CC BY-NC-ND 4.0 · Laryngorhinootologie 2018; 97(S 02): S11-S12
DOI: 10.1055/s-0038-1639755
Abstracts
Aerodigestivtrakt: Aerodigestive tract

Recurrent respiratory papillomatosis (RRP)-time for a reckoning?

C Meyer
1   HNO Klinik Bielefeld Mitte, Bielefeld
,
P Kin Cho Goon
2   Department of Dermatology (P.K.C.G.) Norfolk and Norwich University HospitalColne, Norwich, Großbritannien
,
LU Scholtz
1   HNO Klinik Bielefeld Mitte, Bielefeld
,
H Sudhoff
3   HNO Klinik Bielefel Mitte, Bielefeld
› Author Affiliations
 

Introduction:

Recurrent respiratory papillomatosis (RRP) is a rare disease. The aetiological agent is human papillomavirus (HPV), and HPV types 6 and 11 account for over 90% of all cases. In the active phase of the disease, patients require multiple hospital admissions for surgical removal or ablation of these benign tumors, which are likely to obstruct the airways if left unchecked. Long-term sequelae include scarring of the vocal cords, change in voice timbre, or even muteness if a tracheostomy is required. The aim of this study was to determine if adjuvant vaccination with the quadrivalent HPV L1 vaccine (Gardasil™) would decrease numbers of surgical treatments post-vaccination.

Methods:

A prospective pilot study following a cohort of 12 RRP patients. All patients with type 6 or 11 were vaccinated at the time of first surgical treatment in the hospital, according to the manufacturer's protocols. Patients were followed up closely with 3 or 6 month follow-up visits.

Results:

We found a > 7-fold decrease in the incidence rates of papillomatosis requiring surgical intervention from the pre-vaccination period (47.44/1000 patient-months) compared to the post-vaccination period (6.71/1000 patient-months).

Conclusion:

Surgical treatments for RRP are robust markers for papillomata which require treatment because of the dangers of obstruction of the airway. Despite the small size of this cohort (due to the rarity of this disease), the data suggests that adjuvant use of quadrivalent HPV L1 vaccine imparts significant benefit to this group of patients. A large multi-center randomized placebo controlled trial is required to definitively establish whether this hypothesis is true and can become the new standard of therapy.



Publication History

Publication Date:
18 April 2018 (online)

© 2018. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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