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:189
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.
最长约 10秒,即可获得该文献文件

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
铭铭子发布了新的文献求助10
刚刚
刚刚
honey完成签到 ,获得积分10
1秒前
风汐5423完成签到,获得积分10
1秒前
aspiling完成签到,获得积分10
1秒前
六神曲发布了新的文献求助10
2秒前
mxy完成签到,获得积分10
2秒前
3秒前
打打应助xinxin采纳,获得10
3秒前
4秒前
4秒前
5秒前
5秒前
LUCA完成签到 ,获得积分10
6秒前
dihou111完成签到,获得积分10
7秒前
hongyeZhang完成签到 ,获得积分10
9秒前
哈喽哈喽发布了新的文献求助10
9秒前
feike完成签到,获得积分10
9秒前
大意的安白完成签到,获得积分10
10秒前
七小七发布了新的文献求助10
10秒前
铭铭子发布了新的文献求助10
13秒前
机灵的成协完成签到,获得积分10
13秒前
酷波er应助顺顺过过采纳,获得10
13秒前
14秒前
15秒前
15秒前
19秒前
哈喽哈喽完成签到,获得积分10
19秒前
19秒前
甜甜的黑猫完成签到,获得积分10
19秒前
炙热睿渊发布了新的文献求助10
19秒前
21秒前
21秒前
cjc完成签到,获得积分10
23秒前
证明发布了新的文献求助10
24秒前
铭铭子发布了新的文献求助10
25秒前
李健应助步美采纳,获得10
28秒前
28秒前
我是老大应助276868sxzz采纳,获得10
29秒前
科目三应助QianqianZhang采纳,获得10
32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
Reducing Compassion Fatigue, Secondary Traumatic Stress and Burnout 600
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Mammalian Synthetic Biology 500
Auslegungsgeschichte 500
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 500
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 7638224
求助须知:如何正确求助?哪些是违规求助? 9211551
关于积分的说明 19759122
捐赠科研通 7205251
什么是DOI,文献DOI怎么找? 3275822
关于科研通互助平台的介绍 2437416
邀请新用户注册赠送积分活动 2273004