Survival Benefits of Second-line Axitinib Versus Everolimus After First Line Sunitinib Treatment in Metastatic Renal Cell Carcinoma

作者
Lajos Géczi,G. Bodoky,György Rokszin,Ibolya Fábián,László Torday
出处
期刊:Pathology & Oncology Research [Springer Science+Business Media]
卷期号:26 (4): 2201-2207 被引量:9
标识
DOI:10.1007/s12253-020-00809-z
摘要

BACKGROUND: Targeted therapies significantly improve clinical outcomes among patients with metastatic renal cell carcinoma (mRCC). Several new agents have been approved for first- and second-line use. However, there is a lack of compelling evidence comparing sequencing strategies, and available comparative data regarding the real-world effectiveness of different therapeutic sequences are limited. MATERIALS AND METHODS: We identified mRCC patients who initiated targeted therapy between January 1, 2008 and May 31, 2017 from the National Health Insurance Fund (NHIF) database of Hungary. Overall survival (OS) and duration of first-line treatment (DFT) were obtained for patients receiving sunitinib-everolimus, sunitinib-axitinib, or pazopanib-everolimus treatment sequences. OS of sunitinib-everolimus and sunitinib-axitinib sequences was also determined for patients having better or worse response to sunitinib first-line therapy. RESULTS: Median OS was significantly longer among patients treated with sunitinib-axitinib compared to those receiving sunitinib-everolimus. Median DFT was also significantly longer in the sunitinib-axitinib vs. sunitinib-everolimus group. Sunitinib-axitinib was associated with significantly longer median OS compared to sunitinib-everolimus in patients with better response to first-line sunitinib in the pooled sunitinib population. In patients with worse response to sunitinib, sunitinib-axitinib was associated with a trend towards greater OS compared to sunitinib-everolimus, but the difference did not reach statistical significance. CONCLUSIONS: In this nationwide database analysis, mRCC patients treated with the sunitinib-axitinib sequence had significantly longer OS compared to those receiving sunitinib-everolimus therapy. The OS benefits of second-line axitinib were consistent among patients with better response to sunitinib defined by DFT values.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
蜜蜜芪完成签到 ,获得积分10
刚刚
1秒前
高高从霜完成签到 ,获得积分10
1秒前
1秒前
莫天枫完成签到,获得积分10
1秒前
AFFAFDFDFDDF完成签到,获得积分20
1秒前
1秒前
yz应助Ml采纳,获得10
1秒前
dtcao完成签到,获得积分10
1秒前
zdesfsfa完成签到,获得积分10
2秒前
2秒前
小马完成签到,获得积分10
2秒前
Eugene完成签到 ,获得积分10
2秒前
。。。完成签到,获得积分10
2秒前
机灵太君发布了新的文献求助10
2秒前
2秒前
哈哈哈发布了新的文献求助10
2秒前
震动的平蝶完成签到,获得积分10
3秒前
水煮牛牛完成签到,获得积分10
3秒前
科研通AI6.2应助蕊蕊蕊采纳,获得10
3秒前
拟晓汁发布了新的文献求助10
3秒前
与心爱的你行至世界尽头完成签到,获得积分10
3秒前
慕青应助生动绫采纳,获得10
3秒前
铛铛完成签到,获得积分10
4秒前
李健的粉丝团团长应助lqy采纳,获得10
4秒前
红3完成签到,获得积分10
4秒前
modric完成签到,获得积分10
4秒前
Rocky完成签到 ,获得积分10
5秒前
FragrantHill发布了新的文献求助20
5秒前
茉云发布了新的文献求助10
5秒前
TY完成签到,获得积分10
5秒前
5秒前
呼呼虫完成签到,获得积分10
6秒前
6秒前
自由芷云完成签到,获得积分10
6秒前
0077发布了新的文献求助10
6秒前
红3发布了新的文献求助10
6秒前
小糊涂仙发布了新的文献求助10
6秒前
充电宝应助Snowy采纳,获得10
6秒前
7秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Les chinois de jakarta: temples et vie collective 1000
Autoparametric Resonance in Mechanical Systems 1000
基于锂离子电池正极材料回收的绿色溶剂开发及工程化应用研究 800
Social Psychology 600
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 600
Management and the Arts 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7646591
求助须知:如何正确求助?哪些是违规求助? 9218830
关于积分的说明 19782955
捐赠科研通 7211387
什么是DOI,文献DOI怎么找? 3277115
关于科研通互助平台的介绍 2438656
邀请新用户注册赠送积分活动 2275331