New England Journal of Medicine· 2026Q1
Sacituzumab Tirumotecan plus Pembrolizumab in PD-L1–Negative Advanced NSCLC
- 2citations
- Q1SCImago
- 2026year
Short summary
First-line sacituzumab tirumotecan plus pembrolizumab significantly improved progression-free survival (15.0 months vs. 5.7 months) in PD-L1–negative advanced NSCLC patients compared to chemotherapy plus pembrolizumab.
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Key points
- Sacituzumab tirumotecan plus pembrolizumab extended median progression-free survival to 15.0 months from 5.7 months in PD-L1–negative advanced NSCLC patients.
- The hazard ratio for disease progression or death was 0.49 (95% CI, 0.36 to 0.65; P<0.001) with the new combination.
- Objective response rates were similar (50.2% vs. 47.3%), but duration of response was longer with sacituzumab tirumotecan plus pembrolizumab (13.6 months vs. 6.8 months).
- Grade 3 or higher adverse events occurred less frequently with sacituzumab tirumotecan plus pembrolizumab (47.6%) compared to chemotherapy plus pembrolizumab (60.6%).
AI-generated from the title and abstract; the full text is not read.
Abstract
BACKGROUND: Pembrolizumab plus chemotherapy with a platinum-based agent and pemetrexed is a widely used standard first-line treatment option for patients with programmed death ligand 1 (PD-L1)-negative advanced nonsquamous non-small-cell lung cancer (NSCLC) without targetable genomic alterations, but outcomes remain suboptimal. METHODS: In this phase 3, open-label, randomized trial, we evaluated sacituzumab tirumotecan plus pembrolizumab in patients with previously untreated locally advanced or metastatic nonsquamous NSCLC without targetable genomic alterations and a PD-L1 tumor proportion score of less than 1%. Patients were randomly assigned in a 1:1 ratio to receive sacituzumab tirumotecan plus pembrolizumab or chemotherapy plus pembrolizumab. The primary end point was progression-free survival as assessed by blinded independent central review. Overall survival was a secondary end point. This report presents the results of the prespecified interim analysis. RESULTS: A total of 455 patients were randomly assigned to receive sacituzumab tirumotecan plus pembrolizumab (229 patients) or chemotherapy plus pembrolizumab (226 patients). After a median follow-up of 9.7 months, the median progression-free survival was significantly longer with sacituzumab tirumotecan plus pembrolizumab than with chemotherapy plus pembrolizumab (15.0 months vs. 5.7 months; hazard ratio for disease progression or death, 0.49; 95% confidence interval [CI], 0.36 to 0.65; P<0.001). An objective response occurred in 50.2% and 47.3% of the patients, respectively, and the median duration of response was 13.6 months and 6.8 months. Overall survival data were immature; the hazard ratio for death was 0.58 (95% CI, 0.38 to 0.88). Adverse events of grade 3 or higher that occurred after the start of treatment were reported in 47.6% of the patients assigned to receive sacituzumab tirumotecan plus pembrolizumab and in 60.6% of those assigned to receive chemotherapy plus pembrolizumab. Stomatitis was common with sacituzumab tirumotecan plus pembrolizumab, but the events were predominantly grade 1 or 2. CONCLUSIONS: Among patients with PD-L1-negative advanced nonsquamous NSCLC without targetable genomic alterations, first-line treatment with sacituzumab tirumotecan plus pembrolizumab led to significantly longer progression-free survival than chemotherapy plus pembrolizumab. (Funded by Sichuan Kelun-Biotech Biopharmaceutical; OptiTROP-Lung06 ClinicalTrials.gov number, NCT06711900.).
The authors' abstract, as published at the source. New England Journal of Medicine, 2026 · DOI ↗
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Field: Oncology
OncologyMedicine