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ANCA Associated Vasculitis Subtypes: Response [Letter]
Authors Merkel PA, Jayne DRW , Bekker P
Received 7 August 2022
Accepted for publication 20 August 2022
Published 9 September 2022 Volume 2022:15 Pages 5161—5162
DOI https://doi.org/10.2147/JIR.S385293
Checked for plagiarism Yes
Editor who approved publication: Professor Ning Quan
Peter A Merkel,1 David RW Jayne,2 Pirow Bekker3
1University of Pennsylvania, Philadelphia, PA, USA; 2University of Cambridge, Cambridge, England; 3ChemoCentryx Inc, San Carlos, CA, USA
Correspondence: Peter A Merkel, Division of Rheumatology, University of Pennsylvania, White Building, Fifth Floor, 3400 Spruce Street, Philadelphia, PA, 19104, USA, Email [email protected]
View the original paper by Dr Austin and colleagues
A Response to Letter has been published for this article.
Dear editor
We read the review article entitled “ANCA Associated Vasculitis Subtypes: Recent Insights and Future Perspectives” by Austin K et al published in the Journal of Inflammation Research 2022;15:2567–2582. We congratulate the authors for this interesting and comprehensive article. However, we respectfully want to elaborate on one statement in the article.1 In the management section, the authors reference the ADVOCATE trial and suggest that background immunosuppressive therapy and ANCA type should influence decisions on use of avacopan to treat ANCA-associated vasculitis.
ADVOCATE was a randomized, double-blind, double-dummy trial conducted in 143 study centers in 20 countries in which avacopan replaced an oral prednisone taper regimen in a standard of care regimen for ANCA-associated vasculitis.2 The choice of background immunosuppressive therapy was not randomized, and the study was not powered, nor the analyses designed, to determine the efficacy of avacopan based on background immunosuppressive therapy. Additionally, patients with both PR3- and MPO-ANCA benefited from treatment with avacopan, based on results at both week 26 and week 52.2
Thus, while we agree that we are in an era of moving towards a personalized medicine approach for treating vasculitis, the current data do not indicate such an approach is ready for use with avacopan with respect to background immunosuppressive therapy or ANCA type.
Disclosure
Dr Peter A Merkel reports grants from ChemoCentryx, during the conduct of the study; grants, personal fees from AbbVie, grants, personal fees from AstraZeneca, grants, personal fees from Boehringer-Ingelheim, grants, personal fees from Bristol-Meyers Squibb, grants, personal fees from ChemoCentryx, personal fees from CSL Behring, personal fees from Dynacure, personal fees from EMD Serono, grants, personal fees from Forbius, grants, personal fees from Genentech/Roche, grants, personal fees from GSK, personal fees from Immagene, grants, personal fees from InflaRx, personal fees from Jannsen, personal fees from Kiniksa, personal fees from Kyverna, personal fees from Magenta, personal fees from MiroBio, personal fees from Mitsubishi, personal fees from Neutrolis, personal fees from Novartis, personal fees from NS Pharma, personal fees from Pfizer, personal fees from Q32, personal fees from Regeneron, personal fees from Sparrow, grants, personal fees from Takeda, grants from Eicos, grants from Electra, grants from Sanofi, personal fees from UpToDate, outside the submitted work. Dr David RW Jayne reports personal fees from ChemoCentryx, grants from Vifor, during the conduct of the study; personal fees from AstraZeneca, other from Aurinia, grants from GSK, personal fees from Takeda, personal fees from Roche, outside the submitted work. Dr Pirow Bekker reports personal fees from ChemoCentryx, outside the submitted work. The authors report no other conflicts of interest in this communication.
References
1. Austin K, Janagan S, Wells M, et al. ANCA associated vasculitis subtypes: recent insights and future perspectives. J Inflamm Res. 2022;15:2567–2582. doi:10.2147/JIR.S284768
2. Jayne DR, Merkel PA, Schall TJ, Bekker P; ADVOCATE Study Group. Avacopan for the treatment of ANCA-associated vasculitis. N Eng J Med. 2021;384(7):599–609. doi:10.1056/NEJMoa2023386
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