Immunoglobulin Replacement Therapy is critical and cost-effective in increasing life expectancy and quality of life in patients suffering from Common Variable Immunodeficiency Disorders (CVID): A health-economic assessment
Common variable immunodeficiency disorders (CVID), the most common form of primary antibody deficiency, are rare conditions associated with considerable morbidity and mortality. The clinical benefit of immunoglobulin replacement therapy (IgGRT) is substantial: timely treatment with appropriate doses...
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Abstract | Common variable immunodeficiency disorders (CVID), the most common form of primary antibody deficiency, are rare conditions associated with considerable morbidity and mortality. The clinical benefit of immunoglobulin replacement therapy (IgGRT) is substantial: timely treatment with appropriate doses significantly reduces mortality and the incidence of CVID-complications such as major infections and bronchiectasis. Unfortunately, CVID-patients still face a median diagnostic delay of 4 years. Their disease burden, expressed in annual loss of disability-adjusted life years, is 3-fold higher than in the general population. Hurdles to treatment access and reimbursement by healthcare payers may exist because the value of IgGRT is poorly documented. This paper aims to demonstrate cost-effectiveness and cost-utility (on life expectancy and quality) of IgGRT in CVID.
With input from a literature search, we built a health-economic model for cost-effectiveness and cost-utility assessment of IgGRT in CVID. We compared a mean literature-based dose (≥450mg/kg/4wks) to a zero-or-low dose (0 to ≤100 mg/kg/4wks) in a simulated cohort of adult patients from time of diagnosis until death; we also estimated the economic impact of diagnostic delay in this simulated cohort. Compared to no or minimal treatment, IgGRT showed an incremental benefit of 17 life-years (LYs) and 11 quality-adjusted life-years (QALYs), resulting in an incremental cost-effectiveness ratio (ICER) of €29,296/LY and €46,717/QALY. These results were robust in a sensitivity analysis. Reducing diagnostic delay by 4 years provided an incremental benefit of six LYs and four QALYs compared to simulated patients with delayed IgGRT initiation, resulting in an ICER of €30,374/LY and €47,495/QALY.
The health-economic model suggests that early initiation of IgGRT compared to no or delayed IgGRT is highly cost-effective. CVID-patients' access to IgGRT should be facilitated, not only because of proven clinical efficacy, but also due to the now demonstrated cost-effectiveness. |
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AbstractList | BackgroundCommon variable immunodeficiency disorders (CVID), the most common form of primary antibody deficiency, are rare conditions associated with considerable morbidity and mortality. The clinical benefit of immunoglobulin replacement therapy (IgGRT) is substantial: timely treatment with appropriate doses significantly reduces mortality and the incidence of CVID-complications such as major infections and bronchiectasis. Unfortunately, CVID-patients still face a median diagnostic delay of 4 years. Their disease burden, expressed in annual loss of disability-adjusted life years, is 3-fold higher than in the general population. Hurdles to treatment access and reimbursement by healthcare payers may exist because the value of IgGRT is poorly documented. This paper aims to demonstrate cost-effectiveness and cost-utility (on life expectancy and quality) of IgGRT in CVID.Methods and findingsWith input from a literature search, we built a health-economic model for cost-effectiveness and cost-utility assessment of IgGRT in CVID. We compared a mean literature-based dose (≥450mg/kg/4wks) to a zero-or-low dose (0 to ≤100 mg/kg/4wks) in a simulated cohort of adult patients from time of diagnosis until death; we also estimated the economic impact of diagnostic delay in this simulated cohort. Compared to no or minimal treatment, IgGRT showed an incremental benefit of 17 life-years (LYs) and 11 quality-adjusted life-years (QALYs), resulting in an incremental cost-effectiveness ratio (ICER) of €29,296/LY and €46,717/QALY. These results were robust in a sensitivity analysis. Reducing diagnostic delay by 4 years provided an incremental benefit of six LYs and four QALYs compared to simulated patients with delayed IgGRT initiation, resulting in an ICER of €30,374/LY and €47,495/QALY.ConclusionsThe health-economic model suggests that early initiation of IgGRT compared to no or delayed IgGRT is highly cost-effective. CVID-patients' access to IgGRT should be facilitated, not only because of proven clinical efficacy, but also due to the now demonstrated cost-effectiveness. Background Common variable immunodeficiency disorders (CVID), the most common form of primary antibody deficiency, are rare conditions associated with considerable morbidity and mortality. The clinical benefit of immunoglobulin replacement therapy (IgGRT) is substantial: timely treatment with appropriate doses significantly reduces mortality and the incidence of CVID-complications such as major infections and bronchiectasis. Unfortunately, CVID-patients still face a median diagnostic delay of 4 years. Their disease burden, expressed in annual loss of disability-adjusted life years, is 3-fold higher than in the general population. Hurdles to treatment access and reimbursement by healthcare payers may exist because the value of IgGRT is poorly documented. This paper aims to demonstrate cost-effectiveness and cost-utility (on life expectancy and quality) of IgGRT in CVID. Methods and findings With input from a literature search, we built a health-economic model for cost-effectiveness and cost-utility assessment of IgGRT in CVID. We compared a mean literature-based dose ([greater than or equal to]450mg/kg/4wks) to a zero-or-low dose (0 to [less than or equal to]100 mg/kg/4wks) in a simulated cohort of adult patients from time of diagnosis until death; we also estimated the economic impact of diagnostic delay in this simulated cohort. Compared to no or minimal treatment, IgGRT showed an incremental benefit of 17 life-years (LYs) and 11 quality-adjusted life-years (QALYs), resulting in an incremental cost-effectiveness ratio (ICER) of [euro]29,296/LY and [euro]46,717/QALY. These results were robust in a sensitivity analysis. Reducing diagnostic delay by 4 years provided an incremental benefit of six LYs and four QALYs compared to simulated patients with delayed IgGRT initiation, resulting in an ICER of [euro]30,374/LY and [euro]47,495/QALY. Conclusions The health-economic model suggests that early initiation of IgGRT compared to no or delayed IgGRT is highly cost-effective. CVID-patients' access to IgGRT should be facilitated, not only because of proven clinical efficacy, but also due to the now demonstrated cost-effectiveness. Common variable immunodeficiency disorders (CVID), the most common form of primary antibody deficiency, are rare conditions associated with considerable morbidity and mortality. The clinical benefit of immunoglobulin replacement therapy (IgGRT) is substantial: timely treatment with appropriate doses significantly reduces mortality and the incidence of CVID-complications such as major infections and bronchiectasis. Unfortunately, CVID-patients still face a median diagnostic delay of 4 years. Their disease burden, expressed in annual loss of disability-adjusted life years, is 3-fold higher than in the general population. Hurdles to treatment access and reimbursement by healthcare payers may exist because the value of IgGRT is poorly documented. This paper aims to demonstrate cost-effectiveness and cost-utility (on life expectancy and quality) of IgGRT in CVID. With input from a literature search, we built a health-economic model for cost-effectiveness and cost-utility assessment of IgGRT in CVID. We compared a mean literature-based dose (≥450mg/kg/4wks) to a zero-or-low dose (0 to ≤100 mg/kg/4wks) in a simulated cohort of adult patients from time of diagnosis until death; we also estimated the economic impact of diagnostic delay in this simulated cohort. Compared to no or minimal treatment, IgGRT showed an incremental benefit of 17 life-years (LYs) and 11 quality-adjusted life-years (QALYs), resulting in an incremental cost-effectiveness ratio (ICER) of €29,296/LY and €46,717/QALY. These results were robust in a sensitivity analysis. Reducing diagnostic delay by 4 years provided an incremental benefit of six LYs and four QALYs compared to simulated patients with delayed IgGRT initiation, resulting in an ICER of €30,374/LY and €47,495/QALY. The health-economic model suggests that early initiation of IgGRT compared to no or delayed IgGRT is highly cost-effective. CVID-patients' access to IgGRT should be facilitated, not only because of proven clinical efficacy, but also due to the now demonstrated cost-effectiveness. About the Authors: Philippe van Wilder Roles Conceptualization, Data curation, Formal analysis, Methodology, Validation, Visualization, Writing – original draft, Writing – review & editing Affiliation: Research Centre in Health Economics, School of Public Health, Université Libre de Bruxelles, Brussels, Belgium Irina Odnoletkova Roles Conceptualization, Funding acquisition, Methodology, Writing – review & editing Affiliation: Research Centre in Health Economics, School of Public Health, Université Libre de Bruxelles, Brussels, Belgium Mehdi Mouline Roles Formal analysis, Writing – review & editing Affiliation: Research Centre in Health Economics, School of Public Health, Université Libre de Bruxelles, Brussels, Belgium Esther de Vries Roles Data curation, Methodology, Supervision, Visualization, Writing – original draft, Writing – review & editing * E-mail: e.devries@tilburguniversity.edu Affiliations Dept Tranzo, Tilburg School of Social and Behavioral Sciences, Tilburg University, Tilburg, The Netherlands, Laboratory of Medical Microbiology and Immunology, Elisabeth-Tweesteden Hospital, Tilburg, The Netherlands ORCID logo https://orcid.org/0000-0003-4311-3550 Introduction A rare disease is often characterized by high morbidity and mortality [1] and is defined as a condition with a low number of affected patients (typically <5/10,000) by regulatory authorities [2]. [...]analysis of the European Society for Immunodeficiencies (ESID) Registry database, containing data on 2,700 European patients with CVID, identified that current practice shows a significant variation in monthly IgGRT-doses across European countries with a mean (standard deviation; SD) of 454 (196) mg/kg; the analysis also showed that a diagnostic delay of several years occurred in over 80% of the cohort [3]. [...]decision makers and clinicians make coverage and treatment decisions based solely on cost estimations rather than on the cost-effectiveness assessment of IgGRT. Age, time horizon and the dose of ≥450mg/kg/4 weeks were selected based on the mean age at diagnosis, the median life expectancy on IgGRT and the mean IgG-dose administered in the ESID Registry study, respectively [3]; the limit of ≤100mg/kg/4 weeks was selected because this was the lowest dose in a meta-analysis of clinical studies that evaluated the incidence of pneumonia based on IgGRT-dose and IgG trough levels in antibody deficient patients [13]. Common variable immunodeficiency disorders (CVID), the most common form of primary antibody deficiency, are rare conditions associated with considerable morbidity and mortality. The clinical benefit of immunoglobulin replacement therapy (IgGRT) is substantial: timely treatment with appropriate doses significantly reduces mortality and the incidence of CVID-complications such as major infections and bronchiectasis. Unfortunately, CVID-patients still face a median diagnostic delay of 4 years. Their disease burden, expressed in annual loss of disability-adjusted life years, is 3-fold higher than in the general population. Hurdles to treatment access and reimbursement by healthcare payers may exist because the value of IgGRT is poorly documented. This paper aims to demonstrate cost-effectiveness and cost-utility (on life expectancy and quality) of IgGRT in CVID. With input from a literature search, we built a health-economic model for cost-effectiveness and cost-utility assessment of IgGRT in CVID. We compared a mean literature-based dose ([greater than or equal to]450mg/kg/4wks) to a zero-or-low dose (0 to [less than or equal to]100 mg/kg/4wks) in a simulated cohort of adult patients from time of diagnosis until death; we also estimated the economic impact of diagnostic delay in this simulated cohort. The health-economic model suggests that early initiation of IgGRT compared to no or delayed IgGRT is highly cost-effective. CVID-patients' access to IgGRT should be facilitated, not only because of proven clinical efficacy, but also due to the now demonstrated cost-effectiveness. |
Audience | Academic |
Author | de Vries, Esther Mouline, Mehdi van Wilder, Philippe Odnoletkova, Irina |
AuthorAffiliation | University of South Carolina College of Pharmacy, UNITED STATES 1 Research Centre in Health Economics, School of Public Health, Université Libre de Bruxelles, Brussels, Belgium 2 Dept Tranzo, Tilburg School of Social and Behavioral Sciences, Tilburg University, Tilburg, The Netherlands 3 Laboratory of Medical Microbiology and Immunology, Elisabeth-Tweesteden Hospital, Tilburg, The Netherlands |
AuthorAffiliation_xml | – name: 3 Laboratory of Medical Microbiology and Immunology, Elisabeth-Tweesteden Hospital, Tilburg, The Netherlands – name: University of South Carolina College of Pharmacy, UNITED STATES – name: 1 Research Centre in Health Economics, School of Public Health, Université Libre de Bruxelles, Brussels, Belgium – name: 2 Dept Tranzo, Tilburg School of Social and Behavioral Sciences, Tilburg University, Tilburg, The Netherlands |
Author_xml | – sequence: 1 givenname: Philippe surname: van Wilder fullname: van Wilder, Philippe organization: Research Centre in Health Economics, School of Public Health, Université Libre de Bruxelles, Brussels, Belgium – sequence: 2 givenname: Irina surname: Odnoletkova fullname: Odnoletkova, Irina organization: Research Centre in Health Economics, School of Public Health, Université Libre de Bruxelles, Brussels, Belgium – sequence: 3 givenname: Mehdi surname: Mouline fullname: Mouline, Mehdi organization: Research Centre in Health Economics, School of Public Health, Université Libre de Bruxelles, Brussels, Belgium – sequence: 4 givenname: Esther orcidid: 0000-0003-4311-3550 surname: de Vries fullname: de Vries, Esther organization: Laboratory of Medical Microbiology and Immunology, Elisabeth-Tweesteden Hospital, Tilburg, The Netherlands |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33661975$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_cveq_2024_04_005 crossref_primary_10_1016_j_jaip_2022_08_041 crossref_primary_10_1177_17534666241253945 crossref_primary_10_1007_s00467_022_05757_1 crossref_primary_10_3390_jcm13061717 crossref_primary_10_3389_fimmu_2024_1413231 crossref_primary_10_1007_s00430_022_00759_0 crossref_primary_10_1016_j_jaip_2022_05_017 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Competing Interests: I have read the journal’s policy and the authors of this manuscript have the following competing interests: both EdV and PvW received funding from PPTA to perform the work. EdV has received a research grant from Shire/Takeda for performing independent research on unclassified antibody deficiency. This does not alter our adherence to PLOS ONE policies on sharing data and materials. |
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Snippet | Common variable immunodeficiency disorders (CVID), the most common form of primary antibody deficiency, are rare conditions associated with considerable... Background Common variable immunodeficiency disorders (CVID), the most common form of primary antibody deficiency, are rare conditions associated with... BACKGROUNDCommon variable immunodeficiency disorders (CVID), the most common form of primary antibody deficiency, are rare conditions associated with... BackgroundCommon variable immunodeficiency disorders (CVID), the most common form of primary antibody deficiency, are rare conditions associated with... About the Authors: Philippe van Wilder Roles Conceptualization, Data curation, Formal analysis, Methodology, Validation, Visualization, Writing – original... |
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SubjectTerms | Antibodies Biology and Life Sciences Care and treatment Chronic illnesses Clinical decision making Common variable immunodeficiency Common Variable Immunodeficiency - economics Common Variable Immunodeficiency - therapy Cost analysis Cost-Benefit Analysis Decision making Disease Economic analysis Economic aspects Economic models Economics Editing Estimates Genetic aspects Health economics Humans Immunoglobulin G Immunoglobulins Immunoglobulins - administration & dosage Immunoglobulins - economics Immunoglobulins - therapeutic use Immunological deficiency syndromes Immunology Infections Life Expectancy Life span Mean Medicine and Health Sciences Meta-analysis Methodology Microbiology Models, Economic Morbidity Mortality Patients Physical sciences Physiological aspects Pneumonia Public health Quality of Life Quality-Adjusted Life Years Rare diseases Regulatory agencies Research and analysis methods Research facilities Social Sciences Society Testing Treatment Outcome Visualization |
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Title | Immunoglobulin Replacement Therapy is critical and cost-effective in increasing life expectancy and quality of life in patients suffering from Common Variable Immunodeficiency Disorders (CVID): A health-economic assessment |
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