Cost-effectiveness Analysis of Ado-trastuzumab Emtansine (T-DM1) for the Adjuvant Treatment of Patients With Residual Invasive HER2+ Early Breast Cancer in the United States

医学 曲妥珠单抗 曲妥珠单抗 乳腺癌 队列 肿瘤科 内科学 质量调整寿命年 成本效益 癌症 风险分析(工程)
作者
Jesse Sussell,Gurleen Jhuti,Vincent Antao,Oscar Herrera-Restrepo,Elizabeth Wehler,S. Pinar Bilir
出处
期刊:American Journal of Clinical Oncology [Lippincott Williams & Wilkins]
卷期号:44 (7): 340-349 被引量:9
标识
DOI:10.1097/coc.0000000000000816
摘要

Ado-trastuzumab emtansine (T-DM1) was recently approved for patients with human epidermal growth factor receptor 2 positive (HER2+) early breast cancer (eBC) with residual invasive disease after neoadjuvant taxane and trastuzumab-based treatment. Cost-effectiveness analysis was conducted to compare T-DM1 versus trastuzumab in the United States.A Markov cohort-based model tracked clinical and economic outcomes over a lifetime horizon from a US payer perspective. The model included 6 health states: invasive disease-free, nonmetastatic (locoregional) recurrence, remission, first-line and second-line metastatic BC and death. Model state transitions were based on statistical extrapolation of the head-to-head KATHERINE study and published sources. Dosing and treatment duration reflected prescribing information and trials. Costs (2019 US dollars) associated with pharmaceutical treatment (wholesale acquisition costs), health state specific care, adverse events, and end-of-life care were included. Health state utilities were obtained from KATHERINE and published literature.T-DM1 dominated trastuzumab, yielding lower lifetime costs (-$40,271), and higher life-years (2.980) and quality-adjusted life-years (2.336). Results were driven by patients receiving T-DM1 spending less time in more costly downstream health states, as these patients are less likely to experience a recurrence overall, despite having a higher likelihood of metastatic disease (distant recurrence) in the subset of patients who experience recurrence. Probabilistic sensitivity analysis indicated robust results, with 96.7% of 5000 stochastic simulations producing dominance for T-DM1. The most influential variables were related to treatment costs, off treatment utilities, and health state costs. Additional scenario analyses tested a range of model inputs and assumptions, and produced consistent results.Relative to trastuzumab, T-DM1 treatment for patients with HER2+ eBC who have residual invasive disease after neoadjuvant taxane and trastuzumab-based treatment is likely to reduce the overall financial burden of cancer, while simultaneously improving patient outcomes.
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
1秒前
2秒前
舒小胖发布了新的文献求助10
7秒前
8秒前
Rr发布了新的文献求助10
9秒前
wangbq发布了新的文献求助30
9秒前
9秒前
所所应助67采纳,获得10
10秒前
云墨完成签到 ,获得积分10
13秒前
任性糖豆完成签到,获得积分10
13秒前
脑洞疼应助HSD采纳,获得10
14秒前
李爱国应助逆游的鱼采纳,获得10
17秒前
CUN完成签到,获得积分10
17秒前
FashionBoy应助ww采纳,获得10
17秒前
FashionBoy应助小尾巴采纳,获得10
17秒前
咿呀咿呀完成签到 ,获得积分10
18秒前
科研通AI5应助优雅的白山采纳,获得10
18秒前
19秒前
19秒前
Lucas应助fhbsdufh采纳,获得10
21秒前
烟花应助舒小胖采纳,获得10
22秒前
22秒前
布鲁爱思发布了新的文献求助10
25秒前
和谐的阁完成签到,获得积分10
25秒前
kkkay完成签到,获得积分10
26秒前
今后应助morry5007采纳,获得10
27秒前
27秒前
28秒前
布鲁爱思完成签到,获得积分10
29秒前
Hello应助和谐的阁采纳,获得10
31秒前
Epiphany完成签到,获得积分10
32秒前
tan_sg完成签到,获得积分10
32秒前
小七完成签到,获得积分10
33秒前
lanheqingniao发布了新的文献求助10
34秒前
Cinema完成签到,获得积分10
34秒前
棉花糖发布了新的文献求助10
35秒前
章北海发布了新的文献求助10
35秒前
田様应助tan_sg采纳,获得10
37秒前
看不见的蛋炒饭完成签到 ,获得积分10
37秒前
38秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
Continuum Thermodynamics and Material Modelling 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 1000
CRC Handbook of Chemistry and Physics 104th edition 1000
Izeltabart tapatansine - AdisInsight 600
An International System for Human Cytogenomic Nomenclature (2024) 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3769292
求助须知:如何正确求助?哪些是违规求助? 3314477
关于积分的说明 10171824
捐赠科研通 3029644
什么是DOI,文献DOI怎么找? 1662409
邀请新用户注册赠送积分活动 794898
科研通“疑难数据库(出版商)”最低求助积分说明 756421