RELAY+: Final Overall Survival With Ramucirumab Plus Gefitinib in Patients With Untreated -Mutated Metastatic NSCLC.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
환자: metastatic -mutated NSCLC
I · Intervention 중재 / 시술
RAM plus osimertinib (80 mg once daily) (period 2)
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Treatment-emergent T790M rate post progression was 81.3%. [CONCLUSIONS] RELAY+ revealed a favorable benefit-risk profile for RAM plus GEF in East Asian patients with untreated -mutated metastatic NSCLC, supporting RAM plus GEF as an alternative first-line treatment option, particularly in those with an L858R mutation.
[INTRODUCTION] Ramucirumab (RAM) plus gefitinib (GEF) exhibited favorable efficacy and safety as first-line treatment in the primary analysis of the RELAY+ study of East Asian patients with metastatic
APA
Nishio M, Seto T, et al. (2025). RELAY+: Final Overall Survival With Ramucirumab Plus Gefitinib in Patients With Untreated -Mutated Metastatic NSCLC.. JTO clinical and research reports, 6(12), 100912. https://doi.org/10.1016/j.jtocrr.2025.100912
MLA
Nishio M, et al.. "RELAY+: Final Overall Survival With Ramucirumab Plus Gefitinib in Patients With Untreated -Mutated Metastatic NSCLC.." JTO clinical and research reports, vol. 6, no. 12, 2025, pp. 100912.
PMID
41278399
Abstract
[INTRODUCTION] Ramucirumab (RAM) plus gefitinib (GEF) exhibited favorable efficacy and safety as first-line treatment in the primary analysis of the RELAY+ study of East Asian patients with metastatic -mutated NSCLC. We report the final overall survival (OS) and safety.
[METHODS] This open-label, two-period, single-arm exploratory study included patients with untreated NSCLC having ex19del or L858R mutations and no central nervous system metastasis or T790M mutation. Patients received RAM (10 mg/kg every 2 wk) plus GEF (250 mg once daily) until disease progression (period 1); patients with disease progression who acquired a T790M mutation received RAM plus osimertinib (80 mg once daily) (period 2).
[RESULTS] At final OS data cutoff (October 20, 2023; median follow-up: 42.5 mo), median (95% confidence interval [CI]) OS was 47.4 (35.9‒57.6) months, and the 3-year OS rate was 61.8%. In the L858R and ex19del subgroups, median OS was 51.9 and 38.4 months, and 3-year OS rates were 70.2% and 52.8%, respectively. Overall, 85.4% of patients received subsequent systemic therapy post study treatment discontinuation. Grade 3 or higher treatment-related adverse events (AEs) were reported by 51 (62.2%) patients. The most common grade 3 or higher treatment-emergent AE of special interest was hypertension (25.6%; grade 3 event only). Treatment-emergent T790M rate post progression was 81.3%.
[CONCLUSIONS] RELAY+ revealed a favorable benefit-risk profile for RAM plus GEF in East Asian patients with untreated -mutated metastatic NSCLC, supporting RAM plus GEF as an alternative first-line treatment option, particularly in those with an L858R mutation.
[METHODS] This open-label, two-period, single-arm exploratory study included patients with untreated NSCLC having ex19del or L858R mutations and no central nervous system metastasis or T790M mutation. Patients received RAM (10 mg/kg every 2 wk) plus GEF (250 mg once daily) until disease progression (period 1); patients with disease progression who acquired a T790M mutation received RAM plus osimertinib (80 mg once daily) (period 2).
[RESULTS] At final OS data cutoff (October 20, 2023; median follow-up: 42.5 mo), median (95% confidence interval [CI]) OS was 47.4 (35.9‒57.6) months, and the 3-year OS rate was 61.8%. In the L858R and ex19del subgroups, median OS was 51.9 and 38.4 months, and 3-year OS rates were 70.2% and 52.8%, respectively. Overall, 85.4% of patients received subsequent systemic therapy post study treatment discontinuation. Grade 3 or higher treatment-related adverse events (AEs) were reported by 51 (62.2%) patients. The most common grade 3 or higher treatment-emergent AE of special interest was hypertension (25.6%; grade 3 event only). Treatment-emergent T790M rate post progression was 81.3%.
[CONCLUSIONS] RELAY+ revealed a favorable benefit-risk profile for RAM plus GEF in East Asian patients with untreated -mutated metastatic NSCLC, supporting RAM plus GEF as an alternative first-line treatment option, particularly in those with an L858R mutation.
🏷️ 키워드 / MeSH
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