Two-year cost-effectiveness of different COBRA-like intensive remission induction schemes in early rheumatoid arthritis: a piggyback study on the pragmatic randomised controlled CareRA trial

被引:15
作者
Pazmino, Sofia [1 ]
Boonen, Annelies [2 ,3 ]
Stouten, Veerle [1 ]
De Cock, Diederik [1 ]
Joly, Johan [4 ]
Van der Elst, Kristien [4 ]
Westhovens, Rene [1 ,4 ]
Verschueren, Patrick [1 ,4 ]
机构
[1] Katholieke Univ Leuven, Dept Dev & Regenerat, Skeletal Biol & Engn Res Ctr, B-3000 Leuven, Flanders, Belgium
[2] Maastricht Univ, Med Ctr, Dept Internal Med, Div Rheumatol, Maastricht, Netherlands
[3] Maastricht Univ, Care & Publ Hlth Res Inst CAPHRI, Maastricht, Netherlands
[4] Univ Hosp Leuven, Dept Rheumatol, Leuven, Belgium
关键词
MODIFYING ANTIRHEUMATIC DRUGS; TREATMENT STRATEGIES; MULTIPLE IMPUTATION; CLINICAL-TRIALS; DISEASE; METHOTREXATE; COMBINATION; EQ-5D; QUESTIONNAIRE; UTILITIES;
D O I
10.1136/annrheumdis-2019-216874
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives To evaluate the cost-effectiveness of treat-to-target strategies among recently diagnosed patients with rheumatoid arthritis (RA) using methotrexate (MTX) and a step-down glucocorticoid (GC) scheme (COBRA Slim) compared with (1) this combination with either sulphasalazine (COBRA Classic) or leflunomide (COBRA Avant-G arde) in high-risk patients and (2) MTX without GCs (Tight-S tep-Up, TSU) in low-risk patients. Methods The incremental cost-utility was calculated from a healthcare perspective in the intention-to-treat population (n=379) of the 2-year open-label pragmatic randomised controlled Care in early RA trial. Healthcare costs were collected prospectively through electronic trial records. Quality-adjusted life years (QALYs) were estimated using mapping algorithms for EuroQoL-5 Dimension. Multiple imputation was used to handle missing data and bootstrapping to calculate CIs. Robustness was tested with biological disease-modifying antirheumatic drugs at biosimilar prices. Results In the high-risk group, Classic (Delta k(sic)1.464, 95%CI -0.198 to 3.127) and Avant-G arde (Delta k(sic)0.636, 95%CI -0.987 to 2.258) were more expensive compared with Slim and QALYs were slightly worse for Classic (Delta-0.002, 95%CI -0.086 to 0.082) and Avant-Garde (Delta-0.009, 95%CI -0.102 to 0.084). This resulted in the domination of Classic and Avant-G arde by Slim. In the low-risk group, Slim was cheaper (Delta k(sic)-0.617, 95%CI -2.799 to 1.566) and QALYs were higher (Delta 0.141, 95%CI 0.008 to 0.274) compared with TSU, indicating Slim dominated. Results were robust against the price of biosimilars. Conclusions The combination of MTX with a GC bridging scheme is less expensive with comparable health utility than more intensive step-down combination strategies or a conventional step-up approach 2 years after initial treatment.
引用
收藏
页码:556 / 565
页数:10
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