Use of angiotensin converting enzyme inhibitors is associated with reduced risk of late bladder toxicity following radiotherapy for prostate cancer
Kerns, S. L. Amidon Morlang, A. Lee, S. M. Peterson, D. R. Marples, B. Zhang, H. Bylund, K. Rosenzweig, D. Hall, W. De Ruyck, K.
Kerns, S. L.
Amidon Morlang, A.
Lee, S. M.
Peterson, D. R.
Marples, B.
Zhang, H.
Bylund, K.
Rosenzweig, D.
Hall, W.
De Ruyck, K.
Citations
Altmetric:
Abstract
Background and purpose Genome-wide association studies (GWAS) of late hematuria following prostate cancer radiotherapy identified single nucleotide polymorphisms (SNPs) near AGT, encoding angiotensinogen. We tested the hypothesis that patients taking angiotensin converting enzyme inhibitors (ACEi) have a reduced risk of late hematuria. We additionally tested genetically-defined hypertension. Materials and methods Prostate cancer patients undergoing potentially-curative radiotherapy were enrolled onto two multi-center observational studies, URWCI (N = 256) and REQUITE (N = 1,437). Patients were assessed pre-radiotherapy and followed prospectively for development of toxicity for up to four years. The cumulative probability of hematuria was estimated by the Kaplan-Meier method. Multivariable grouped relative risk models assessed the effect of ACEi on time to hematuria adjusting for clinical factors and stratified by enrollment site. A polygenic risk score (PRS) for blood pressure was tested for association with hematuria in REQUITE and our Radiogenomics Consortium GWAS. Results Patients taking ACEi during radiotherapy had a reduced risk of hematuria (HR 0.51, 95%CI 0.28 to 0.94, p = 0.030) after adjusting for prior transurethral prostate and/or bladder resection, heart disease, pelvic node radiotherapy, and bladder volume receiving 70 Gy, which are associated with hematuria. A blood pressure PRS was associated with hypertension (odds ratio per standard deviation 1.38, 95%CI 1.31 to 1.46, n = 5,288, p < 0.001) but not hematuria (HR per standard deviation 0.96, 95%CI 0.87 to 1.06, n = 5,126, p = 0.41). Conclusions Our study is the first to show a radioprotective effect of ACEi on bladder in an international, multi-site study of patients receiving pelvic radiotherapy. Mechanistic studies are needed to understand how targeting the angiotensin pathway protects the bladder.
Authors
Kerns, S. L.
Amidon Morlang, A.
Lee, S. M.
Peterson, D. R.
Marples, B.
Zhang, H.
Bylund, K.
Rosenzweig, D.
Hall, W.
De Ruyck, K.
Rosenstein, B. S.
Stock, R. G.
Gómez-Caamaño, A.
Vega, A.
Sosa-Fajardo, P.
Taboada-Valladares, B.
Aguado-Barrera, M. E.
Parker, C.
Veldeman, L.
Fonteyne, V.
Bultijnck, R.
Talbot, C. J.
Symonds, R. P.
Johnson, K.
Rattay, T.
Webb, A.
Lambrecht, M.
de Ruysscher, D.
Vanneste, B.
Choudhury, Ananya
Elliott, R. M.
Sperk, E.
Herskind, C.
Veldwijk, M. R.
Rancati, T.
Avuzzi, B.
Valdagni, R.
Azria, D.
Farcy Jacquet, M. P.
Chang-Claude, J.
Seibold, P.
West, Catharine M L
Janelsins, M.
Chen, Y.
Messing, E.
Morrow, G.
Amidon Morlang, A.
Lee, S. M.
Peterson, D. R.
Marples, B.
Zhang, H.
Bylund, K.
Rosenzweig, D.
Hall, W.
De Ruyck, K.
Rosenstein, B. S.
Stock, R. G.
Gómez-Caamaño, A.
Vega, A.
Sosa-Fajardo, P.
Taboada-Valladares, B.
Aguado-Barrera, M. E.
Parker, C.
Veldeman, L.
Fonteyne, V.
Bultijnck, R.
Talbot, C. J.
Symonds, R. P.
Johnson, K.
Rattay, T.
Webb, A.
Lambrecht, M.
de Ruysscher, D.
Vanneste, B.
Choudhury, Ananya
Elliott, R. M.
Sperk, E.
Herskind, C.
Veldwijk, M. R.
Rancati, T.
Avuzzi, B.
Valdagni, R.
Azria, D.
Farcy Jacquet, M. P.
Chang-Claude, J.
Seibold, P.
West, Catharine M L
Janelsins, M.
Chen, Y.
Messing, E.
Morrow, G.
Description
Date
2022
Publisher
Collections
Keywords
Type
Article
Citation
Kerns SL, Amidon Morlang A, Lee SM, Peterson DR, Marples B, Zhang H, et al. Use of angiotensin converting enzyme inhibitors is associated with reduced risk of late bladder toxicity following radiotherapy for prostate cancer. Vol. 168, Radiotherapy and Oncology. Elsevier BV; 2022. p. 75–82.