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 [Lippincott Williams & Wilkins]
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
77发布了新的文献求助10
刚刚
1秒前
hmh完成签到,获得积分10
2秒前
5秒前
bamboo完成签到,获得积分10
6秒前
immm完成签到 ,获得积分10
6秒前
诚心的剑身完成签到,获得积分10
7秒前
拉长的傲菡完成签到,获得积分10
9秒前
小L同学完成签到,获得积分10
10秒前
华仔应助一定行采纳,获得10
11秒前
12秒前
星辰大海应助Jeremy采纳,获得10
12秒前
盲点完成签到,获得积分10
13秒前
13秒前
Guowei完成签到,获得积分10
13秒前
14秒前
科研通AI6.1应助刘高峰采纳,获得30
15秒前
施宇宙完成签到 ,获得积分10
16秒前
小杜完成签到 ,获得积分10
16秒前
More应助Nicole采纳,获得10
16秒前
曾丽红发布了新的文献求助20
16秒前
17秒前
小马甲应助加贝峥采纳,获得10
18秒前
fengzhang完成签到,获得积分10
18秒前
wubobo发布了新的文献求助10
20秒前
windmill发布了新的文献求助10
20秒前
搜集达人应助悠南采纳,获得10
21秒前
挽风完成签到 ,获得积分10
21秒前
23秒前
吴小利完成签到,获得积分10
23秒前
25秒前
26秒前
思源应助sdzylx7采纳,获得30
27秒前
眼睛大的冰岚完成签到,获得积分10
27秒前
烟花应助111采纳,获得10
27秒前
如常发布了新的文献求助10
28秒前
小马甲应助windmill采纳,获得10
28秒前
wubobo完成签到,获得积分10
29秒前
77完成签到,获得积分10
29秒前
29秒前
高分求助中
液晶指向矢仿真分析数据集 8888
Invited Discussant 63O and 64O 1000
Ideology and Meaning-Making under the Putin Regime 750
Petrology and Plate Tectonics 500
Writing Systems 500
A Handbook of User Experience Research & Design in Libraries 400
Understanding Modeling and Simulation of Polymerization Reactions 400
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 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6899576
求助须知:如何正确求助?哪些是违规求助? 8594709
关于积分的说明 18247254
捐赠科研通 6298759
什么是DOI,文献DOI怎么找? 3061751
关于科研通互助平台的介绍 2082162
邀请新用户注册赠送积分活动 2039616