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Carboplatin + Paclitaxel + Cetuximab (PCC) after failure of first line Immune checkpoint inhibitor with or without chemotherapy in recurrent/metastatic squamous cell carcinoma of the head and neck: CARPACCIO (CARboplatin PAClitaxel Cetuximab IO immuno-oncology)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-512297-96-01
Enrollment
46
Registered
2024-10-30
Start date
2024-11-26
Completion date
Unknown
Last updated
2026-01-16

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

Conditions

Head and neck squamous cell carcinoma

Brief summary

Number of patients who had an objective response within 12 months

Detailed description

Progression events (loco-regional progression, metastatic progression or death whatever the cause) will be collected beyond 12 months of patient participation according to local practices., The patient's condition (alive, deceased from whatever cause or lost to follow-up) will be collected beyond 12 months of patient participation. Patients alive at the time of analysis will be censored on the date of last contact, Time from date of first documented response (complete or partial response) to date of first subsequent progression or death from any cause, Incidence of treatment-emergent adverse events, serious adverse events according to CTCAE V5.0 criteria and deaths, Taking the QLQ-C30 and QLQ-HN35 questionnaires

Interventions

DRUGsolution à diluer pour perfusion
DRUGErbitux 5 mg/mL solution for infusion

Sponsors

Centre Regional Lutte Contre Le Cancer
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Number of patients who had an objective response within 12 months

Secondary

MeasureTime frame
Progression events (loco-regional progression, metastatic progression or death whatever the cause) will be collected beyond 12 months of patient participation according to local practices., The patient's condition (alive, deceased from whatever cause or lost to follow-up) will be collected beyond 12 months of patient participation. Patients alive at the time of analysis will be censored on the date of last contact, Time from date of first documented response (complete or partial response) to date of first subsequent progression or death from any cause, Incidence of treatment-emergent adverse events, serious adverse events according to CTCAE V5.0 criteria and deaths, Taking the QLQ-C30 and QLQ-HN35 questionnaires

Countries

France

Outcome results

None listed

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