Cost-minimization analysis of a phase III trial comparing concurrent versus sequential radiochemotherapy for locally advanced non-small-cell lung cancer (GFPC-GLOT 95–01)

Background: We conducted an economic analysis of a phase III clinical trial comparing sequential radiochemotherapy (RT-CT) with concurrent RT-CT in patients with locally advanced non-small-cell lung cancer. Patients and methods: The trial was a randomized multicenter study comparing three cycles of...

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Published inAnnals of oncology Vol. 17; no. 8; pp. 1269 - 1274
Main Authors Vergnenegre, A., Combescure, C., Fournel, P., Bayle, S., Gimenez, C., Souquet, P. J., Lena, H., Perol, M., Delhoume, J. Y.
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 01.08.2006
Oxford Publishing Limited (England)
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Summary:Background: We conducted an economic analysis of a phase III clinical trial comparing sequential radiochemotherapy (RT-CT) with concurrent RT-CT in patients with locally advanced non-small-cell lung cancer. Patients and methods: The trial was a randomized multicenter study comparing three cycles of chemotherapy (arm A) followed by radiotherapy against an RT-CT combination (two cycles of platinum etoposide) followed by two cycles of platinum-vinorelbine (arm B). The economic analysis adopted the payer's perspective and only included direct costs. Costs (€, 1996–2003) were recorded until the cut-off date. A cost minimization analysis and a sensitivity analysis were carried out. Results: Data from 173 patients were used in the economic study. Protocol costs tended to be higher in arm B, while relapse costs were significantly higher in arm A. The total number of hospital days was higher in arm B. The average total cost per patient was €16 074 in arm A and €15 245 in arm B (P = 0.15). The cost minimization analysis favored arm B. This advantage persisted in the sensitivity analysis. Conclusions: Concurrent RT-CT was not the more costly strategy in this phase III trial, despite lengthier hospitalization for toxicity. Other studies of similar design are needed to confirm these results in future randomized trials.
Bibliography:local:mdl100
istex:40C1F8DACD58B4695CA4497A685C5A604373495D
Correspondence to: Prof. A. Vergnenegre, Service de Pathologie Respiratoire, Hôpital Universitaire du Cluzeau, 87042 Limoges cedex, France. Tel: +33-5-55-05-66-29; Fax: +33-5-55-05-68-15; E-mail: avergne@unilim.fr
ark:/67375/HXZ-PGH4G6T9-7
ISSN:0923-7534
1569-8041
DOI:10.1093/annonc/mdl100