scholarly journals Chasing the survival curve tail: The effect on cost-effectiveness of nivolumab for second-line treatment of advanced renal cell carcinoma

2017 ◽  
Vol 28 ◽  
pp. v401
Author(s):  
M. Sarfaty ◽  
A. Moore ◽  
V. Neiman ◽  
E. Rosenbaum ◽  
D. Goldstein
2010 ◽  
Vol 13 (1) ◽  
pp. 55-60 ◽  
Author(s):  
Martin Hoyle ◽  
Colin Green ◽  
Jo Thompson-Coon ◽  
Zulian Liu ◽  
Karen Welch ◽  
...  

2017 ◽  
Vol 35 (15_suppl) ◽  
pp. e18338-e18338
Author(s):  
Michal Sarfaty ◽  
Moshe Leshno ◽  
Noa Gordon ◽  
Assaf Moore ◽  
Victoria Neiman ◽  
...  

e18338 Background: In recent years, new drugs have been introduced to the second line setting of advanced renal cell carcinoma (RCC). Nivolumab increases overall survival and is associated with less toxicity compared to everolimus in this setting based on the Checkmate 025 study. However, due to nivolumab's high cost there is a need to define its value by considering both efficacy and cost. The objective of this study was to estimate the cost-effectiveness of nivolumab for the second-line treatment of advanced RCC from the US payer perspective. Methods: A Markov model was developed to compare the costs and effectiveness of nivolumab with those of everolimus or placebo in the second-line treatment of advanced RCC. Health outcomes were measured in life-years and quality-adjusted life-years (QALYs). Drug costs were based on Medicare reimbursement rates in 2016. Model robustness was addressed in univariable and probabilistic sensitivity analyses. We addressed the controversial issue of the extensive duration of immunotherapy treatment amongst long term survivors, which may or may not be approved by payers. Results: The total mean cost per-patient of nivolumab versus everolimus was $101,070 and $50,935, respectfully. Nivolumab generated a gain of 0.24 LYs (0.34 QALYs) over everolimus and 0.89 LYs (0.96 QALYs) over placebo. The incremental cost-effectiveness ratio (ICER) for nivolumab was $146,532/QALY versus everolimus and $105,232/QALY versus placebo. Limiting the maximal treatment duration of nivolumab to two years lowered the ICER to $121,788/QALY versus everolimus and $96,418/QALY versus placebo. Conclusions: Our analysis established an ICER of $146,532/QALY for nivolumab versus everolimus in second-line advanced RCC treatment.


2015 ◽  
Vol 7 (5) ◽  
pp. 286-294 ◽  
Author(s):  
Daniele Alesini ◽  
Claudia Mosillo ◽  
Giuseppe Naso ◽  
Enrico Cortesi ◽  
Roberto Iacovelli

2020 ◽  
Vol 36 (9) ◽  
pp. 1507-1517
Author(s):  
Arielle G. Bensimon ◽  
Yichen Zhong ◽  
Umang Swami ◽  
Allison Briggs ◽  
Joshua Young ◽  
...  

2014 ◽  
Vol 100 (6) ◽  
pp. e282-e285
Author(s):  
Roberto Iacovelli ◽  
Elena Verzoni ◽  
Paolo Grassi ◽  
Alessio Farcomeni ◽  
Filippo de Braud ◽  
...  

2018 ◽  
Vol 4 (Supplement 2) ◽  
pp. 71s-71s
Author(s):  
K.A.R. Ku Nurhasni ◽  
J. Sabirin ◽  
S.E. Wan Puteh ◽  
M. Dahlui

Background: Axitinib has been suggested to be effective as a second line treatment of metastatic renal cell carcinoma. However, its adoption may be limited by its financial consequences. Therefore, a cost-utility analysis was conducted to estimate the economic value of axitinib as a second line treatment of metastatic renal cell carcinoma. Aim: This analysis will informed the decision makers on the potential use of axitinib in this population within the Ministry of Health facilities. Methods: A state transition model was developed using Microsoft Excel 2010 to simulate a hypothetical cohort of patient receiving axitinib or best supportive care over 5 years of time horizon. A monthly cycle was chosen without a half cycle correction. Three health states were included in the model as progression free, disease progression and dead. A 3% discount rate was applied as recommended in the Pharmacoeconomic Guidelines for Malaysia. Total costs were estimated using unit costs from local sources and published data. The clinical and utility parameters were derived from the published literatures. Results: The mean probabilistic incremental discounted cost and QALY for axitinib were RM 113,576.29 and 0.35413 respectively, yielded a probabilistic incremental cost-effectiveness ratio (ICER) of RM 320,719. Unavailability of the local price for axinitib may play a part in the higher estimation of ICER. Conclusion: Axitinib may not be considered as a cost-effective second line treatment of metastatic renal cell carcinoma as the ICER is beyond the value of 3 GDP per capita.


2010 ◽  
Vol 13 (1) ◽  
pp. 61-68 ◽  
Author(s):  
Martin Hoyle ◽  
Colin Green ◽  
Jo Thompson-Coon ◽  
Zulian Liu ◽  
Karen Welch ◽  
...  

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