | Lazertinib 240 mg once daily oral (PO); SBRT to oligometastatic sites | PFS, OS, distant PFS, ORR, DOR, CTCAE | 2023/12/25 |
NCT04764214 | Phase II | 56 | Oligometastatic EGFR-mutant NSCLC | Osimertinib 80 mg once daily; consolidative SBRT to all residual disease | PFS, OS, CTCAE v. 5.0 | 2023/12/31 |
NCT05583409 | Not applicable | 72 | EGFR-mutant NSCLC with fewer than 5 metastatic focus | Received SBRT after 3 months of osimertinib treatment; osimertinib 80 mg once daily | PFS, OS | 2025/12/30 |
EGFR, epidermal growth factor receptor; TKI, tyrosine kinase inhibitor; SBRT, stereotactic radiation therapy; NSCLC, non-small cell lung cancer; PFS, progression-free survival; RECIST, Response Evaluation Criteria in Solid Tumors; PO, per os; OS, overall survival; ORR, objective response rate; DOR, duration of response; CTCAE, Common Terminology Criteria for Adverse Events.