drugset / Trial / NCT02997332

Durvalumab in Combination With Docetaxel, Cisplatin and 5-FU for Locally Advanced Head and Neck Squamous Cell Carcinoma

NCT02997332 ↗

NaSingle-groupOpen-labelTreatment

Summary

The prognosis of patients with locally advanced SCCHN is poor. Results of recent randomized trials evaluating induction chemotherapy by docetaxel, cisplatin, 5 fluorouracil are conflicting, and benefit on overall survival is uncertain. Improve efficacy of induction chemotherapy is important without increase toxicities. Durvalumab is a promising agent in SSCHN. The safety of combination of docetaxel, cisplatin, 5 fluorouracil with durvalumab is unknown. The aim of the study is to evaluate the feasibility and the safety of the association of DCF (standard regimen for induction in SSCCHN) and durvalumab. The safety profile of DCF and durvalumab are different, so the expected toxicities should not be additive. The addition of durvalumab to DCF could improve the efficacy of induction chemotherapy and the prognostic of patients with SSCCHN. Concerning the translational research, the aim will be to explore the relationships between immune capacity, specificity, activation state and clinical outcome to help elucidate the determinants of response to immunotherapy.

Timeline

Start
2017-03-30
Primary completion
2020-03-17
Completion
2022-12-01

Outcome

Outcome not reported

Stopped (Enrollment): “Toxicities due to the treatment, stop of enrollment”

Drugs

EvaluationDrugModalityDoseRoute
Subject Durvalumab Monoclonal antibody 750 mg —
Subject Durvalumab Monoclonal antibody 1120 mg —
Background Cisplatin Other / unclassified 75 mg/m2 Intravenous
Background Docetaxel Small molecule 75 mg/m2 Intravenous
Background fluorouracil Small molecule 750 mg/m2 Intravenous

Indications