A systematic review of the effectiveness of adalimumab
A systematic review of the effectiveness of adalimumab
A systematic review of the effectiveness of adalimumab
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80<br />
Health economics<br />
TABLE 24 Summary <strong>of</strong> methods used in industry economic analyses<br />
Submission Abbott Laboratories Wyeth Schering-Plough<br />
features Adalimumab (Humira ® ) Etanercept (Enbrel ® ) Infliximab (Remicade ® )<br />
Choice <strong>of</strong> TNF Adalimumab in combination with Six-line drug sequence with Infliximab in combination with<br />
inhibitor MTX etanercept/MTX combination MTX<br />
1st line, 2nd line or 3rd line<br />
Comparator Three-line drug sequence Six-line drug sequence without MTX alone<br />
without use <strong>of</strong> <strong>adalimumab</strong> use <strong>of</strong> etanercept<br />
Patient Patients with RA, average age Patients with RA, average age Two patient groups: (1) active<br />
characteristics 55 years, 77% women, who 53 years, (in line with patients RA despite treatment with<br />
have failed three DMARDs in TEMPO) DMARDs; (2) severe active<br />
including MTX early RA<br />
Form <strong>of</strong> analysis Cost–utility analysis Cost–utility analysis Cost–utility analysis<br />
Model used Patient-based transition-state Markov model with 6-monthly Markov model with 6-monthly<br />
model with 10,000 patients cycles and 10,000 patients cycles, based on ARAMIS<br />
Time-horizon <strong>of</strong> Lifetime Lifetime Lifetime<br />
model<br />
Base-case results £17,860 per QALY 1st line: £16,000 per QALY MTX experienced:<br />
2nd line: £20,000 per QALY £6228 per QALY<br />
3rd line: £18,000 per QALY MTX-naïve: £16,766 per QALY<br />
MTX-naïve with high CRP:<br />
£13,000 per QALY<br />
ethical and distributional issues in any <strong>of</strong> <strong>the</strong><br />
included studies.<br />
● All but one economic analysis used a decisionanalytic<br />
model. Published models vary in some<br />
important aspects; for example, <strong>the</strong> type <strong>of</strong><br />
model used, whe<strong>the</strong>r switching <strong>of</strong> <strong>the</strong>rapy is<br />
considered, drug combinations, comparator<br />
<strong>the</strong>rapies, and time-horizon and cycle length.<br />
● One study carried out a cost-<strong>effectiveness</strong><br />
analysis using patient-level data on costs and<br />
outcomes from a patient cohort. However,<br />
results for two separate TNF inhibitors were<br />
combined.<br />
● Six studies report costs that include both those<br />
from a healthcare perspective and indirect costs<br />
including losses <strong>of</strong> productivity; inclusion <strong>of</strong><br />
<strong>the</strong>se productivity costs improves <strong>the</strong> cost<strong>effectiveness</strong><br />
<strong>of</strong> TNF inhibitors.<br />
● One study carried out a cost-<strong>effectiveness</strong><br />
analysis, with <strong>the</strong> remaining nine conducting a<br />
cost–utility analysis. Two studies obtained<br />
preference weights from VAS, considered to be a<br />
less acceptable method for obtaining<br />
preference. The remaining seven studies used<br />
EQ-5D, in some cases using regression analysis<br />
to convert HAQ scores to EQ-5D.<br />
● In model-based analyses, costs and benefits<br />
were modelled over a number <strong>of</strong> different time-<br />
horizons: 6 months (one study), 1 year (one<br />
study), 5 years (one study), 10 years (two<br />
studies) and lifetime (four studies). However,<br />
<strong>the</strong>re was no association between ICER values<br />
and time-horizon used.<br />
Review <strong>of</strong> industry cost<strong>effectiveness</strong><br />
submissions<br />
A detailed summary <strong>of</strong> <strong>the</strong> economic analyses and<br />
models included in <strong>the</strong> company submissions to<br />
NICE for <strong>the</strong> appraisal <strong>of</strong> <strong>adalimumab</strong>, etanercept<br />
and infliximab carried out in 2005–6 is reported<br />
in this section. All three companies provided an<br />
electronic model.<br />
The methods used in <strong>the</strong> economic analyses are<br />
presented in Table 24.<br />
Abbott submission (<strong>adalimumab</strong>)<br />
A patient-based, state-transition model was<br />
developed to assess <strong>the</strong> cost-<strong>effectiveness</strong> <strong>of</strong><br />
<strong>adalimumab</strong> in combination with methotrexate<br />
compared with a sequence <strong>of</strong> traditional DMARDs<br />
in patients with moderate to severe RA. The main<br />
treatment sequences considered are shown in<br />
Table 25. Adalimumab mono<strong>the</strong>rapy and o<strong>the</strong>r TNF