Volume 127, Issue 10 pp. 2225-2229
Broncho-Esophagology

Systemic bevacizumab for recurrent respiratory papillomatosis: A national survey

Simon R. Best MD

Corresponding Author

Simon R. Best MD

Department of Otolaryngology–Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland, U.S.A

Send correspondence to Simon Best, MD, 601 North Caroline Street, Room 6210, Baltimore, MD 21287. E-mail: [email protected]Search for more papers by this author
Michael Mohr MD

Michael Mohr MD

Department of Medicine, Hematology, Oncology and Pneumology, University Hospital Muenster, Muenster, Germany

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Karen B. Zur MD

Karen B. Zur MD

Pediatric Otolaryngology, The Children's Hospital of Philadelphia, The University of Pennsylvania, Philadelphia, Pennsylvania, U.S.A

Department of Otolaryngology–Head and Neck Surgery, The University of Pennsylvania, Philadelphia, Pennsylvania, U.S.A

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First published: 28 June 2017
Citations: 72

Financial support for this study was provided by the National Institute on Deafness and Other Communication Disorders, Mentored Patient-Oriented Research Career Development Award (1K23DC014758 [S. Best]).

The authors have no other funding, financial relationships, or conflicts of interest to disclose.

Abstract

Objectives/Hypothesis

Aggressive laryngeal, tracheal, and pulmonary papilloma is an extremely challenging clinical problem without proven treatment options. A recent German report documented promising results with systemic bevacizumab. The objective of this study is to report the initial experience of this novel treatment in the United States for recurrent respiratory papillomatosis (RRP).

Study Design

Cases series.

Methods

Electronic survey of the RRP Task Force of the American Society of Pediatric Otolaryngology, American Broncho-Esophagological Association, and physicians known to the authors to have used systemic bevacizumab for RRP.

Results

Eleven completed surveys were obtained. In three cases, systemic bevacizumab was considered clinically but not administered. Eight patients were treated with systemic bevacizumab, all for aggressive papillomatosis uncontrolled by surgical and adjuvant therapy, including seven of eight with pulmonary disease. Treatment dosing ranged from 5 to 10 mg/kg every 2 to 4 weeks, with all patients responding (7/8 partial response, 1/8 complete response). In four patients who had postbevacizumab chest imaging, three demonstrated improvement of disease and one stabilization. Treatment interval could be lengthened in seven patients and clinical response maintained. One patient with long-standing pulmonary disease (>10 years) was diagnosed with malignant transformation while on treatment, and bevacizumab was discontinued in lieu of other chemotherapeutic agents. All other patients continue on systemic bevacizumab with minimal complications (hemoptysis n = 1, proteinuria n = 1).

Conclusions

Systemic bevacizumab appears to have significant promise in the most treatment-resistant and aggressive forms of papillomatosis with a low complication profile. These results suggest bevacizumab should be studied in a formal clinical trial for RRP.

Level of Evidence

4. Laryngoscope, 127:2225–2229, 2017

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