Testing the Addition of Anti-Cancer Drug, Cetuximab, to Standard of Care Treatment (Pembrolizumab) for Returning or Spreading Head and Neck Cancer After Previous Treatment

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorNational Cancer Institute (NCI)

About this trial

This phase III trial compares the effect of adding cetuximab to pembrolizumab versus pembrolizumab alone in treating patients with head and neck squamous cell carcinoma (HNSCC) that has come back after a period of improvement (recurrent) and/or that has spread from where it first started (primary site) to other places in the body (metastatic). Cetuximab is in a class of medications called monoclonal antibodies. It binds to a protein called EGFR, which is found on some types of tumor cells. This may help keep tumor cells from growing. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the tumor, and may interfere with the ability of tumor cells to grow and spread. Giving cetuximab and pembrolizumab together may be more effective at treating patients with recurrent and/or metastatic HNSCC than pembrolizumab alone.

Eligibility criteria

Qualifiers

Histologically confirmed diagnosis head and neck squamous cell carcinomas (HNSCC).

Previously untreated for recurrent and/or metastatic disease incurable by local therapies.

Primary tumor location of oral cavity, oropharynx, larynx, or hypopharynx.

Note: Other primary tumor sites of HNSCC, including nasopharynx primary tumor are not eligible. Unknown primary tumors may be eligible and can be enrolled at the discretion of the treatment team with approval by the study chair.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Biospecimen Collection
  • Cetuximab
  • Computed Tomography
  • Magnetic Resonance Imaging
  • Pembrolizumab
  • Positron Emission Tomography

Treatment groups

158 Participants
are divided into 2 treatment groups