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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.
Pasello, Giulia; Lorenzi, Martina; Scattolin, Daniela; Del Conte, Alessandro; Cecere, Fabiana; Pavan, Alberto; Macerelli, Marianna; Polo, Valentina; Pilotto, Sara; Santarpia, Mariacarmela; Cumerlato, Enrico; Da Ros, Valentina; Targato, Giada; Bortolami, Alberto; Bonanno, Laura; Ferro, Alessandra; Dal Maso, Alessandro; Frega, Stefano; Guarneri, Valentina.
Afiliação
  • Pasello G; Department of Surgery, Oncology, and Gastroenterology, University of Padova, Padova, Italy.
  • Lorenzi M; Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.
  • Scattolin D; Department of Surgery, Oncology, and Gastroenterology, University of Padova, Padova, Italy.
  • Del Conte A; Department of Surgery, Oncology, and Gastroenterology, University of Padova, Padova, Italy.
  • Cecere F; Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.
  • Pavan A; Medical Oncology and Immunorelated Tumors, National Cancer Institute Centro di Riferimento Oncologico (CRO) - IRCCS, Aviano (PN), Italy.
  • Macerelli M; Oncology 1, Regina Elena National Cancer Institute - IRCCS, Roma, Italy.
  • Polo V; Medical Oncology Department, Azienda Unità Locale Socio Sanitaria (AULSS 3) Serenissima, Mestre-Venezia, Italy.
  • Pilotto S; Department of Oncology, Azienda Sanitaria Universitaria Friuli Centrale (ASUFC), Udine, Italy.
  • Santarpia M; Oncology Unit, AULSS 2 Marca Trevigiana, Ca' Foncello Hospital, Treviso, Italy.
  • Cumerlato E; 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.
  • Da Ros V; Medical Oncology Unit, Department of Human Pathology "G. Barresi," Messina, Italy.
  • Targato G; Medical Oncology, AULSS 6 Euganea, South Padua Hospital, Monselice (PD), Italy.
  • Bortolami A; Medical Oncology and Immunorelated Tumors, National Cancer Institute Centro di Riferimento Oncologico (CRO) - IRCCS, Aviano (PN), Italy.
  • Bonanno L; Department of Oncology, Azienda Sanitaria Universitaria Friuli Centrale (ASUFC), Udine, Italy.
  • Ferro A; Veneto Oncology Network, Istituto Oncologico Veneto, I.R.C.C.S., Padua, Italy.
  • Dal Maso A; Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.
  • Frega S; Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.
  • Guarneri V; Division of Medical Oncology 2, Veneto Institute of Oncology - IRCCS, Padova, Italy.
Oncologist ; 29(7): 596-608, 2024 Jul 05.
Article em En | MEDLINE | ID: mdl-38520745
ABSTRACT

INTRODUCTION:

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.

METHODS:

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.

RESULTS:

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.

CONCLUSIONS:

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Acrilamidas / Carcinoma Pulmonar de Células não Pequenas / Receptores ErbB / Compostos de Anilina / Neoplasias Pulmonares Limite: Aged80 Idioma: En Revista: Oncologist Assunto da revista: NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Acrilamidas / Carcinoma Pulmonar de Células não Pequenas / Receptores ErbB / Compostos de Anilina / Neoplasias Pulmonares Limite: Aged80 Idioma: En Revista: Oncologist Assunto da revista: NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália