Pembrolizumab and nivolumab (with or without chemotherapy) are used to treat head and neck cancer. The middle part of the throat (oropharynx) is a common location for head and neck cancer. This cancer is known as oropharyngeal squamous cell carcinoma (OPSCC) and is most often caused by human papillomavirus (HPV) infection. This real-world evidence study carried out in the United States (US) will assess patient demographic and clinical characteristics, treatment patterns, and effectiveness of pembrolizumab and nivolumab (with or without chemotherapy) in patients with HPV positive (HPV+) OPSCC after their cancer spread (metastatic) and/or returned (recurrent). The collected real-world data can be compared with data derived from matched study populations in clinical studies that test new therapies in patients with HPV+ OPSCC. This will allow a more reliable evaluation of the clinical benefits and better-informed design of future clinical studies in this patient population.
Age range
18 Years
Sex
ALL
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Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Patient demographics with ECA 1
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
Clinical characteristics with ECA 1
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
Treatment patterns with ECA 1
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
1L treatment outcomes with ECA 1
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
Patient demographics with ECA 2
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
Clinical characteristics with ECA 2
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
1L treatment outcomes with ECA 2
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
Treatment patterns with ECA 2
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
Patient demographics with ECA3
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
Clinical characteristics with ECA3
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
Treatment patterns with ECA3
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
1L treatment outcomes with ECA3
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
Patient demographics with ECA 4
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
Clinical characteristics with ECA 4
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
Treatment patterns with ECA 4
Timeframe: Whole study period (05 June 2024 through 30 April 2025)
1L treatment outcomes with ECA 4
Timeframe: Whole study period (05 June 2024 through 30 April 2025)