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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

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