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转移性肾细胞癌患者接受三线靶向治疗的临床结局:来自大型患者队列的结果。

Clinical outcomes in patients receiving three lines of targeted therapy for metastatic renal cell carcinoma: results from a large patient cohort.

机构信息

Sapienza University of Rome, Department of Radiology, Oncology and Human Pathology, Rome, Italy.

Oncology Unit, A. Cardarelli Hospital, Naples, Italy.

出版信息

Eur J Cancer. 2013 Jun;49(9):2134-42. doi: 10.1016/j.ejca.2013.02.032. Epub 2013 Mar 18.

DOI:10.1016/j.ejca.2013.02.032
PMID:23518211
Abstract

AIM

A number of targeted therapies (TTs) are effective in metastatic renal cell carcinoma (mRCC) but clinical outcomes with the sequential use of three TTs have been poorly investigated, this study evaluates their outcome.

METHODS

Patients with clear cells mRCC treated with three TTs were retrospectively studied. Therapies were classified as vascular endothelial growth factor (VEGF)/vascular endothelial growth factor receptor (VEGFR) or mammalian target of rapamycin inhibitors (mTORi). Progression free survival (PFS), overall survival (OS) and total PFS (tPFS)--defined as the time from start of first-line to progression on third-line treatment--were estimated using the Kaplan-Meier method and curves were compared with log-rank test.

RESULTS

A total of 2065 patients with mRCC were consecutively treated with first-line TT in 23 centres in Italy. Overall 281/2065 patients (13%) were treated with three TTs. Median OS and tPFS were 44.7 and 34.1 months, respectively and were longer in patients receiving the sequence vascular endothelial growth factor inhibitors (VEGFi)-VEGFi-mTORi compared with those receiving VEGFi-mTORi-VEGFi with a statistical difference in OS (50.7 versus 37.8 months, p = 0.004; 36.5 versus 29.3 months, p = 0.059, respectively).

CONCLUSIONS

Few patients received three lines of TTs. The sequence VEGFi-VEGFi-mTORi was associated with improved survival with respect to VEGFi-mTORi-VEGFi and primary resistance to first-line was a negative predictive and prognostic factor.

摘要

目的

一些靶向治疗(TTs)在转移性肾细胞癌(mRCC)中有效,但对三种 TTs 序贯使用的临床结果研究甚少,本研究评估其结果。

方法

回顾性研究接受三种 TTs 治疗的 clear cells mRCC 患者。治疗分为血管内皮生长因子(VEGF)/血管内皮生长因子受体(VEGFR)或哺乳动物雷帕霉素靶蛋白抑制剂(mTORi)。使用 Kaplan-Meier 法估计无进展生存期(PFS)、总生存期(OS)和总 PFS(tPFS)——定义为从一线治疗开始到三线治疗进展的时间——并用对数秩检验比较曲线。

结果

意大利 23 个中心共 2065 例 mRCC 患者连续接受一线 TT 治疗。共有 281/2065 例(13%)患者接受三种 TTs 治疗。中位 OS 和 tPFS 分别为 44.7 和 34.1 个月,接受 VEGFi-VEGFi-mTORi 序贯治疗的患者 OS 和 tPFS 均长于接受 VEGFi-mTORi-VEGFi 序贯治疗的患者,差异具有统计学意义(OS:50.7 与 37.8 个月,p=0.004;36.5 与 29.3 个月,p=0.059)。

结论

很少有患者接受三种 TTs 治疗。VEGFi-VEGFi-mTORi 序贯治疗与 VEGFi-mTORi-VEGFi 序贯治疗相比,生存情况得到改善,一线原发性耐药是一个负面预测和预后因素。

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