Understanding the Natural History of Chronic Hepatitis D: Proposal of a Model for Cost-Effectiveness Studies.

IF 2 Q2 ECONOMICS
PharmacoEconomics Open Pub Date : 2024-03-01 Epub Date: 2024-01-03 DOI:10.1007/s41669-023-00466-3
Ankita Kaushik, Geoffrey Dusheiko, Chong Kim, Nathaniel J Smith, Csilla Kinyik-Merena, Gian Luca Di Tanna, Robert J Wong
{"title":"Understanding the Natural History of Chronic Hepatitis D: Proposal of a Model for Cost-Effectiveness Studies.","authors":"Ankita Kaushik, Geoffrey Dusheiko, Chong Kim, Nathaniel J Smith, Csilla Kinyik-Merena, Gian Luca Di Tanna, Robert J Wong","doi":"10.1007/s41669-023-00466-3","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>As new therapeutic options become available, better understanding the potential impact of emerging therapies on clinical outcomes of hepatits D virus (HDV) is critical.</p><p><strong>Objective: </strong>The aim of this study was to develop a natural history model for patients with hepatitis D virus.</p><p><strong>Methods: </strong>We developed a model (decision tree followed by a Markov cohort model) in adults with chronic HDV infection to assess the natural history and impact of novel treatments on disease progression versus best supportive care (BSC). The model time horizon was over a lifetime (up to 100 years of age); state transitions and health states were defined by responder status. Patients in fibrosis stages 0 through 4 received treatment; decompensated patients were not treated. Response was defined as the combined response endpoint of achievement of HDV-RNA undetectability/≥2-log<sub>10</sub> decline and alanine aminotransferase normalization; response rates of 50% and 75% were explored. Health events associated with advanced liver disease were modeled as the number of events per 10,000 patients. Scenario analyses of early treatment, alternate treatment response, and no fibrosis regression for treatment responders were also explored.</p><p><strong>Results: </strong>The model was able to reflect disease progression similarly to published natural history studies for patients with HBV/HDV infection. In a hypothetical cohort of patients reflecting a population enrolled in a recent clinical trial, fewer advanced liver disease events were observed with a novel HDV treatment versus BSC. Fewer liver-related deaths were observed under 50% and 75% response (900 and 1,358 fewer deaths, respectively, per 10,000 patients). Scenario analyses showed consistently fewer advanced liver disease events with HDV treatment compared with BSC, with greater reductions observed with earlier treatment.</p><p><strong>Conclusion: </strong>This HDV disease progression model replicated findings from natural history studies. Furthermore, it found that a hypothetical HDV treatment results in better clinical outcomes for patients versus BSC, with greater benefit observed when starting treatment early. This validated natural history model for HBV/HDV infection can serve as a foundation for future clinical and economic analyses of novel HDV treatments that can support healthcare stakeholders in the management of patients with chronic HDV.</p>","PeriodicalId":19770,"journal":{"name":"PharmacoEconomics Open","volume":" ","pages":"333-343"},"PeriodicalIF":2.0000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10884366/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"PharmacoEconomics Open","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s41669-023-00466-3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/3 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ECONOMICS","Score":null,"Total":0}
引用次数: 0

Abstract

Background: As new therapeutic options become available, better understanding the potential impact of emerging therapies on clinical outcomes of hepatits D virus (HDV) is critical.

Objective: The aim of this study was to develop a natural history model for patients with hepatitis D virus.

Methods: We developed a model (decision tree followed by a Markov cohort model) in adults with chronic HDV infection to assess the natural history and impact of novel treatments on disease progression versus best supportive care (BSC). The model time horizon was over a lifetime (up to 100 years of age); state transitions and health states were defined by responder status. Patients in fibrosis stages 0 through 4 received treatment; decompensated patients were not treated. Response was defined as the combined response endpoint of achievement of HDV-RNA undetectability/≥2-log10 decline and alanine aminotransferase normalization; response rates of 50% and 75% were explored. Health events associated with advanced liver disease were modeled as the number of events per 10,000 patients. Scenario analyses of early treatment, alternate treatment response, and no fibrosis regression for treatment responders were also explored.

Results: The model was able to reflect disease progression similarly to published natural history studies for patients with HBV/HDV infection. In a hypothetical cohort of patients reflecting a population enrolled in a recent clinical trial, fewer advanced liver disease events were observed with a novel HDV treatment versus BSC. Fewer liver-related deaths were observed under 50% and 75% response (900 and 1,358 fewer deaths, respectively, per 10,000 patients). Scenario analyses showed consistently fewer advanced liver disease events with HDV treatment compared with BSC, with greater reductions observed with earlier treatment.

Conclusion: This HDV disease progression model replicated findings from natural history studies. Furthermore, it found that a hypothetical HDV treatment results in better clinical outcomes for patients versus BSC, with greater benefit observed when starting treatment early. This validated natural history model for HBV/HDV infection can serve as a foundation for future clinical and economic analyses of novel HDV treatments that can support healthcare stakeholders in the management of patients with chronic HDV.

了解慢性 D 型肝炎的自然病史:关于成本效益研究模型的建议》。
背景:随着新治疗方案的出现,更好地了解新疗法对丁型肝炎病毒(HDV)临床疗效的潜在影响至关重要:本研究旨在为丁型肝炎病毒感染者建立一个自然病史模型:我们以慢性 HDV 感染的成人患者为对象建立了一个模型(决策树后接马尔可夫队列模型),以评估新疗法相对于最佳支持治疗 (BSC) 的自然史及其对疾病进展的影响。该模型的时间跨度为一生(最长 100 岁);状态转换和健康状态由应答者状态定义。纤维化 0 至 4 期的患者接受治疗;失代偿期患者不接受治疗。应答定义为HDV-RNA检测不到/≥2-log10下降和丙氨酸氨基转移酶正常化的综合应答终点;应答率为50%和75%。与晚期肝病相关的健康事件以每 10,000 名患者中发生的事件数建模。还探讨了早期治疗、交替治疗应答以及治疗应答者无纤维化回归的情景分析:结果:该模型能够反映疾病进展,与已发表的 HBV/HDV 感染患者自然史研究结果相似。在反映近期临床试验入组人群的假定患者队列中,观察到新型 HDV 治疗与 BSC 相比,晚期肝病事件更少。在 50%和 75% 的应答率下,观察到的肝脏相关死亡病例较少(每 10,000 名患者中分别减少 900 例和 1,358 例)。情景分析表明,与 BSC 相比,HDV 治疗可持续减少晚期肝病事件的发生,早期治疗可观察到更大程度的减少:结论:这一 HDV 疾病进展模型复制了自然史研究的结果。此外,该模型还发现,与 BSC 相比,假设的 HDV 治疗可为患者带来更好的临床疗效,而且早期开始治疗的患者获益更大。这一经过验证的 HBV/HDV 感染自然史模型可作为未来新型 HDV 治疗方法临床和经济分析的基础,为医疗保健相关方管理慢性 HDV 患者提供支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.50
自引率
0.00%
发文量
64
审稿时长
8 weeks
期刊介绍: PharmacoEconomics - Open focuses on applied research on the economic implications and health outcomes associated with drugs, devices and other healthcare interventions. The journal includes, but is not limited to, the following research areas:Economic analysis of healthcare interventionsHealth outcomes researchCost-of-illness studiesQuality-of-life studiesAdditional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in PharmacoEconomics -Open 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 important medical advances.All manuscripts are subject to peer review by international experts. Letters to the Editor are welcomed and will be considered for publication.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信