Evidence map›Paper›PMID 41712207›Full record

ArticleJAMA network open2026

Cost-Effectiveness of Early vs Delayed Belimumab Treatment for Systemic Lupus Erythematosus.

Sabrina Hundal, Julian Cappelli, Christopher Sjöwall, Mohamed Osman, Zahi Touma, Ioannis Parodis, Stephanie R Goldberg, Elena Netchiporouk

Abstract read
In one paragraph

Article in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Sabrina HundalDepartment of Medicine, University of Calgary, Calgary, Alberta, Canada.
Julian CappelliDepartment of Health Research Methods, McMaster University, Hamilton, Ontario, Canada.
Christopher SjöwallDepartment of Biomedical and Clinical Sciences, Division of Inflammation and Infection, Linköping University, Linköping, Sweden.
Mohamed OsmanDepartment of Rheumatology, University of Alberta, Edmonton, Alberta, Canada.
Zahi ToumaSchroeder Arthritis Institute, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
Ioannis ParodisDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital, and Center for Molecular Medicine, Stockholm, Sweden.
Stephanie R GoldbergDepartment of Surgery, Mary Washington Healthcare, Fredericksburg, Virginia.
Elena NetchiporoukDivision of Dermatology, McGill University Health Centre, Montreal, Quebec, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Belimumab is a biologic therapy for active, autoantibody-positive systemic lupus erythematosus (SLE) that has been shown to reduce disease activity, flare frequency, and glucocorticoid use, thereby preventing organ damage. Belimumab is typically reserved for refractory disease, but emerging evidence suggests earlier initiation may lead to higher response rates, greater achievement of remission or low disease activity, and further reduction in glucocorticoid use. Objective: To evaluate the economic and health-related outcomes of early vs delayed belimumab initiation for biologic-naive patients with clinically active SLE, comparing medical costs and quality-adjusted life-years (QALYs). Design, Setting, and Participants: This economic evaluation using cost-utility analysis from a US payer perspective was conducted with a Markov model with monthly cycles over a 15-year horizon and was informed by studies published from 2013 to 2025, identified through a targeted literature review. Biologic-naive adult SLE patients with active disease (SLE Disease Activity Index 2000 score >0) were included. Patients began in a pretreatment state and transitioned monthly between 5 health states: complete response (per SLE Responder Index-4 [SRI-4]), partial response, nonresponse (failure to meet SRI-4 accompanied by flare or treatment-emergent adverse event), no treatment (standard of care), and death. Exposure: Early (≤2 years of disease duration) or delayed (after failure of standard therapy) initiation of intravenous belimumab. Main Outcomes and Measures: Primary outcomes included total direct medical costs, QALYs, incremental cost-effectiveness ratio (ICER), and incremental net monetary benefit (INMB). The 95% uncertainty intervals (UIs) for incremental costs, QALYs, and INMB were calculated from the 2.5 and 97.5 percentiles of the probabilistic sensitivity analyses. Results: The modeled cohort included 1000 adults (912 female [91.2%]) with a mean (SD) age of 41 (11) years at belimumab initiation. Early initiation provided an additional 0.30 (95% UI, -0.42 to 1.39) QALYs at an incremental cost of -$126 337.12 (95% UI, -$910 010.39 to $168 383.94) per patient relative to delayed initiation, yielding a favorable ICER of -$421 123.73 per QALY. At a $50 000 per QALY threshold, the mean INMB was $141 337.12 (95% UI, -$157 997.53 to $925 019.51), with early initiation preferred in 81.3% of simulations (8125 of 10 000 simulations). Deterministic sensitivity analyses identified time horizon (INMB range, $6351.07 for a 1-year horizon to $156 497.12 for a lifetime horizon) and SRI-4 response odds ratio (INMB range, $69 741.68 for an odds ratio of 1.08 to $209 591.09 for an odds ratio of 3.47) as the most influential parameters. Conclusions and Relevance: In this economic evaluation of early vs delayed belimumab in biologic-naive patients with active SLE, early initiation was associated with improved health outcomes and reduced costs. These findings support earlier clinical adoption and reconsideration of reimbursement criteria to reflect long-term value.

Indexed as

Antibodies, Monoclonal, HumanizedImmunosuppressive AgentsLupus Erythematosus, SystemicAdultCost-Benefit AnalysisCost-Effectiveness AnalysisFemaleHumansMaleMarkov ChainsQuality-Adjusted Life YearsTreatment DelayAntibodies, Monoclonal, HumanizedbelimumabImmunosuppressive Agents

Identifiers

PMID41712207
PMCPMC12921522

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.