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How to carry out retrospective studies in metastatic renal cell cancer: Two caveats that should be avoided

机译:如何进行转移性肾细胞癌的回顾性研究:应避免的两个警告

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Evaluation of: Grünwald V, Seidel C, Fenner M, Ganser A, Busch J, Weikert S. Treatment of everolimus-resistant metastatic renal cell carcinoma with VEGF-targeted therapies. Br. J. Cancer 105(11), 1635-1639 (2011). The results achieved with targeted therapy have changed the natural course of kidney cancer not amenable to local therapy. Sunitinib, bevacizumab and pazopanib are approved in the first-line setting for patients at good/intermediate prognosis, while temsirolimus should be the first-line agent to be used in patients at poor prognosis. The oncology community has been eagerly awaiting results as far as second-line treatment is concerned. The RECORD-1 and AXIS trials provided evidence in favor of everolimus and axitinib, respectively, in patients pretreated with VEGF-directed agents. As the number of available agents grows, so does the possibility of using multiple lines of therapy with a potential benefit in overall survival. The third-line setting has been poorly investigated, and no comparative prospective trials are presently available. Retreatment with VEGF-directed therapy may be an option in everolimus-pretreated patients, with the possibility that mTOR inhibitors may reverse resistance to VEGF-directed therapy. Grunwald et al. presented retrospective data showing that retreatment with VEGF-directed targeted agents, including sunitinib, bevacizumab/interferon, dovitinib and sorafenib, was associated with a progression-free survival time of approximately 5 months. Although the evidence provided by retrospective studies is weak, their role in highlighting matters of clinical relevance deserving investigation is undoubtful, as demonstrated by the retrospective study discussed in this paper.
机译:评价:GrünwaldV,Seidel C,Fenner M,Ganser A,Busch J,WeikertS。用靶向VEGF的疗法治疗依维莫司耐药的转移性肾细胞癌。 Br。 J.癌症105(11),1635-1639(2011)。靶向治疗获得的结果改变了不适合局部治疗的肾癌的自然病程。一线治疗方案中,舒尼替尼,贝伐单抗和帕唑帕尼已被批准用于预后良好/中度的患者,而西罗莫司应作为预后不良的患者的一线药物。就二线治疗而言,肿瘤学界一直在等待结果。 RECORD-1和AXIS试验分别为接受VEGF定向药物治疗的患者分别支持依维莫司和阿昔替尼提供了证据。随着可用药物数量的增加,使用多种疗法对整体存活率具有潜在益处的可能性也在增加。三线研究尚未深入研究,目前尚无可比较的前瞻性试验。在依维莫司治疗的患者中,用VEGF导向疗法进行复治可能是一种选择,而mTOR抑制剂可能会逆转对VEGF导向疗法的耐药性。 Grunwald等。提交的回顾性数据显示,用VEGF导向的靶向药物(包括舒尼替尼,贝伐单抗/干扰素,多维替尼和索拉非尼)进行的再治疗与大约5个月的无进展生存期相关。尽管回顾性研究提供的证据很薄弱,但正如本文讨论的回顾性研究所证明的那样,它们在强调临床相关性值得研究方面的作用是毋庸置疑的。

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