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类风湿关节炎中肿瘤坏死因子抑制剂使用情况的真实世界评估

Real-world evaluation of TNF-inhibitor utilization in rheumatoid arthritis.

作者信息

Harnett J, Wiederkehr D, Gerber R, Gruben D, Koenig A, Bourret J

机构信息

a a Pfizer Inc , New York , NY , USA.

b b Pfizer Inc , Groton , CT , USA.

出版信息

J Med Econ. 2016;19(2):91-102. doi: 10.3111/13696998.2015.1099538. Epub 2015 Oct 27.

Abstract

OBJECTIVES

To evaluate 12-month treatment patterns, healthcare resource use (HCRU), and costs for patients with rheumatoid arthritis (RA), following initiation of index TNF inhibitors (TNFi) and subsequent biologic DMARDs (bDMARDs).

METHODS

This was a retrospective cohort analysis of adults with RA newly initiating TNFi in the Truven Marketscan Commercial Claims and Encounters and Medicare Supplemental Databases during 2010-2013. A sub-group of patients who switched to a bDMARD within 12 months post-index and within 180 days of last index TNFi were subsequently evaluated over 12 months. TNFi/bDMARD treatment patterns were characterized as: continuers, no gap >180 days in prescription/administration of index TNFi; discontinuers, gap >180 days; switchers, initiated new bDMARD. Concomitant conventional synthetic DMARD use, co-morbid chronic illnesses, and RA severity were assessed. All-cause/RA-related HCRU and costs were evaluated 12 months post-index.

RESULTS

Of 9567 identified patients, 67.2%, 17.3%, and 15.4% were continuers, discontinuers, and switchers, respectively. Switchers had the highest 12-month unadjusted mean all-cause costs of $34,585 vs $33,051 for continuers (p = 0.1158) and $24,915 for discontinuers (p < 0.0001; discontinuers vs continuers, p < 0.0001). RA-related costs comprised 82.8%, 31.4%, and 85.7% of total costs for continuers, discontinuers, and switchers, respectively. Of 764 switchers, 68.2% switched to alternative TNFi (cyclers), the rest to non-TNFi bDMARDs; 36.7% of patients who switched to TNFi switched again (to third-line bDMARD) vs 27.6% (p = 0.0313) of those who switched to non-TNFi bDMARDs. Switchers to non-TNFi bDMARDs had higher mean 12-month all-cause costs of $76,580 compared with $50,689 for switchers to alternative TNFi (p < 0.0001); biologic-administration visits comprised 78.8% of the greater total RA-related costs of switchers to non-TNFi bDMARDs.

CONCLUSIONS

Real-world TNFi discontinuation/switching rates correspond to randomized controlled trial non-response rates. TNFi cycling is common and associated with an increased likelihood of switching to third-line bDMARD. Switching to non-TNFi bDMARDs was associated with higher costs, mostly attributed to in-office administrations.

摘要

目的

评估类风湿性关节炎(RA)患者在开始使用首种肿瘤坏死因子抑制剂(TNFi)及后续生物性改善病情抗风湿药(bDMARDs)后12个月的治疗模式、医疗资源使用(HCRU)情况及费用。

方法

这是一项对2010 - 2013年期间在Truven Marketscan商业索赔与病历数据库以及医疗保险补充数据库中首次使用TNFi的成年RA患者进行的回顾性队列分析。对索引后12个月内且在最后一次索引TNFi使用后180天内转而使用bDMARD的患者亚组进行了为期12个月的后续评估。TNFi/bDMARD治疗模式的特征如下:持续使用者,索引TNFi的处方/给药无超过180天的间隔;停用者,间隔超过180天;转换者,开始使用新的bDMARD。评估了同时使用传统合成DMARD的情况、共病慢性病情况以及RA的严重程度。在索引后12个月评估全因/RA相关的HCRU及费用。

结果

在9567名确诊患者中,分别有67.2%、17.3%和15.4%为持续使用者、停用者和转换者。转换者12个月未经调整的平均全因费用最高,为34,585美元,持续使用者为33,051美元(p = 0.1158),停用者为24,915美元(p < 0.0001;停用者与持续使用者相比,p < 0.0001)。RA相关费用分别占持续使用者、停用者和转换者总费用的82.8%、31.4%和85.7%。在764名转换者中,68.2%转换为其他TNFi(循环使用者),其余转换为非TNFi的bDMARD;转换为TNFi的患者中有36.7%再次转换(使用三线bDMARD),而转换为非TNFi的bDMARD的患者中这一比例为27.6%(p = 0.0313)。转换为非TNFi的bDMARD的患者12个月平均全因费用更高,为76,580美元,而转换为其他TNFi的患者为50,689美元(p < 0.0001);生物制剂给药就诊费用占转换为非TNFi的bDMARD的患者更高的RA相关总费用的78.8%。

结论

实际应用中TNFi的停药/转换率与随机对照试验中的无反应率相当。TNFi循环使用很常见,且与转换为三线bDMARD的可能性增加有关。转换为非TNFi的bDMARD与更高的费用相关,主要归因于门诊给药。

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