老年子宫内膜癌妇女泌尿系统不良结局。

C Anderson, J L Lund, J Park, W Brewster, V Bae-Jump, A F Olshan, H B Nichols
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引用次数: 0

摘要

研究目的:子宫内膜癌及其治疗可能对泌尿系统造成损害,但很少有大规模研究调查子宫内膜癌幸存者中泌尿相关结局的发生率。我们调查了患有子宫内膜癌的老年妇女与没有癌症病史的妇女的几种泌尿系统疾病诊断的风险。方法:在2004-2017年期间诊断为子宫内膜癌的66岁及以上女性(N=44,386)和无癌症病史的女性(N=221,219)在年龄,种族/民族和州方面匹配5:1,在监测,流行病学和最终结果-医疗保险相关数据中确定。ICD-9和-10诊断代码用于识别医疗保险索赔数据中的泌尿结局。在有和没有子宫内膜癌的妇女中估计尿结局的累积发生率(IP)。使用多变量Cox比例风险回归模型来估计患有和未患子宫内膜癌的女性泌尿结局的风险比(HR)。hr也被用于确定子宫内膜癌幸存者的泌尿预后相关特征。结果:相对于未患癌症的女性,子宫内膜癌幸存者患泌尿系统诊断的风险增加,包括肾衰竭(5年生存率:25% vs 14%;HR = 1.50;95% CI: 1.47-1.53),慢性肾病(5年IP: 20% vs 14%;HR = 1.25;95% CI: 1.22-1.28),尿路结石(5年IP: 7% vs 4%;HR = 1.55;95% CI: 1.50-1.61),下尿路感染(5年IP: 55% vs 33%;HR = 1.75;95% CI: 1.72, 1.78)和膀胱疾病(5年IP: 10% vs 6%;HR = 1.57;95% ci: 1.52, 1.62)。这些关联在子宫内膜癌诊断后1年以上和5年以上的分析中持续存在。非西班牙裔黑人或西班牙裔人种/民族、较高的合并症指数、较高的癌症分期或分级、非子宫内膜样组织学、化疗和/或放疗通常是子宫内膜癌女性泌尿结局的预测因素。结论:我们的研究结果表明,在老年妇女中,子宫内膜癌后泌尿结局的风险升高。对于有子宫内膜癌病史的老年妇女,监测泌尿系统疾病可能是长期生存护理的关键部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adverse Urinary System Outcomes among Older Women with Endometrial Cancer.

Purpose of the study: Endometrial cancer and its treatment may cause damage to the urinary system, but few large-scale studies have examined the incidence of urinary-related outcomes among endometrial cancer survivors. We investigated the risk of several urinary disease diagnoses among older women with endometrial cancer compared to women without a cancer history.

Methods: Women ages 66 years and older with an endometrial cancer diagnosis during 2004-2017 (N=44,386) and women without a cancer history (N=221,219) matched 5:1 on age, race/ethnicity, and state were identified in the Surveillance, Epidemiology, and End Results-Medicare linked data. ICD-9 and -10 diagnosis codes were used to identify urinary outcomes in the Medicare claims data. Cumulative incidences (IP) of urinary outcomes were estimated among women with and without endometrial cancer. Multivariable Cox proportional hazards regression models were used to estimate hazards ratios (HR) for urinary outcomes comparing women with and without endometrial cancer. HRs were also used to identify characteristics associated with urinary outcomes among endometrial cancer survivors.

Results: Relative to women without cancer, endometrial cancer survivors had an increased risk of urinary system diagnoses, including renal failure (5-year IP: 25% vs 14%; HR=1.50; 95% CI: 1.47-1.53), chronic kidney disease (5-year IP: 20% vs 14%; HR=1.25; 95% CI: 1.22-1.28), calculus of the urinary tract (5-year IP: 7% vs 4%; HR=1.55; 95% CI: 1.50-1.61), lower urinary tract infection (5-year IP: 55% vs 33%; HR=1.75; 95% CI: 1.72, 1.78), and bladder diseases (5-year IP: 10% vs 6%; HR=1.57; 95% CI: 1.52, 1.62). These associations persisted in analyses limited to 1+ and 5+ years after endometrial cancer diagnosis. Non-Hispanic Black or Hispanic race/ethnicity, higher comorbidity index, higher stage or grade cancer, non-endometrioid histology, and treatment with chemotherapy and/or radiation were often predictors of urinary outcomes among women with endometrial cancer.

Conclusions: Our results suggest that, among older women, the risk of urinary outcomes is elevated after endometrial cancer. Monitoring for urinary diseases may be a critical part of long-term survivorship care for older women with an endometrial cancer history.

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