Sriskandarajah Sanjeevan, Bostad Leif, Myklebust Tor Åge, Møller Bjørn, Skrede Steinar, Bjørneklett Rune
Department of Clinical Medicine, University of Bergen, Bergen, Norway.
Department of Pathology, Haukeland University Hospital, Bergen, Norway.
Int J Nephrol. 2017;2017:6013038. doi: 10.1155/2017/6013038. Epub 2017 Dec 18.
Immunosuppressive therapy for antineutrophil cytoplasmic antibody-associated vasculitis has been associated with increased malignancy risk.
To quantify the cancer risk associated with contemporary cyclophosphamide-sparing protocols.
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.
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).
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.
抗中性粒细胞胞浆抗体相关性血管炎的免疫抑制治疗与恶性肿瘤风险增加有关。
量化与当代环磷酰胺替代方案相关的癌症风险。
纳入1988年至2012年挪威肾脏活检登记处中经活检证实为寡免疫性肾小球肾炎且抗中性粒细胞胞浆抗体(ANCA)血清学呈阳性的患者。计算标准化发病率(SIRs)以将研究队列与普通人群进行比较。
研究队列包括419名患者。在3010人年期间,41名患者(9.79%)发生癌症;预期癌症病例数为37.5例(8.95%)。该队列的SIRs如下:所有癌症类型为1.09(95%CI,0.81至1.49);除非黑色素瘤皮肤癌外的所有类型为0.96(95%CI,0.69至1.34);非黑色素瘤皮肤癌为3.40(95%CI,1.62至7.14);血液系统癌症为3.52(95%CI,1.32至9.37);移植后癌症为2.12(95%CI,1.01至4.44);诊断后1至5年随访期间为1.53(95%CI,1.01至2.32)。
该ANCA相关性肾小球肾炎队列中的癌症风险没有显著增加。然而,非黑色素瘤皮肤癌、移植后癌症和血液系统癌症风险增加表明免疫抑制与恶性肿瘤之间存在关联。