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Antiadenovirus Antibodies Predict Response Durability to Nadofaragene Firadenovec Therapy in BCG-unresponsive Non-muscle-invasive Bladder Cancer: Secondary Analysis of a Phase 3 Clinical Trial.

Authors :
Mitra AP
Narayan VM
Mokkapati S
Miest T
Boorjian SA
Alemozaffar M
Konety BR
Shore ND
Gomella LG
Kamat AM
Bivalacqua TJ
Montgomery JS
Lerner SP
Busby JE
Poch M
Crispen PL
Steinberg GD
Schuckman AK
Downs TM
Svatek RS
Mashni J
Lane BR
Guzzo TJ
Bratslavsky G
Karsh LI
Woods ME
Brown GA
Canter D
Luchey A
Lotan Y
Krupski T
Inman BA
Williams MB
Cookson MS
Keegan KA
Andriole GL
Sankin AI
Boyd A
O'Donnell MA
Philipson R
Ylä-Herttuala S
Sawutz D
Parker NR
McConkey DJ
Dinney CPN
Source :
European urology [Eur Urol] 2022 Mar; Vol. 81 (3), pp. 223-228. Date of Electronic Publication: 2021 Dec 18.
Publication Year :
2022

Abstract

A recent phase 3 trial of intravesical nadofaragene firadenovec reported a promising complete response rate for patients with bacillus Calmette-Guérin-unresponsive non-muscle-invasive bladder cancer. This study examined the ability of antiadenovirus antibody levels to predict the durability of therapeutic response to nadofaragene firadenovec. A standardized and validated quantitative assay was used to prospectively assess baseline and post-treatment serum antibody levels among 91 patients from the phase 3 trial, of whom 47 (52%) were high-grade recurrence free at 12 mo (responders). While baseline titers did not predict treatment response, 3-mo titer >800 was associated with a higher likelihood of durable response (p = 0.026). Peak post-treatment titers >800 were noted in 42 (89%) responders versus 26 (59%) nonresponders (p = 0.001; assay sensitivity, 89%; negative predictive value, 78%). Moreover, 22 (47%) responders compared with eight (18%) nonresponders had a combination of peak post-treatment titers >800 and peak antibody fold change >8 (p = 0.004; assay specificity, 82%; positive predictive value, 73%). A majority of responders continued to have post-treatment antibody titers >800 after the first 6 mo of therapy. In conclusion, serum antiadenovirus antibody quantification may serve as a novel predictive marker for nadofaragene firadenovec response durability. Future studies will focus on large-scale validation and clinical utility of the assay. PATIENT SUMMARY: This study reports on a planned secondary analysis of a phase 3 multicenter clinical trial that established the benefit of nadofaragene firadenovec, a novel intravesical gene therapeutic, for the treatment of patients with bacillus Calmette-Guérin (BCG)-unresponsive high-risk non-muscle-invasive bladder cancer. Prospective assessment of serum anti-human adenovirus type-5 antibody levels of patients in this trial indicated that a combination of post-treatment titers and fold change from baseline can predict treatment efficacy. While this merits additional validation, our findings suggest that serum antiadenovirus antibody levels can serve as an important predictive marker for the durability of therapeutic response to nadofaragene firadenovec.<br /> (Copyright © 2021 European Association of Urology. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1873-7560
Volume :
81
Issue :
3
Database :
MEDLINE
Journal :
European urology
Publication Type :
Academic Journal
Accession number :
34933753
Full Text :
https://doi.org/10.1016/j.eururo.2021.12.009