Pharmacoeconomic Analysis of Brigatinib versus Alectinib in First‑Line Treatment of Anaplastic Lymphoma Kinase‑Positive Advanced Non‑Small‑Cell Lung Cancer in China.

IF 3.2 Q2 ONCOLOGY
Oncology and Therapy Pub Date : 2025-09-01 Epub Date: 2025-07-24 DOI:10.1007/s40487-025-00361-3
Qingqing Chai, Congling Gu, Luis Hernandez, Yan-Jun Zhang
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引用次数: 0

Abstract

Introduction: Brigatinib and alectinib are anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitors (ALK-TKIs) approved in China in 2022 and 2018, respectively, for the treatment of patients with ALK-positive, advanced non‑small‑cell lung cancer (NSCLC). The objective of this study is to conduct a comparative pharmacoeconomic analysis of first-line drugs, brigatinib and alectinib, in patients with ALK-positive NSCLC from the perspective of the Chinese healthcare system.

Methods: A partitioned survival model with three health states was used to simulate the health outcomes and costs of brigatinib and alectinib with a 30-year time horizon. Indirect treatment comparisons (ITC) data were used to obtain the comparative efficacy of brigatinib and alectinib, owing to lack of head-to-head trials. As the health benefits were comparable between brigatinib and alectinib on the basis of the ITCs, cost-minimization analysis (CMA) was conducted. Cost-effectiveness analyses (CEA) were also conducted as scenario analyses using the different point estimates from the ITCs. Health state utilities and costs were obtained from public sources or clinical expert opinion. Direct medical costs and quality-adjusted life years (QALYs) were discounted at an annual rate of 5%. One-way sensitivity analyses were conducted for the CMA.

Results: The CMA showed that, over 30 years, brigatinib (63,539 USD) was associated with cost savings of 14,203 USD compared with alectinib (77,742 USD). One-way sensitivity analyses showed that drug costs were the most influential parameter but brigatinib remained cost-saving in all the analyses. In the CEAs, the total cost of brigatinib was lower in all scenarios and also resulted in higher QALYs in 60% of the CEA scenarios.

Conclusions: Brigatinib was a cost-saving (14,203 USD) treatment compared with alectinib in the CMA analysis for the first-line treatment of patients with ALK-positive advanced NSCLC in China.

Abstract Image

Abstract Image

布里加替尼与阿勒替尼一线治疗间变性淋巴瘤激酶阳性晚期非小细胞肺癌的药物经济学分析。
Brigatinib和alectinib是间变性淋巴瘤激酶(ALK)酪氨酸激酶抑制剂(ALK- tkis),分别于2022年和2018年在中国获批,用于治疗ALK阳性的晚期非小细胞肺癌(NSCLC)患者。本研究的目的是从中国医疗体系的角度对一线药物布加替尼和阿勒替尼在alk阳性NSCLC患者中的应用进行比较药物经济学分析。方法:采用具有三种健康状态的分区生存模型,模拟布加替尼和阿勒替尼在30年时间范围内的健康结果和成本。由于缺乏正面试验,采用间接治疗比较(ITC)数据来获得布加替尼和阿勒替尼的比较疗效。基于ITCs,布加替尼和阿勒替尼之间的健康益处具有可比性,因此进行了成本最小化分析(CMA)。成本效益分析(CEA)也作为情景分析进行,使用国际贸易中心的不同点估计。卫生公用事业和费用是从公共资源或临床专家意见中获得的。直接医疗费用和质量调整生命年(QALYs)按5%的年折现率计算。对CMA进行单向敏感性分析。结果:CMA显示,在30年的时间里,布加替尼(63,539美元)与阿勒替尼(77,742美元)相比节省了14,203美元的成本。单向敏感性分析显示,药物成本是影响最大的参数,但布加替尼在所有分析中仍然是节省成本的。在CEA中,布加替尼的总成本在所有情况下都较低,并且在60%的CEA情况下也导致较高的QALYs。结论:在中国一线治疗alk阳性晚期NSCLC患者的CMA分析中,布加替尼比阿勒替尼更节省成本(14203美元)。
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来源期刊
CiteScore
3.40
自引率
0.00%
发文量
31
审稿时长
6 weeks
期刊介绍: Now indexed in PubMed Aims and Scope Oncology and Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality pre-clinical, clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all therapeutic areas. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Oncology and Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research. Rapid Publication The journal’s rapid publication timelines aim for a peer review decision within 2 weeks of submission. If an article is accepted it will be published online 3-4 weeks from acceptance. These rapid timelines are achieved through the combination of a dedicated in-house editorial team, who closely manage article workflow, and an extensive Editorial and Advisory Board who assist with rapid peer review. This allows the journal to support the rapid dissemination of research, whilst still providing robust peer review. Combined with the journal’s open access model this allows for the rapid and efficient communication of the latest research and reviews, allowing the advancement of clinical therapies. Personal Service The journal’s dedicated in-house editorial team offer a personal “concierge service” meaning that authors will always have a personal point of contact able to update them on the status of their manuscript. The editorial team check all manuscripts to ensure that articles conform to the most recent COPE, GPP and ICMJE publishing guidelines. This supports the publication of ethically sound and transparent research. We also encourage pre-submission enquiries and are always happy to provide a confidential assessment of manuscripts. Digital features and plain language summaries Oncology and Therapy offers a range of additional features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by key summary points, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand the scientific content and overall implications of the article. The journal also provides the option to include various types of digital features including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations. All additional features are peer reviewed to the same high standard as the article itself. If you consider that your paper would benefit from the inclusion of a digital feature, please let us know. Our editorial team are able to create high-quality slide decks and infographics in-house, and video abstracts through our partner Research Square, and would be happy to assist in any way we can. For further information about digital features, please contact the journal editor (see ‘Contact the Journal’ for email address), and see the ‘Guidelines for digital features and plain language summaries’ document under ‘Submission guidelines’. Preprints We encourage posting of preprints of primary research manuscripts on preprint servers, authors'' or institutional websites, and open communications between researchers whether on community preprint servers or preprint commenting platforms. Posting of preprints is not considered prior publication and will not jeopardize consideration in our journals. Please see here for further information on preprint sharing: https://www.springer.com/gp/authors-editors/journal-author/journal-author-helpdesk/submission/1302#c16721550 Peer Review Process Upon submission, manuscripts are assessed by the editorial team to ensure they fit within the aims and scope of the journal and are also checked for plagiarism. All suitable submissions are then subject to a comprehensive single-blind peer review. Reviewers are selected based on their relevant expertise and publication history in the subject area. The journal has an extensive pool of editorial and advisory board members who have been selected to assist with peer review based on the afore-mentioned criteria. At least two extensive reviews are required to make the editorial decision, with the exception of some article types such as Commentaries, Editorials and Letters which are generally reviewed by one member of the Editorial Board. Where reviewer recommendations are conflicted, the editorial board will be contacted for further advice and a presiding decision. Manuscripts are then either accepted, rejected or authors are required to make major or minor revisions (both reviewer comments and editorial comments may need to be addressed). Once a revised manuscript is re-submitted, it is assessed along with the responses to reviewer comments and if it has been adequately revised it will be accepted for publication. Accepted manuscripts are then copyedited and typeset by the production team before online publication. Appeals against decisions following peer review are considered on a case by case basis and should be sent to the journal editor. Copyright Oncology and Therapy''s content is published open access under the Creative Commons Attribution-Noncommercial License, which allows users to read, copy, distribute, and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited. The author assigns the exclusive right to any commercial use of the article to Springer. For more information about the Creative Commons Attribution-Noncommercial License, click here: http://creativecommons.org/licenses/by-nc/4.0 Publication Fees Upon acceptance of an article, authors will be required to pay the mandatory Rapid Service Fee of £3650/€4500/$5100. The journal will consider fee discounts for developing countries and this is decided on a case by case basis. Open Access All articles published by Oncology and Therapy are published open access Contact For more information about the journal, including pre-submission enquiries, please contact managing editor Lydia Alborn at lydia.alborn@springer.com.
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