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我们是否在使用用于肾细胞癌分期的最佳肿瘤大小切点?

Are We Using the Best Tumor Size Cut-points for Renal Cell Carcinoma Staging?

作者信息

Bhindi Bimal, Lohse Christine M, Mason Ross J, Westerman Mary E, Cheville John C, Tollefson Matthew K, Boorjian Stephen A, Thompson R Houston, Leibovich Bradley C

机构信息

Department of Urology, Mayo Clinic, Rochester, MN.

Department of Biostatistics, Mayo Clinic, Rochester, MN.

出版信息

Urology. 2017 Nov;109:121-126. doi: 10.1016/j.urology.2017.04.010. Epub 2017 Apr 12.

Abstract

OBJECTIVE

To compare the predictive ability for oncologic outcomes among current tumor size cut-points and clinically relevant alternatives to determine which are optimal.

METHODS

Patients who underwent radical or partial nephrectomy between 1970 and 2010 for T1-2Nx/N0M0 renal cell carcinoma (RCC) were identified. Associations between tumor size and progression-free survival (PFS) and cancer-specific survival (CSS) were evaluated using Kaplan-Meier analyses and Cox models. Predictive ability was assessed using c-indexes.

RESULTS

The cohort included 3304 patients with a median age of 63 years (interquartile range 53, 70). Median follow-up among survivors was 9.9 years (interquartile range 6.9, 14.3). There were 536 patients who progressed and 354 who died from RCC. For RCC tumors ≤3.0 cm, 10-year PFS and CSS rates were 93%-95% and 97%-99%, respectively. For tumors >3.0-4.0 cm, PFS and CSS began to decline (91% and 95%, respectively), with further gradual declines in PFS and CSS with increasing tumor size. Plots of hazard ratios for progression and RCC death as a function of tumor size did not reveal major inflection points. Differences in discrimination based on various combinations of tumor-size cut-points for progression or RCC death were small, with c-indexes ranging between 0.691-0.704 and 0.734-0.750, respectively.

CONCLUSION

RCC tumors ≤3.0 cm in size are associated with favorable outcomes. Thereafter, risks of progression and RCC death increase gradually with tumor size, with no compelling biological reason to endorse a given cut-point over another.

摘要

目的

比较当前肿瘤大小切点及临床相关替代指标对肿瘤学结局的预测能力,以确定哪些是最佳的。

方法

确定1970年至2010年间因T1-2Nx/N0M0肾细胞癌(RCC)接受根治性或部分肾切除术的患者。使用Kaplan-Meier分析和Cox模型评估肿瘤大小与无进展生存期(PFS)和癌症特异性生存期(CSS)之间的关联。使用c指数评估预测能力。

结果

该队列包括3304例患者,中位年龄为63岁(四分位间距53,70)。幸存者的中位随访时间为9.9年(四分位间距6.9,14.3)。有536例患者病情进展,354例死于RCC。对于大小≤3.0 cm的RCC肿瘤,10年PFS和CSS率分别为93%-95%和97%-99%。对于大小>3.0-4.0 cm的肿瘤,PFS和CSS开始下降(分别为91%和95%),随着肿瘤大小增加,PFS和CSS进一步逐渐下降。进展和RCC死亡的风险比随肿瘤大小变化的曲线未显示出主要拐点。基于进展或RCC死亡的肿瘤大小切点的各种组合的区分度差异很小,c指数分别在0.691-0.704和0.734-0.750之间。

结论

大小≤3.0 cm的RCC肿瘤与良好结局相关。此后,进展和RCC死亡风险随肿瘤大小逐渐增加,没有令人信服的生物学原因支持采用某一切点而非其他切点。

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