Ranibizumab, verteporfin photodynamic therapy or observation for the treatment of myopic choroidal neovascularization: cost effectiveness in the UK.

PURPOSE: The aim of this study was to evaluate the cost effectiveness of ranibizumab compared with verteporfin photodynamic therapy (vPDT) or no treatment (observation) in patients with visual impairment due to myopic choroidal neovascularization (CNV).
METHODS: A Markov model with health states defined by best-corrected visual acuity and a 3-month cycle length was developed. It had a healthcare provider (UK National Health Service and personal social services) perspective, a lifetime time horizon, and was based on 2011 prices; future costs and health outcomes were discounted at 3.5 % per annum. Baseline characteristics were based on the phase III RADIANCE (Ranibizumab and vPDT Evaluation in Myopic CNV) study, and year 1 health-state transitions were based on this and the VIP (Verteporfin in Photodynamic Therapy) study. Extensive sensitivity analyses tested the robustness of the model.
RESULTS: The lifetime cost of treating myopic CNV with ranibizumab was £12,866, whereas vPDT and observation were associated with total costs of £14,421 and £8,163, respectively. Ranibizumab treatment produced higher cumulative quality-adjusted life-years (QALYs; 12.99) than vPDT (12.60) or observation (12.45). Ranibizumab treatment was therefore dominant, with greater health gains and lower overall costs than vPDT. Ranibizumab was cost effective compared with observation, with an incremental cost-effectiveness ratio of £8,778/QALY. In the probabilistic sensitivity analysis, ranibizumab had a 100 % and 88 % probability of being cost effective compared with vPDT and observation, respectively, at a willingness-to-pay threshold of £20,000/QALY.
CONCLUSION: This study indicates that ranibizumab therapy is dominant over vPDT for the treatment of visual impairment due to CNV secondary to pathologic myopia in the UK healthcare setting and cost effective compared with observation.

RCT Entities:   Population Interventions Outcomes

Key Points

Introduction

Pathologic myopia is a progressive condition characterized by axial elongation and degenerative changes in the posterior segment of the eye [1]. Choroidal neovascularization (CNV) is characterized by the growth of blood vessels under the retinal pigment epithelium or retina; these vessels can rupture, leading to the accumulation of blood and fluid within layers of the retina [2]. CNV secondary to pathologic myopia, also known as myopic CNV, is one of the major causes of blindness and visual impairment worldwide [3, 4].

Verteporfin (Visudyne®, Novartis Pharma AG, Switzerland) photodynamic therapy (vPDT) has replaced laser photocoagulation as the treatment of choice for myopic CNV for subfoveal lesions [3]. However, vPDT does not significantly improve patients’ vision and may not control the underlying neovascularization disease activity [5, 6]. In the 24-month Verteporfin in Photodynamic Therapy (VIP) trial, the proportion of patients whose best-corrected visual acuity (BCVA) remained stable was higher with vPDT than with placebo at 12 months (72 vs 44 %, p < 0.01), but this was no longer significant at 24 months (64 vs 49 %, p = 0.11) [5]. The median change in BCVA from baseline to 24 months ranged from −1 to 1 letter with vPDT and −5 to −9 letters with placebo (measured using the ETDRS [Early Treatment Diabetic Retinopathy Study] chart). There is therefore an unmet need for treatment that improves vision in patients with visual impairment secondary to myopic CNV.

Ranibizumab (Lucentis®, Novartis Pharma AG, Switzerland) is a recombinant, humanized, monoclonal antibody fragment designed to inhibit the active forms of vascular endothelial growth factor A (VEGF-A) [7]. VEGF-A is important in the pathogenesis of CNV, stimulating the growth of new blood vessels and increasing vascular leakage [8, 9]. Ranibizumab has demonstrated clinical efficacy in patients with visual impairment secondary to wet age-related macular degeneration [10-12], diabetic macular oedema [13-17] and macular oedema following retinal vein occlusion [18-22], and is widely licensed and reimbursed across these indications. The most recent indication is for the treatment of visual impairment due to CNV secondary to pathologic myopia.

The RADIANCE (Ranibizumab and vPDT Evaluation in Myopic CNV) study was a 12-month, phase III study in which patients were randomized to either ranibizumab or vPDT, plus appropriate shams [23]. To avoid denying patients an effective treatment, patients randomized to vPDT could switch to ranibizumab from month 3 onwards at the treating investigator’s discretion. Indeed, 73 % (40/55) of patients randomized to vPDT did switch to ranibizumab during the study, including two patients who switched before month 3. The primary endpoint, the mean average change from baseline in BCVA at 3 months, was +10.5 and +10.6 letters in patients randomized to ranibizumab (administered according to disease stabilization or disease activity criteria, respectively) compared with +2.2 letters in the vPDT group (p < 0.0001 versus ranibizumab, stratified Cochran–Mantel–Haenszel test) [23]. Improvements in BCVA in the ranibizumab groups were sustained for the duration of the study. Patient-reported visual functioning, as measured by the 25-item National Eye Institute Visual Functioning Questionnaire (NEI VFQ-25), was improved in the ranibizumab groups from baseline and the difference compared with vPDT was significant at 3 months (measured using the composite score, p < 0.05 [24]).

Here we present an economic analysis of ranibizumab in the treatment of visual impairment due to myopic CNV. We have used a Markov health-state transition model and have incorporated findings from the RADIANCE study and VIP trial to compare the costs and benefits of treating patients with ranibizumab with those of vPDT treatment or observation only, adopting a UK healthcare provider perspective.

Methods

Model Structure

A Markov decision-analytical model was developed to predict the long-term costs and health outcomes of ranibizumab treatment for visual impairment due to myopic CNV compared with vPDT or observation only. In the Markov structure, patients were categorized by health state and could move between states at the end of each 3-month cycle according to their level of visual acuity. Half-cycle correction was used. The model had eight health states defined by the BCVA in the treated eye and a ninth absorbing death state (Fig. 1). The BCVA health states are defined by 10-letter (two-line) BCVA ranges between 25 letters or less and 86–100 letters (on the ETDRS chart). A 10-letter gain is associated with clinically relevant changes in the patient’s vision and vision-related quality of life [25].

Fig. 1

Markov model of health states and possible patient transitions. The transition probabilities were based on patients moving between any two states, so the arrows as depicted on this schematic would extend to all other states. The arrows have not been completed here for every possible state to maintain legibility. BCVA best-corrected visual acuity, ETDRS Early Treatment Diabetic Retinopathy study

BCVA scores at baseline were taken from the RADIANCE study (treated eyes of patients receiving ranibizumab by disease activity criterion, full analysis set). The starting age of patients was 55 years based on the mean age of patients in the RADIANCE study [23] and 15 % were assumed to have bilateral disease at the start of the model [26, 27]. Patients received either ranibizumab or vPDT over 2 years and treatment was resumed only in cases of recurrence (Table 1). The annual recurrence rate was based on expert opinion (two international advisory boards comprising experts chosen for their high level of expertise in retinal disease) and assumed to be 6 % following treatment completion (consensus was reached by discussion). This was a conservative estimate and is supported by recurrence data from a long-term study in which 46 % of eyes treated with vPDT and/or anti-VEGF experienced at least one recurrence over a mean follow-up of 71 months [28]. At baseline, 21 % of patients were treated in their better-seeing eye (BSE; defined as such when the BCVA letter score at baseline was higher than the score for the non-study eye) [29] estimated from the RADIANCE study.

Table 1

Model inputs for treatment and monitoring frequencies and data sources for baseline BCVA the base-case scenario

Time period	Treatment	BCVA data source	Mean number of treatments administered	Mean number of monitoring visits
Year 1	Ranibizumab	RADIANCE study (0–12 months) [23]	3.5 [23]	8.5a (assumption)
	vPDT	RADIANCE study (0–3 months) [23] VIP trial (4–12 months) [5]	3.4 [5]	4.0 [48]
	Observation	VIP trial (0–12 months) [5]	0	4.0 [5]
Year 2	Ranibizumab	Natural history [30]	1.0b (expert advice)	4.0 (assumption)
	vPDT	Natural history [30]	1.7 (VIP trial) [6]	4.0 [48]
	Observation	Natural history [30]	0	4.0 (assumption)
Year 3+	Ranibizumab	Natural history [30]	0b (expert advice)	0b (expert advice)
	vPDT	Natural history [30]	0 (VIP trial) [6]	0 (VIP trial) [6]
	Observation	Natural history [30]	0	4.0 (assumption)c

BCVA best-corrected visual acuity, mCNV myopic choroidal neovascularization, RADIANCE Ranibizumab and vPDT Evaluation in Myopic Choroidal Neovascularization, SmPC Summary of Product Characteristics, VIP Verteporfin in Photodynamic Therapy, vPDT verteporfin photodynamic therapy

aThis is a conservative assumption; the ranibizumab SmPC states that about 5.5 monitoring visits are expected in year 1 of ranibizumab treatment

bExpert advice was taken from an advisory board of 11 UK ophthalmologists

cFor patients undergoing observation, as the disease is not actively being treated it was assumed that they will continue to be monitored up to year 3, as their disease was unlikely to have been cured. For patients receiving treatment, in the absence of long-term data, and informed by expert advice, it was assumed that mCNV has a limited course, requiring no monitoring visits in year 3

The proportion of patients treated in their BSE in each health state is shown in Table 2. The model is dynamic in that it allows the treated eye to change from being the worse-seeing eye (WSE) to the BSE as BCVA improves. This was modelled using a probability matrix of the study eye being the BSE by level of visual acuity (Table 2).

Table 2

Baseline distributions of patients treated in their better-seeing eye (BSE) or worse-seeing eye (WSE) and utility values by BSE/WSE

BCVA health state (letters)	Patients at model entry (%)	Patients whose treated eye was their BSE (%)	Utility when treated eye was the BSE	Utility when treated eye was the WSE
86–100	0	50a	0.850	0.850
76–85	4	50	0.758	0.836
66–75	20	22	0.685	0.821
56–65	33	22	0.611	0.807
46–55	20	21	0.537	0.793
36–45	13	15	0.464	0.779
26–35	9	10	0.390	0.764
≤25	1	0a	0.353	0.750
Death	0	–	0.000	0.000

Utilities for the BSE were from a published study; WSE utilities were assumed to be proportional to those for the BSE [33]

BCVA best-corrected visual acuity, RADIANCE Ranibizumab and vPDT Evaluation in Myopic Choroidal Neovascularization

aAssumption, no patients were in these groups at baseline in the RADIANCE study

Transition probabilities (TPs) were calculated for each 3-month cycle depending on the treatment received. Patients could transition between any health state in each cycle, according to their change in BCVA score over the cycle. For the first year, patient-level data were used to calculate separate TPs for each BCVA health state, allowing for 64 unique TPs (8 × 8) for each 3-month time period (see electronic supplementary material [ESM], Online Resource 1). The 8 × 8 matrix was able to model the ‘ceiling effect’ of gains in visual acuity, as patients with high baseline visual acuity have less potential for improvement than those with poor baseline vision. Consequently, this method predicted the trial results more accurately than two other methods tested (constant TPs across all BCVA levels or constant probabilities for all states other than the two highest health states). The base-case TPs in each cycle in year 1 were varied in sensitivity analysis by multiplying by a factor of 0.5–2.0.

The effect of ranibizumab, vPDT or observation on BCVA was modelled over 1 year. Thereafter, it was assumed that BCVA declined at the same rate irrespective of initial treatment, according to natural history data. In the base-case analysis, a second set of TPs was calculated using data from the natural history study with the longest available follow-up [30] and applied from year 2 onwards to capture the natural decline in BCVA without treatment. The overall probability of a patient’s vision deteriorating over the follow-up period was converted to a monthly rate and in turn converted into a 3-monthly probability. A probability of all-cause mortality was included in the model [31] and an increased mortality risk was applied when BCVA was 55 letters or less to reflect increased mortality in patients with BCVA below this level (relative risk of 1.23, increasing to 1.54 when BCVA was ≤35 letters) [32].

Utilities

Each BCVA health state was assigned a utility weight dependent on whether the treated eye was the patient’s BSE or WSE. The proportion of patients whose treated eye was their BSE was matched to baseline BCVA in the RADIANCE study and was modelled dynamically as described earlier [23] (Table 2). Utility weights for the BSE were taken from a study in which visual impairment was simulated using specially designed contact lenses worn by healthy volunteers from the UK and in which time trade-off was used to assess participant’s valuation of their health state prior to and following lens installation [33] (Table 2). Utilities for patients treated in the WSE were not available from the literature and various assumptions were required. In the base-case scenario, utility weights for the WSE were assumed to be higher than, or the same as, for the BSE, because visual impairment in the WSE is considered less serious than visual impairment in the BSE. A 0.1 maximum difference in utility values was assumed for the WSE between the best and worst possible BCVA health states, as good vision in both eyes is considered ‘worth’ an additional utility of 0.1 compared with good vision in only one eye. This assumption was based on the National Institute for Health and Care Excellence (NICE) Evidence Review Group guidance issued for ranibizumab in the treatment of visual impairment caused by macular oedema secondary to retinal vein occlusion [34]. The WSE utility curve was anchored at the highest BCVA health state, at which point the utility was the same for the WSE and BSE (ESM, Online Resource 2).

The probability that the study eye is the BSE improves as vision improves. When the BCVA in the treated eye improves to such an extent that it becomes the BSE, the utility value is changed and can be lower than the utility when the eye was the WSE (even though this appears counterintuitive because one might predict that improving vision would result in increased utility). For patients with bilateral disease, utility values were assigned according to BCVA in the BSE as health-related quality of life (HRQoL) is driven by visual acuity in the BSE [35]. For patients who had a recurrence, no change in visual acuity or utility was assumed to occur from the recurrence.

Patients were assumed to experience adverse events (AEs) based on the rates reported in the RADIANCE study for ranibizumab [23] or the VIP trial for vPDT or observation [5] (ESM, Online Resource 3). All AEs that were reported for five or more patients or were suspected to be related to treatment were included. AEs were associated with temporary reductions in utility based on published literature or assumption (range of 0 to −0.02, see ESM, Online Resource 3). Because timings for AEs were not available, disutilities were calculated as one-off events per patient and applied at entry to the model with the following durations: conjunctival haemorrhage, 1 month; intraocular pressure increase, 1 day; injection site reaction, 8.2 days. In order to assess the comparability of the RADIANCE study and VIP trial populations, baseline characteristics are compared in Online Resource 4 and inclusion/exclusion criteria are compared in Online Resource 5 (ESM). These suggest that the two studies were sufficiently similar to warrant the chosen methodology.

Costs

A full breakdown of costs and sources is given in ESM, Online Resource 6. A UK healthcare provider (National Health Service [NHS] and personal social services [PSS]) perspective was adopted, and a lifetime time horizon used. Future costs and health outcomes were discounted at 3.5 % per annum according to NICE recommendations. Costs from earlier years were inflated to 2011 prices using the Hospital and Community Services Inflation Index [36]. The health-state costs included cost of treatment, administration, monitoring, management of AEs and recurrences, and the long-term cost of blindness. The costs of drug acquisition did not include the ranibizumab patient access scheme discount that is in place in the UK. The cost of administration included the cost of optical coherence tomography plus an injection visit for ranibizumab or an ophthalmologist consultation visit for vPDT. Frequencies of treatment and monitoring were taken from the RADIANCE study or VIP trial (Table 1). The frequency of treatment and the cost and frequency of monitoring were varied extensively in sensitivity analyses. For patients with recurrence, the numbers of treatment and monitoring visits were assumed to correspond to those for year 1 of initial treatment. For patients with bilateral disease, the cost of treatment and monitoring visits was doubled since the fellow eye would incur additional treatment and monitoring visits. The cost of blindness was included when the BSE had a BCVA below 35 letters (that is, both eyes were affected). Resource utilization was based on published data [37] and was higher in the year following diagnosis than in subsequent years as in previous NICE assessments [34].

Economic Analysis

The incremental cost-effectiveness ratio (ICER) was calculated as the ratio of the mean incremental cost and the mean number of incremental quality-adjusted life-years (QALYs) for ranibizumab compared with either vPDT or observation. Net monetary benefit (NMB) was calculated assuming a willingness-to-pay of £20,000/QALY [38]. Using this formulation, higher NMB indicates greater value: NMB greater than £0 is equivalent to an ICER of less than £20,000/QALY. Thus, in the context of this analysis, ‘cost effective’ is defined as meeting accepted standards of cost effectiveness based on a willingness-to-pay threshold of £20,000/QALY. Deterministic sensitivity analysis was used to explore uncertainty around individual input values to the model, and the effect on the resultant NMB calculated. Probabilistic sensitivity analysis was used to assess the overall level of uncertainty in the model (see ESM, Online Resource 7 for parameters and distributions). The internal validity of the model was checked by a health economist not involved in the development or use of the model. Face validity of the model was validated by two UK ophthalmologists.

Results

The model predicted that the gain in BCVA in year 1 was greater with ranibizumab than with vPDT (in agreement with the trial data); for both treatments, BCVA gradually decreased over subsequent years (Fig. 2). The number of life-years gained was slightly higher with ranibizumab than with vPDT or observation (difference of 0.15 and 0.24 years, respectively), reflecting the higher mortality in patients with low BCVA. Ranibizumab was associated with a QALY gain of 0.39 over vPDT and a QALY gain of 0.54 over observation (Table 3). Lifetime costs were slightly lower for ranibizumab than for vPDT (−£1,555) but higher than for observation (+£4,703, Table 3). As ranibizumab led to greater health gains at lower cost, it was dominant over vPDT (Table 3). The NMB was £9,289 at a willingness-to-pay threshold of £20,000/QALY. Comparison of ranibizumab with observation gave an ICER of £8,778/QALY (Table 3), which is lower than the threshold of £20,000–30,000/QALY often applied in the UK [38]. The NMB was £6,013.

Fig. 2

Visual acuity modelled over time. BCVA best-corrected visual acuity, ETDRS Early Treatment Diabetic Retinopathy study, vPDT verteporfin photodynamic therapy

Table 3

Base-case cost-effectiveness results using deterministic values

	Ranibizumab	vPDT	Observation	Ranibizumab versus vPDT	Ranibizumab versus observation
Cost (£)	12,866	14,421	8,163	−1,555	+4,703
QALYs	12.99	12.60	12.45	+0.39	+0.54
Life-years	16.85	16.70	16.61	+0.15	+0.24
NMB (£)	–	–	–	9,289	6,013
ICER (£/QALY)	–	–	–	Dominant	8,778

The model followed a cohort of 1,000 patients over a lifetime time horizon. The healthcare provider perspective was adopted. Future costs and health outcomes were discounted at 3.5 % per annum

ICER incremental cost-effectiveness ratio, NMB net monetary benefit, QALY quality-adjusted life-year, vPDT verteporfin photodynamic therapy

There were differences in the cost of blindness between treatments. The lifetime cost of blindness was lower for patients receiving ranibizumab (−£3,920) or vPDT (−2,138) than for patients under observation. Costs of AEs incurred with ranibizumab (£106) or vPDT (£10) were negligible and did not impact on the overall costs.

One-way sensitivity analysis showed that the model results were robust. Comparing with vPDT (Fig. 3a), the model was most sensitive to the maximum utility gain for the WSE, with higher utility values increasing NMB. Ranibizumab was cost effective even when assuming 12 ranibizumab injections in the first year (NMB, £596) and only ceased to be cost effective if 11 or more injections were administered in year 2, or at a cost over £1,100 per monitoring visit or a cost over £1,300 per injection visit at the base case number of injections. Extensive variation of the TPs in year 1 gave results that were consistent with the base-case scenario. Comparing with observation (Fig. 3b), the model was also sensitive to the maximum utility gain for the WSE. Ranibizumab ceased being cost effective when ten injections were administered in the first year, or seven in year 2, or at a cost over £1,100 per monitoring visit or a cost over £900 per injection visit.

Fig. 3

Tornado plots showing results of one-way sensitivity analysis for ranibizumab compared with a vPDT and b observation. The X axis represents the net monetary benefit, which for the base-case scenario is £9,289 for ranibizumab versus vPDT, and £6,013 for ranibizumab versus observation. Parameters varied are listed in the Y axis. Low value, lower limit of parameter varied for sensitivity analysis; high value, upper limit of parameter varied for sensitivity analysis; multiplier, multiplication factor for base-case value of parameter. BSE better-seeing eye, vPDT verteporfin photodynamic therapy, WSE worse-seeing eye

The probabilistic sensitivity analysis showed that ranibizumab has a 100 and 88 % probability of being cost effective compared with vPDT and observation, respectively, at a willingness-to-pay threshold of £20,000/QALY (Fig. 4). Validation of the model by detailed examination of the Markov traces confirmed that the model produced similar results to the study data on which it was based.

Fig. 4

Scatter plots for probabilistic sensitivity analysis showing cost effectiveness of ranibizumab compared with a vPDT and b observation. QALY quality-adjusted life-year, vPDT verteporfin photodynamic therapy

Discussion

This is the first study to evaluate the cost effectiveness of ranibizumab compared with vPDT or observation for the treatment of patients with visual impairment due to myopic CNV. The analysis showed that ranibizumab is dominant over vPDT and was associated with lower lifetime costs and an incremental QALY gain. Ranibizumab was cost effective compared with observation, with an ICER of £8,778/QALY. One-way sensitivity analysis showed that the model results were robust, but sensitive to the maximum utility gain for the WSE and number of ranibizumab injections received. Probabilistic sensitivity analysis showed that ranibizumab has a 100 and 88 % probability of being cost effective compared with vPDT and observation, respectively, at a willingness-to-pay threshold of £20,000/QALY.

The anti-VEGF bevacizumab was not included as a comparator in this analysis because it is unlicensed for the treatment of myopic CNV and its use is not considered by NICE to be routine practice across the NHS. Furthermore, after reviewing the quality of evidence for bevacizumab in myopic CNV, the NICE committee concluded that there was insufficient evidence to allow bevacizumab to be included with confidence in a clinical and cost-effectiveness analysis [39].

The improvements in BCVA with ranibizumab compared with vPDT in the RADIANCE study (+10.5 and +10.6 letters, respectively, for the disease stabilization and disease activity criteria groups at 3 months) translated to higher utility values in the model, reflecting improved HRQoL after treatment. This gain was achieved with relatively few injections. In the ‘disease activity’ treatment group, whose characteristics were incorporated into the model and whose treatment corresponded to the ranibizumab myopic CNV label, 50 % of patients required 1–2 injections, 36 % required 3–5 injections and 14 % required 6–12 injections over the 12-month study [40]. This translated into a mean treatment frequency of 3.5 ranibizumab injections in year 1 of the model. The 3.4 vPDT treatments in year 1 were calculated from treatment frequency in the large VIP trial [5, 6]. We used a very conservative assumption of 8.5 monitoring visits in year 1, which is likely to overestimate visits compared with clinical practice. In deterministic sensitivity analysis, increasing the frequency of injections and follow-up visits had a strong effect on the cost effectiveness. However, even assuming 12 injections in year 1, ranibizumab remained cost effective compared with vPDT given 3.4 times per year.

Myopic CNV is a relatively acute condition with a reduced requirement for retreatment compared with other retinal conditions such as neovascular age-related macular degeneration; this is reflected in the low number of ranibizumab injections required in year 2. During the 12-month follow-up in the RADIANCE study, over 50 % of patients treated with ranibizumab according to disease activity criteria required only 1–2 injections and over 60 % did not require further injections from month 6 to month 12 [41]. The NICE review of the model suggested that 1.7 injections in year 2 would be a more reasonable assumption than the one injection included in the model [39]. However, the number of treatments in years 1 and 2 were varied in deterministic and probabilistic sensitivity analyses and did not affect the cost-effectiveness decision. Compared with vPDT, ranibizumab only ceased to be cost effective if 11 or more injections were administered in year 2. Compared with observation, ranibizumab only ceased being cost effective when seven or more injections were administered in year 2.

The RADIANCE results were used to estimate BCVA for year 1 for ranibizumab and for 0–3 months for vPDT as patients from the vPDT arm were allowed to cross over after 3 months to enable them to benefit from ranibizumab treatment. Thus, data from the VIP trial were used to model BCVA for patients receiving vPDT after 3 months, and the placebo arm data were used to simulate patients under observation only [6]. After 1 year, the decline in BCVA was modelled with the same rate across treatments. This is a conservative approach as recurrence after treatment is likely to be more common in the vPDT group than with ranibizumab [28]. The slow rate of decline in BCVA in subsequent years is consistent with several studies showing that visual acuity gains are maintained over 3–5 years in a high proportion of patients treated with anti-VEGF therapy [42-44]. Bilateral disease was only modelled by prevalence as patients entered the model because accurate estimation of the incidence rate was not possible owing to the lack of long-term natural history data. Bilateral disease was assumed to double the cost of treatment at the start of the model; for recurrence, the additional costs occurred at the time of the recurrence and included 1 year of treatment and monitoring (overestimating what would happen in clinical practice). Neither variations in the rate of recurrence (0–12 %) nor the baseline rate of bilateral disease (0–30 %) affected the dominance of ranibizumab over vPDT. As the mean age of the cohort increased, ranibizumab became less cost effective compared with vPDT or observation as cost savings from avoidance of blindness were not realized.

Utility estimates for the BSE were obtained from a published study that had simulated visual impairment associated with age-related macular degeneration using specially designed contact lenses [33]. BCVA was defined for the BSE and the ‘health states’ valued by a representative sample of the UK population using the time trade-off technique [33]. The resultant utility values were adjusted to control for important factors known to affect utility (including age and sex). NICE has previously judged that, in the absence of studies reporting utility values for the specific ocular condition, these utility values most accurately reflect the HRQoL associated with visual impairment [34]. The 5-domain European Quality of Life questionnaire was used in the RADIANCE study but the results were not used in the present analysis as the instrument is acknowledged as being insensitive to changes in visual acuity [13]. In sensitivity analysis, varying the utility values by a factor of 0.3–1.3 had little effect on the overall results.

The relationship between utility and BCVA in the WSE is a major source of uncertainty and there are no published studies that can be used to estimate utilities in the WSE. Our approach was to assume that utilities would be the same for the BSE and WSE in the highest BCVA health state, while for all other BCVA health states, utilities for the WSE would be proportional to but higher than utilities for the BSE, with the greatest difference between the BSE and WSE at the lowest BCVA health state. Essentially, visual impairment in the BSE has a greater negative effect on utility than impairment in the WSE. This is supported by visual functioning findings [35]. In the base case there was a 0.1 maximum difference in utility values for the WSE between the best and worst possible health states, as good binocular vision is considered ‘worth’ an additional utility of 0.1 compared with good vision in only one eye [34]. In sensitivity analyses, the maximum utility gain in the WSE had a bigger impact on the results than the other parameters tested. For values of 0.5 or more, the WSE actually had worse utility values than the BSE for the same level of BCVA, which is counterintuitive. At these high estimations, ranibizumab was more cost effective compared with vPDT or observation than in the base-case estimate. Varying the probability that the study eye was the BSE had little effect on the dominance versus vPDT or cost effectiveness versus observation.

Previous models using BCVA health states have maintained a constant proportion of patients whose treated eye is their BSE over the period of the model. The current model is dynamic in that, although the proportion of patients whose treated eye is their BSE is fixed within a health state, as patients transition across health states the overall proportion whose treated eye is their BSE can change over time in the model. Thus, for patients whose treated eye is the WSE, if treatment improves the visual acuity of the treated eye to such an extent that it exceeds the BCVA of the fellow eye, the treated eye becomes the BSE. This can appear counterintuitive, as higher visual acuity in the treated eye may decrease the patient-level utility value, but can be considered a conservative approach as it would underestimate total QALY gain. Furthermore, modelling both BSE and WSE allows more accurate estimations of utility for the patient, reflecting the relative gain from binocular vision.

The study was undertaken from a UK perspective and used UK-specific costs; however, the trial data from the RADIANCE study and VIP trial were international, and the efficacy and safety results are considered to have good generalizability between populations and healthcare systems. Apart from treatment and visit-related costs, the factors that had the greatest impact on the cost effectiveness were unlikely to be country dependent. The effect of increased mortality associated with low BCVA was not tested in sensitivity analyses. However, the Evidence Review Group on behalf of NICE conducted an exploratory analysis that did vary the mortality multiplier for blindness (BCVA ≤35 letters), with no effect on the cost-effectiveness decision [39].

There is little previous work around the cost effectiveness of treatments in myopic CNV. The one published study in this indication compared vPDT and observation from a US managed care perspective [45]. The base case estimated a QALY gain of 0.037 and an ICER of US$214,085/QALY over 1 year. The results are not comparable with the current study because of significant differences in methodology, including a 1-year time horizon, perspective and the absence of costs of blindness in the US study. In wet age-related macular degeneration, diabetic macular oedema and retinal vein occlusion, ranibizumab has been shown to be cost effective (e.g. [34, 37, 46, 47]).

In summary, this economic evaluation shows that ranibizumab is dominant over vPDT and cost effective compared with observation for the treatment of visual impairment due to myopic CNV using a UK healthcare perspective. This analysis suggests that ranibizumab should be adopted in this patient population.

Below is the link to the electronic supplementary material (ESM).

Online Resource 1: Transition probability matrices for patients treated with ranibizumab, vPDT or observation (DOCX 56 kb)

Online Resource 2: Utility values for the better-seeing eye (BSE) and worse-seeing eye (WSE); for the base-case scenario, the WSE curve is anchored at the highest health state (DOCX 100 kb)

Online Resource 3: Adverse event rates and the disutility values applied (DOCX 42 kb)

Online Resource 4: Baseline characteristics of populations in RADIANCE and VIP studies (DOCX 40 kb)

Online Resource 5: Key inclusion/exclusion criteria for RADIANCE and VIP studies (DOCX 42 kb)

Online Resource 6: Costs—sources and rationale (DOCX 54 kb)

Online Resource 7: Inputs for probabilistic sensitivity analysis (DOCX 44 kb)

Ranibizumab is a vascular endothelial growth factor A inhibitor licensed for the treatment of visual impairment due to choroidal neovascularization (CNV) secondary to pathologic myopia.

A cost-utility model was developed using the pivotal phase III RADIANCE study results. This indicated that the health gains associated with ranibizumab treatment over a patient’s lifetime are higher than those associated with the previous standard of care, verteporfin photodynamic therapy (vPDT), or managing patients through observation.

Ranibizumab treatment was associated with lower lifetime costs than vPDT and is therefore an economically dominant alternative to vPDT for the treatment of myopic CNV in the UK healthcare setting. Ranibizumab treatment is cost effective compared with observation.