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Published in: BMC Musculoskeletal Disorders 1/2019

Open Access 01-12-2019 | Osteoarthrosis | Research article

Incidence of total hip and total knee replacements from the prospective epidemiologic risk factor study: considerations for event driven clinical trial design

Authors: Cecilie L. Bager, Morten Karsdal, Asger Bihlet, Christian Thudium, Inger Byrjalsen, Anne C. Bay-Jensen

Published in: BMC Musculoskeletal Disorders | Issue 1/2019

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Abstract

Background

Osteoarthritis (OA) leads to joint failure and total joint replacement (TJR, either hip (H) or knee (K)). Worsening of pain and joint space narrowing are believed to be surrogates for joint failure; however, we hypothesize that TJR, as a reflection of joint failure, can be used as an endpoint in event-driven clinical trials within a reasonable duration. We explored the incidence of TJR in the Prospective Epidemiologic Risk Factor (PERF I) study.

Methods

A total of 5855 Danish postmenopausal women aged 49–88 enrolled in the PERF I study during 1999–2001 (baseline). Three-, six- and twelve-year follow-up data from the Danish National Patient Registry was collected, including occurrence of TJR and OA diagnosis. At baseline the women were asked whether they had OA.

Results

The women with a TJR diagnosis before or after baseline were on average 1 year older (p < 0.001) and heavier (p < 0.001), compared to women with no TJR. The 3-, 6- and 12-year cumulative incidences were 1.1, 2.4 and 6.0% for TKR, and 2.1, 4.4 and 9.3% for THR. For those with an OA diagnosis at baseline the respective incidences were 2.7, 5.6 and 11.7% and 3.9, 7.2 and 13.6%

Conclusions

Within 3, 6 or 12 years TJR incidences were double for women with an OA diagnosis compared to the all-comer population. TJRs are frequent amongst elderly women with OA and it is, therefore, feasible to conduct event-driven clinical trials where TJR is the endpoint demonstrating clinical benefit of a novel disease-modifying OA drug (DMOAD).
Literature
2.
go back to reference Karsdal MA, Michaelis M, Ladel C, Siebuhr AS, Bihlet AR, Andersen JR, et al. Disease-modifying treatments for osteoarthritis (DMOADs) of the knee and hip: lessons learned from failures and opportunities for the future. Osteoarthr Cartil. 2016;24.CrossRef Karsdal MA, Michaelis M, Ladel C, Siebuhr AS, Bihlet AR, Andersen JR, et al. Disease-modifying treatments for osteoarthritis (DMOADs) of the knee and hip: lessons learned from failures and opportunities for the future. Osteoarthr Cartil. 2016;24.CrossRef
3.
go back to reference Kraus VB, Blanco FJ, Englund M, Karsdal MA, Lohmander LS. Call for standardized definitions of osteoarthritis and risk stratification for clinical trials and clinical use. Osteoarthr Cartil. 2015;23.CrossRef Kraus VB, Blanco FJ, Englund M, Karsdal MA, Lohmander LS. Call for standardized definitions of osteoarthritis and risk stratification for clinical trials and clinical use. Osteoarthr Cartil. 2015;23.CrossRef
4.
go back to reference Karsdal MA, Bihlet A, Byrjalsen I, Alexandersen P, Ladel C, Michaels M, et al. OA phenotypes, rather than disease stage, drive structural progression - identification of structural progressors from 2 phase III randomized clinical studies with symptomatic knee OA. Osteoarthr Cartil. 2015;23.CrossRef Karsdal MA, Bihlet A, Byrjalsen I, Alexandersen P, Ladel C, Michaels M, et al. OA phenotypes, rather than disease stage, drive structural progression - identification of structural progressors from 2 phase III randomized clinical studies with symptomatic knee OA. Osteoarthr Cartil. 2015;23.CrossRef
6.
go back to reference Kraus VB, Simon LS, Katz JN, Neogi T, Hunter D, Guermazi A, et al. Proposed study designs for approval based on a surrogate endpoint and a post-marketing confirmatory study under FDA’s accelerated approval regulations for disease modifying osteoarthritis drugs. Osteoarthr Cartil [Internet]. 2019;27:571–9 Available from: http://www.ncbi.nlm.nih.gov/pubmed/30465809.CrossRef Kraus VB, Simon LS, Katz JN, Neogi T, Hunter D, Guermazi A, et al. Proposed study designs for approval based on a surrogate endpoint and a post-marketing confirmatory study under FDA’s accelerated approval regulations for disease modifying osteoarthritis drugs. Osteoarthr Cartil [Internet]. 2019;27:571–9 Available from: http://​www.​ncbi.​nlm.​nih.​gov/​pubmed/​30465809.CrossRef
8.
go back to reference Karsdal MA, Byrjalsen I, Alexandersen P, Bihlet A, Andersen JR, Riis BJ, et al. Treatment of symptomatic knee osteoarthritis with oral salmon calcitonin: results from two phase 3 trials. Osteoarthr Cartil. 2015;23.CrossRef Karsdal MA, Byrjalsen I, Alexandersen P, Bihlet A, Andersen JR, Riis BJ, et al. Treatment of symptomatic knee osteoarthritis with oral salmon calcitonin: results from two phase 3 trials. Osteoarthr Cartil. 2015;23.CrossRef
9.
go back to reference Wirth W, Hunter DJ, Nevitt MC, Sharma L, Kwoh CK, Ladel CZ, et al. Predictive and concurrent validity of cartilage thickness change as a marker of knee osteoarthritis progression: data from the Osteoarthritis initiative. Osteoarthr Cartil [Internet]. 2017;25:2063–2071. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28838858.CrossRef Wirth W, Hunter DJ, Nevitt MC, Sharma L, Kwoh CK, Ladel CZ, et al. Predictive and concurrent validity of cartilage thickness change as a marker of knee osteoarthritis progression: data from the Osteoarthritis initiative. Osteoarthr Cartil [Internet]. 2017;25:2063–2071. Available from: http://​www.​ncbi.​nlm.​nih.​gov/​pubmed/​28838858.CrossRef
11.
go back to reference FDA. title:osteoarthritis: Structural Endpoints for the Development of Drugs, Devices, and Biological Products for Treatment Guidance for Industry. 2018. p. 1–6. FDA. title:osteoarthritis: Structural Endpoints for the Development of Drugs, Devices, and Biological Products for Treatment Guidance for Industry. 2018. p. 1–6.
12.
go back to reference Jonsson H, Olafsdottir S, Sigurdardottir S, Aspelund T, Eiriksdottir G, Sigurdsson S, et al. Incidence and prevalence of total joint replacements due to osteoarthritis in the elderly: risk factors and factors associated with late life prevalence in the AGES-Reykjavik study. BMC Musculoskelet Disord [Internet]. 2016;17:14 Available from: http://www.ncbi.nlm.nih.gov/pubmed/4711057.CrossRef Jonsson H, Olafsdottir S, Sigurdardottir S, Aspelund T, Eiriksdottir G, Sigurdsson S, et al. Incidence and prevalence of total joint replacements due to osteoarthritis in the elderly: risk factors and factors associated with late life prevalence in the AGES-Reykjavik study. BMC Musculoskelet Disord [Internet]. 2016;17:14 Available from: http://​www.​ncbi.​nlm.​nih.​gov/​pubmed/​4711057.CrossRef
14.
go back to reference Gossec L, Paternotte S, Maillefert JF, Combescure C, Conaghan PG, Davis AM, et al. The role of pain and functional impairment in the decision to recommend total joint replacement in hip and knee osteoarthritis: an international cross-sectional study of 1909 patients. Report of the OARSI-OMERACT task force on total joint replacement. Osteoarthr Cartil [Internet]. 2011;19:147–54 Available from: http://www.ncbi.nlm.nih.gov/pubmed/21044689.CrossRef Gossec L, Paternotte S, Maillefert JF, Combescure C, Conaghan PG, Davis AM, et al. The role of pain and functional impairment in the decision to recommend total joint replacement in hip and knee osteoarthritis: an international cross-sectional study of 1909 patients. Report of the OARSI-OMERACT task force on total joint replacement. Osteoarthr Cartil [Internet]. 2011;19:147–54 Available from: http://​www.​ncbi.​nlm.​nih.​gov/​pubmed/​21044689.CrossRef
15.
16.
go back to reference Neergaard JS, Dragsbæk K, Kehlet SN, Hansen HB, Hansen G, Byrjalsen I, et al. Cohort profile: the prospective epidemiological risk factor (PERF) study. Int J Epidemiol. 2017;46. Neergaard JS, Dragsbæk K, Kehlet SN, Hansen HB, Hansen G, Byrjalsen I, et al. Cohort profile: the prospective epidemiological risk factor (PERF) study. Int J Epidemiol. 2017;46.
18.
go back to reference Henriksen K, Byrjalsen I, Andersen JR, Bihlet AR, Russo LA, Alexandersen P, et al. A randomized, double-blind, multicenter, placebo-controlled study to evaluate the efficacy and safety of oral salmon calcitonin in the treatment of osteoporosis in postmenopausal women taking calcium and vitamin D. Bone. 2016;91. Henriksen K, Byrjalsen I, Andersen JR, Bihlet AR, Russo LA, Alexandersen P, et al. A randomized, double-blind, multicenter, placebo-controlled study to evaluate the efficacy and safety of oral salmon calcitonin in the treatment of osteoporosis in postmenopausal women taking calcium and vitamin D. Bone. 2016;91.
20.
go back to reference Niu J, Nevitt M, McCulloch C, Torner J, Lewis CE, Katz JN, et al. Comparing the functional impact of knee replacements in two cohorts. BMC Musculoskelet Disord. 2014. Niu J, Nevitt M, McCulloch C, Torner J, Lewis CE, Katz JN, et al. Comparing the functional impact of knee replacements in two cohorts. BMC Musculoskelet Disord. 2014.
25.
go back to reference Lenguerrand E, Whitehouse MR, Beswick AD, Kunutsor SK, Foguet P, Porter M, et al. Risk factors associated with revision for prosthetic joint infection following knee replacement: an observational cohort study from England and Wales. Lancet Infect Dis [Internet]. 2019; Available from: http://www.ncbi.nlm.nih.gov/pubmed/31005559. Lenguerrand E, Whitehouse MR, Beswick AD, Kunutsor SK, Foguet P, Porter M, et al. Risk factors associated with revision for prosthetic joint infection following knee replacement: an observational cohort study from England and Wales. Lancet Infect Dis [Internet]. 2019; Available from: http://​www.​ncbi.​nlm.​nih.​gov/​pubmed/​31005559.
27.
29.
go back to reference Singh JA, Dohm M, Choong PF. Consensus on draft OMERACT core domains for clinical trials of Total joint replacement outcome by orthopaedic surgeons: a report from the international consensus on outcome measures in TJR trials (I-COMiTT) group. BMC Musculoskelet Disord [Internet]. 2017;18:45. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28125985. Singh JA, Dohm M, Choong PF. Consensus on draft OMERACT core domains for clinical trials of Total joint replacement outcome by orthopaedic surgeons: a report from the international consensus on outcome measures in TJR trials (I-COMiTT) group. BMC Musculoskelet Disord [Internet]. 2017;18:45. Available from: http://​www.​ncbi.​nlm.​nih.​gov/​pubmed/​28125985.
30.
go back to reference Singh JA, Dowsey MM, Dohm M, Goodman SM, Leong AL, Scholte Voshaar MMJH, et al. Achieving consensus on Total joint replacement trial outcome reporting using the OMERACT filter: endorsement of the final Core domain set for Total hip and Total knee replacement trials for Endstage arthritis. J Rheumatol [Internet]. 2017;44:1723–1726. Available from: http://www.ncbi.nlm.nih.gov/pubmed/28089984.CrossRef Singh JA, Dowsey MM, Dohm M, Goodman SM, Leong AL, Scholte Voshaar MMJH, et al. Achieving consensus on Total joint replacement trial outcome reporting using the OMERACT filter: endorsement of the final Core domain set for Total hip and Total knee replacement trials for Endstage arthritis. J Rheumatol [Internet]. 2017;44:1723–1726. Available from: http://​www.​ncbi.​nlm.​nih.​gov/​pubmed/​28089984.CrossRef
31.
go back to reference Kanis JA, Johnell O, Oden A, Johansson H, McCloskey E. FRAX™ and the assessment of fracture probability in men and women from the UK. Osteoporos Int. 2008. Kanis JA, Johnell O, Oden A, Johansson H, McCloskey E. FRAX™ and the assessment of fracture probability in men and women from the UK. Osteoporos Int. 2008.
32.
go back to reference Arends RHGP, Karsdal MA, Verburg KM, West CR, Bay-Jensen AC, Keller DS. Identification of serological biomarker profiles associated with total joint replacement in osteoarthritis patients. Osteoarthr Cartil. 2017:25. Arends RHGP, Karsdal MA, Verburg KM, West CR, Bay-Jensen AC, Keller DS. Identification of serological biomarker profiles associated with total joint replacement in osteoarthritis patients. Osteoarthr Cartil. 2017:25.
Metadata
Title
Incidence of total hip and total knee replacements from the prospective epidemiologic risk factor study: considerations for event driven clinical trial design
Authors
Cecilie L. Bager
Morten Karsdal
Asger Bihlet
Christian Thudium
Inger Byrjalsen
Anne C. Bay-Jensen
Publication date
01-12-2019
Publisher
BioMed Central
Published in
BMC Musculoskeletal Disorders / Issue 1/2019
Electronic ISSN: 1471-2474
DOI
https://doi.org/10.1186/s12891-019-2680-3

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