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肾癌的靶向治疗:让艺术在算法周围。

Targeted therapy of kidney cancer: keeping the art around the algorithms.

机构信息

Genitourinary Oncology Program, Moffitt Cancer Center, Tampa, FL 33612, USA.

出版信息

Cancer Control. 2013 Jul;20(3):222-32. doi: 10.1177/107327481302000310.

Abstract

BACKGROUND

Therapy for metastatic kidney cancer is actively evolving, particularly in the results of registration drug trials that have led to the approval of vascular endothelial growth factor pathway drugs such as sorafenib, sunitinib, pazopanib, bevacizumab, and axitinib, with focus on patients with good- or intermediate-risk criteria and clear cell histology. Mammalian target of rapamycin (mTOR) drugs such as everolimus and temsirolimus pivotal trials emphasize experiences in the setting of prior treatment or high-risk features. Interferon and interleukin 2 also are part of the treatment algorithms.

METHODS

The results of pivotal trials and the underlying context for the development of a cogent, cohesive treatment plan for an individual are reviewed, touching on decision points such as nephrectomy, metastasectomy, and medical initiation and discontinuation time points.

RESULTS

To the extent that these drug therapies are essential for achieving best outcomes for patients, these pivotal trial results and associated guidelines exist within a multidimensional, multidisciplinary context of many other disease features, comorbid features, and non-drug treatment decisions. Other dimensions include investigational targeted therapies, patient selection strategies, surgical strategies, and immunotherapies, some of which are in active development.

CONCLUSIONS

Clinicians should work toward the best use of drug sequencing and selection strategies based on core data derived from prospective randomized trials. To address individual patient needs, they should also recognize and emphasize individualized goals, to the extent that these are different from issues that were directly addressed in the trials.

摘要

背景

转移性肾细胞癌的治疗方法正在不断发展,特别是在注册药物试验的结果中,这些试验导致了血管内皮生长因子通路药物(如索拉非尼、舒尼替尼、帕唑帕尼、贝伐珠单抗和阿昔替尼)的批准,这些药物主要针对具有良好或中等风险标准和透明细胞组织学的患者。哺乳动物雷帕霉素靶蛋白(mTOR)药物(如依维莫司和替西罗莫司)的关键试验强调了既往治疗或高危特征的经验。干扰素和白细胞介素 2也是治疗方案的一部分。

方法

回顾了关键试验的结果以及为个体制定有力、连贯的治疗计划的背景,涉及到诸如肾切除术、转移切除术以及药物起始和停药时间点等决策点。

结果

在这些药物治疗对患者获得最佳结果至关重要的程度上,这些关键试验结果和相关指南存在于多维、多学科的背景下,涉及许多其他疾病特征、合并症特征和非药物治疗决策。其他维度包括研究性靶向治疗、患者选择策略、手术策略和免疫疗法,其中一些正在积极开发中。

结论

临床医生应根据前瞻性随机试验得出的核心数据,努力优化药物序贯和选择策略的使用。为了满足个体患者的需求,他们还应认识到并强调个体化目标,只要这些目标与试验中直接解决的问题不同。

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