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A phase II study of presurgical sunitinib in patients with metastatic clear-cell renal carcinoma and the primary tumor in situ.

机译:舒尼替尼在转移性透明细胞肾癌和原发灶原位癌患者中的II期临床研究。

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OBJECTIVE: To investigate response rate (RR) of the primary tumor after presurgical sunitinib before planned cytoreductive nephrectomy (CN) in patients with metastatic renal cell carcinoma (mRCC). Secondary endpoints were safety and if this strategy can be used to identify patients who progress rapidly and may not benefit from CN. METHODS: Prospective study to detect a 25% response evaluation criteria in solid tumors RR (RECIST-RR) in the primary tumor (Simon two-stage design). CN was performed after 2 cycles of sunitinib 50 mg/d. Response in the primary tumor and metastatic sites, change of longest diameter of the primary tumor (Delta-LDT), progression-free survival (PFS), and adverse events were assessed. RESULTS: Twenty-two patients with primary mRCC were included. The trial did not enter the second stage because only 1 primary tumor responded partially in the first stage (4.5%). Median Delta-LDT was -9.5% (range 2.2 to -36%). A >10% Delta-LDT was significantly associated with a high probability to survive 2 years (P = .01). At metastatic sites, 7 patients developed a partial response (31.8%), 7 stable disease (31.8%), and 8 progressive disease (36.4%). Subsequently 3 (13.6%) developed a complete response after CN and continued taking sunitinib. Median PFS is 7 months (range 0-41). Median follow-up is 23 months (range 2-41). Median overall survival has not been reached. CONCLUSIONS: Downsizing of primary tumors after 2 cycles of sunitinib is modest but associated with long-term survival. Patients with progression of metastases after pretreatment have short survival and are unlikely to benefit from CN.
机译:目的:研究转移性肾细胞癌(mRCC)患者术前舒尼替尼在计划细胞减灭性肾切除术(CN)之前的原发肿瘤反应率(RR)。次要终点是安全性,如果可以使用该策略来识别进展迅速且可能无法从CN中受益的患者。方法:前瞻性研究在原发性肿瘤(Simon两阶段设计)中检测到实体瘤RR(RECIST-RR)中25%的反应评估标准。在舒尼替尼50 mg / d的2个周期后进行CN。评估了原发肿瘤和转移部位的反应,原发肿瘤最长直径的变化(Delta-LDT),无进展生存期(PFS)以及不良事件。结果:包括22例原发性mRCC患者。该试验未进入第二阶段,因为在第一阶段只有1例原发性肿瘤部分缓解(4.5%)。 Delta-LDT中位数为-9.5%(范围为2.2至-36%)。大于10%的Delta-LDT与存活2年的高可能性显着相关(P = 0.01)。在转移部位,有7例患者出现部分缓解(31.8%),7例稳定疾病(31.8%)和8例进行性疾病(36.4%)。随后3(13.6%)位患者在CN后出现了完全缓解,并继续服用舒尼替尼。 PFS中位数为7个月(范围0-41)。中位随访时间为23个月(范围2-41)。尚未达到中位总体生存率。结论:舒尼替尼2个周期后原发肿瘤的缩小是适度的,但与长期生存有关。预处理后发生转移的患者生存期短,不太可能受益于CN。

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