Medical Oncology Service, Hospital Universitari Vall d'Hebron, Passeig de la Vall d'Hebron, 119-129, 08035, Barcelona, Spain.
Cancer Metastasis Rev. 2012 Sep;31 Suppl 1:S3-9. doi: 10.1007/s10555-012-9353-0.
The approval and use of molecular targeted agents for the first-line treatment of metastatic renal cell carcinoma (mRCC) has substantially improved the clinical outcome of patients. Although eventually all patients progress, hopes have been renewed with the approval of everolimus for patients who progress on or after treatment with tyrosine kinase inhibitors. In order to improve the prognosis for these patients, it is imperative to understand the reasons why patients with mRCC fail on first-line treatment. Currently, progression is assessed on the basis of the Response Evaluation Criteria in Solid Tumors, but it is known that targeted agents tend to cause disease stabilization rather than a significant decrease in tumor mass. Therefore, it may be time to evaluate the need to incorporate additional diagnostic methods in the assessment of disease response. Equally important is the study of the factors that determine the success or failure of second-line therapy in order to increase the chances of delivering the most effective and personalized therapy possible. In this article, we review the evidence related to the evaluation of patients with mRCC who fail on first-line treatment with targeted agents, including the systems to assess response and progression, the prognostic factors, the prognostic models that have been created based on these factors, and what is known about predictive biomarkers of disease outcome.
分子靶向药物在转移性肾细胞癌(mRCC)一线治疗中的批准和应用极大地改善了患者的临床结局。尽管最终所有患者都会进展,但随着依维莫司在酪氨酸激酶抑制剂治疗后进展的患者中的批准,希望再次燃起。为了改善这些患者的预后,了解 mRCC 患者在一线治疗中失败的原因至关重要。目前,进展是基于实体瘤反应评估标准进行评估的,但已知靶向药物往往会导致疾病稳定,而不是肿瘤体积显著减小。因此,评估在疾病反应评估中纳入额外诊断方法的必要性可能是时候了。同样重要的是研究决定二线治疗成败的因素,以增加提供最有效和个性化治疗的机会。在本文中,我们回顾了与评估接受靶向药物一线治疗失败的 mRCC 患者相关的证据,包括评估反应和进展的系统、预后因素、基于这些因素创建的预后模型,以及对疾病结果的预测生物标志物的了解。