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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorStanford University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Refuse or unable to sign an IRB approved consent form.

Refuse to be contacted in the future for follow up.

Trial population

Newly diagnosed patients with head and neck cancer

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Tumor biopsy

    Procedure/Surgery

    For patients who undergo tumor biopsy or resection at Stanford, approximately 500 mg of the tumor will be removed from the resection specimen

  • Phlebotomy

    Procedure/Surgery

    Blood draw (approximately 20 cc) prior to any anticancer therapy Weekly blood draw (approximately 20cc) only for patients who are undergoing radiation treatment at Stanford University

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Identification of Secreted Markers for Tumor Hypoxia through tissue collection

Time frame
before therapy, weekly during therapy

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Stanford University

Lead sponsor

National Institutes of Health (NIH)

Collaborator

National Institute of Dental and Craniofacial Research (NIDCR)

Collaborator