Osimertinib in Patients With Treatment-Naive EGFR-Mutant Non-small Cell Lung Cancer: Overall Survival, Post-progression Management and Budget Impact Analysis in Real-World.

cost effectiveness epidermal growth factor receptor non-small-cell lung cancer osimertinib real-world study

Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
23 Mar 2024
Historique:
received: 17 10 2023
accepted: 05 02 2024
medline: 23 3 2024
pubmed: 23 3 2024
entrez: 23 3 2024
Statut: aheadofprint

Résumé

The observational multicenter prospective FLOWER study (NCT04965701) confirmed effectiveness and safety of osimertinib in the real-world (RW) management of untreated EGFR-mutant advanced non-small cell lung cancer (aNSCLC) patients. Herein, we report updated survival data, post-progression management, cost/effectiveness and budget impact (BI) of osimertinib compared with a RW population receiving gefitinib or erlotinib. Overall, 189 Caucasian patients receiving first-line osimertinib were included. After a follow-up of 20.7 months, 74(39.2%) patients discontinued osimertinib, median time-to-treatment discontinuation (mTTD) was 27.9 months, overall survival 36.8 months. At progression, tissue biopsy was performed in 29 (56.9%), liquid biopsy in 15 (29.4%) and both in 7 (13.7%) cases. The most frequent resistant mechanism was MET amplification (N = 14, 29.8%). At data cutoff, 13 (6.9%) patients were continuing osimertinib beyond progression; 52 (67.5%) received second-line treatment; no further treatments were administered in 25 (32.5%) cases. Thirty-three (63.4%) patients received chemotherapy, 12(23.1%) TKIs combination. Cost-effectiveness analysis showed a total cost per patient based on RW mTTD of 98,957.34€, 21,726.28€ and 19,637.83€ for osimertinib, erlotinib and gefitinib, respectively. The incremental cost-effectiveness ratio (ICER)/month for osimertinib was 359,806.0€/life-year-gained (LYG) and 197,789.77€/LYG compared to erlotinib and gefitinib. For osimertinib, the BI-gap between RW-TTD and theoretical-TTD was 16,501.0€ per patient. This updated analysis confirms the effectiveness of osimertinib in RW. Although the ICER of osimertinib seems not cost-effective, additional costs for the management of disease progression to old generation TKIs were not considered in this study. The BI-gap suggests RW mTTD as a more reliable measure for expense estimation.

Identifiants

pubmed: 38520745
pii: 7634234
doi: 10.1093/oncolo/oyae043
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Ricerca Corrente Istituto Oncologico Veneto

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press.

Auteurs

Giulia Pasello (G)

Department of Surgery, Oncology, and Gastroenterology, University of Padova, Padova, Italy.
Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.

Martina Lorenzi (M)

Department of Surgery, Oncology, and Gastroenterology, University of Padova, Padova, Italy.

Daniela Scattolin (D)

Department of Surgery, Oncology, and Gastroenterology, University of Padova, Padova, Italy.
Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.

Alessandro Del Conte (A)

Medical Oncology and Immunorelated Tumors, National Cancer Institute Centro di Riferimento Oncologico (CRO) - IRCCS, Aviano (PN), Italy.

Fabiana Cecere (F)

Oncology 1, Regina Elena National Cancer Institute - IRCCS, Roma, Italy.

Alberto Pavan (A)

Medical Oncology Department, Azienda Unità Locale Socio Sanitaria (AULSS 3) Serenissima, Mestre-Venezia, Italy.

Marianna Macerelli (M)

Department of Oncology, Azienda Sanitaria Universitaria Friuli Centrale (ASUFC), Udine, Italy.

Valentina Polo (V)

Oncology Unit, AULSS 2 Marca Trevigiana, Ca' Foncello Hospital, Treviso, Italy.

Sara Pilotto (S)

Section of Innovation Biomedicine - Oncology Area, Department of Engineering for Innovation Medicine (DIMI), University of Verona and University and Hospital Trust (AOUI) of Verona, Verone, Italy.

Mariacarmela Santarpia (M)

Medical Oncology Unit, Department of Human Pathology "G. Barresi", Messina, Italy.

Enrico Cumerlato (E)

Medical Oncology, AULSS 6 Euganea, South Padua Hospital, Monselice (PD), Italy.

Valentina Da Ros (V)

Medical Oncology and Immunorelated Tumors, National Cancer Institute Centro di Riferimento Oncologico (CRO) - IRCCS, Aviano (PN), Italy.

Giada Targato (G)

Department of Oncology, Azienda Sanitaria Universitaria Friuli Centrale (ASUFC), Udine, Italy.

Alberto Bortolami (A)

Veneto Oncology Network, Istituto Oncologico Veneto, I.R.C.C.S., Padua, Italy.

Laura Bonanno (L)

Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.

Alessandra Ferro (A)

Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.

Alessandro Dal Maso (A)

Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.

Stefano Frega (S)

Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.

Valentina Guarneri (V)

Department of Surgery, Oncology, and Gastroenterology, University of Padova, Padova, Italy.
Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.

Classifications MeSH