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Sunitinib efficacy against advanced renal cell carcinoma.

机译:舒尼替尼对晚期肾细胞癌的疗效。

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PURPOSE: We assessed the efficacy of the oral multitargeted tyrosine kinase inhibitor sunitinib in patients with metastatic clear cell renal cell carcinoma. MATERIALS AND METHODS: Patients with metastatic clear cell renal cell carcinoma were enrolled in this multicenter, phase II clinical trial. Major eligibility requirements were clear cell renal cell carcinoma histology, prior nephrectomy, measurable metastases and failed prior cytokine therapy as a result of disease progression. Sunitinib was given orally as second line therapy in 6-week cycles of 50 mg daily for 4 weeks, followed by 2 weeks off drug per treatment cycle. Response to sunitinib was rigorously assessed by an independent third party core imaging laboratory (central review). RESULTS: Of 106 patients enrolled in the study 105 were evaluated for response. As determined by independent third party assessment, the objective response rate was 33% (95% CI 24%-43%) with a median response duration of 14.0 months. Median time to progression and median progression-free survival in the 105 evaluable patients was 10.7 and 8.8 months, respectively. Median survival was 23.9 months and 43 patients remained alive at a median followup of 29.7 months. CONCLUSIONS: The results of this trial demonstrate the efficacy of sunitinib for metastatic renal cell carcinoma. The optimal integration of surgery and sunitinib treatment requires further prospective investigation.
机译:目的:我们评估了口服多靶点酪氨酸激酶抑制剂舒尼替尼在转移性透明细胞肾细胞癌患者中的疗效。材料与方法:转移性透明细胞肾细胞癌患者参加了该多中心II期临床试验。资格的主要要求是清除细胞肾细胞癌的组织学,先前的肾切除术,可测量的转移以及由于疾病进展而先前的细胞因子治疗失败。舒尼替尼以二线疗法口服,以6周为周期口服,每天50 mg,持续4周,然后每个治疗周期停药2周。一个独立的第三方核心影像实验室严格评估了对舒尼替尼的反应(中心评估)。结果:在研究的106名患者中,有105名接受了评估。由独立的第三方评估确定,客观缓解率为33%(95%CI 24%-43%),中位缓解期为14.0个月。 105名可评估患者的中位进展时间和中位无进展生存期分别为10.7和8.8个月。中位生存期为23.9个月,有43名患者活着,平均随访29.7个月。结论:该试验的结果证明了舒尼替尼治疗转移性肾细胞癌的疗效。手术和舒尼替尼治疗的最佳整合需要进一步的前瞻性研究。

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