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血管内皮生长因子受体酪氨酸激酶抑制剂在转移性肾细胞癌且具有高危特征患者中的疗效和安全性。

Efficacy and safety of vascular endothelial growth factor receptor tyrosine kinase inhibitors in patients with metastatic renal cell carcinoma and poor risk features.

机构信息

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-Ro 43-Gil, Songpa-gu, Seoul 138-736, Korea.

出版信息

J Cancer Res Clin Oncol. 2012 Apr;138(4):687-93. doi: 10.1007/s00432-012-1148-8. Epub 2012 Jan 12.

DOI:10.1007/s00432-012-1148-8
PMID:22237457
Abstract

BACKGROUND

Temsirolimus is a standard of care in patients with metastatic renal cell carcinoma (mRCC) with poor risk factors. The role of vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitors (TKI) remains poorly defined in this setting.

METHODS

Records of our center were examined to identify patients with mRCC and 3 or more poor prognosis factors, as determined in the Advanced Renal Cell Carcinoma (ARCC) trial, who had been treated with VEGFR TKIs. Their baseline characteristics, radiologic response, adverse events, and survival status were assessed.

RESULTS

The 88 patients who met our inclusion criteria had a median age of 56 years (range 17-83 years). We observed clear cell histology in 71 (81%) patients, and 52 (59%) underwent prior nephrectomy. Seventy-six patients (86%) were treated with sunitinib and 10 (11%) with sorafenib. Of 85 patients with measurable lesions, 19 (22%) showed objective response, with disease control achieved in 49 (56%). At a median follow-up of 29.6 months, the median time to progression was 5.0 months (95% CI, 3.5-6.5 months) and the median overall survival (OS) was 9.3 months (95% CI, 7.1-11.5 months). Neutrophil count (>ULN), bone metastasis, and lymph node metastasis were independent prognostic factors for OS, whereas prior nephrectomy was not.

CONCLUSIONS

VEGFR TKIs, especially sunitinib, are active and tolerated by mRCC patients with poor risk features.

摘要

背景

替西罗莫司是一种标准的治疗方法,适用于伴有不良预后因素的转移性肾细胞癌(mRCC)患者。在这种情况下,血管内皮生长因子受体(VEGFR)酪氨酸激酶抑制剂(TKI)的作用仍未得到充分明确。

方法

检查我们中心的记录,以确定患有 mRCC 且符合 ARCC 试验中确定的 3 个或更多不良预后因素的患者,这些患者曾接受过 VEGFR TKI 治疗。评估他们的基线特征、影像学反应、不良事件和生存状况。

结果

符合我们纳入标准的 88 名患者的中位年龄为 56 岁(范围 17-83 岁)。我们观察到 71 名(81%)患者存在透明细胞组织学,52 名(59%)患者接受了肾切除术。76 名(86%)患者接受舒尼替尼治疗,10 名(11%)患者接受索拉非尼治疗。在 85 名可测量病变的患者中,19 名(22%)显示出客观缓解,49 名(56%)达到疾病控制。在中位随访 29.6 个月时,中位无进展生存期为 5.0 个月(95%CI,3.5-6.5 个月),中位总生存期(OS)为 9.3 个月(95%CI,7.1-11.5 个月)。中性粒细胞计数(>ULN)、骨转移和淋巴结转移是 OS 的独立预后因素,而肾切除术并非如此。

结论

VEGFR TKI,特别是舒尼替尼,对伴有不良预后特征的 mRCC 患者有效且耐受良好。

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