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Biosimilar pegfilgrastim may offer affordable treatment options for patients in France: a budget impact analysis on the basis of clinical trial and real-world data
被引:6
|作者:
Yang, Jingyan
[1
,2
]
Liu, Rongzhe
[3
]
Granghaud, Anna
[4
]
Zaidi, Omer
[5
]
Stephens, Jennifer
[3
]
机构:
[1] Pfizer Inc, Patient Hlth & Impact PHI, 235 East 42nd St, New York, NY 10017 USA
[2] Columbia Univ, Inst Social & Econ Res & Policy, New York, NY USA
[3] Pharmerit, Bethesda, MD USA
[4] Pfizer SAS, Paris, France
[5] Pharmerit, Boston, MA USA
关键词:
Budget impact model;
G-CSF;
pegfilgrastim;
filgrastim;
biosimilar;
cancer;
COLONY-STIMULATING FACTORS;
INDUCED FEBRILE NEUTROPENIA;
CANCER-PATIENTS;
PROSPECTIVE MULTICENTER;
CHEMOTHERAPY;
PROPHYLAXIS;
FILGRASTIM;
HOSPITALIZATION;
PREVENTION;
PATTERNS;
D O I:
10.1080/13696998.2021.1922252
中图分类号:
F [经济];
学科分类号:
02 ;
摘要:
Background NYVEPRIA, a pegfilgrastim (a long-acting granulocyte colony-stimulating factor [G-CSF]) biosimilar, was recently recommended for marketing authorization in Europe for decreasing the incidence of febrile neutropenia (FN) in patients with non-myeloid malignancies receiving myelosuppressive anti-cancer drugs. The present study aimed to evaluate the financial impact of introducing a new pegfilgrastim biosimilar from a French healthcare system perspective. Methods An Excel-based budget impact model was developed to estimate the financial impact by introducing a new pegfilgrastim biosimilar (NYVEPRIA) to France over a 5-year time horizon. Comparators included existing long-acting and short-acting G-CSFs. The burden of FN was obtained from existing literature. Costs (2021 Euros) included drug acquisition and administration, estimated based on drug dosage in both clinical trial and real-world settings. Scenario analyses were conducted to examine the robustness of key model assumptions. Results In a total French population of 67.19 million, 79,873 patients were estimated to be treated with G-CSFs annually. The annual number of patients to be treated with NYVEPRIA was estimated to be 1593, 3195, 3674, 3782, and 4052 in years 1 to 5, respectively. Using real-world data, NYVEPRIA resulted in total annual cost savings of euro8,620, euro868,498, euro868,498, euro814,102, and euro958,952 over years 1 to 5, respectively, leading to a cumulative 5-year cost savings of euro3,518,669. Using data from clinical trials, NYVEPRIA resulted in total annual cost savings of euro14,366, euro1,447,496, euro1,447,496, euro1,356,836, and euro1,598,253 over years 1 to 5, respectively, leading to a cumulative 5-year cost savings of euro5,864,448. Conclusions The introduction of a new pegfilgrastim biosimilar (NYVEPRIA) is potentially associated with substantial cost savings for the French healthcare system.
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页码:665 / 674
页数:10
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