Development of a Decision Model to Estimate the Outcomes of Treatment Sequences in Advanced Melanoma

BackgroundA decision model for patients with advanced melanoma to estimate outcomes of a wide range of treatment sequences is lacking.ObjectivesTo develop a decision model for advanced melanoma to estimate outcomes of treatment sequences in clinical practice with the aim of supporting decision making. The article focuses on methodology and long-term health benefits.MethodsA semi-Markov model with a lifetime horizon was developed. Transitions describing disease progression, time to next treatment, and mortality were estimated from real-world data (RWD) as a function of time since starting treatment or disease progression and patient characteristics. Transitions were estimated separately for melanoma with and without a BRAF mutation and for patients with favorable and intermediate prognostic factors. All transitions can be adjusted using relative effectiveness of treatments derived from a network meta-analysis of randomized controlled trials (RCTs). The duration of treatment effect can be adjusted to obtain outcomes under different assumptions.ResultsThe model distinguishes 3 lines of systemic treatment for melanoma with a BRAF mutation and 2 lines of systemic treatment for melanoma without a BRAF mutation. Life expectancy ranged from 7.8 to 12.0 years in patients with favorable prognostic factors and from 5.1 to 8.7 years in patients with intermediate prognostic factors when treated with sequences consisting of targeted therapies and immunotherapies. Scenario analyses illustrate how estimates of life expectancy depend on the duration of treatment effect.ConclusionThe model is flexible because it can accommodate different treatments and treatment sequences, and the duration of treatment effects and the transitions influenced by treatment can be adjusted. We show how using RWD and data from RCTs can harness advantages of both data sources, guiding the development of future decision models.HighlightsThe model is flexible because it can accommodate different treatments and treatment sequences, and the duration of treatment effects as well as the transitions that are influenced by treatment can be adjusted.The long-term health benefits of treatment sequences depend on the place of different therapies within a treatment sequence.Assumptions about the duration of relative treatment effects influence the estimates of long-term health benefits.We show how the use of real-world data and data from randomized controlled trials harness the advantages of both data sources, guiding the development of future decision models.

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Journal
Medical Decision Making
Published
2025-02-22
DOI
https://doi.org/10.1177/0272989x251319338
Citations
1
Primary Topic
Health Systems, Economic Evaluations, Quality of Life
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article
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article

Development of a Decision Model to Estimate the Outcomes of Treatment Sequences in Advanced Melanoma

Astrid A.M. van der Veldt, Geke A.P. Hospers, Hedwig M. Blommestein, John B.A.G. Haanen et al.
1 citations
Medical Decision Making
Health Systems, Economic Evaluations, Quality of Life
article

Development of a Decision Model to Estimate the Outcomes of Treatment Sequences in Advanced Melanoma

Astrid A.M. van der Veldt, Geke A.P. Hospers, Hedwig M. Blommestein, John B.A.G. Haanen, Willeke A.M. Blokx, Jan Willem B. de Groot, Pieter van Baal, Ellen Kapiteijn, Carin A. Uyl‐de Groot, Michel W.J.M. Wouters, F. Van den Berkmortel, B Leeneman, Alfons J.M. van den Eertwegh, Maureen J.B. Aarts, Saskia de Groot, Olivier J. van Not, Karijn P.M. Suijkerbuijk, Marye J. Boers‐Sonderen
article en
1 citations

Abstract

BackgroundA decision model for patients with advanced melanoma to estimate outcomes of a wide range of treatment sequences is lacking.ObjectivesTo develop a decision model for advanced melanoma to estimate outcomes of treatment sequences in clinical practice with the aim of supporting decision making. The article focuses on methodology and long-term health benefits.MethodsA semi-Markov model with a lifetime horizon was developed. Transitions describing disease progression, time to next treatment, and mortality were estimated from real-world data (RWD) as a function of time since starting treatment or disease progression and patient characteristics. Transitions were estimated separately for melanoma with and without a BRAF mutation and for patients with favorable and intermediate prognostic factors. All transitions can be adjusted using relative effectiveness of treatments derived from a network meta-analysis of randomized controlled trials (RCTs). The duration of treatment effect can be adjusted to obtain outcomes under different assumptions.ResultsThe model distinguishes 3 lines of systemic treatment for melanoma with a BRAF mutation and 2 lines of systemic treatment for melanoma without a BRAF mutation. Life expectancy ranged from 7.8 to 12.0 years in patients with favorable prognostic factors and from 5.1 to 8.7 years in patients with intermediate prognostic factors when treated with sequences consisting of targeted therapies and immunotherapies. Scenario analyses illustrate how estimates of life expectancy depend on the duration of treatment effect.ConclusionThe model is flexible because it can accommodate different treatments and treatment sequences, and the duration of treatment effects and the transitions influenced by treatment can be adjusted. We show how using RWD and data from RCTs can harness advantages of both data sources, guiding the development of future decision models.HighlightsThe model is flexible because it can accommodate different treatments and treatment sequences, and the duration of treatment effects as well as the transitions that are influenced by treatment can be adjusted.The long-term health benefits of treatment sequences depend on the place of different therapies within a treatment sequence.Assumptions about the duration of relative treatment effects influence the estimates of long-term health benefits.We show how the use of real-world data and data from randomized controlled trials harness the advantages of both data sources, guiding the development of future decision models.

Medical Decision MakingVol. 45(3)
University Medical Center Groningen (NL), Radboud University Nijmegen (NL), University of Groningen (NL), Leiden University Medical Center (NL), Erasmus MC (NL), Radboud University Medical Center (NL), The Netherlands Cancer Institute (NL), University Medical Center Utrecht (NL), Maastricht University (NL), Dutch Institute for Clinical Auditing (NL), Zuyderland Medisch Centrum (NL), Isala (NL), Cancer Center Amsterdam (NL), Amsterdam UMC Location Vrije Universiteit Amsterdam (NL), Erasmus University Rotterdam (NL)
Amgen, Bristol-Myers Squibb, Pfizer, AstraZeneca, Sanofi, Gilead Sciences, Celgene, Les Laboratories Pierre Fabre, Roche Nederland, ZonMw, Erasmus Medisch Centrum, Astellas Pharma, Medical Delta, National Institutes of Health, Erasmus Universitair Medisch Centrum Rotterdam, Cilag
Good health and well-being
Openalex Percentile: Top 95%
Health Systems, Economic Evaluations, Quality of Life
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