Objective:To assess the cost-effectiveness of pembrolizumab monotherapy compared with standard chemotherapy for the treatment of advanced non-small cell lung cancer (NSCLC) in previously untreated adults who have a high programmed death ligand 1 (PD-L1) tumor proportion score of 50% or greater in Singapore. Materials and methods:A partitioned-survival analysis model was developed from a healthcare system's perspective that extrapolated clinical and economic outcomes of first-line pembrolizumab (maximum treatment duration of 2 years) versus platinum doublet chemotherapy over a 10-year time horizon for patients with advanced NSCLC. The model consisted of three health states: alive with no progression, alive with progression, and dead. Key clinical inputs were based on Kaplan-Meier survival curves from the interim (median follow-up = 11.2 months) and updated analysis (median follow-up = 25.2 months) of the KEYNOTE-024 randomized controlled trial. Local cost data were applied. Utilities were derived from published international estimates. Both one-way and multivariate probabilistic sensitivity analyses (PSA) were conducted to identify key drivers of the results. Results:Using the results from the updated analysis of KEYNOTE-024, patients treated with pembrolizumab experienced more quality adjusted life-years (QALYs), but incurred higher costs compared to chemotherapy over a 10-year time horizon (pembrolizumab: 1.9983 QALYs, SGD215,761; chemotherapy: 1.1317 QALYs, SGD70,444). The base-case incremental cost-effectiveness ratio (ICER) was SGD167,692 per QALY gained. One-way sensitivity analysis showed the ICER was most sensitive to the cost of pembrolizumab, followed by the time horizon. Multivariate PSA indicated that pembrolizumab had 0% probability of being cost-effective at a hypothetical willingness-to-pay threshold of SGD100,000 per QALY gained. Conclusion:While pembrolizumab is superior to standard chemotherapy in improving overall survival and progression-free survival, results suggest that it is unlikely to be cost-effective at its current price in Singapore. Factors including clinical effectiveness, safety, and budget impact should also be considered when making national funding decisions.
机构:
Univ Lisbon, Ctr Estudos Med Baseada Evidencia, Fac Med, Lisbon 11, PortugalUniv Lisbon, Ctr Estudos Med Baseada Evidencia, Fac Med, Lisbon 11, Portugal
Pinheiro, B.
Silva Miguel, L.
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Univ Lisbon, Ctr Estudos Med Baseada Evidencia, Fac Med, Lisbon 11, PortugalUniv Lisbon, Ctr Estudos Med Baseada Evidencia, Fac Med, Lisbon 11, Portugal
Silva Miguel, L.
Alarcao, J.
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Univ Lisbon, Ctr Estudos Med Baseada Evidencia, Fac Med, Lisbon 11, PortugalUniv Lisbon, Ctr Estudos Med Baseada Evidencia, Fac Med, Lisbon 11, Portugal
Alarcao, J.
Paracha, N.
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F Hoffmann La Roche Ltd, Basel, SwitzerlandUniv Lisbon, Ctr Estudos Med Baseada Evidencia, Fac Med, Lisbon 11, Portugal
Paracha, N.
Felizzi, F.
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F Hoffmann La Roche, Basel, SwitzerlandUniv Lisbon, Ctr Estudos Med Baseada Evidencia, Fac Med, Lisbon 11, Portugal
Felizzi, F.
Pereira, C.
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Roche Farmaceut Quim, Lda, Amadora, PortugalUniv Lisbon, Ctr Estudos Med Baseada Evidencia, Fac Med, Lisbon 11, Portugal
Pereira, C.
Borges, M.
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Univ Lisbon, Ctr Estudos Med Baseada Evidencia, Fac Med, Lisbon 11, PortugalUniv Lisbon, Ctr Estudos Med Baseada Evidencia, Fac Med, Lisbon 11, Portugal
机构:
Univ Birmingham, Inst Canc Studies, Canc Res UK, Trials Unit, Birmingham B15 2TT, W Midlands, EnglandUniv Birmingham, Inst Canc Studies, Canc Res UK, Trials Unit, Birmingham B15 2TT, W Midlands, England
Billingham, LJ
Bathers, S
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机构:Univ Birmingham, Inst Canc Studies, Canc Res UK, Trials Unit, Birmingham B15 2TT, W Midlands, England
Bathers, S
Burton, A
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机构:Univ Birmingham, Inst Canc Studies, Canc Res UK, Trials Unit, Birmingham B15 2TT, W Midlands, England
Burton, A
Bryan, S
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机构:Univ Birmingham, Inst Canc Studies, Canc Res UK, Trials Unit, Birmingham B15 2TT, W Midlands, England
Bryan, S
Cullen, MH
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机构:Univ Birmingham, Inst Canc Studies, Canc Res UK, Trials Unit, Birmingham B15 2TT, W Midlands, England