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Dig Dis Sci. 2017 Oct;62(10):2704-2712. doi: 10.1007/s10620-017-4714-8. Epub 2017 Sep 6.
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Curing Chronic Hepatitis C: A Cost Comparison of the Combination Simeprevir Plus Sofosbuvir vs. Protease-Inhibitor-Based Triple Therapy.治愈慢性丙型肝炎:simeprevir联合索非布韦与基于蛋白酶抑制剂的三联疗法的成本比较
Ann Hepatol. 2017 May-Jun;16(3):366-374. doi: 10.5604/16652681.1235479.
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Antivir Ther. 2017;22(6):481-493. doi: 10.3851/IMP3117. Epub 2016 Dec 9.
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Am Health Drug Benefits. 2016 Sep;9(6):327-335.
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Hepatology. 2016 Aug;64(2):405-14. doi: 10.1002/hep.28625. Epub 2016 Jun 7.
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基于索非布韦的方案治疗美国高保险人群中的慢性丙型肝炎:患者特征、治疗依从性、疗效和医疗保健费用,2013-2015 年。

Sofosbuvir-Based Regimens for Chronic Hepatitis C in a Well-Insured U.S. Population: Patient Characteristics, Treatment Adherence, Effectiveness, and Health Care Costs, 2013-2015.

机构信息

1 Division of Viral Hepatitis, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia.

出版信息

J Manag Care Spec Pharm. 2019 Feb;25(2):195-210. doi: 10.18553/jmcp.2019.25.2.195.

DOI:10.18553/jmcp.2019.25.2.195
PMID:30698086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6753523/
Abstract

BACKGROUND

Chronic hepatitis C (CHC) is a leading cause of morbidity and mortality and has imposed a high health care burden in the United States. Direct-acting antiviral (DAA) regimens are well tolerated and highly effective for CHC therapy but were initially marketed at a high price. Studies of their real-world use with a nationwide population are limited.

OBJECTIVE

To examine patient characteristics, treatment adherence, effectiveness, and health care costs in a large U.S. population with commercial and Medicare supplemental insurance plans who received simeprevir (SIM), sofosbuvir (SOF), or ledipasvir/sofosbuvir (LED/SOF) during the years 2013-2015.

METHODS

Patients with at least 1 diagnosis code for CHC and at least 1 claim for SIM, SOF, or LED/SOF prescriptions were selected. The date of the first claim for SIM, SOF, or LED/SOF was defined as the index date. Analyses were stratified by 4 regimens: SOF + SIM ± ribavirin (RBV), SOF + peginterferon alpha-2a or 2b (PEG) + RBV, SOF + RBV, and LED/SOF ± RBV. Adherence was defined by the proportion of days covered (PDC) ≥ 80%. Sustained virologic response (SVR12) was defined as a hepatitis C virus (HCV) RNA load of ≤ 25 IU/mL measured at ≥ 12 weeks following the end of the days supply of the last DAA refill. Health care costs such as DAA drug costs and medical costs (inpatient costs plus outpatient costs) were described.

RESULTS

Of 10,808 CHC patients, approximately two thirds were male, and mean age was 55 years. The proportion of patients with compensated cirrhosis among each regimen ranged from 7.4% in LED/SOF ± RBV to 13.8% in SOF + SIM ± RBV, and the proportion of patients with decompensated cirrhosis ranged from 3.9% in LED/SOF ± RBV to 10.7% in SOF + SIM ± RBV. The majority of patients (89.0%) used the newer regimen LED/SOF ± RBV in 2015. Adherence rates were estimated at 80.5%, 81.5%, 85.7%, and 91.4% for SOF + SIM ± RBV (n = 1,761); SOF + PEG + RBV (n = 1,314); SOF + RBV (n = 1,994); and LED/SOF ± RBV (n = 5,739), respectively. Regimen-specific adherence predictors included sex, age group, payer type, health plan, and treatment option with RBV. Being born during 1945-1965, liver disease severity, and Charlson Comorbidity Index levels did not predict adherence in any regimen. Overall SVR12 was 92.6% in 203 patients with available HCV RNA results: 100% (41/41) in SOF + SIM ± RBV; 83.3% (25/30) in SOF + PEG + RBV; 90.6% (29/32) in SOF + RBV; and 93% (93/100) in LED/SOF ± RBV. While the drug costs for these DAA regimens were initially high, they had decreased 18.9% (P < 0.001) during 2013-2015. Medical costs decreased 9.2% (P < 0.001) 1 year after the index dates.

CONCLUSIONS

These results indicate that DAA drug costs decreased steadily during 2013-2015 and that 89% of patients on SOF-based DAA regimens took newer, lower-cost regimens with adherence rates above 80%. Available data show that SVR12 rates were close to those obtained in clinical studies. Medical costs also significantly decreased 1 year after the index dates.

DISCLOSURES

No outside funding supported this study. All authors are U.S. federal employees of the Centers for Disease Control and Prevention. The authors declare that they have no competing interests. The findings and conclusions in this research are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.

摘要

背景

慢性丙型肝炎(CHC)是发病率和死亡率的主要原因,并给美国的医疗保健带来了沉重负担。直接作用抗病毒(DAA)方案对 CHC 治疗具有良好的耐受性和高度有效性,但最初的市场价格很高。对具有全国性人群的真实世界使用情况进行研究的情况有限。

目的

在接受simeprevir(SIM)、sofosbuvir(SOF)或 ledipasvir/sofosbuvir(LED/SOF)治疗的具有商业和医疗保险补充计划的美国大型人群中,研究患者特征、治疗依从性、有效性和医疗保健费用,时间范围为 2013-2015 年。

方法

选择至少有 1 个 CHC 诊断代码和至少 1 次 SIM、SOF 或 LED/SOF 处方的患者。首次开具 SIM、SOF 或 LED/SOF 处方的日期定义为索引日期。分析分为 4 种方案:SOF + SIM ± ribavirin(RBV)、SOF + peginterferon alpha-2a 或 2b(PEG)+ RBV、SOF + RBV 和 LED/SOF ± RBV。依从性定义为比例≥ 80%。持续病毒学应答(SVR12)定义为在最后一次 DAA 续药的最后一天供应后至少 12 周时,HCV RNA 载量≤ 25 IU/mL。描述了直接抗病毒药物成本和医疗成本(住院成本加门诊成本)等医疗保健费用。

结果

在 10808 例 CHC 患者中,约三分之二为男性,平均年龄为 55 岁。每种方案中代偿性肝硬化患者的比例范围为 LED/SOF ± RBV 方案的 7.4%至 SOF + SIM ± RBV 方案的 13.8%,失代偿性肝硬化患者的比例范围为 LED/SOF ± RBV 方案的 3.9%至 SOF + SIM ± RBV 方案的 10.7%。2015 年,大多数患者(89.0%)使用更新的 LED/SOF ± RBV 方案。SOF + SIM ± RBV(n = 1761)、SOF + PEG + RBV(n = 1314)、SOF + RBV(n = 1994)和 LED/SOF ± RBV(n = 5739)方案的估计依从率分别为 80.5%、81.5%、85.7%和 91.4%。方案特异性依从性预测因素包括性别、年龄组、付款人类型、健康计划和 RBV 治疗选择。出生于 1945-1965 年、肝病严重程度和 Charlson 合并症指数水平在任何方案中均不能预测依从性。在有 HCV RNA 结果的 203 例患者中,总体 SVR12 为 92.6%:SOF + SIM ± RBV 方案为 100%(41/41);SOF + PEG + RBV 方案为 83.3%(25/30);SOF + RBV 方案为 90.6%(29/32);LED/SOF ± RBV 方案为 93%(93/100)。尽管这些 DAA 方案的药物成本最初很高,但在 2013-2015 年期间已下降 18.9%(P < 0.001)。索引日期后 1 年,医疗成本下降 9.2%(P < 0.001)。

结论

这些结果表明,2013-2015 年期间 DAA 药物成本稳步下降,89%的 SOF 为基础的 DAA 方案患者使用了新的、成本较低、依从性高于 80%的方案。现有数据表明,SVR12 率接近临床研究获得的结果。索引日期后 1 年,医疗成本也显著下降。

披露

本研究无外部资金支持。所有作者均为美国疾病控制与预防中心的联邦雇员。作者声明他们没有利益冲突。研究结果是作者的结果,不一定代表疾病控制与预防中心的立场。