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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Main Authors: Sanjeevan Sriskandarajah, Leif Bostad, Tor Åge Myklebust, Bjørn Møller, Steinar Skrede, Rune Bjørneklett
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:International Journal of Nephrology
Online Access:http://dx.doi.org/10.1155/2017/6013038
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author Sanjeevan Sriskandarajah
Leif Bostad
Tor Åge Myklebust
Bjørn Møller
Steinar Skrede
Rune Bjørneklett
author_facet Sanjeevan Sriskandarajah
Leif Bostad
Tor Åge Myklebust
Bjørn Møller
Steinar Skrede
Rune Bjørneklett
author_sort Sanjeevan Sriskandarajah
collection DOAJ
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 doaj-art-1bd7021d924e4bf1bccb9a1816614b732025-02-03T05:44:16ZengWileyInternational Journal of Nephrology2090-214X2090-21582017-01-01201710.1155/2017/60130386013038Cancer in ANCA-Associated Glomerulonephritis: A Registry-Based Cohort StudySanjeevan Sriskandarajah0Leif Bostad1Tor Åge Myklebust2Bjørn Møller3Steinar Skrede4Rune Bjørneklett5Department of Clinical Medicine, University of Bergen, Bergen, NorwayDepartment of Clinical Medicine, University of Bergen, Bergen, NorwayDepartment of Clinical and Registry-Based Research, Cancer Registry of Norway, Institute of Population-Based Cancer Research, Oslo, NorwayDepartment of Clinical and Registry-Based Research, Cancer Registry of Norway, Institute of Population-Based Cancer Research, Oslo, NorwayDepartment of Clinical Science, University of Bergen, Bergen, NorwayDepartment of Clinical Medicine, University of Bergen, Bergen, NorwayBackground. 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.http://dx.doi.org/10.1155/2017/6013038
spellingShingle Sanjeevan Sriskandarajah
Leif Bostad
Tor Åge Myklebust
Bjørn Møller
Steinar Skrede
Rune Bjørneklett
Cancer in ANCA-Associated Glomerulonephritis: A Registry-Based Cohort Study
International Journal of Nephrology
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
url http://dx.doi.org/10.1155/2017/6013038
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