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Cancer in ANCA-Associated Glomerulonephritis: A Registry-Based Cohort Study

BACKGROUND: Immunosuppressive therapy for antineutrophil cytoplasmic antibody-associated vasculitis has been associated with increased malignancy risk. OBJECTIVES: To quantify the cancer risk associated with contemporary cyclophosphamide-sparing protocols. METHODS: Patients from the Norwegian Kidney...

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Autores principales: Sriskandarajah, Sanjeevan, Bostad, Leif, Myklebust, Tor Åge, Møller, Bjørn, Skrede, Steinar, Bjørneklett, Rune
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748316/
https://www.ncbi.nlm.nih.gov/pubmed/29403663
http://dx.doi.org/10.1155/2017/6013038
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author Sriskandarajah, Sanjeevan
Bostad, Leif
Myklebust, Tor Åge
Møller, Bjørn
Skrede, Steinar
Bjørneklett, Rune
author_facet Sriskandarajah, Sanjeevan
Bostad, Leif
Myklebust, Tor Åge
Møller, Bjørn
Skrede, Steinar
Bjørneklett, Rune
author_sort Sriskandarajah, Sanjeevan
collection PubMed
description BACKGROUND: Immunosuppressive therapy for antineutrophil cytoplasmic antibody-associated vasculitis has been associated with increased malignancy risk. OBJECTIVES: To quantify the cancer risk associated with contemporary cyclophosphamide-sparing protocols. METHODS: Patients from the Norwegian Kidney Biopsy Registry between 1988 and 2012 who had biopsy-verified pauci-immune glomerulonephritis and positive antineutrophil cytoplasmic antibody (ANCA) serology were included. Standardised incidence ratios (SIRs) were calculated to compare the study cohort with the general population. RESULTS: The study cohort included 419 patients. During 3010 person-years, cancer developed in 41 patients (9.79%); the expected number of cancer cases was 37.5 (8.95%). The cohort had SIRs as follows: 1.09, all cancer types (95% CI, 0.81 to 1.49); 0.96, all types except nonmelanoma skin cancer (95% CI, 0.69 to 1.34); 3.40, nonmelanoma skin cancer (95% CI, 1.62 to 7.14); 3.52, hematologic cancer (95% CI, 1.32 to 9.37); 2.12, posttransplant cancer (95% CI, 1.01 to 4.44); and 1.53, during the 1–5-year follow-up after diagnosis (95% CI, 1.01 to 2.32). CONCLUSIONS: Cancer risk did not increase significantly in this cohort with ANCA-associated glomerulonephritis. However, increased risk of nonmelanoma skin cancer, posttransplant cancer, and hematologic cancer indicates an association between immunosuppression and malignancy.
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spelling pubmed-57483162018-02-05 Cancer in ANCA-Associated Glomerulonephritis: A Registry-Based Cohort Study Sriskandarajah, Sanjeevan Bostad, Leif Myklebust, Tor Åge Møller, Bjørn Skrede, Steinar Bjørneklett, Rune Int J Nephrol Research Article BACKGROUND: Immunosuppressive therapy for antineutrophil cytoplasmic antibody-associated vasculitis has been associated with increased malignancy risk. OBJECTIVES: To quantify the cancer risk associated with contemporary cyclophosphamide-sparing protocols. METHODS: Patients from the Norwegian Kidney Biopsy Registry between 1988 and 2012 who had biopsy-verified pauci-immune glomerulonephritis and positive antineutrophil cytoplasmic antibody (ANCA) serology were included. Standardised incidence ratios (SIRs) were calculated to compare the study cohort with the general population. RESULTS: The study cohort included 419 patients. During 3010 person-years, cancer developed in 41 patients (9.79%); the expected number of cancer cases was 37.5 (8.95%). The cohort had SIRs as follows: 1.09, all cancer types (95% CI, 0.81 to 1.49); 0.96, all types except nonmelanoma skin cancer (95% CI, 0.69 to 1.34); 3.40, nonmelanoma skin cancer (95% CI, 1.62 to 7.14); 3.52, hematologic cancer (95% CI, 1.32 to 9.37); 2.12, posttransplant cancer (95% CI, 1.01 to 4.44); and 1.53, during the 1–5-year follow-up after diagnosis (95% CI, 1.01 to 2.32). CONCLUSIONS: Cancer risk did not increase significantly in this cohort with ANCA-associated glomerulonephritis. However, increased risk of nonmelanoma skin cancer, posttransplant cancer, and hematologic cancer indicates an association between immunosuppression and malignancy. Hindawi 2017 2017-12-18 /pmc/articles/PMC5748316/ /pubmed/29403663 http://dx.doi.org/10.1155/2017/6013038 Text en Copyright © 2017 Sanjeevan Sriskandarajah et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sriskandarajah, Sanjeevan
Bostad, Leif
Myklebust, Tor Åge
Møller, Bjørn
Skrede, Steinar
Bjørneklett, Rune
Cancer in ANCA-Associated Glomerulonephritis: A Registry-Based Cohort Study
title Cancer in ANCA-Associated Glomerulonephritis: A Registry-Based Cohort Study
title_full Cancer in ANCA-Associated Glomerulonephritis: A Registry-Based Cohort Study
title_fullStr Cancer in ANCA-Associated Glomerulonephritis: A Registry-Based Cohort Study
title_full_unstemmed Cancer in ANCA-Associated Glomerulonephritis: A Registry-Based Cohort Study
title_short Cancer in ANCA-Associated Glomerulonephritis: A Registry-Based Cohort Study
title_sort cancer in anca-associated glomerulonephritis: a registry-based cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748316/
https://www.ncbi.nlm.nih.gov/pubmed/29403663
http://dx.doi.org/10.1155/2017/6013038
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