Current and Future Management of HER2-Positive Metastatic Breast Cancer

帕妥珠单抗 曲妥珠单抗 曲妥珠单抗 医学 紫杉烷 来那替尼 肿瘤科 转移性乳腺癌 内科学 乳腺癌 卡培他滨 拉帕蒂尼 癌症 结直肠癌
作者
Olga Martínez‐Sáez,Aleix Prat
出处
期刊:JCO oncology practice [American Society of Clinical Oncology]
卷期号:17 (10): 594-604 被引量:143
标识
DOI:10.1200/op.21.00172
摘要

Human epidermal growth factor receptor 2 (HER2) is overexpressed and/or amplified in approximately 20% of breast cancers, conferring an aggressive tumor behavior but also an opportunity for targeted therapies. In the advanced setting, the prognosis of patients suffering from this disease has greatly improved after the introduction of new anti-HER2 drugs beyond trastuzumab. For most patients, a taxane combined with trastuzumab and pertuzumab in the first-line setting, followed by trastuzumab-emtansine in second line, should be considered the standard of care today. However, chemo-free anti-HER2 strategies in hormone receptor-positive, HER2-positive breast cancer could also be considered in selected patients. In the third-line setting and beyond, several emerging anti-HER2 therapies are becoming available, including tucatinib, fam-trastuzumab deruxtecan-nxki (DS-8201a), neratinib, and margetuximab-cmkb. In addition, new compounds and combinations are showing promising results in the late-line setting. The treatment landscape of HER2-positive advanced disease is evolving constantly, active drugs such as pertuzumab and trastuzumab-emtansine are moving to early-stage, many biomarkers, including quantification of HER2 itself, are being explored to improve patient selection, and patient populations with specific needs are emerging, such as those with brain metastasis. Here, we provide an overview of the current and future management of HER2-positive advanced breast cancer.

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
刚刚
梧桐完成签到,获得积分10
刚刚
1秒前
Frankll发布了新的文献求助10
1秒前
1秒前
2秒前
不摇头的向日葵完成签到,获得积分10
2秒前
小蘑菇应助xin采纳,获得10
3秒前
5秒前
重要的水壶完成签到,获得积分10
6秒前
7秒前
灿烂千阳发布了新的文献求助10
8秒前
橙子青发布了新的文献求助10
8秒前
9秒前
仁爱嫣完成签到,获得积分20
10秒前
11秒前
Chichien完成签到,获得积分10
11秒前
leranlily完成签到 ,获得积分10
11秒前
Orange应助月亮不知道采纳,获得10
13秒前
迟策完成签到,获得积分10
13秒前
13秒前
14秒前
Chichien发布了新的文献求助10
14秒前
16秒前
mufulee完成签到,获得积分10
16秒前
16秒前
17秒前
Dream完成签到 ,获得积分10
18秒前
Wymbol完成签到,获得积分10
18秒前
19秒前
qizhang完成签到,获得积分10
19秒前
ljj完成签到,获得积分10
20秒前
bluesama发布了新的文献求助10
21秒前
123应助你好采纳,获得10
21秒前
22秒前
秋雨梧桐完成签到 ,获得积分10
22秒前
22秒前
24秒前
甜美阁完成签到,获得积分10
24秒前
24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
Modern Epidemiology, Fourth Edition 5000
Handbook of pharmaceutical excipients, Ninth edition 5000
Digital Twins of Advanced Materials Processing 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
Social Cognition: Understanding People and Events 1000
Polymorphism and polytypism in crystals 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6028957
求助须知:如何正确求助?哪些是违规求助? 7696731
关于积分的说明 16188640
捐赠科研通 5176175
什么是DOI,文献DOI怎么找? 2769918
邀请新用户注册赠送积分活动 1753285
关于科研通互助平台的介绍 1639050