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Metastatic clear cell renal carcinoma – an unusual responseto Temsirolimus in second line therapy

机译:转移性透明细胞肾癌–异常反应二线治疗中使用替莫罗莫司

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摘要

Renal cell carcinoma (RCC) represents 3% of all cancers, with the highest incidence occurring in the most developed countries and representing the seventh most common cancer in men and the ninth most common cancer in women. The understanding of the tumor molecular biology and the discovery of new drugs that target molecular pathways have increased the arsenal against advanced renal cell carcinoma and improved the outcomes in the patients suffering from these affections. Studying the molecular signaling that controls the tumor growth and the progression has led to the development of molecular therapies targeting the vascular endothelial growth factor (VEGF) and mammalian target of rapamycin (mTOR) pathways, resulting in a significant improvement in the overall survival and quality of life. Sunitinib represents an inhibitor of VEGFR 1-3, c-kit, FLT-3 and PDGFR. We present the case of a patient with metastatic clear cell RCC with a treatment effect following sequential VEGF and mTOR inhibitor treatment. Under sunitinib treatment, the patient had a progression free survival (PFS) of approximately 9 months, similar to the PFS observed in clinical trials. Sunitinib was well tolerated by this patient. Temsirolimus, an mTOR inhibitor, is currently only approved for the first-line treatment of mRCC patients with poor prognosis. This study analyzes a treatment effect of second line temsirolimus in a patient with metastatic renal cell carcinoma (mRCC).
机译:肾细胞癌(RCC)占所有癌症的3%,发生率最高的国家是最发达国家,在男性中排名第七,在女性中排名第九。对肿瘤分子生物学的了解和靶向分子途径的新药的发现增加了抵抗晚期肾细胞癌的药库,并改善了患有这些疾病的患者的预后。研究控制肿瘤生长和进展的分子信号传导已导致针对血管内皮生长因子(VEGF)和哺乳动物雷帕霉素靶标(mTOR)途径的分子疗法的开发,从而导致总体存活率和质量显着提高生活。舒尼替尼代表VEGFR 1-3,c-kit,FLT-3和PDGFR的抑制剂。我们介绍了具有转移性透明细胞RCC的患者的情况,该患者在连续VEGF和mTOR抑制剂治疗后具有治疗效果。在舒尼替尼治疗下,患者的无进展生存期(PFS)约为9个月,类似于在临床试验中观察到的PFS。该患者对舒尼替尼耐受良好。 mTOR抑制剂Temsirolimus目前仅被批准用于预后较差的mRCC患者的一线治疗。这项研究分析了二线西罗莫司对转移性肾细胞癌(mRCC)患者的治疗效果。

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