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Cost-Effectiveness Analysis of REBYOTA™ (Fecal Microbiota, Live-jslm [FMBL]) Versus Standard of Care for the Prevention of Recurrent Clostridioides Difficile Infection in the USA

Overview
Journal Adv Ther
Date 2023 Apr 24
PMID 37093359
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Abstract

Introduction: Recurrent Clostridioides difficile infection (rCDI) is common and associated with considerable clinical and economic consequences. REBYOTA™ (fecal microbiota, live-jslm [FMBL]) is a microbiota-based live biotherapeutic approved for the prevention of rCDI following antibiotic treatment for rCDI. We sought to evaluate cost-effectiveness of FMBL compared to standard of care (SOC) from a US third-party payer perspective among patients with one or more (≥ 1) recurrences.

Methods: A Markov model with a lifetime time horizon was developed. The model population included adult patients who had ≥ 1 recurrence after a primary CDI episode and had completed ≥ 1 round of antibiotics, or had ≥ 2 severe CDI episodes resulting in hospitalization within the last year. The model consisted of six health states with an 8-week model cycle: rCDI, absence of CDI after recurrence, colectomy, ileostomy, ileostomy reversal, and death. Drug costs and rCDI-related medical costs were estimated in 2022 US dollars and discounted at 3% annually. Deterministic sensitivity analyses were performed.

Results: Compared to SOC, FMBL at $9000/course resulted in an incremental cost-effectiveness ratio (ICER) of $18,727 per quality-adjusted life year (QALY) gained. The incremental cost was $5336 (FMBL $79,236, SOC $73,900) and the incremental effectiveness was 0.285 QALYs (FMBL 10.346, SOC 10.061). The cumulative drug acquisition and administration costs for the FMBL and SOC arms were $24,245 and $16,876, while rCDI-related medical costs for FMBL and SOC were $54,991 and $57,024, respectively. The ICER in the subgroup of patients at first recurrence was $13,727 per QALY gained. FMBL remained cost-effective across all sensitivity analyses.

Conclusions: FMBL was found to be cost-effective compared to SOC for the prevention of rCDI with more benefits among patients at first recurrence, with an ICER far below the payer ICER threshold of $100,000. Patients treated with FMBL experienced higher total QALYs and reduced healthcare resource utilization, including reduced hospitalizations.

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References
1.
Lessa F, Mu Y, Bamberg W, Beldavs Z, Dumyati G, Dunn J . Burden of Clostridium difficile infection in the United States. N Engl J Med. 2015; 372(9):825-34. PMC: 10966662. DOI: 10.1056/NEJMoa1408913. View

2.
Leong C, Zelenitsky S . Treatment Strategies for Recurrent Clostridium difficile Infection. Can J Hosp Pharm. 2013; 66(6):361-8. PMC: 3867563. DOI: 10.4212/cjhp.v66i6.1301. View

3.
Cornely O, Miller M, Louie T, Crook D, Gorbach S . Treatment of first recurrence of Clostridium difficile infection: fidaxomicin versus vancomycin. Clin Infect Dis. 2012; 55 Suppl 2:S154-61. PMC: 3388030. DOI: 10.1093/cid/cis462. View

4.
Khanna S, Assi M, Lee C, Yoho D, Louie T, Knapple W . Efficacy and Safety of RBX2660 in PUNCH CD3, a Phase III, Randomized, Double-Blind, Placebo-Controlled Trial with a Bayesian Primary Analysis for the Prevention of Recurrent Clostridioides difficile Infection. Drugs. 2022; 82(15):1527-1538. PMC: 9607700. DOI: 10.1007/s40265-022-01797-x. View

5.
Orenstein R, Dubberke E, Khanna S, Lee C, Yoho D, Johnson S . Durable reduction of Clostridioides difficile infection recurrence and microbiome restoration after treatment with RBX2660: results from an open-label phase 2 clinical trial. BMC Infect Dis. 2022; 22(1):245. PMC: 8917640. DOI: 10.1186/s12879-022-07256-y. View