James Buchanan Brady Urological Institute and Department of Urology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
James Buchanan Brady Urological Institute and Department of Urology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Eur Urol Oncol. 2019 Jul;2(4):343-348. doi: 10.1016/j.euo.2018.08.023. Epub 2018 Sep 25.
The rising incidence of renal cell carcinoma (RCC) since the 1980s has been accompanied by stage migration toward early-stage (stage I) cancers. Stage migration drove an apparent increase in survival for RCC since the 1980s, but it is unclear whether it remains a contributor more recently.
To determine whether clinical stage migration has persisted and the relative impact of stage migration versus improvements in treatment on survival for RCC.
DESIGN, SETTING, AND PARTICIPANTS: An epidemiologic assessment of stage migration and survival for 262 597 patients at diagnosis of RCC (2004-2015) across >1500 facilities in the National Cancer Database.
Proportion of patients over time was assessed by clinical stage at diagnosis via Cochran-Armitage chi-square tests and linear regression. Mortality data were assessed with the Kaplan-Meier method for 5-yr overall survival, Cox proportional hazards regression, and propensity score matching to differentiate the impact of treatment including systemic therapy from stage migration.
Greater diagnosis of clinical stage I disease (70%; p<0.001) was observed, with decreased diagnosis of stage III (8%; p<0.001) and stage IV (11%; p<0.001) up to 2007 followed by stabilization through 2015. Tumor size continues to decrease for localized tumors (mean-0.22cm stage I and-1.24cm stage II, 2004-2015). Histology demonstrated significant associations with stage. Five-year overall survival improved (67.9% [2004] to 72.3% [2010]) with gains in advanced RCC but not localized tumors. Models confirmed improved survival in recent years for stage IV patients. Systemic therapy was associated with improved survival (hazard ratio 0.811 [0.786-0.837], p<0.001). National Cancer Database limitations apply.
The proportion of patients presenting with stage I RCC has stabilized (70%), suggesting that stage migration may have ended. Localized tumors are detected with decreasing size, while advanced cancers have remained stable. Only 11% of patients now present with distant metastatic disease, but 5-yr overall survival is improving in recent years due to improved treatments rather than stage migration.
In this study, we found that stage migration toward early-stage cancers has ended for renal cell carcinoma (RCC). However, improved treatment for advanced RCC appears to be responsible for improved survival in recent years.
自 20 世纪 80 年代以来,肾细胞癌(RCC)的发病率不断上升,同时伴有向早期(I 期)癌症的分期转移。自 20 世纪 80 年代以来,分期转移导致 RCC 的生存率明显提高,但尚不清楚这种情况最近是否仍然存在。
确定临床分期转移是否持续存在,以及分期转移相对于治疗进展对 RCC 生存率的相对影响。
设计、设置和参与者:对 2004 年至 2015 年间,国家癌症数据库中 1500 多家医疗机构的 262597 例 RCC 患者的分期转移和生存情况进行了一项流行病学评估。
通过 Cochran-Armitage 卡方检验和线性回归评估随时间推移诊断时临床分期的患者比例。使用 Kaplan-Meier 方法评估 5 年总生存率,Cox 比例风险回归和倾向评分匹配,以区分治疗(包括系统治疗)和分期转移对生存率的影响。
观察到临床 I 期疾病的诊断比例增加(70%;p<0.001),诊断为 III 期(8%;p<0.001)和 IV 期(11%;p<0.001)的比例下降,直到 2007 年,然后在 2015 年之前稳定下来。局限性:适用于国家癌症数据库。
I 期 RCC 患者的比例已稳定(70%),提示分期转移可能已经结束。局部肿瘤的检测尺寸减小,而晚期癌症保持稳定。现在只有 11%的患者出现远处转移疾病,但由于治疗进展而非分期转移,近年来 5 年总生存率有所提高。
在这项研究中,我们发现肾细胞癌(RCC)向早期癌症的分期转移已经结束。然而,晚期 RCC 的治疗进展似乎是近年来生存率提高的原因。