Cancers of the kidney and urinary tract in patients on dialysis for end-stage renal disease: Analysis of data from the United States, Europe, and Australia and New Zealand

被引:219
作者
Stewart, JH
Buccianti, G
Agodoa, L
Gellert, R
McCredie, MRE
Lowenfels, AB
Disney, APS
Wolfe, RA
Boyle, P
Maisonneuve, P
机构
[1] Univ Otago, Dept Med & Surg Sci, Dunedin, New Zealand
[2] Osped Bassini, Div Nefrol & Dialisi, Azienda Osped San Gerardo, Cinisello Balsamo, Italy
[3] NIDDKD, Div Kidney Urol & Heamtol Dis, Bethesda, MD 20892 USA
[4] CSK AM Banacha, Dept Internal Med & Nephrol, Warsaw, Poland
[5] Univ Otago, Sch Med, Dept Prevent & Social Med, Dunedin, New Zealand
[6] New York Med Coll, Valhalla, NY 10595 USA
[7] Queen Elizabeth Hosp, ANZDATA Registry, Adelaide, SA, Australia
[8] Univ Michigan, USRDS Coordinating Ctr, Ann Arbor, MI 48109 USA
[9] European Inst Oncol, Div Epidemiol & Biostat, I-20141 Milan, Italy
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2003年 / 14卷 / 01期
关键词
D O I
10.1097/01.ASN.0000039608.81046.81
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Patients on maintenance dialysis have increased risk for cancer, especially in the kidney and urinary tract. In a retrospective cohort of 831,804 patients starting dialysis during 1980 to 1994 in the United States, Europe, or Australia and New Zealand, standardized incidence ratios (SIR) with 95% confidence intervals (CI) were calculated for kidney and bladder cancers. Risks for cancers of the kidney (SIR 3.6; CI 3.5 to 3.8) and bladder (SIR 1.5; CI 1.4 to 1.6) were increased, relatively more in younger than older patients and more in female patients (kidney: SIR 4.6, CI 4.3 to 4.9; bladder: SIR 2.7, CI 2.4 to 2.9) than male patients (kidney: SIR 3.2, CI 3.0 to 3.4; bladder: SIR 1.3, CI 1.2 to 1.3). SIR for kidney cancer were raised in all categories of primary renal disease, and for bladder cancer in all but diabetes and familial, hereditary diseases. Notably high SIR occurred in toxic nephropathies (chiefly analgesic nephropathy) and miscellaneous conditions (a category that includes Balkan nephropathy), the excess of kidney cancer in these conditions being urothelial in origin. SIR for kidney cancer rose significantly, and those for bladder cancer fell (not reaching significance) with time on dialysis. There was no association with type of dialysis. The pattern of increased risk for renal parenchymal cancer in dialysis patients is consistent with causation through acquired renal cystic disease and of urothelial cancers of the kidney and bladder with the carcinogenic effects of certain primary renal diseases.
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页码:197 / 207
页数:11
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