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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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Detalles Bibliográficos
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
Descripción
Sumario: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.