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一线酪氨酸激酶抑制剂治疗后转移性肾细胞癌患者 1 年内早期死亡的新型预测模型。

Novel Predictive Models of Early Death Less Than 1 Year in Patients With Metastatic Renal Cell Carcinoma After Treatment With First-line Tyrosine Kinase Inhibitors.

机构信息

Jincheon Public Health Care Center, Chungbuk, South Korea.

Department of Urology, Sungkyunkwan University College of Medicine, Samsung Medical Center, Seoul, South Korea.

出版信息

Clin Genitourin Cancer. 2019 Dec;17(6):e1137-e1146. doi: 10.1016/j.clgc.2019.07.014. Epub 2019 Aug 6.

Abstract

BACKGROUND

We aimed to develop a modified International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) model that can predict early death less than 1 year in patients with metastatic renal cell carcinoma (mRCC) after receiving first-line tyrosine kinase inhibitors (TKIs).

PATIENTS AND METHODS

We retrospectively reviewed records of patients with mRCC treated with first-line TKIs at our institution between 2007 and 2012. The primary endpoint was the rate of early death within 1 year after first-line TKI administration. We determined statistically significant factors predicting early death by performing multiple logistic regression. The modified IMDC model 1 was developed using new variables in addition to the risk criteria of the IMDC model, and model 2 was developed using new variables irrespective of the risk classification of IMDC model.

RESULTS

Early mortality within 1 year of first-line TKI treatment was 19.7% (n = 98) in 462 patients. Although the C-index of the IMDC model for early death was 0.655, the C-index of model 1, which includes 5 variables (previous nephrectomy, body mass index, multiple metastases, previous metastasectomy, and serum albumin level) in addition to the Heng criteria, was 0.823. The C-index of model 2, which includes 7 variables (hemoglobin, neutrophil level, and the 5 variables of model 1) was 0.822. Of note, there was no significant difference in net reclassification index between the 2 models.

CONCLUSION

This is the first study suggesting novel prediction models for early death less than 1 year in patients with mRCC treated with first-line TKI.

摘要

背景

我们旨在开发一种改良的国际转移性肾细胞癌数据库联盟(IMDC)模型,以预测接受一线酪氨酸激酶抑制剂(TKI)治疗后转移性肾细胞癌(mRCC)患者 1 年内的早期死亡。

患者与方法

我们回顾性分析了 2007 年至 2012 年在我院接受一线 TKI 治疗的 mRCC 患者的记录。主要终点是一线 TKI 治疗后 1 年内早期死亡的发生率。我们通过多元逻辑回归分析确定了预测早期死亡的统计学显著因素。改良的 IMDC 模型 1 在 IMDC 模型的风险标准之外增加了新的变量,模型 2 则在不考虑 IMDC 模型风险分类的情况下使用新的变量开发。

结果

在 462 例患者中,有 19.7%(n=98)在接受一线 TKI 治疗后 1 年内早期死亡。虽然 IMDC 模型对早期死亡的 C 指数为 0.655,但包含 Heng 标准以外的 5 个变量(既往肾切除术、体重指数、多发转移、既往转移切除术和血清白蛋白水平)的模型 1 的 C 指数为 0.823。包含血红蛋白、中性粒细胞水平和模型 1 的 5 个变量的模型 2 的 C 指数为 0.822。值得注意的是,这两个模型的净重新分类指数没有显著差异。

结论

这是第一项关于接受一线 TKI 治疗的 mRCC 患者 1 年内早期死亡的新预测模型的研究。

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