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碳酸酐酶 IX 和病理特征可预测接受血管内皮生长因子靶向治疗的转移性透明细胞肾细胞癌患者的结局。

Carbonic anhydrase IX and pathological features as predictors of outcome in patients with metastatic clear-cell renal cell carcinoma receiving vascular endothelial growth factor-targeted therapy.

机构信息

Dana-Farber/Harvard Cancer Center, Boston, MA, USA.

出版信息

BJU Int. 2010 Sep;106(6):772-8. doi: 10.1111/j.1464-410X.2010.09218.x. Epub 2010 Mar 2.

Abstract

OBJECTIVE

To investigate the utility of tumour carbonic anhydrase IX (CAIX) expression and histological features for predicting the outcome in patients with metastatic clear-cell renal cell carcinoma (mRCC) treated with vascular endothelial growth factor (VEGF)-targeted therapy.

PATIENTS AND METHODS

We identified 118 patients with mRCC initiating first-line VEGF-targeted therapy, including 94 with clinical and histological data, and available tissue. The primary endpoint was to detect an interaction between sorafenib vs sunitinib treatment and CAIX status on tumour shrinkage. Other treatment outcomes were also assessed.

RESULTS

There was heterogeneity in tumour responsiveness to sunitinib or sorafenib according to CAIX status; the mean shrinkage was -17% vs -25% for sunitinib-treated patients with high vs low tumour CAIX expression, compared to -13% vs +9% for sorafenib-treated patients (P interaction, 0.05). A higher tumour clear-cell component was independently associated with greater tumour shrinkage (P= 0.02), response (P= 0.02) and treatment duration (P= 0.02).

CONCLUSIONS

Although CAIX expression had no prognostic value in patients with clear-cell mRCC treated with VEGF-targeted therapy, it might be a predictive biomarker for response to sorafenib treatment. Patients with a higher clear-cell component in their tumours are likely to have a superior clinical benefit from VEGF-targeted therapy.

摘要

目的

探讨肿瘤碳酸酐酶 IX(CAIX)表达和组织学特征在预测接受血管内皮生长因子(VEGF)靶向治疗的转移性透明细胞肾细胞癌(mRCC)患者预后中的作用。

患者与方法

我们确定了 118 例接受一线 VEGF 靶向治疗的 mRCC 患者,其中 94 例具有临床和组织学数据以及可用组织。主要终点是检测索拉非尼与舒尼替尼治疗与肿瘤缩小中 CAIX 状态之间的相互作用。还评估了其他治疗结果。

结果

根据 CAIX 状态,肿瘤对舒尼替尼或索拉非尼的反应存在异质性;与低肿瘤 CAIX 表达的舒尼替尼治疗患者相比,高肿瘤 CAIX 表达的患者肿瘤缩小率分别为-17%和-25%,而索拉非尼治疗患者分别为-13%和+9%(P 交互=0.05)。肿瘤透明细胞成分较高与肿瘤缩小(P=0.02)、反应(P=0.02)和治疗持续时间(P=0.02)独立相关。

结论

尽管 CAIX 表达在接受 VEGF 靶向治疗的透明细胞 mRCC 患者中没有预后价值,但它可能是预测索拉非尼治疗反应的生物标志物。肿瘤透明细胞成分较高的患者可能从 VEGF 靶向治疗中获得更好的临床获益。

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