BENITIONSClinical Trial Intelligence

A Study of Pembrolizumab (MK-3475) With or Without Lenvatinib (E7080/MK-7902) as First Line (1L) Intervention in a Programmed Cell Death-ligand 1 (PD-L1) Selected Population With Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma (R/M HNSCC) (MK-7902-010/LEAP-010)-China Extension

Фаза 3 Завершено NCT05523323

ЗаболеваниеHead and Neck Squamous Cell Carcinoma
ФазаФаза 3
СпонсорMerck Sharp & Dohme LLC
СтатусЗавершено
Участники112 участн.
ВмешательствоLenvatinib, Pembrolizumab
Дата начала30.10.2020
Дата завершения25.08.2023
Публикация результатов18.10.2024

Кратко

This is a study of pembrolizumab (MK-3475) with or without lenvatinib (E7080/MK-7902) as a first line intervention in a PD-L1 selected population with participants with recurrent or metastatic head and neck squamous cell carcinoma. Hypotheses include: * Pembrolizumab + lenvatinib is superior to pembrolizumab + placebo with respect to Objective Response Rate (ORR) per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) by blinded independent central review (BICR). * Pembrolizumab + lenvatinib is superior to pembrolizumab + placebo with respect to Progression Free Survival (PFS) per RECIST 1.1 as assessed by BICR. * Pembrolizumab + lenvatinib is superior to pembrolizumab + placebo with respect to overall survival (OS).

Objective Response Rate (ORR) Per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) as Assessed by Blinded Independent Central Review (BICR)

Up to approximately 33 months · Percentage of participants

Pembrolizumab + Lenvatinib39.3 Percentage of participants
Pembrolizumab + Placebo9.8 Percentage of participants
p-value0.0002014
Estimate difference29.5 (95% CI 14.0–43.9)

Progression Free Survival (PFS) Per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) as Assessed by Blinded Independent Central Review (BICR)

Up to approximately 33 months · Months

Pembrolizumab + Lenvatinib7.0 Months
Pembrolizumab + Placebo1.5 Months
p-value0.0000037
Hazard Ratio (HR)0.34 (95% CI 0.21–0.55)

Overall Survival (OS)

Up to approximately 33 months · Months

Pembrolizumab + Lenvatinib10.9 Months
Pembrolizumab + Placebo11.9 Months
p-value0.30933
Hazard Ratio (HR)0.86 (95% CI 0.49–1.54)

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