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Record W2792338314 · doi:10.1093/jcag/gwy009.073

A73 COST-EFFECTIVENESS OF INFLIXIMAB BIOSIMILAR COMPARED TO ORIGINATOR INFLIXIMAB FOR THE MANAGEMENT OF CROHN’S DISEASE

2018· article· en· W2792338314 on OpenAlexaffabout
Candace L. Beilman, Christopher Ma, Christopher McCabe, Richard N. Fedorak, Brendan P. Halloran

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2018
Typearticle
Languageen
FieldImmunology and Microbiology
TopicBiosimilars and Bioanalytical Methods
Canadian institutionsUniversity of CalgaryUniversity of Alberta
Fundersnot available
KeywordsInfliximabBiosimilarMedicineCrohn's diseaseIntensive care medicineInternal medicineDisease

Abstract

fetched live from OpenAlex

Originator infliximab (marketed as Remicade) was the first biological therapy approved in patients with Crohn’s Disease (CD), and has been proven to be effective for the induction and maintenance of remission in patients with moderate-to-severe disease. Due to its recent patent expiry, an infliximab biosimilar (infliximab-dyyb, marketed as Inflectra) has been introduced in Canada. Recent trials have shown that switching from originator infliximab to its biosimilar is not inferior to continued treatment with originator infliximab, however the molecular complexity and sensitivity to changes in manufacturing of biologics makes it difficult to verify the similarity of biosimilars to their respective originator biologic. Nevertheless, the lower price of infliximab biosimilar compared to originator infliximab has the potential to result in large cost savings for patients with CD. The aim of our study was to compare the cost-effectiveness of infliximab biosimilar (Inflectra) to originator infliximab (Remicade) for the management of CD. A Markov model was developed to simulate the clinical pathway of patients with moderate-to-severe CD after initiating either originator infliximab or infliximab-dyyb. We calculated the cost and effectiveness of both treatments arms over a 5-year time horizon. Loss of response rates were obtained using the CD data from the NOR-SWITCH non-inferiority trial. Transition probabilities between health states and utility values for each health state were obtained from a review of the literature. The cost of health states were accessed with the CIHI patient cost estimator, and the drug costs of Remicade and Inflectra were determined by the Alberta Health and Wellness Drug Benefit List. Deterministic and probabilistic sensitivity analysis was performed on all key variables. Using a 5-year time horizon, originator infliximab costs $190,632 per patient and yields 3.63 quality-adjusted life years (QALYs). Infliximab-dyyb costs $128,306 per patient and yields 3.15 QALYs. Using a willingness-to-pay (WTP) threshold of $50,000 per QALY, infliximab-dyyb has a 83% probability of being cost-effective, whereas originator infliximab has a 17% probability of being cost-effective. The cost-effectiveness of each treatment at a range of WTP thresholds is shown in Figure 1. Infliximab biosmilar resulted in large cost savings despite similar effectiveness to originator infliximab for patients with moderate-to-severe CD. Based on the results of our model, the mainstream usage of infliximab biosimilar (Inflectra) may help reduce the economic burden associated with CD. Cost-effectiveness acceptability curve demonstrating the probability that each treatment option is cost-effective at a range of willingness-to-pay thresholds. The Centre of Excellence for Gastrointestinal Inflammation and Immunity Research

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.064
Threshold uncertainty score0.509

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0020.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.021
GPT teacher head0.296
Teacher spread0.275 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2018
Admission routes2
Has abstractyes

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