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Identification of Secreted Markers for Tumor Hypoxia in Patients With Head and Neck or Lung Cancers

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Stanford University

Status

Enrolling

Conditions

Head and Neck Cancers
Lip Cancer
Lung Cancer
Lip Neoplasms
Head and Neck Cancer

Treatments

Procedure: Phlebotomy
Procedure: Tumor biopsy

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT00568490
IRB-10564
R01DE029672-01A1 (U.S. NIH Grant/Contract)
SU-11052007-801 (Other Identifier)
73995 (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to identify and confirm new blood and tissue markers for prognosis and tumor hypoxia. Tumor hypoxia, or the condition of low oxygen in the tumor, has been shown to increase the risk of tumor spread and enhance tumor resistance to the standard treatment of radiation and chemotherapy in head and neck and lung cancers. We have recently identified several proteins or markers in the blood and in tumors (including osteopontin, lysyl oxidase, macrophage inhibiting factor and proteomic technology) in the laboratory that may be able to identify tumors with low oxygen levels or more aggressive behaving tumors.

Full description

The endpoints of the study are

  1. To validate the prognostic significance of OPN in H&N and lung cancer patients and to monitor its level during active therapy and follow up for cancer surveillance.
  2. To identify a gene and protein signature for hypoxia in H&N and lung cancer patients.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Histologically confirmed squamous cell carcinoma of the head and neck sites or non-small cell lung cancer, or relatives of patients with histologically confirmed squamous cell carcinoma of the head and neck.
  • Able to sign a Stanford IRB approved consent form

Exclusion criteria

  • Refuse or unable to sign an IRB approved consent form.
  • Refuse to be contacted in the future for follow up.

Trial contacts and locations

1

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Central trial contact

Eyiwunmi Laseinde

Data sourced from clinicaltrials.gov

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