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Cost-Effectiveness of Baloxavir Marboxil Versus Oseltamivir or no Treatment for the Management of Influenza in the United States.
Kommandantvold, Svenn Alexander; Chang, Shih-Chen; Surinach, Andy; Yau, Vincent; Best, Jennie H; Zaraket, Hassan; Zhou, Hao; Frimpter, Jeff; Blanchet Zumofen, Marie-Helene.
Affiliation
  • Kommandantvold SA; Roche Norway, F. Hoffmann-La Roche AG, Roche Norge AS, Brynsengfaret 6B, 0667, Oslo, Norway. svenn.kommandantvold@roche.com.
  • Chang SC; Genentech Inc, South San Francisco, CA, USA.
  • Surinach A; Genesis Research, Hoboken, NJ, USA.
  • Yau V; Genentech Inc, South San Francisco, CA, USA.
  • Best JH; Genentech Inc, South San Francisco, CA, USA.
  • Zaraket H; Roche Products Ltd., Welwyn Garden City, UK.
  • Zhou H; Genentech Inc, South San Francisco, CA, USA.
  • Frimpter J; Health Interactions, an Inizio Company, San Francisco, CA, USA.
  • Blanchet Zumofen MH; F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Infect Dis Ther ; 13(9): 2071-2087, 2024 Sep.
Article in En | MEDLINE | ID: mdl-39150658
ABSTRACT

INTRODUCTION:

This study sought to evaluate the cost-effectiveness of baloxavir marboxil compared with oseltamivir or no antiviral treatment from a US payer perspective using data from a real-world US administrative claims study. Given baloxavir's ability to rapidly stop viral shedding, the potential health economic implications of a baloxavir-induced population-level reduction in viral transmission was also explored.

METHODS:

A decision tree cost-effectiveness model was developed for seasonal influenza (2018-2020) using a lifetime time horizon with 3.0% discounting for costs and quality-adjusted life-years (QALYs). Patients aged ≥ 12 years could receive baloxavir, oseltamivir or no antiviral treatment. Patient characteristics, complications, and costs were derived from the Merative™ MarketScan® Research Databases including US commercial claims and Medicare and Medicaid Supplemental databases. A scenario analysis explored the impact of reduced viral transmission with baloxavir.

RESULTS:

In the base case analysis, baloxavir was cost-effective within a willingness-to-pay threshold of US$100,000/QALY compared with oseltamivir [incremental cost-effectiveness ratio (ICER), $6813/QALY gained] or no antiviral treatment (ICER, $669/QALY gained). The net monetary benefit (NMB) of baloxavir was $1180 and $6208 compared with oseltamivir and no treatment, respectively. The NMB of baloxavir increased linearly with reductions in viral transmission, where a 5% transmission reduction yielded an NMB of $2592 versus oseltamivir and $7621 versus no treatment. Baloxavir became dominant (more effective and less costly, with ICERs < 0) starting with a 12.0% reduction in viral transmission versus oseltamivir and 6.0% versus no antiviral treatment.

CONCLUSION:

Baloxavir was cost-effective compared with oseltamivir or no antiviral treatment. The potential of baloxavir to reduce viral transmission offers a substantial economic benefit from a US payer perspective.
Baloxavir is a prescription medicine that reduces the duration of flu symptoms and reduces the likelihood of complications from the flu, including serious complications that may require hospitalization. Baloxavir may reduce the spread of the flu to healthy people by reducing the amount and duration of virus shedding from infected people. We designed a model to estimate the cost benefits of using baloxavir versus another flu treatment, known as oseltamivir, or no flu treatment at all. Using baloxavir led to more cost savings than oseltamivir or no treatment for people in the US who have commercial health insurance. Baloxavir was even more cost-effective in the scenario where it reduced the number of flu cases (transmission benefit). This could ultimately have a meaningful benefit across a large health insurance population.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Infect Dis Ther Year: 2024 Document type: Article Affiliation country: Norway Country of publication: New Zealand

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Infect Dis Ther Year: 2024 Document type: Article Affiliation country: Norway Country of publication: New Zealand