BENITIONSClinical Trial Intelligence

Study of Pembrolizumab Given Prior to Surgery and in Combination With Radiotherapy Given Post-surgery for Advanced Head and Neck Squamous Cell Carcinoma (MK-3475-689)

Phase 3 Active, not recruiting NCT03765918

ConditionHead and Neck Neoplasms
PhasePhase 3
SponsorMerck Sharp & Dohme LLC
StatusActive, not recruiting
Enrollment714 participants
InterventionsPembrolizumab 200 mg, Radiotherapy 60 Gray, Radiotherapy 66 Gray, Radiotherapy 70 Gray, Cisplatin 100 mg/m^2
Start dateDec 17, 2018
Completion dateJul 25, 2024
Results postedAug 20, 2025

Summary

This is a randomized, active-controlled, open-label study of pembrolizumab given prior to surgery and pembrolizumab in combination with standard of care radiotherapy (with or without cisplatin), as post-surgical therapy in treatment naïve participants with newly diagnosed Stage III/IVA, resectable, locoregionally advanced, head and neck squamous cell carcinoma (LA-HNSCC). Efficacy outcomes will be stratified by programmed cell death ligand 1 (PD-L1) combined positive score (CPS) status. The primary hypothesis is that pembrolizumab given before surgery and after surgery in combination with radiotherapy (with or without cisplatin) improves event-free survival compared to radiotherapy (with or without cisplatin) given after surgery alone.

Event-free Survival (EFS)

Up to ~66 months · Months

Pembrolizumab + Standard of Care (SOC)51.8 Months
Standard of Care (SOC)30.4 Months
p-value0.00411
Hazard Ratio (HR)0.73 (95% CI 0.58–0.92)

EFS in Participants With Programmed Cell Death Ligand 1 (PD-L1) Combined Positive Score (CPS) ≥10

Up to ~66 months · Months

Pembrolizumab + Standard of Care (SOC)59.7 Months
Standard of Care (SOC)26.9 Months
p-value0.00217
Hazard Ratio (HR)0.66 (95% CI 0.49–0.88)

EFS in Participants With PD-L1 CPS ≥1

Up to ~66 months · Months

Pembrolizumab + Standard of Care (SOC)59.7 Months
Standard of Care (SOC)29.6 Months
p-value0.00140
Hazard Ratio (HR)0.70 (95% CI 0.55–0.89)

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