首页> 外文期刊>The lancet oncology >Activity of a multitargeted chemo-switch regimen (sorafenib, gemcitabine, and metronomic capecitabine) in metastatic renal-cell carcinoma: a phase 2 study (SOGUG-02-06).
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Activity of a multitargeted chemo-switch regimen (sorafenib, gemcitabine, and metronomic capecitabine) in metastatic renal-cell carcinoma: a phase 2 study (SOGUG-02-06).

机译:多靶点化学转换方案(索拉非尼,吉西他滨和节律性卡培他滨)在转移性肾细胞癌中的活性:一项2期研究(SOGUG-02-06)。

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BACKGROUND: Maximum tolerated dose (MTD) chemotherapy followed by metronomic chemotherapy (low doses given on a frequent schedule) acts on tumour vascular endothelial cells by increasing the anti-tumour effect of anti-angiogenic agents. This multicentre, phase 2 study investigated the effectiveness of MTD gemcitabine combined with metronomic capecitabine plus the multikinase inhibitor sorafenib for the treatment of metastatic renal-cell carcinoma (RCC). METHODS: Patients were enrolled at eight centres across Spain between Dec 13, 2006, and April 17, 2008. Patients were aged 18 years or older, had confirmed metastatic RCC with clear-cell histology, had an Eastern Cooperative Oncology Group performance status of 0 or 1, had not undergone previous therapy, and were unsuitable for, or intolerant to, immunotherapy. Treatment consisted of intravenous gemcitabine 1000 mg/m(2) (days 1 and 8), oral capecitabine 500 mg/m(2) twice a day (final dose after adjustment, days 1-14), and oral sorafenib 400 mg twice a day (days 1-21), for six cycles, followed by sorafenib monotherapy (at the investigator's discretion if clinical benefit was maintained). The primary endpoint was median progression-free survival (PFS) analysed in a population of all patients who received treatment. The trial is registered with ClinicalTrials.gov, number NCT00496301. FINDINGS: 44 patients enrolled in the study, 40 of whom received treatment. Median PFS for these patients was 11.1 months (95% CI 7.9-17.1). A partial response was achieved in 20 patients, and stable disease in 17 patients. Most adverse events were grade 1 or 2. Grade 3 adverse events were fatigue or asthenia (n=9), hand-foot skin reaction (n=11), mucositis (n=3), diarrhoea (n=2), infection (n=2), and allergic reaction, hypertension, and rash (all n=1). Grade 3 haematological toxicity was noted in nine patients. One death due to pulmonary embolism was reported as grade 5 dyspnoea possibly related to study drug. INTERPRETATION: PFS and response rates were greater than those previously observed with gemcitabine and capecitabine or sorafenib monotherapy in patients with metastatic RCC. Adverse events were manageable in most patients. These findings provide preliminary confirmation of the synergistic activity of the chemo-switch concept seen in preclinical studies, and merit further exploration. FUNDING: Spanish Oncology Genitourinary Group (SOGUG).
机译:背景:最大耐受​​剂量(MTD)化疗后再进行节律性化疗(按经常性计划给予低剂量)可通过增加抗血管生成剂的抗肿瘤作用来作用于肿瘤血管内皮细胞。这项多中心的2期研究调查了MTD吉西他滨联合节律性卡培他滨联合多激酶抑制剂索拉非尼治疗转移性肾细胞癌(RCC)的有效性。方法:患者于2006年12月13日至2008年4月17日在西班牙的8个中心入组。年龄在18岁或18岁以上,已确诊转移性RCC和透明细胞组织学,东部合作肿瘤小组的工作状态为0的患者或1,之前未曾接受过治疗,并且不适合或不耐受免疫治疗。治疗包括静脉内吉西他滨1000 mg / m(2)(第1和8天),口服卡培他滨500 mg / m(2)每天两次(调整后的最终剂量,第1-14天)和口服索拉非尼400 mg两次每天(1-21天),共六个周期,然后进行索拉非尼单药治疗(如果能够维持临床获益,则由研究者决定)。主要终点是接受治疗的所有患者群体的中位无进展生存期(PFS)。该试验已在ClinicalTrials.gov上注册,编号为NCT00496301。结果:44名患者参加了研究,其中40名接受了治疗。这些患者的PFS中位数为11.1个月(95%CI 7.9-17.1)。 20例患者获得部分缓解,17例患者疾病稳定。大多数不良反应为1级或2级。3级不良反应为疲劳或虚弱(n = 9),手足皮肤反应(n = 11),粘膜炎(n = 3),腹泻(n = 2),感染( n = 2),以及过敏反应,高血压和皮疹(所有n = 1)。在9例患者中发现3级血液学毒性。据报道,由于肺栓塞导致的1例死亡为5级呼吸困难,可能与研究药物有关。结论:转移性RCC患者的PFS和缓解率均高于吉西他滨和卡培他滨或索拉非尼单药治疗之前的观察。在大多数患者中不良事件是可以控制的。这些发现为临床前研究中所观察到的化学转换概念的协同活性提供了初步确认,值得进一步探索。资金来源:西班牙肿瘤泌尿生殖科(SOGUG)。

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