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Metastatic Renal Cell Carcinoma: Sunitinib as First-Line Treatment; Results of a Retrospective Study

机译:转移性肾细胞癌:舒尼替尼作为一线治疗;回顾性研究的结果

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Background: Targeted agents were introduced over past years because of better understanding of oncogenetic mechanisms in metastatic renal cell carcinoma (mRCC). These agents include tyrosine kinase inhibitors (TKIs) such as sorafenib, sunitinib, pazopanib and axitinib. Methods: Review of recorded data from patients’ files with mRCC were analysed during the period from August 2008 to December 2014. Those patients were treated by sunitinib as first-line therapy. The data included patients characteristics such as age, sex, ECOG performance status (ECOG PS), number and sites of metastasis and pathological type. Also, we reviewed response to sunitinib therapy, its adverse events and progression-free survival (PFS). Results: This study included 26 patients; median age was 56 years with male predominance (76.9%) and 61.5% of patients were of ECOG PS0. Lymph nodes were the most common site of metastasis (38.5%) and 46.2% presented with ≥3 sites of disease. Clear cell pathology was reported in 96.2%. No grade IV adverse events to sunitinib reactions were observed. Thrombocytopenia was the most predominant haematological reaction (46%) followed by neutropenia (38.6%), whilst fatigue was the most reported non-haematological one (50%) followed by diarrhoea (42.3%). Partial response (PR) was found in 30.8% and stable disease (SD) in 46.2%. One-year PFS was 57.7% with median PFS time of 12 months. Conclusion: This study proved effectiveness and safety of sunitinib as first-line treatment for mRCC. However, this is a retrospective study and relatively small numbers of patients were included, so prospective studies with larger number of patients are needed for further evaluation.
机译:背景:由于对转移性肾细胞癌(mRCC)的致癌机制有了更深入的了解,近年来引入了靶向药物。这些药物包括酪氨酸激酶抑制剂(TKI),例如索拉非尼,舒尼替尼,帕唑帕尼和阿西替尼。方法:从2008年8月至2014年12月,分析mRCC患者档案的记录数据。这些患者接受舒尼替尼作为一线治疗。数据包括患者特征,例如年龄,性别,ECOG表现状态(ECOG PS),转移的数量和部位以及病理类型。此外,我们回顾了对舒尼替尼治疗的反应,其不良事件和无进展生存期(PFS)。结果:这项研究包括26例患者。中位年龄为56岁,男性占优势(76.9%),其中61.5%的患者为ECOG PS0。淋巴结是最常见的转移部位(38.5%),占46.2%且≥3个疾病部位。透明细胞病理学报道为96.2%。没有观察到舒尼替尼反应的IV级不良事件。血小板减少是最主要的血液学反应(46%),其次是中性粒细胞减少症(38.6%),而疲劳是报告最多的非血液学反应(50%),其次是腹泻(42.3%)。部分反应(PR)占30.8%,稳定疾病(SD)占46.2%。一年PFS为57.7%,中位PFS时间为12个月。结论:本研究证明了舒尼替尼作为mRCC的一线治疗的有效性和安全性。但是,这是一项回顾性研究,纳入的患者相对较少,因此需要对更多患者进行前瞻性研究以进行进一步评估。

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