Impact on health outcomes of treating all eligible large B-cell lymphoma patients with axicabtagene ciloleucel in Portugal – A modeling approach

AIM: This study aimed to quantify the health benefits that can be achieved by treating axicabtagene-ciloleucel (axi-cel)-eligible large B-cell lymphoma patients with axi-cel instead of historical standard of care (hSoC) in Portugal. "Estimated Opportunity Lost" quantified the difference in outcomes in 2024 if all axi-cel-eligible patients were treated with axi-cel versus if only a fraction received axi-cel and the remaining patients received hSoC. "Potential Future Gains" quantified the difference in outcomes in 2026-2028 if all axi-cel-eligible patients receive axi-cel versus all patients receiving hSoC. METHODS: A Population Level Health Impact model was developed to obtain the weighted average results for 2L and 3L + models. Both underlying models used a partitioned survival model with extrapolations performed using mixture cure assumption. At model entry, patients were treated with axi-cel or hSoC. Each cohort of "year of entry/line of entry" was followed for 5 years. Outcomes were life years (LY), progression-free survival years (PFSY), quality-adjusted life-years (QALY), and absolute number and proportion of patients alive at 5 years and potentially cured (not progressed) at 5 years. Model inputs were based on publicly available literature, a modified Delphi panel, and real-world data. Utilities and mortality data were Portuguese-specific. RESULTS: Of 284 axi-cel-eligible patients in 2024, 23 (8%) received axi-cel. Over 5 years, the Estimated Opportunity Lost by not treating all eligible patients with axi-cel was 203 LY, 45 deaths, and 36 patients that could have been potentially cured. The Potential Future Gains from treating all eligible patients with axi-cel are an estimated 527 more PFSY, 582 more LY, 119 more patients alive, and 85 more potentially cured. CONCLUSION: The model suggests that limited axi-cel uptake in Portugal resulted in lost health benefits for axi-cel-eligible patients. When considering the next 3 years, substantial health benefits may be gained if all eligible patients receive axi-cel treatment.

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Publication Details

Journal
Journal of Medical Economics
Published
2026-08-14
DOI
https://doi.org/10.1080/13696998.2026.2714649
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00

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article

Impact on health outcomes of treating all eligible large B-cell lymphoma patients with axicabtagene ciloleucel in Portugal – A modeling approach

Filipa Moita, Cláudia Claudino, Filipa Aragão, Ana Carneiro et al.
Journal of Medical Economics
CAR-T cell therapy research
article

Impact on health outcomes of treating all eligible large B-cell lymphoma patients with axicabtagene ciloleucel in Portugal – A modeling approach

Filipa Moita, Cláudia Claudino, Filipa Aragão, Ana Carneiro, Susana Carvalho, Sónia Pereira, Alexandra Santos, Maria João Silva, Eduardo Espada
article en

Abstract

AIM: This study aimed to quantify the health benefits that can be achieved by treating axicabtagene-ciloleucel (axi-cel)-eligible large B-cell lymphoma patients with axi-cel instead of historical standard of care (hSoC) in Portugal. "Estimated Opportunity Lost" quantified the difference in outcomes in 2024 if all axi-cel-eligible patients were treated with axi-cel versus if only a fraction received axi-cel and the remaining patients received hSoC. "Potential Future Gains" quantified the difference in outcomes in 2026-2028 if all axi-cel-eligible patients receive axi-cel versus all patients receiving hSoC. METHODS: A Population Level Health Impact model was developed to obtain the weighted average results for 2L and 3L + models. Both underlying models used a partitioned survival model with extrapolations performed using mixture cure assumption. At model entry, patients were treated with axi-cel or hSoC. Each cohort of "year of entry/line of entry" was followed for 5 years. Outcomes were life years (LY), progression-free survival years (PFSY), quality-adjusted life-years (QALY), and absolute number and proportion of patients alive at 5 years and potentially cured (not progressed) at 5 years. Model inputs were based on publicly available literature, a modified Delphi panel, and real-world data. Utilities and mortality data were Portuguese-specific. RESULTS: Of 284 axi-cel-eligible patients in 2024, 23 (8%) received axi-cel. Over 5 years, the Estimated Opportunity Lost by not treating all eligible patients with axi-cel was 203 LY, 45 deaths, and 36 patients that could have been potentially cured. The Potential Future Gains from treating all eligible patients with axi-cel are an estimated 527 more PFSY, 582 more LY, 119 more patients alive, and 85 more potentially cured. CONCLUSION: The model suggests that limited axi-cel uptake in Portugal resulted in lost health benefits for axi-cel-eligible patients. When considering the next 3 years, substantial health benefits may be gained if all eligible patients receive axi-cel treatment.

Journal of Medical EconomicsVol. 29(1)
ActionAid (US), University of St Andrews (GB), Research for Action (US), Administração Regional de Saúde de Lisboa e Vale do Tejo (PT), IPO Porto (PT), Gilead Sciences (Spain) (ES), Centro Hospitalar de Lisboa Ocidental (PT), Gilead Sciences (United States) (US), Gilead Sciences (Australia) (AU), Universidade Nova de Lisboa (PT)
Gilead Sciences
Good health and well-being
Openalex Percentile: Top 12%
CAR-T cell therapy research
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