Phase II study of ramucirumab plus erlotinib for treatment-naïve patients with EGFR-mutant non-squamous non-small cell lung cancer and pleural effusion (RELAY-Effusion)
Mené sur 40 patients atteints d'un cancer du poumon non à petites cellules non épidermoïde avec mutation au niveau du gène EGFR et présentant un épanchement pleural (durée médiane de suivi : 29,5 mois), cet essai multicentrique de phase II évalue l'efficacité, du point de vue de la survie sans progression, et la toxicité d'un traitement de première ligne combinant ramucirumab et erlotinib
Introduction: Malignant pleural effusion (MPE) develops in approximately 30–40% of patients with non-small cell lung cancer (NSCLC), including those harboring epidermal growth factor receptor (EGFR) mutations, and is generally associated with reduced responsiveness to EGFR tyrosine kinase inhibitors. This study aimed to investigate the efficacy of ramucirumab in the context of MPE, which remains unexplored.
Methods: In this single-arm, multicenter, phase II study, we enrolled treatment-naïve patients with EGFR-mutant NSCLC complicated by MPE. They received ramucirumab (10 mg/kg) every 2 weeks plus erlotinib (150 mg) daily until disease progression or unacceptable toxicity. The primary endpoint was progression-free survival (PFS), and the secondary endpoints were objective response rate (ORR), overall survival (OS), and safety.
Results: Forty patients were enrolled between December 2021 and December 2023 (median follow-up, 29.5 months). The median PFS and OS were 12.9 (95% confidence interval [CI], 7.3–16.7) and 36.3 (95% CI: 28.5– not available [NA]) months, respectively, with a 12-month OS rate of 87.5% and ORR of 77.5% (95% CI, 61.5–89.2%). The median drainage-free survival was 33.0 months (95% CI: 26.0–NA). Treatment-related adverse events occurred in 85% of patients (grade 5 = 0%; grade 3 or 4 = 22.5%); the most common were acneiform dermatitis (60.0%), decreased appetite (30.0%), increased aspartate aminotransferase concentration (25.0%), paronychia (22.5%), hypertension (22.5%), proteinuria (22.5%), and anemia (22.5%).
Conclusions: Although the primary endpoint was not met, the combination provided durable control of MPE and was well tolerated, suggesting potential value in symptom-focused management of this high-risk subgroup.
Lung Cancer , résumé, 2026