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Clinical Trials/NCT06412172
NCT06412172
Recruiting
Not Applicable

The Natural History and Biological Study of Pulmonary Recurrent Respiratory Papillomatosis (pRRP)

Massachusetts General Hospital1 site in 1 country100 target enrollmentApril 15, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Recurrent Respiratory Papillomatosis
Sponsor
Massachusetts General Hospital
Enrollment
100
Locations
1
Primary Endpoint
Number of Participants with HPV 6 or 11 infection in the pulmonary lesions
Status
Recruiting
Last Updated
8 months ago

Overview

Brief Summary

Recurrent respiratory papillomatosis (RRP) is an orphan disease that affects approximately 20,000 people in the United States and is caused by infection with human papillomavirus (HPV) types 6 and 11. Since RRP is an orphan disease, it is an understudied disease entity with correspondingly few treatment options. The investigators hypothesize that by understanding the biology of RRP and the failed host immune responses against HPV, novel and rational therapies can be developed. This study will examine the genetic and immunologic alterations found in these rare tumors and distant metastatic involved sites (such as the lung) in patients diagnosed with RRP.

Detailed Description

Since RRP is an orphan disease, any single institution or hospital treats a limited number of RRP patients. The primary purpose for establishing a tissue repository is to collect RRP tissue from various institutions and hospitals and to provide investigators access to a large number of RRP tissues to perform genetic and immunologic studies of these rare tumors. This is both a prospective and retrospective tissue collection repository. Tissue that will be collected will include excess fresh or archived human tissue, either normal or pathological, that was removed as part of standard of care clinical procedures and/or during procedures performed for separate research purposes, such as a therapeutic clinical trial. Prospectively collected and archived pathology samples will be obtained under informed consent from those patients who are still living. The tissue repository will be de-identified. The PI and the RRP Foundation will collaborate and serve as the gatekeepers of the repository and oversee any tissue requests. Any academic collaborator(s) or for-profit collaborator(s) can request access to the tissue specimens. The investigator or collaborators should submit a letter to express interest in obtaining tissue from the tissue repository to the RRP Foundation and the PI.

Registry
clinicaltrials.gov
Start Date
April 15, 2024
End Date
April 15, 2030
Last Updated
8 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sara Pai, MD, PhD

Associate Surgeon

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • History of HPV-associated Recurrent Respiratory Papillomatosis
  • Has pulmonary lesions

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Number of Participants with HPV 6 or 11 infection in the pulmonary lesions

Time Frame: 24 months

HPV 6 and 11 genotyping will be done via polymerase chain reaction

Number of Participants with different mutational profiles in the matched laryngeal and pulmonary lesions

Time Frame: 24 months

Sequencing of the HPV genome in the matched laryngeal and pulmonary lesions will be performed.

Study Sites (1)

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