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A Multicenter Open-Label Randomized Phase II Study of Osimertinib With and Without Ramucirumab in Tyrosine Kinase
Xiuning Le1, Jyoti D Patel2, Elaine Shum3
1UT MD Anderson Cancer Center, Houston, TX.
Purpose:
Preclinical studies demonstrated that dual inhibition of epidermal growth factor receptor (EGFR) and vascular endothelial growth factor (VEGF) pathways delay the emergence of resistance to EGFR tyrosine kinase inhibitors (TKIs), and in trials with first-generation EGFR TKIs, the combination of EGFR VEGF pathway inhibitors prolonged progression-free survival (PFS).
Methods:
The RAMOSE trial (ClinicalTrials.gov identifier: NCT03909334, HCRN LUN-18-335) is a randomized, open-label multicenter phase II study comparing osimertinib with ramucirumab (arm A) to osimertinib (arm B) for initial treatment of metastatic EGFR-mutant non-small cell lung cancer (NSCLC) with 2:1 random assignment. The primary end point is PFS for evaluable patients; secondary end points include objective response rates (ORRs), disease control rate (DCR), overall survival, and safety. The stratification criteria were EGFR mutation type and the presence of CNS metastasis.
Results:
At data cutoff on August 29, 2023, 160 patients consented, 147 patients received treatment, and 139 patients were evaluable with at least one scan. In this preplanned interim analysis, the median follow-up was 16.6 months. Among the evaluable patients, 57 PFS events occurred. The median PFS was 24.8 (A) versus 15.6 (B) months (hazard ratio, 0.55 [95% CI, 0.32 to 0.93]; log-rank P = .023), 12-month PFS rate was 76.7% (A) versus 61.9% (B; P = .026). No significant difference was observed in the ORRs and DCRs between arms. Any-grade (G) adverse events (AEs) occurred in 100% (A) and 98% (B) of patients, with no G5 treatment-related AE (TRAE), one G4 TRAE (hyponatremia, A), and 53% (A) versus 41% (B) G3 TRAEs. AE-related discontinuation occurred in 13 patients (9.7% in A and 8.7% in B). The safety profile was in line with known safety of each drug.
Conclusion:
Ramucirumab plus osimertinib significantly prolonged PFS compared with osimertinib alone in patients with TKI-naïve EGFR-mutant NSCLC. The combination is safe and well tolerated.
Insights
Ramucirumab plus osimertinib significantly improved progression-free survival (PFS) in patients with EGFR-mutant non-small cell lung cancer. This combination therapy is safe and well-tolerated for initial treatment.
Area of Science:
- Oncology
- Pharmacology
- Genetics
Background:
- Dual inhibition of EGFR and VEGF pathways may overcome resistance to EGFR TKIs.
- Previous trials with first-generation EGFR TKIs showed improved PFS with combined EGFR and VEGF pathway inhibitors.
Purpose of the Study:
- To compare the efficacy and safety of osimertinib plus ramucirumab versus osimertinib alone as initial treatment for metastatic EGFR-mutant non-small cell lung cancer (NSCLC).
Main Methods:
- The RAMOSE trial is a randomized, open-label, multicenter phase II study.
- 147 patients received either osimertinib with ramucirumab (arm A) or osimertinib alone (arm B) with a 2:1 random assignment.
- Primary endpoint was progression-free survival (PFS); secondary endpoints included objective response rates (ORRs), disease control rate (DCR), overall survival, and safety.
Main Results:
- Median PFS was significantly longer with ramucirumab plus osimertinib (24.8 months) compared to osimertinib alone (15.6 months).
- The 12-month PFS rate was 76.7% in arm A versus 61.9% in arm B.
- Adverse events were manageable and consistent with known drug profiles; no significant difference in ORRs or DCRs was observed.
Conclusions:
- Ramucirumab plus osimertinib significantly prolonged PFS in TKI-naïve EGFR-mutant NSCLC patients.
- The combination demonstrated a safe and well-tolerated profile for initial treatment.
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