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Title: | Cost effectiveness analysis of afatinib versus pemetrexed-cisplatin for first-line treatment of locally advanced or metastatic EGFR mutation positive non-small-cell lung cancer from the Singapore healthcare payer's perspective | Authors: | Tan, P.-T Aziz, M.I.A Pearce, F Lim, W.-T Wu, D.B.-C Ng, K |
Keywords: | afatinib cisplatin epidermal growth factor receptor pemetrexed afatinib antineoplastic agent cisplatin epidermal growth factor receptor pemetrexed advanced cancer Article cancer chemotherapy cancer growth comparative effectiveness controlled study cost effectiveness analysis death drug cost drug effect drug efficacy drug response drug safety EGFR gene gene mutation human major clinical study medical decision making multiple cycle treatment non small cell lung cancer overall survival phase 3 clinical trial progression free survival quality of life randomized controlled trial sensitivity analysis Singapore survival rate treatment outcome cancer staging clinical trial cost benefit analysis genetics health care cost lung tumor metastasis mortality mutation non small cell lung cancer pathology prognosis Afatinib Antineoplastic Combined Chemotherapy Protocols Carcinoma, Non-Small-Cell Lung Cisplatin Cost-Benefit Analysis ErbB Receptors Health Care Costs Humans Lung Neoplasms Mutation Neoplasm Metastasis Neoplasm Staging Pemetrexed Prognosis Singapore Treatment Outcome |
Issue Date: | 2018 | Citation: | Tan, P.-T, Aziz, M.I.A, Pearce, F, Lim, W.-T, Wu, D.B.-C, Ng, K (2018). Cost effectiveness analysis of afatinib versus pemetrexed-cisplatin for first-line treatment of locally advanced or metastatic EGFR mutation positive non-small-cell lung cancer from the Singapore healthcare payer's perspective. BMC Cancer 18 (1) : 352. ScholarBank@NUS Repository. https://doi.org/10.1186/s12885-018-4223-y | Rights: | Attribution 4.0 International | Abstract: | Background: Non-small-cell lung cancer (NSCLC) accounts for 85% of all lung cancers and is associated with a poor prognosis. Afatinib is an irreversible ErbB family blocker recommended in clinical guidelines as a first-line treatment for NSCLC which harbours an epidermal growth factor receptor (EGFR) mutation. The objective of this study was to evaluate the cost-effectiveness of afatinib versus pemetrexed-cisplatin for first-line treatment of locally advanced or metastatic EGFR mutation positive NSCLC in Singapore. Methods: A partitioned survival model with three health states (progression-free, progressive disease and death) was developed from a healthcare payer perspective. Survival curves from the LUX-Lung 3 trial (afatinib versus pemetrexed-cisplatin chemotherapy) were extrapolated beyond the trial period to estimate the underlying progression-free survival and overall survival parametric distributions. Rates of adverse reactions were also estimated from LUX-Lung 3 while health utilities from overseas were derived from the literature in the absence of local estimates. Direct costs were sourced from public healthcare institutions in Singapore. Incremental cost-effectiveness ratios (ICERs) were calculated over a 5 year time horizon. Deterministic and probabilistic sensitivity analyses and additional scenario analyses were conducted to explore the impact of uncertainties and assumptions on the cost-effectiveness results. Results: In the base-case analysis, the ICER for afatinib versus pemetrexed-cisplatin was SG$137,648 per quality-adjusted life year (QALY) gained and SG$109,172 per life-year gained. One-way sensitivity analysis showed the ICER was most sensitive to variations in the utility values, the cost of afatinib and time horizon. Scenario analyses showed that even reducing the cost of afatinib by 50% led to a high ICER which was unlikely to represent a cost-effective use of healthcare resources. Conclusions: Compared with pemetrexed-cisplatin, afatinib is not cost-effective as a first-line treatment for advanced EGFR mutation-positive NSCLC in Singapore. The findings from our study will be useful to inform local healthcare decision-making and resource allocations for NSCLC treatments, together with other considerations such as clinical effectiveness, safety and affordability of TKIs. © 2018 The Author(s). | Source Title: | BMC Cancer | URI: | https://scholarbank.nus.edu.sg/handle/10635/181206 | ISSN: | 14712407 | DOI: | 10.1186/s12885-018-4223-y | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
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