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

RecruitingObservational study

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

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* ≥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 Criteria:

* Non-squamous histologies (eg, nasopharynx or salivary gland)
* Relapse or recurrence within 6 months of first line chemotherapy and / or chemoradiotherapy
* Tumors that are PD-L1 negative (CPS \<1)
* 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
* Unable to comply with study procedures (i.e., not willing or able to have additional blood samples collected)

About the study

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.

Sponsor: Tempus AI · Participants: 500 · Started: Aug 1, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06163534

Locations in the U.S.

CaliforniaCity of Hope, Duarte
USC/Norris Comprehensive Cancer Center, Los Angeles
University of California, Los Angeles, Los Angeles
Stanford, Palo Alto
Providence Medical Foundation, Santa Rosa
FloridaMayo Clinic Florida, Jacksonville
GeorgiaMorehouse, Atlanta
Piedmont Healthcare, Atlanta
Winship Cancer Institute, Emory University, Atlanta
IllinoisNorthwestern University Feinberg School of Medicine, Chicago
Cancer Care Specialists of Illinois, Decatur
Illinois Cancer Care, Peoria
KansasUniversity of Kansas, Westwood
MarylandUniversity of Maryland, Baltimore
MassachusettsDana Farber Cancer Institute, Boston
MichiganHenry Ford, Detriot
Karmanos Cancer Institute, Detroit
MinnesotaMayo Clinic Rochester, Rochester
MissouriOncology Hematology Associates, Springfield
Washington University in St. Louis, St Louis
New YorkMount Sinai Hospital, New York
North DakotaSanford Fargo, Fargo
OhioUniversity of Cincinnati, Cincinnati
Cleveland Clinic, Cleveland
Ohio State University, Columbus
PennsylvaniaUniversity of Pennsylvania, Philadelphia
Cancer Care Associates of York, York
South DakotaSanford Sioux Falls, Sioux Falls
TennesseeVanderbilt University, Nashville
WashingtonUniversity of Washington, Seattle
WisconsinThedaCare, Appleton

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.