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DOI 10.33393/grhta.2025.3306

Медицинская библиотека · Global & regional health technology assessment · 2025

[Not Available].

Marcellusi Andrea, Bini Chiara, Fioravanti Laura, Ripoli Silvia, Morelli Paolo

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Аннотация

OBJECTIVE

: Systemic anaplastic large cell lymphoma (sALCL) is a rare and severe non-Hodgkin lymphoma. Despite its clinical relevance, the aetiology of this disease is unknown, not allowing the patient to prevent and counteract it. This study investigates the cost-effectiveness of Brentuximab Vedotin (BV) in combination with cyclophosphamide, doxorubicin and prednisone (CHP) for the front-line treatment of patients with sALCL in Italy.

METHODS

: The analysis was conducted from the perspective of the National Health Service using a three-state partitioned survival model with cycles lasting 21 days and a lifetime time horizon. The survival curves were taken from three-year follow-up data of ECHELON-2 trial. Costs were obtained from published literature and national tariffs. For all drugs, ex-factory prices net of the mandatory reductions required by law were considered.

RESULTS

: Compared with CHOP, BV in combination with CHP was associated with an increase of € 46,349 total costs, 2.3 life years and 1.8 quality-adjusted life-years (QALYs) respectively. The incremental cost-utility ratios (ICUR) were estimated equal to € 25,367/QALY compared with CHOP, resulting below the value of € 41,411/QALY for severe diseases in Italy.

CONCLUSIONS

: Based on data from 3 years of follow-up from the ECHELON-2 trial, BV in combination with CHP is estimated a cost-effective option versus CHOP for the front-line treatment of sALCL in Italy. Data from 5-year from the ECHELON-2 trial confirmed the advantage in terms of PFS and OS. The analysis also suggested that treatment with BV+CHP may be cost-effective compared with CHOEP.

Для цитирования: Marcellusi Andrea, Bini Chiara, Fioravanti Laura, Ripoli Silvia, Morelli Paolo. [Not Available].. Global & regional health technology assessment. 2025. DOI: 10.33393/grhta.2025.3306.
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