# The Health Impacts of Better Access to Axicabtagene Ciloleucel: The Case of Spain

**Authors:** Raúl Córdoba, Lucía López-Corral, María Presa, Victoria Martín-Escudero, Sachin Vadgama, Miguel Ángel Casado, Carlos Pardo

PMC · DOI: 10.3390/cancers16152712 · Cancers · 2024-07-30

## TL;DR

This study shows that better access to axicabtagene ciloleucel in Spain could significantly improve survival and quality of life for lymphoma patients.

## Contribution

The study quantifies the health benefits of expanding access to axi-cel in Spain using real-world data and survival models.

## Key findings

- Treating all eligible patients with axi-cel could gain 2173 life years and 1706 quality-adjusted life years.
- Expanding access could result in 85 more patients alive and 78 without disease progression at 5 years.
- Current treatment rates in Spain are below eligibility estimates, leading to significant health losses.

## Abstract

Axicabtagene ciloleucel (axi-cel) has been shown to improve the health outcomes of patients with relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL); however, the actual number of patients treated in Spain is lower than the epidemiology estimations. The aim of our study was to assess the value of axi-cel versus chemotherapy in patients with R/R DLBCL after ≥2 lines of therapy based on the number of patients treated. Considering that the entire cohort was eligible for treatment with axi-cel (n = 490) compared to the currently treated population (n = 187), the use of axi-cel rather than chemotherapy in all eligible patients could lead to 2173 life years gained and 1706 quality-adjusted life years. Furthermore, if all eligible patients were treated with CAR T-cell therapy, an additional 85 patients would be alive, and 78 patients would be alive without disease progression at 5 years.

In this study, the health impacts of improving access to treatment with axicabtagene ciloleucel (axi-cel) was assessed in patients with relapsed/refractory diffuse large B-cell lymphoma after ≥2 lines of therapy in Spain. A partitioned survival mixture cure model was used to estimate the lifetime accumulated life years gained (LYG) and quality-adjusted life years (QALYs) per patient treated with axi-cel versus chemotherapy. Efficacy data were extracted from the ZUMA-1 trial for axi-cel and from the SCHOLAR-1 study for chemotherapy. In the base case, the incremental outcomes of axi-cel versus chemotherapy were evaluated in a cohort of 187 patients treated with CAR T-cell therapies, as reported by the “Spanish National Health System Plan for Advanced Therapies”, and in the alternative scenario in the full eligible population based on epidemiological estimates (n = 490). Taking those currently treated with axi-cel, compared with chemotherapy, axi-cel provided an additional 1341 LYGs and 1053 QALYs. However, when all eligible patients (n = 490) were treated, axi-cel provided an additional 3515 LYs and 2759 QALYs. Therefore, if all eligible patients were treated with axi-cel rather than those currently treated as per the registry (n = 187), there would have been an additional 303 patients treated, resulting in an additional 2173 LYGs and 1706 QALYs in total. The lack of access in Spain has led to a loss of a substantial number of LYGs and QALYs, and efforts should be made to improve access for all eligible patients.

## Linked entities

- **Diseases:** diffuse large B-cell lymphoma (MONDO:0018905)

## Full-text entities

- **Genes:** CXADRP1 (CXADR pseudogene 1) [NCBI Gene 653108] {aka CAR, CXADRP}
- **Diseases:** diffuse large B-cell lymphoma (MESH:D016403)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** SCHOLAR-1 — Mus musculus (Mouse), Hybridoma (CVCL_C7RB)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11311991/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC11311991/full.md

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Source: https://tomesphere.com/paper/PMC11311991