Trastuzumab deruxtecan (DS-8201a) in patients with advanced HER2-positive breast cancer previously treated with trastuzumab emtansine: a dose-expansion, phase 1 study

医学 曲妥珠单抗 曲妥珠单抗 内科学 乳腺癌 肿瘤科 癌症
作者
Kenji Tamura,Junji Tsurutani,Shunji Takahashi,Hiroji Iwata,Ian E. Krop,Charles H. Redfern,Yasuaki Sagara,Toshihiko Doi,Haeseong Park,Rashmi K. Murthy,Rebecca Redman,Takahiro Jikoh,Caleb Lee,Masahiro Sugihara,Javad Shahidi,Antoine Yver,Shanu Modi
出处
期刊:Lancet Oncology [Elsevier BV]
卷期号:20 (6): 816-826 被引量:345
标识
DOI:10.1016/s1470-2045(19)30097-x
摘要

Summary

Background

Trastuzumab deruxtecan (DS-8201a) is a novel HER2-targeted antibody–drug conjugate with a humanised anti-HER2 antibody, cleavable peptide-based linker, and potent topoisomerase I inhibitor payload. A phase 1, non-randomised, open-label, multiple-dose study was done to assess the safety, tolerability, and activity of trastuzumab deruxtecan in HER2-expressing, advanced solid tumours. The dose escalation (part 1) has previously been reported and the recommended doses for expansion of 5·4 mg/kg or 6·4 mg/kg were established. In this Article, we report the safety and preliminary activity results from this phase 1 trial in all patients with HER2-positive advanced-stage breast cancer with previous trastuzumab emtansine treatment who received trastuzumab deruxtecan at the recommended doses for expansion.

Methods

We did an open-label, dose-escalation and dose-expansion phase 1 trial at eight hospitals and clinics in the USA and six in Japan. Eligible patients were at least 18 years old in the USA and at least 20 years of age in Japan and had advanced solid tumours (regardless of HER2 expression in dose escalation or HER2 expression or mutation in dose expansion). The recommended doses for expansion of 5·4 mg/kg or 6·4 mg/kg trastuzumab deruxtecan were administered intravenously to patients once every 3 weeks until withdrawal of consent, unacceptable toxicity, or progressive disease. In this Article, all patients with HER2-positive advanced-stage breast cancer with previous trastuzumab emtansine treatment who received trastuzumab deruxtecan at the recommended doses for expansion were analysed together. The primary endpoints of the study were safety and preliminary activity (proportion of patients who achieved an objective response as assessed by the investigators). The activity evaluable set included all patients who received at least one dose of trastuzumab deruxtecan at the recommended doses for expansion, and for whom both baseline and post-treatment activity data were available. The safety analysis set included all patients who received at least one dose of trastuzumab deruxtecan at the recommended doses for expansion. Enrolment for patients with HER2-positive breast cancer has been completed. This trial is registered at ClinicalTrials.gov, number NCT02564900, and ClinicalTrials.jp, number JapicCTI-152978.

Findings

Between Aug 28, 2015, and Aug 10, 2018, 115 of 118 patients with HER2-positive breast cancer were treated with at least one dose of trastuzumab deruxtecan at the recommended doses for expansion. All patients had at least one treatment-emergent adverse event. Frequent grade 3 or worse treatment-emergent adverse events included anaemia (19 [17%] of 115) and decreased neutrophil (16 [14%]), white blood cell (ten [9%]), and platelet (nine [8%]) counts. At least one serious treatment-emergent adverse event occurred for 22 (19%) patients. Investigators reported 20 cases of interstitial lung disease, pneumonitis, or organising pneumonia, including one grade 3 event and two treatment-related deaths due to pneumonitis. One death unrelated to study treatment was due to progressive disease. 66 (59·5%; 95% CI 49·7–68·7) of 111 patients had a confirmed objective response.

Interpretation

Trastuzumab deruxtecan had a manageable safety profile and showed preliminary activity in trastuzumab emtansine-pretreated patients with HER2-positive breast cancer. These results suggest that further development in phase 2 and 3 clinical trials for HER2-positive breast cancer is warranted.

Funding

Daiichi Sankyo Co, Ltd.
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
刚刚
1秒前
搜集达人的应助被Wendy含采纳,获得10
1秒前
1秒前
乐空思的应助被djbj2022采纳,获得20
1秒前
Hello的应助被前度刘郎采纳,获得10
2秒前
olivia完成签到,获得积分10
3秒前
Christina发布了新的文献求助10
3秒前
一觉醒来发现自己身在学校完成签到,获得积分10
3秒前
张康发布了新的文献求助10
5秒前
booniang发布了新的文献求助10
6秒前
蛋蛋发布了新的文献求助10
7秒前
fancyplain发布了新的文献求助10
7秒前
zdp827完成签到 ,获得积分10
7秒前
8秒前
科研通AI6.2的应助被酒筱采纳,获得10
9秒前
vmformation完成签到,获得积分10
9秒前
汪Hiver完成签到,获得积分10
9秒前
研友_VZG7GZ的应助被可爱初瑶采纳,获得10
11秒前
12秒前
wan发布了新的文献求助10
13秒前
情怀的应助被不是秋刀鱼采纳,获得10
14秒前
16秒前
FashionBoy的应助被谢谢采纳,获得10
17秒前
小满完成签到 ,获得积分10
17秒前
飞快的书南完成签到 ,获得积分10
17秒前
18秒前
18秒前
18秒前
薛吃梨发布了新的文献求助10
18秒前
18秒前
Orange的应助被阿白采纳,获得30
19秒前
蹲儿关注了科研通微信公众号
19秒前
脑洞疼的应助被lzz采纳,获得10
19秒前
19秒前
molihuakai的应助被阿鑫采纳,获得10
19秒前
19秒前
19秒前
20秒前
完美世界的应助被檐下猫采纳,获得10
21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
Energie-Contracting 1500
Klimaschutzrecht durch den Energiesektor im Mehrebenensystem – Ein Rechtsvergleich 1000
Oncology Clinical Trials: Successful Design, Conduct, and Analysis, Second Edition 800
Stochastic Models in Operations Research,Vol. 2 600
Organizational Behavior 510
Comprehensive Heterocyclic Chemistry IV 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 计算机科学 工程类 有机化学 化学工程 生物化学 物理 复合材料 内科学 催化作用 光电子学 人工智能 细胞生物学 无机化学 物理化学 数学
热门帖子
关注 科研通微信公众号,转发送积分 8047083
求助须知:如何正确求助?哪些是违规求助? 9477261
关于积分的说明 21288257
捐赠科研通 7613569
什么是DOI,文献DOI怎么找? 3392519
关于科研通互助平台的介绍 2523786
邀请新用户注册赠送积分活动 2430516