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HPV in Sinonasal Ca: Retrospective Analysis Association of Human Papilloma Virus (HPV) Serology and Behavioral Risk Factors

HPV in Sinonasal Ca: Retrospective Analysis Association of Human Papilloma Virus (HPV) Serology and Behavioral Risk Factors

Non Recruiting
18 years and older
All
Phase N/A

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Overview

This is a case-control study designed to evaluate the role of anatomic site, gender and race in human papillomavirus-associated head and neck squamous cell cancers (HNSCC). We will explore the role of HPV, tobacco, alcohol and drug use, in HNSCC by tumor site with particular emphasis on the sinonasal cavity as well as differences in risk factors for HPV-positive HNSCC by gender and race.

Eligibility

Inclusion Criteria:

  • Cases:
    • Patients must be 18 years of age or older with a confirmed or suspected diagnosis of sinonasal cancer
    • Patients must have either a routine diagnostic biopsy of primary tumor or surgical resection planned as part of routine care (to allow for the collection of tumor sample for the study) or grant access to archival material, from a previously performed biopsy.
    • Willing to provide 20 mL blood sample
    • Ability to understand and the willingness to sign a written informed consent document
  • Controls:
    • Must be 18 years of age or older within the categories of age, gender, and race needed to match cases
    • Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria:

  • Cases:
    • Presence of medical or psychiatric condition affecting ability to give voluntary, informed consent
    • Participants who do not speak English and do not agree to use of a telephone or video interpreter will be excluded. However, if there is a hearing, literally or minor fluency issue and the participant requests assistance from a family member or the study coordinator, this individual may still enroll and receive this assistance to ensure they fully hear and understand everything being asked
  • Controls:
    • Presence of medical or psychiatric condition affecting ability to give voluntary, informed consent
    • Participants who do not speak English and do not agree to use of a telephone or video interpreter will be excluded. However, if there is a hearing, literacy or minor fluency issue and the participant requests assistance from a family member or the study coordinator, this individual may still enroll and receive this assistance to ensure they fully hear and understand everything being asked
    • No prior diagnosis of head and neck cancer, except basal cell cancer
    • No previous radiation therapy of the head and neck

Study details
    Sinonasal Carcinoma
    HPV-Related Squamous Cell Carcinoma

NCT04979000

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

21 October 2025

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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