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RELAY+: Final Overall Survival With Ramucirumab Plus Gefitinib in Patients With Untreated -Mutated Metastatic NSCLC.

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JTO clinical and research reports 📖 저널 OA 100% 2025 Vol.6(12) p. 100912
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 3/4)

유사 논문
P · 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.

Nishio M, Seto T, Reck M, Garon EB, Nishio K, Kasahara K, Nishino K, Satouchi M, Yoh K, Hayashi H, Sakai K, Enatsu S, Matsui T, Varughese SC, Carlsen M, Visseren-Grul C, Nakagawa K

📝 환자 설명용 한 줄

[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

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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.

🏷️ 키워드 / MeSH

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