Healthcare-Related Costs Associated with Switching Subcutaneous Tumor Necrosis Factor-α Inhibitor in the Treatment of Inflammatory Arthritis: a Retrospective Study

被引:2
作者
Dalen, Johan [1 ]
Luttropp, Karin [1 ]
Svedbom, Axel [1 ]
Black, Christopher M. [2 ]
Kachroo, Sumesh [2 ]
机构
[1] ICON Plc, Stockholm, Sweden
[2] Merck & Co Inc, Ctr Observat & Real World Evidence, Kenilworth, NJ USA
关键词
Ankylosing spondylitis; Biologics; Cost; Inflammatory arthritis; Psoriatic arthritis; Rheumatoid arthritis; Rheumatology; Subcutaneous TNF alpha inhibitors; Switching; Treatment persistence; MODIFYING ANTIRHEUMATIC DRUGS; RHEUMATOID-ARTHRITIS; TREATMENT PERSISTENCE; PROPENSITY SCORE; REGISTER; BIOLOGICS; OUTCOMES; IMPACT; SAFETY; RATES;
D O I
10.1007/s12325-020-01425-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Introduction: Subsequent lines of subcutaneous tumor necrosis factor alpha inhibitor (SC-TNFi) treatment may be well motivated in the management of rheumatoid arthritis (RA), ankylosing spondylitis (AS), and psoriatic arthritis (PsA)-collectively named inflammatory arthritis (IA). However, the costs associated with switching SC-TNFis are largely unknown. The objective of this retrospective observational study was to explore costs of healthcare resource utilization (HCRU) associated with switching SC-TNFi treatment among biologicnaive Swedish patients with IA. Methods: Using population-based register data, adult patients filling prescriptions between May 6, 2010 and December 31, 2014 for an SCTNFi (adalimumab, etanercept, certolizumab, and golimumab) were included. Patients switching treatment (cyclers) were matched to treatment persistent patients on the basis of propensity score and follow-up time. HCRU-associated costs were captured and compared 12 months before and 12 months after the index date (defined as the date of the switch). Results: A balanced cohort of 594 matched pairs was derived. Prior to the index date, cyclers had significantly higher non-treatment HCRU costs compared to persistent patients ($3815 [3498-4147] vs. $2900; 95%CI [2565-3256]). However, 12 months after the index date, cyclers had significantly increased their non-treatment HCRU costs while persistent patients lowered theirs ($822 [232-1490] vs. $- 313 [- 664-36]). This resulted in a statistically significant difference in difference of $1135 between the groups. Conclusions: In biologic-naive patients treated with SC-TNFi for IA, cyclers significantly increased their non-treatment HCRU costs 12 months after switching treatment while persistent patients lowered their costs during the same time period. As these findings indicate that differences in treatment persistence may have an impact on costs, further research utilizing more comprehensive data sources in alternate settings is warranted.
引用
收藏
页码:3746 / 3760
页数:15
相关论文
共 50 条
  • [31] Efficacy predictors of a second tumor necrosis factor inhibitor in the treatment of rheumatoid arthritis
    Reams, Jennifer
    Berger, Andrea
    Denio, Alfred
    MEDICINE, 2020, 99 (35)
  • [32] Tumor necrosis factor-α antagonist therapy for concomitant rheumatoid arthritis and hepatitis C virus infection: a case series study
    Lin, Ko-Ming
    Cheng, Tien-Tsai
    Lin, Jing-Chi
    Chen, Chung-Jen
    CLINICAL RHEUMATOLOGY, 2015, 34 (06) : 1039 - 1046
  • [33] Secukinumab after first-line tumor necrosis factor-alpha inhibitor therapy in psoriatic arthritis: A real-world retrospective cohort study
    Ak, Tumay
    Mustafayeva, Leyla
    Ayla, Ali Yagiz
    Celik, Yeliz
    Can, Gunay
    Ugurlu, Serdal
    ARCHIVES OF RHEUMATOLOGY, 2024, 39 (01) : 71 - 80
  • [34] Treatment Sequences After Discontinuing a Tumor Necrosis Factor Inhibitor in Patients With Rheumatoid Arthritis: A Comparison of Cycling Versus Swapping Strategies
    Matusevich, Aliza R. Karpes
    Duan, Zhigang
    Zhao, Hui
    Lal, Lincy S.
    Chan, Wenyaw
    Suarez-Almazor, Maria E.
    Giordano, Sharon H.
    Swint, J. Michael
    Lopez-Olivo, Maria A.
    ARTHRITIS CARE & RESEARCH, 2021, 73 (10) : 1461 - 1469
  • [35] Ustekinumab for skin reactions associated with anti-tumor necrosis factor-α agents in patients with inflammatory bowel diseases: A single-center retrospective study
    Ezzedine, Khaled
    Visseaux, Laetitia
    Cadiot, Guillaume
    Brixi, Hedia
    Bernard, Philippe
    Reguiai, Ziad
    JOURNAL OF DERMATOLOGY, 2019, 46 (04) : 322 - 327
  • [36] Polymorphism in the tumor necrosis factor-α gene promoter is associated with severity of rheumatoid arthritis in the Czech population
    Petr Nemec
    Monika Pavkova-Goldbergova
    Martina Stouracova
    Anna Vasku
    Miroslav Soucek
    Jindra Gatterova
    Clinical Rheumatology, 2008, 27 : 59 - 65
  • [37] Tumor necrosis factor-α production is associated with less body cell mass in women with rheumatoid arthritis
    Walsmith, J
    Abad, L
    Kehayias, J
    Roubenoff, R
    JOURNAL OF RHEUMATOLOGY, 2004, 31 (01) : 23 - 29
  • [38] Polymorphism in the tumor necrosis factor-α gene promoter is associated with severity of rheumatoid arthritis in the Czech population
    Nemec, Petr
    Pavkova-Goldbergova, Monika
    Stouracova, Martina
    Vasku, Anna
    Soucek, Miroslav
    Gatterova, Jindra
    CLINICAL RHEUMATOLOGY, 2008, 27 (01) : 59 - 65
  • [39] Hepatitis-B reactivation during treatment with tumor necrosis factor-α blocker adalimumab in a patient with psoriasis arthritis
    Kouba, M.
    Rudolph, S. E.
    Hrdlicka, P.
    Zuber, M. A.
    DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 2012, 137 (1-2) : 23 - 26
  • [40] Elevation of serum KL-6 levels during treatment with tumor necrosis factor-α inhibitor in patients with psoriasis
    Mabuchi, Tomotaka
    Yamaoka, Hanako
    Kawai, Mayu
    Ota, Tami
    Ozawa, Akira
    JOURNAL OF DERMATOLOGY, 2014, 41 (12) : 1136 - 1137