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A Phase II Randomized Clinical Trial Comparing Two Cycles Versus Four Cycles of Combination Therapy with Cetuximab, Avelumab, Cisplatin, and Docetaxel in Patients with Recurrent Metastatic Head and Neck Cancer - AVETUX-HN

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-521738-27-00
Acronym
MS062202_0168
Enrollment
126
Registered
2025-11-17
Start date
2025-12-15
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent Metastatic Head and Neck Cancer

Brief summary

Assessment of quality of life (QoL) regarding role functioning at 18 weeks after the initiation of treatment, measured by the standardized QLQ-C30 questionnaire.

Detailed description

Progression-Free Survival (PFS): PFS is defined as the time from the date of randomization to the date of the first documentation of objective disease progression or death due to any cause, whichever occurs first. To assess the difference between treatment arm A and treatment arm B in terms of progression-free survival (PFS), an exploratory analysis of the HR including a two-sided 95% CI will be carried out., Overall Survival (OS): OS is defined as the time from the date of randomization to the date of death due to any cause. To assess the difference between treatment arm A and treatment arm B in terms of overall survival (OS), an exploratory analysis of the HR including a two-sided 95% CI will be carried out., Objective Response Rate (ORR): ORR is defined as the proportion of patients who have a complete response (CR) or partial response (PR) according to RECIST 1.1 criteria. To assess the difference between treatment arm A and treatment arm B in terms of Objective Response Rate (ORR) an exploratory analysis of the HR including a two-sided 95% CI will be carried out., Duration of Response (DOR): DOR is defined as the time from the first documentation of response (CR or PR) to the date of the first documentation of disease progression or death due to any cause, whichever occurs first. To assess whether the difference between treatment arm A and treatment arm B in terms of Duration of Response an exploratory analysis of the HR including a two-sided 95% CI will be carried out., Exploratory: Quality of Life (QoL): Additional exploratory QoL assessments are conducted using other validated instruments to capture a broader range of patient-reported outcomes which will be assessed with EORTC QLQ H&N35., Exploratory: Perceived Stress Questionnaire (PSQ-20): The German version of the Perceived Stress Questionnaire (PSQ-20) by Fliege, Rose, Arck, Levenstein and Klapp (2001) was provided as an instrument for recording stress. The aim is to record the extent of the currently perceived stress factors and the experience of one's own stress on a cognitive and emotional level. It is not the source of the stress that should be stated, but the reaction to it. The factors worry, tension, joy and demands ar

Interventions

DRUGCARBOPLATIN
DRUGCISPLATIN
DRUGErbitux 5 mg/mL solution for infusion
DRUGDOCETAXEL

Sponsors

Charite Universitaetsmedizin Berlin KöR
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Assessment of quality of life (QoL) regarding role functioning at 18 weeks after the initiation of treatment, measured by the standardized QLQ-C30 questionnaire.

Secondary

MeasureTime frame
Progression-Free Survival (PFS): PFS is defined as the time from the date of randomization to the date of the first documentation of objective disease progression or death due to any cause, whichever occurs first. To assess the difference between treatment arm A and treatment arm B in terms of progression-free survival (PFS), an exploratory analysis of the HR including a two-sided 95% CI will be carried out., Overall Survival (OS): OS is defined as the time from the date of randomization to the date of death due to any cause. To assess the difference between treatment arm A and treatment arm B in terms of overall survival (OS), an exploratory analysis of the HR including a two-sided 95% CI will be carried out., Objective Response Rate (ORR): ORR is defined as the proportion of patients who have a complete response (CR) or partial response (PR) according to RECIST 1.1 criteria. To assess the difference between treatment arm A and treatment arm B in terms of Objective Response Rate (ORR)

Countries

Germany

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026