Recurrent Respiratory Papillomatosis (RPP) is an orphan disease with approximately 20,000 active cases in the United States and with an incidence of approximately 4.3 per 100,000 children and 1.8 per 100,000 adults. RRP is caused by infection with human papillomavirus (HPV) types 6 and 11 and is characterized by mucosal tumors that grow in the respiratory tract, impacting breathing, swallowing, and speech. In 3-5% of patients, the lesions can undergo malignant transformation and the prognosis for patients who develop cancers derived from their RRP is poor. There is no effective systemic therapy for RRP, despite the fact that it typically involves multiple sites. Thus, there is a strong unmet need to develop novel treatment options for RRP patients. We and others have shown that RPP is a disease characterized by an ineffective host immune response to HPV, in part, through the upregulation of the PD1:PDL1 axis. Thus, we hypothesize that administration of a blocking PD-1 monoclonal antibody, pembrolizumab, can re-activate host anti-tumor responses, leading to the regression of existing RPP lesions, clearance of chronic HPV infection, and prevention of new disease as a means to improve the quality of life and achieve possible cure. To test this hypothesis, we have opened an investigator-initiated phase II clinical trial administering pembrolizumab to subjects diagnosed with advanced RPP to evaluate the effectiveness of immunotherapy as a novel treatment option. In this study, biopsies and peripheral blood samples are obtained every 12 weeks while receiving study treatment, which provides a unique longitudinal sampling of tissue to understand how the tumor, tumor immune microenvironment, and host immune responses may evolve over time. We seek support to perform key correlative analyses of the pre- and on-treatment human samples to generate essential data, investigating the role of immunotherapy as a novel and effective treatment option for RRP patients.

Public Health Relevance

Human papillomavirus (HPV) associated recurrent respiratory papillomatosis (RRP) is a rare disease in which no definitive therapy or cure exists. RRP is a disease characterized by ineffective host immune responses against HPV. In a phase II clinical trial, we evaluate the efficacy of anti-PD-1 therapy in patients diagnosed with RRP as well as define the risks of administering this therapy to a non-cancer patient population.

Agency
National Institute of Health (NIH)
Institute
Food and Drug Administration (FDA)
Type
Research Project (R01)
Project #
1R01FD006341-01
Application #
9644859
Study Section
Special Emphasis Panel (ZFD1)
Program Officer
Johnson, Lloyd
Project Start
2019-09-01
Project End
2022-08-31
Budget Start
2019-09-01
Budget End
2020-08-31
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02114