- Open Access
Cost-effectiveness of lung volume reduction coil treatment in patients with severe emphysema: results from the 2-year follow-up crossover REVOLENS study (REVOLENS-2 study)
- Julie Bulsei1Email author,
- Sylvie Leroy2,
- Jeanne-Marie Perotin3,
- Hervé Mal4,
- Charles-Hugo Marquette2,
- Hervé Dutau5,
- Arnaud Bourdin6,
- Jean-Michel Vergnon7,
- Christophe Pison8,
- Romain Kessler9,
- Vincent Jounieaux10,
- Mathieu Salaün11,
- Armelle Marceau4,
- Sylvain Dukic12,
- Coralie Barbe13,
- Margaux Bonnaire14,
- Gaëtan Deslee3,
- Isabelle Durand-Zaleski1 and
- the REVOLENS study group
© The Author(s). 2018
- Received: 22 March 2018
- Accepted: 29 April 2018
- Published: 9 May 2018
The REVOLENS study compared lung volume reduction coil treatment to usual care in patients with severe emphysema at 1 year, resulting in improved quality-adjusted life-year (QALY) and higher costs. Durability of the coil treatment benefit and its cost-effectiveness at 2 years are now assessed.
After one year, the REVOLENS trial’s usual care group patients received coil treatment (second-line coil treatment group). Costs and QALYs were assessed in both arms at 2 years and an incremental cost-effectiveness ratio in cost per QALY gained was calculated. The uncertainty of the results was estimated by probabilistic bootstrapping.
The average cost of coil treatment in both groups was estimated at €24,356. The average total cost at 2 years was €9655 higher in the first-line coil treatment group (p = 0.07) and the difference in QALY between the two groups was 0.127 (p = 0.12) in favor of first-line coil treatment group. The 2-year incremental cost-effectiveness ratio (ICER) was €75,978 / QALY. The scatter plot of the probabilistic bootstrapping had 92% of the replications in the top right-hand quadrant.
First-line coil treatment was more expensive but also more effective than second-line coil treatment at 2 years, with a 2-year ICER of €75,978 / QALY.
ClinicalTrials.gov Identifier NCT01822795.
- Coil treatment
- Severe emphysema
Usual medical treatments have limited effectiveness in patients with severe emphysema, justifying the development of alternative interventional treatments such as endobronchial lung volume reduction treatments including valves, coils, and thermal vapor ablation . Endobronchial coil treatment (ECT) consists on placing non-blocking shape-memory nitinol coils into subsegmental airways to reduce dynamic lung hyperinflation . Three randomized studies demonstrated that ECT is associated with improvements in exercise capacity, lung function and quality of life [3–5]. Only one economic evaluation was carried out by the REVOLENS study (réduction volumique endobronchique par spirales; NCT01822795) . The economic evaluation’s goal is to evaluate the joint distribution of costs and benefits in order to assess the efficiency of a new intervention and therefore determine whether it would be a good use of healthcare resources. As such, they inform decision-makers who decide if a new technology should be reimbursed. The REVOLENS study found a mean cost difference between groups at 1 year of €36,123 per patient (p < 0.001), a mean quality-adjusted life year (QALY) difference of 0.061 (p = 0.02) and an incremental cost-effectiveness ratio (ICER) of €590,079 per QALY . However, the one-year duration of the follow-up precluded any robust conclusions regarding the long-term cost-effectiveness of ECT. In addition, it did not address the question of the benefit (or lack thereof) of an early ECT management. The aim of the REVOLENS-2 study was therefore to estimate the 2-year cost-effectiveness of first-line lung volume reduction coil treatment compared to second-line coil treatment in patients with severe emphysema included in the REVOLENS trial.
Study design and patients
The design of the REVOLENS trial has been previously reported and will be briefly summarized . In this prospective randomized open blinded end-point trial conducted in ten French sites, patients with bilateral emphysema, post bronchodilator forced expiratory volume in one second (FEV1) < 50% pred., residual volume > 220% pred., and formal pulmonary rehabilitation within the previous 12 months, were randomly assigned in a 1:1 ratio to coils treatment or to usual care. This study was approved by the Ethics Committee of Dijon Est I (N°2012-A01477–36), and by the French Agency for Medicines and Health Products (ANSM). The coils were purchased from the manufacturer (PneumRx/BTG, Mountain View, CA) which had no involvement in the study design. All participants signed a written informed consent to participate to the study. The primary endpoint of the REVOLENS trial was the improvement of at least 54 m in the 6-min walk test at 6 months.
In the REVOLENS protocol, patients of the usual care group were offered coil treatment after one year. In the REVOLENS-2 study, this group of patients is referred to as the second-line coil treatment group and is compared to the first-line coil treatment group. According to the protocol, patients in both groups were followed during 5 years post treatment. During this follow-up period, medical data (e.g. intervention data, biological analysis, imaging, respiratory function tests results) and economic data (e.g. quality of life, hospitalizations and consultations) were collected prospectively in a Case Report Form (CRF).
Data for the economic evaluation were prospectively collected during the trial, in accordance with the Consolidated Health Economic Evaluation Reporting Standards (CHEERS) statement . Costs and QALYs were assessed in both arms at 2 years and an incremental cost-effectiveness ratio in cost per QALY gained was calculated. The uncertainty of the results was analyzed using a non-parametric bootstrap which provided multiple estimates of the ICER by randomly re-sampling the patient population 1000 times and results were presented as a scatter plot of 1000 ICERs on the cost-effectiveness plane and transformed into a cost-effectiveness acceptability curve based on the decision-makers’ willingness to pay for an additional QALY. The analysis was conducted from the French healthcare perspective (mandatory health insurance, complementary health insurance and patient co-payments) using tariffs and hospital production costs for coil treatment. The time horizon was 2 years.
Only direct costs were included as recommended by the French National Authority for Health (HAS) . Both hospital and non-hospital resources were considered.
Initial hospitalization and monitoring data were obtained from the CRF and from the local hospital claims database. In addition, for interventional procedure data, a bottom-up micro-costing based on 5 French participating hospital visits was carried out.
The number and type of staff and medical devices required for the procedure (coils, delivery catheter, mucus vacuum cleaner and antibiotic therapy), procedures’ duration, the type of operating room and the type and length of hospital stay but also, the number and type of consultations (anesthesiologist, general practitioner, pulmonologist and physiotherapist), biology act (microbiological analysis of endobronchial aspirates), imaging (chest X-ray, chest computed tomography), medication (long term oxygen therapy), monitoring tests (walk test, blood gas test and respiratory function tests), transportation and readmission were all used as variables to calculate costs.
Staff costs per hour were calculated using the average salary costs which includes charges for each type of staff for full-time contracts of 1607 h per year . Medical devices costs were valued by the manufacturer price. Consultations, laboratory tests, imaging, medication, monitoring tests and transportation costs were valued using the statutory health insurance tariffs [9–13]. Operating room costs were derived from the cost accounting of an operating room in one hospital visited. Hospital stays were valued using the French national hospital cost study (Etude Nationale de Coûts à méthodologie Commune, ENCC) adjusted to the length of stay observed in the study . Readmissions costs were valued using the tariff of the corresponding diagnosis related groups  to which were added intensive care daily supplements .
Unit costs are presented in eTable 1 of the REVOLENS clinical trial article. Since 2017, the price of coils decreased from €1424 to €1080 per unit with a maximum of 10 coils charged per treated lobe. The current price for the economic evaluation was used. All other costs were in 2016 Euros (€) or inflated to 2016 using the health-specific inflation index . A discount rate of 4% was applied to both outcomes and costs beyond the first year .
The effectiveness was expressed as the difference in QALYs during the 2-years follow-up period between the two arms. QALY represents a patient’s survival time weighted by the quality of life, represented by utility. Utility values were collected in the CRF from the EQ-5D-5 L health-related quality of life questionnaire. The EQ-5D-5 L comprises a descriptive system which is composed of five health dimensions (mobility, self-care, usual activities, pain/discomfort and anxiety/depression) with 5 levels of health state (no problems to extreme problems). The participant’s answers are combined to produce a five-digit number describing the participant’s health status which is converted to a utility value from the country specific value set. The French EQ-5D-5 L value set has utility between − 0.530 (worst possible health) and 1 (best possible health) [18–20].
The statistical analyses were performed on the intention-to-treat (ITT) population. Qualitative data were presented using frequencies (percentages) and compared with the Chi-square test. Quantitative data were presented using means (standard deviations) and compared using Student t test or Mann-Whitney test depending on the variables’ distribution. Missing data were imputed either by the average in the case of quantitative variables or by the weighted frequency in the case of qualitative variables. A p-value less than 0.05 was considered significant. SAS (Version 9.3, SAS Institute, Cary, NC, USA) was used for analysis.
Patients and procedures
Costs (inflated and discounted) in € by randomization group over a 2-year period
Average cost per patient in € (SD)
First-line coil treatment group
Second-line coil treatment group
0–12 months after randomization
N = 50
N = 50
First coil procedure
Second coil procedure (N = 47)
Average total cost during the first year a
12–24 months after randomization
N = 46 b
N = 47 b
First coil procedure (N = 40)
Second coil procedure (N = 36)
Average total cost during the second year for patients alive a
0–24 months after randomization
N = 50
N = 50
Total cost for 50 patients per groupc
Average total cost per patient
This health economic analysis of the REVOLENS study results was prospectively designed to inform healthcare payers in France.
The results showed that the mean 2-year treatment cost was estimated at €27,800 per patient in the first-line coil treatment group and at €20,912 in the second-line coil treatment group. Patients in the second-line treatment group received coil treatment at 1 year and the cost difference between the two groups decreased from €28,941 at 1 year to €9655 at 2 years. The non-significant €9655 cost difference between the 2 groups was due to rehospitalization and coil treatment costs which tended to be higher in the first-line coil treatment group. This can be explained by the fact that only 40 out of 50 patients had the procedure. The cost of the intervention was thus zero euro for the remaining 10 patients.
Furthermore, there was an improvement in the post-treatment quality of life in both groups. However in the second-line coil treatment group, quality of life significantly decreased during the first year (pre-treatment) and did not increase to the level of the first-line coil treatment group’s quality of life at one year after coil treatment, suggesting that early lung volume reduction coil treatment might be associated with better quality of life outcome.
The decrease in incremental cost and the increase in incremental QALY had led to an ICER of €75,978 / QALY at 2 years compared to an ICER of €472,759 / QALY at 1 year. The difference between the 1-year ICER of the REVOLENS-2 study and the 1-year ICER of the primary economic evaluation (€590,079 / QALY) was explained by the lower price of coils and 2015/2016 inflation.
The probabilistic bootstrapping, by graphically demonstrating an ICER variation when resampling the patients 1000 times, showed a large dispersion, resulting from the uncertainty surrounding the clinical results. 92% of the replications were in the top right-hand quadrant, indicating a higher cost for greater effectiveness of fist-line coil treatment.
These results provide important data for healthcare payers appraising the cost-effectiveness of ECT in severe emphysema. Indeed, literature regarding cost-effectiveness in endobronchial lung volume reduction is scarce, limited to a model-based assessment of valves , showing an estimated 5-year ICER of €46,322 / QALY and a 10-year of €25,142 / QALY. The REVOLENS study is focused on ECT and was carefully designed to overcome the methodological shortcomings of model-based assessment. Estimation of the 2-year ICER of endobronchial coils is based on rigorous methodology from prospective data and following the international standards of health-economic assessments which allows this study to have a high internal validity. However the external validity is more moderate because of the high cost of the medical device and the variability of the operators’ skills.
The time horizon chosen for the economic evaluation is 2 years. Because patients of the usual care group were offered coil treatment after one year of follow-up, it can be assumed that the difference in cost between the two groups remained unchanged and the difference in utility either remained unchanged or vanished after the second year of follow-up. In the first case, the stabilization of the utility 1 year after the coil treatment in the first-line coil treatment group suggests there could be a similar stabilization in the second-line coil treatment group after year 2. At 5 years, the utility difference between the 2 groups present at 2 years could therefore be maintained. Likewise, the cost difference after the second year of follow-up has no reason to change based on the non-significant difference between the 2 groups in rehospitalizations and home oxygen costs during the second year of follow-up, which are the 2 major costs. As such, we would expect the incremental cost-effectiveness ratio at 5 years to be lower than the ICER at 2 years, making early treatment more cost-effective in the long-term. In the latter case, the ICER would also decrease, but not as much. An 18 month utility measurement would have refined our assumption. In order to answer this question, data at 5 years will be available soon but it might be challenging to obtain hospital data in the long term. The PneumRx endobronchial coil system in treatment of subjects with severe emphysema study (ELEVATE study) will start in 2018. This international study aims to improve patient selection in order to reduce the number needed to treat and improve the cost effectiveness .
Finally, there is limited availability of this technology across the world but due to the lack of effective therapies for patients with severe emphysema, studies on endobronchial lung volume reduction are of interest for pulmunologists internationally.
In conclusion, REVOLENS-2 study results showed that first-line coil treatment was more expensive but also more effective than second-line coil treatment at 2 years, with a 2-year ICER of €75,978 / QALY.
The members of the REVOLENS Study Group includes all authors and Sandra Dury, MD, Hervé Vallerand MD, François Lebargy MD PhD, Claire Launois MD (Hôpital Universitaire de Reims), Johanna Pradelli MD, Jonathan Benzaquen MD, Matthieu Buscot MD, Celine Sanfiorenzo MD, Sylvia Korzeniewski MD, Andrea Mazzetta MD, Jennifer Griffonnet, Ariane Guillemart, Demosthenes Makris MD (Hôpital Universitaire de Nice), Marie Christine Dombret MD, Frédérique Servin MD, Marie Pierre Debray MD (Hôpital Universitaire Bichat, Paris), Sophie Laroumagne MD, Fabienne Bregeon MD PhD, Carine Gomez MD, Philippe Astoul MD PhD (Hôpital Universitaire de Marseille), Nathalie Lesavre MD (Centre d’Investigation Clinique 1409, AP-HM, Marseille), Jean Pierre Mallet MD, Anne Sophie Gamez MD, Philippe Tarodo MD, Christophe Brousse MD, Clément Broissin MD (Hôpital Universitaire de Montpellier), Yoann Thibout MD, Fabrice Di Palma MD, Frédéric Costes MD (Hôpital Universitaire de Saint Etienne), Amandine Briault MD, François Arbib MD, Emilie Reymond MD, G. Ferrettti, Md, PhD (Hôpital Universitaire Grenoble Alpes), Michele Porzio MD, Benjamin Renaud-Picard MD (Hôpital Universitaire de Strasbourg), Bénédicte Toublanc MD, Géraldine François MD (Hôpital Universitaire d’Amiens), Luc Thiberville, MD PhD, Antoine Cuvelier MD PhD, Samy Lachkar MD (Hôpital Universitaire de Rouen), Delphine Gras PhD (Monitoring team, Hôpital Universitaire de Reims), Philippe Benoit MD (Pharmacie, Hôpital Universitaire de Reims), Annick Leclainche, Damien Jolly MD PhD (Pôle recherche et innovation, Hôpital Universitaire de Reims), François Fourrier MD PhD, Eric Hachulla MD PhD, Nicolas Roche MD PhD, Daniel Dusser MD PhD (Data and Safety Management Board). These collaborators did not receive any compensation for their contributions.
The REVOLENS Study was supported by an academic grant from the French Ministry of Health (Direction Générale de l’Offre de Soins, PSTIC-2012) which required a randomized trial design associated with an economic evaluation including a cost-effectiveness analysis. The coils were purchased from the manufacturer (PneumRx/BTG, Mountain View, CA). PneumRx/BTG provided financial support for the follow-up of the patients after one year which had no involvement in the study design and conduct of the study, collection, management, analysis, and interpretation of the data, preparation, review, or approval of the manuscript, and decision to submit the manuscript for publication.
The French Ministry of Health had full access to the results of the study, but had no involvement in the design and conduct of the study, collection, management, analysis, and interpretation of the data, preparation, review, or approval of the manuscript, and decision to submit the manuscript for publication.
Availability of data and materials
The datasets analysed during the current study are available from the Delegation of Clinical Research and Innovation of Reims University Hospital Center (Délégation à la Recherche Clinique et à l’Innovation, firstname.lastname@example.org) on reasonable request.
JB, GD and IDZ had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of data analysis. Study concept and design: JB, GD, CHM, CB, IDZ; Acquisition of data: JB, SL, JMP, HM, CHM, HD, AB, JMV, CP, RK, VJ, MS, AM, SD, CB, MB, GD, IDZ; Analysis and interpretation of data: JB, IDZ; Drafting of the manuscript: JB, CHM, GD, IDZ; Critical revision of the manuscript for important intellectual content: JB, SL, JMP, HM, CHM, HD, AB, JMV, CP, RK, VJ, MS, AM, SD, CB, MB, GD, IDZ Statistical analysis: JB, IDZ, CB; Study supervision: GD, IDZ. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The Ethics Committee of Dijon Est I and the French Agency for Medicines and Health Products Health approved the study protocol.
Hervé Mal received honorarium from Boehringer, Bayer, Roche, Astellas, Chiesi, Actellion, Pfizer, Novartis, GSK outside the submitted work; Charles Hugo Marquette has been involved as investigators in previous studies sponsored by BTG/PneumRx, and received travel reimbursements and speaker fees for educational sessions and consulting from BTG/PneumRx; Hervé Dutau received travel reimbursements and speaker fees for educational sessions and consulting from BTG/PneumRx; Arnaud Bourdin received honorarium from Astra Zeneca, GSK, Boehringer, Novartis, Teva, Chiesi, Actellion, Gilead, Roche outside the submitted work; Jean Michel Vergnon received travel reimbursements and speaker fees for educational sessions from BTG/PneumRx; Christophe Pison received honorarium from BTG/PneumRx and his hospital funds to conduct trials from Nuvaira, PulmonX, BTG/PneumRx; Vincent Jounieaux received travel reimbursements and speaker fees for educational sessions and consulting from BTG/PneumRx; Armelle Marceau received honorarium from BTG/PneumRx; Gaëtan Deslée has been involved as investigator in previous studies sponsored by BTG/PneumRx, and received travel reimbursements and speaker fees for educational sessions and consulting from BTG/PneumRx; Sylvie Leroy, Jeanne Marie Perotin, Romain Kessler, Mathieu Salaün, Margaux Bonnaire, Sylvain Dukic, Coralie Barbe, Isabelle Durand-Zaleski indicated no conflicts of interest.
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