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Tracks molecular markers in people with head and neck squamous cell cancer

Collects tissue and blood samples to profile molecular markers during standard treatment.

Plain-language title generated from the registry record
Registry title: A Longitudinal Multi-Omic Biomarker Profiling Study of Patients With Head & Neck Squamous Cell Carcinoma (HNSCC)

Key facts

Where
San Juan, Puerto RicoSee the site

Where in Puerto Rico

  • Pan American Cancer for OncologySan Juan, Puerto RicoNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Tempus AI
Trial code
NCT06163534
Record updated
3 September 2026
Original description
The study is a prospective, longitudinal, non-interventional, multicenter study of participants with HNSCC who will have tissue and blood based molecular biomarker profiling during their standard of care treatment.Read full original descriptionShow less

TEMPUS PHOENIX HNSCC STUDY: A Longitudinal Multi-Omic Biomarker Profiling Study of Patients With Head & Neck Squamous Cell Carcinoma (HNSCC)

The study is a prospective, longitudinal, non-interventional, multicenter study of participants with HNSCC who will have tissue and blood based molecular biomarker profiling during their standard of care treatment.

Inclusion: ≥18 years of age; Willing and able to provide informed consent; Histologically- or cytologically-confirmed metastatic or unresectable, recurrent HNSCC unsuitable for local therapies; Intended for first line anti-PD1 or PDL1 monotherapy or combination therapy; Must submit tumor tissue sample representative of current disease per laboratory manual.

Exclusion: Relapse or recurrence within 6 months of first line chemotherapy and / or chemoradiotherapy; Clinical evidence of an active second invasive malignancy within <2 years of enrollment with the exception of stable prostate cancer on watchful waiting, in situ cervical cancer, in situ breast carcinoma or localized non-melanoma skin cancers; Non-squamous histologies (eg, nasopharynx or salivary gland); Tumors that are PD-L1 negative (CPS <1); Unable to comply with study procedures (i.e., not willing or able to have additional blood samples collected).

ClinicalTrials.gov NCT06163534