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子宫内膜癌免疫治疗联合疗法的成本效益

Cost effectiveness of immunotherapy combination therapies for endometrial cancer.

作者信息

Benjamin David J, Padula William V, Hsu Robert C

机构信息

Hoag Family Cancer Institute, Newport Beach, CA, USA.

Department of Pharmaceutical and Health Economics, Alfred E. Mann School of Pharmacy and Pharmaceutical Sciences, University of Southern California, Los Angeles, CA, USA.

出版信息

Gynecol Oncol Rep. 2024 Mar 1;52:101351. doi: 10.1016/j.gore.2024.101351. eCollection 2024 Apr.

DOI:10.1016/j.gore.2024.101351
PMID:38449799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10915342/
Abstract

Over the past five years (2019-2023), several new targeted therapies and immunotherapy has been approved in treating relapsed cervical, ovarian, and endometrial cancers. Concurrently, there has been growing recognition of financial toxicity associated with cancer care during this time period. As such, we reviewed FDA approvals from 2019 to 2013 and identified the following approvals in gynecologic oncology: pembrolizumab plus lenvatinib, pembrolizumab for recurrent endometrial cancer that is MSI-H/dMMR, tisotumab vedotin, dostarlimab as single-agent therapy, and dostarlimab plus chemotherapy. We focused on approvals for endometrial cancer, and conducted a cost-effectiveness analysis for combination options approved in treating recurrent or advanced endometrial cancer (i.e. pembrolizumab plus lenvatinib versus placebo; dostarlimab plus chemotherapy versus placebo), and found neither regimen was cost-effective at a willingness-to-pay of $100,000 per Equal Value of Life Years Gained (evLYG). While these costs may not necessarily be translated to an individual patient, these costs are absorbed by healthcare systems and insurance providers on a larger scale with downstream effects on individuals contributing to healthcare costs a whole.

摘要

在过去五年(2019 - 2023年)中,几种新的靶向治疗和免疫疗法已被批准用于治疗复发性宫颈癌、卵巢癌和子宫内膜癌。与此同时,在此期间,人们越来越认识到癌症治疗相关的经济毒性。因此,我们回顾了2019年至2023年美国食品药品监督管理局(FDA)的批准情况,并确定了妇科肿瘤学中的以下批准:帕博利珠单抗联合乐伐替尼、用于微卫星高度不稳定/错配修复缺陷(MSI-H/dMMR)复发性子宫内膜癌的帕博利珠单抗、替索单抗维托辛、作为单药疗法的多斯塔利单抗,以及多斯塔利单抗联合化疗。我们重点关注了子宫内膜癌的批准情况,并对批准用于治疗复发性或晚期子宫内膜癌的联合方案(即帕博利珠单抗联合乐伐替尼与安慰剂对比;多斯塔利单抗联合化疗与安慰剂对比)进行了成本效益分析,发现在每获得一个质量调整生命年(evLYG)支付意愿为10万美元的情况下,这两种方案都不具有成本效益。虽然这些成本不一定会转化为个体患者的费用,但这些成本在更大规模上由医疗系统和保险提供商承担,对整个医疗费用的个体产生下游影响。

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本文引用的文献

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Cost-Effectiveness Analysis of Trastuzumab Deruxtecan Versus Trastuzumab Emtansine for Patients With Human Epidermal Growth Factor Receptor 2 Positive Metastatic Breast Cancer in the United States.曲妥珠单抗-德鲁替康与曲妥珠单抗-美坦新用于美国人表皮生长因子受体 2 阳性转移性乳腺癌患者的成本-效果分析。
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Dostarlimab for Primary Advanced or Recurrent Endometrial Cancer.度伐利尤单抗治疗原发性晚期或复发性子宫内膜癌。
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Clinical outcome and biomarker assessments of a multi-centre phase II trial assessing niraparib with or without dostarlimab in recurrent endometrial carcinoma.多中心 II 期临床试验评估尼拉帕利联合或不联合度伐利尤单抗治疗复发性子宫内膜癌的临床结局和生物标志物评估。
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Lenvatinib Plus Pembrolizumab vs. Chemotherapy in Pretreated Patients With Advanced Endometrial Cancer: A Cost-Effectiveness Analysis.仑伐替尼联合帕博利珠单抗与化疗治疗晚期子宫内膜癌患者:成本效果分析。
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Cancer Drug Approvals That Displaced Existing Standard-of-Care Therapies, 2016-2021.2016-2021 年取代现有标准治疗药物的癌症治疗药物批准情况。
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Safety and antitumor activity of dostarlimab in patients with advanced or recurrent DNA mismatch repair deficient/microsatellite instability-high (dMMR/MSI-H) or proficient/stable (MMRp/MSS) endometrial cancer: interim results from GARNET-a phase I, single-arm study.多塔利单抗治疗晚期或复发性 DNA 错配修复缺陷/微卫星不稳定高(dMMR/MSI-H)或 proficient/stable(MMRp/MSS)子宫内膜癌患者的安全性和抗肿瘤活性:GARNET 研究的初步结果,一项 I 期单臂研究。
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