Background Strontium ranelate is currently used for osteoporosis. The international, double-blind, randomised, placebo-controlled Strontium ranelate Efficacy in Knee OsteoarthrItis triAl evaluated its effect on radiological progression of knee osteoarthritis.
Methods Patients with knee osteoarthritis (Kellgren and Lawrence grade 2 or 3, and joint space width (JSW) 2.5–5 mm) were randomly allocated to strontium ranelate 1 g/day (n=558), 2 g/day (n=566) or placebo (n=559). The primary endpoint was radiographical change in JSW (medial tibiofemoral compartment) over 3 years versus placebo. Secondary endpoints included radiological progression, Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score, and knee pain. The trial is registered (ISRCTN41323372).
Results The intention-to-treat population included 1371 patients. Treatment with strontium ranelate was associated with smaller degradations in JSW than placebo (1 g/day: −0.23 (SD 0.56) mm; 2 g/day: −0.27 (SD 0.63) mm; placebo: −0.37 (SD 0.59) mm); treatment-placebo differences were 0.14 (SE 0.04), 95% CI 0.05 to 0.23, p<0.001 for 1 g/day and 0.10 (SE 0.04), 95% CI 0.02 to 0.19, p=0.018 for 2 g/day. Fewer radiological progressors were observed with strontium ranelate (p<0.001 and p=0.012 for 1 and 2 g/day). There were greater reductions in total WOMAC score (p=0.045), pain subscore (p=0.028), physical function subscore (p=0.099) and knee pain (p=0.065) with strontium ranelate 2 g/day. Strontium ranelate was well tolerated.
Conclusions Treatment with strontium ranelate 1 and 2 g/day is associated with a significant effect on structure in patients with knee osteoarthritis, and a beneficial effect on symptoms for strontium ranelate 2 g/day.
- Knee Osteoarthritis
- Outcomes research
This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/3.0/ and http://creativecommons.org/licenses/by-nc/3.0/legalcode
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Osteoarthritis is characterised by degeneration of cartilage and other structures in the joint, including subchondral bone.1 It is the most prevalent joint disease, and up to 40% of those over 65 may suffer from knee or hip osteoarthritis.2 Current management strategies focus on relieving symptoms and improving function through non-pharmacological and pharmacological approaches, and surgical procedures, including osteotomy, subchondral bone stimulation and possibly joint distraction, with the final option of joint replacement if these efforts fail.1 ,3 Pharmacological approaches include analgesics, anti-inflammatory agents, intra-articular corticosteroids or hyaluronic acid, glucosamine sulphate, chondroitin sulphate or some experimental treatments, none of which are registered as structure-modifying.
Strontium ranelate is currently indicated for the management of postmenopausal osteoporosis, and may be hypothesised to act on both cartilage and subchondral bone. Preclinical in vitro studies indicate that it inhibits subchondral bone resorption4 and stimulates cartilage matrix formation in normal and osteoarthritic human chondrocytes.5 ,6 Exploratory analyses suggest that 3 years’ treatment with strontium ranelate attenuates radiological progression of spinal osteoarthritis and improves back pain.7 The aim of the 3-year international, double-blind, randomised, placebo-controlled trial—Strontium ranelate Efficacy in Knee OsteoarthrItis triAl (SEKOIA)—described herein was to evaluate the effect of strontium ranelate on radiological and clinical progression of knee osteoarthritis.
Study design and patients
SEKOIA was an international, multicentre, randomised, double-blind, placebo-controlled phase 3 trial in outpatients with knee osteoarthritis mainly in secondary care. This 3-year study was performed in 98 centres in 18 countries. The selection criteria defined eligible patients as Caucasian ambulatory men and women aged ≥50 years with knee osteoarthritis according to American College of Rheumatology criteria,8 with pain on at least half of the days of the previous month (intensity ≥40 mm on a 100-mm visual analogue scale). On radiography, included patients were Kellgren and Lawrence9 grade 2 (ie, definite osteophytes and possible narrowing of joint space) or grade 3 (ie, moderate multiple osteophytes, definite narrowing of joint space and some sclerosis, and possible deformity of bone ends), and had joint space width (JSW) of 2.5 to 5 mm with predominant knee osteoarthritis of the medial tibiofemoral compartment. The investigator defined the target knee at selection. If both knees fulfilled the selection criteria, the target knee was the most painful; if both were equally painful, the target had the highest Kellgren and Lawrence grade and/or the lowest JSW; and if both had the same radiological score, the target knee was defined by the investigator's judgement. Exclusion criteria included knee prosthesis, recent intra-articular injection (notably glucocorticoids <3 months previously or hyaluronic acid <6 months previously), clinical deformities, secondary knee osteoarthritis, previous treatments acting on cartilage or bone metabolism (eg, oral or intravenous bisphosphonates <1 year previously, teriparatide or raloxifene <7 days prior to selection, and oral glucosamine ≥1500 mg/day and chondroitin sulphate <3 months previously), and a medical history or a high risk of venous thromboembolism (contraindication for strontium ranelate). Further details of other inclusion and exclusion criteria, and more information on trial design, have been published elsewhere.10
The study conformed to the principles of the Declaration of Helsinki; it was approved by the ethics committee or institutional review board of every site. All patients provided written informed consent before randomisation. The trial is registered (ISRCTN41323372).
Treatment allocation and masking
At inclusion, patients were randomly allocated to three treatment groups (strontium ranelate 1 or 2 g/day or placebo) using a centralised interactive voice response system with balanced randomisation stratified by centre and gender (block size, 3). Patients were instructed to take one sachet daily of study treatment with water at bedtime after a 2-h fast. Patients and investigators were blinded to treatment allocation, and study treatments had identical appearance. During the study, patients were allowed physiotherapy, rehabilitation, alternative medicines and pain relief as necessary. Except for study medication, any pain medication was to be stopped at least five half-lives before a visit for symptom assessment. The investigators instructed their patients how long they had to stop pain medication prior to a visit, giving a number of days defined for each available treatment in a specific country. Treatments acting on cartilage (chondroitin, glucosamine sulphate ≥1500 mg) or bone metabolism (bisphosphonates), and glucocorticoids (oral, inhaled >1500 μg/day, or intra-articular, except in cases of medical need) were not allowed.10 The first patient visit was on 28 April 2006 and recruitment ended on 10 March 2008. The last visit was on 17 February 2011.
Interventions and outcomes
Knee radiographs were performed on both knees at selection and then annually on the target knee alone or upon withdrawal (patients treated >6 months), using a standardised technique described elsewhere.10 Briefly, the radiographer recorded a fixed flexion posterioanterior view (fixed angle 10°), using a SynaFlexer positioning frame (Synarc Inc, San Francisco, California, USA).11 Quality control procedures (Synarc Inc, Hamburg) included specifications related to image acquisition and collection (eg, depiction, positioning and beam angle); regular training for radiology technicians; determination of radiographical eligibility; and onsite and centralised digitisation and quality control of radiographs.10 All radiographs were measured centrally (INSERM UMR 1033, Lyon, France) by a single reader blinded to treatment allocation and patient identity. Each blinded post-baseline image was measured in comparison with the inclusion image to optimise reproducibility and sensitivity.12–14
Minimal JSW (mm) at the medial tibiofemoral compartment was measured using a standardised computer-assisted method, as described elsewhere.10 ,15 In short, magnification was determined (radio-opaque ruler) and a region of interest was delimited by a horizontal tangent to the inferior edges of each femoral condyle and two perpendiculars to the condylar margins. Within an area defined automatically by two parallel lines 15mm apart (with one 10 mm from the condyle line), the observer delineated the tibial and femoral bone margins, to depict a polygon; JSW was the diameter of the smallest circle (automatically calculated) included in this polygon. Intrareader reproducibility was evaluated at yearly intervals, using 70 knee radiographs unlinked to the study; it was satisfactory (intraclass correlation coefficient for JSW >0.90).12 A second reading was performed by a single reader in another centre (Liege, Belgium), independently of the first centre, using the same method; inter-reader reproducibility was good (intraclass correlation coefficient for JSW >0.90).
Other investigations included Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and global knee pain (visual analogue scale) at inclusion and six monthly intervals. WOMAC evaluates osteoarthritis health status and outcomes via 24 questions,16 expressed as a total score and pain, stiffness and physical function subscores. Each subscore is normalised to 100 mm and the total WOMAC score is the sum of the three normalised subscores, that is, maximal value is 300 mm, with the lower scores indicating a better status. Urine samples were collected at baseline, at 3, 6 and 12 months, and at yearly intervals thereafter, for assessment of C telopeptide of type II procollagen (CTX-II), a biomarker for cartilage turn-over (performed by Supreme SA, Liege, Belgium, using an ELISA, Urine CartiLaps, ImmunDiagnostic System Nordic, Denmark). Compliance was evaluated by sachet counts. Safety assessment included recording of adverse events and clinical and laboratory parameters.
The primary endpoint was radiographical change in JSW from baseline to last evaluation over 3 years in treatment groups versus placebo. Secondary endpoints included radiological progression (joint space narrowing (JSN) ≥0.5 mm over 3 years); radioclinical progression (JSN ≥0.5 mm, and lack of improvement in WOMAC pain (≤20%) over 3 years); WOMAC scores; global knee pain; and urinary CTX-II levels.
At the time of the study design, the literature data on JSN progression were unclear, and a possible extension of the follow-up time to 3 years was planned if radiological progression was lower than expected. The initial sample size calculation estimated that 960 patients would be necessary for >90% power, assuming an SD of 0.7 and a 40% dropout rate to detect a significant between-group difference in JSN of 0.3 mm at 2 years (two-sided Dunnett test, 5% type I error). This was amended to 0.2 mm (±10%, ie, between 0.18 and 0.22 mm) in May 2007, following new findings of a lower progression in JSN in the placebo group than previously published,17 leading to an estimated sample size of 2127 patients. In March 2008, the Executive Committee decided to prolong the study to 3 years, in view of results of a blinded re-estimation of radiological progression (212 patients) indicating JSN of 0.06±0.42 mm after 1 year. The final estimated sample size was therefore 1600 patients allowing a treatment-placebo difference in JSN of 0.2 mm (±10%) at 3 years with an SD of 0.5 mm.
All efficacy analyses were conducted according to the intention-to-treat (ITT) principle. The ITT population included all randomised patients who had taken at least one dose of treatment and who had an assessable baseline and one post-baseline evaluation of JSW.
Baseline characteristics are presented as numbers (%) or mean±SD. Treatment-placebo difference in primary endpoint from baseline to last value was analysed using a general linear model with baseline, centre and gender as covariates, producing estimates and SEs of the adjusted differences, 95% CIs (Dunnett type) and p values (adjusted according to Dunnett-Hsu18). A range of sensitivity analyses (described in online supplementary table S1) were conducted to investigate the impact of missing data on treatment effect. For secondary outcomes, treatment-placebo differences in radiological and radioclinical progression from baseline to last value were analysed as estimates of the between-group difference (SE) with associated 95% CI and p value (χ2 test). Treatment-placebo differences in WOMAC scores and global knee pain were analysed using mixed model for repeated measurements and the adjusted general linear model. Treatment effect was studied using a Mann-Whitney-Wilcoxon test for CTX-II (non-Gaussian distribution). Safety data are presented as number (%) of events.
The two-sided type I error rate was set at 5%. The results were analysed by the Biostatistics Division of the Institut de Recherches Internationales Servier, using SAS (V.9.1). The main analysis was confirmed by the Department of Public Health Epidemiology and Health Economics, University of Liege, Belgium.
Role of the funding source
The Executive Committee was responsible for the study design, interpretation of the results, and manuscript preparation; they had full access to study data. The sponsor was responsible for data management and statistical analyses. The sponsor supported the work of the Executive Committee, but made no scientific or research decisions independent of this committee.
Three thousand four hundred and thirty-eight patients were selected, 1683 were included and allocated to treatment (558 strontium ranelate 1 g/day; 566 strontium ranelate 2 g/day; and 559 placebo) and 974 (58%) patients completed the study (figure 1). The ITT population included 1371 patients (82% of randomised patients) followed for 29.8±10.5 months (mean±SD).
There were no relevant between-group differences at baseline (table 1). Mean age of the randomised patients was 62.9±7.5 years with a majority of women (70%). Body mass index was 29.9±5.0 kg/m2. The target knee JSW was 3.50±0.84 mm at baseline, patients were Kellgren and Lawrence grade 2 (62%) or 3 (38%) and total WOMAC score was 132.4±62.4 mm. The mean duration of knee osteoarthritis was 76.7±77.7 months (about 6.4 years). One thousand three hundred and four (76%) patients reported a medical history of musculoskeletal or connective tissue disorders, mainly back pain (9%), arthralgia (8%), osteopenia (5%) and osteoporosis (5%). At inclusion, 1148 (68%) patients were taking treatment for osteoarthritis, mainly propionic acid-related treatments (18%), acetic acid derivatives (12%) or anilides (32%). Only seven patients were taking glucosamine and one chondroitin sulphate. In general, 39% of the patients were receiving analgesics, and three patients systemic corticosteroids for their osteoarthritis. There were no relevant differences in baseline characteristics between completed and withdrawn patients, between randomised and ITT populations or between ITT groups at baseline (table 1).
Mean compliance was 93.3±9.3% (ITT population). During the study, 1278 patients (76% of the randomised set) received at least one concomitant treatment for osteoarthritis, mainly propionic acid derivatives (25%), acetic acid derivatives (18%) and anilides (39%). Forty-six per cent of the patients took analgesics with an indication for osteoarthritis, 13 patients received glucosamine, three chondroitin sulphate, and two a combination of the two agents; 5% of the patients received systemic corticoids for their osteoarthritis. There was no relevant between-group difference (see online supplementary table S2).
JSN in the placebo group was −0.37±0.59 mm over the study. Treatment with strontium ranelate was associated with significantly attenuated JSN versus placebo, with −0.23±0.56 mm for 1 g/day and −0.27±0.63 mm for 2 g/day from baseline to end (table 2). The estimate of the treatment-placebo difference was significant for both dosages (p<0.001 for 1 g/day and p=0.018 for 2 g/day) (figure 2). Similar results were found in the second reading and a range of sensitivity analyses to assess the impact of missing data (see online supplementary table S1).
There were significantly fewer radiological and radioclinical progressors with strontium ranelate 1 and 2 g/day (table 2). Treatment with strontium ranelate 2 g/day was associated with significantly lower WOMAC total score (p=0.045) and pain subscore (p=0.028), and a trend toward lower physical function subscore (p=0.099) and global knee pain (p=0.065) (table 2, figure 2). None of these reductions was significant at 1 g/day. Urinary CTX-II decreased in all groups, and the between-group difference in the relative change was significant for both dosages versus placebo (p=0.003 for 1 g/day and p=0.021 for 2 g/day).
The change in JSW from baseline was significantly different from placebo in both treatment groups at 12, 24 and 36 months, with no difference between the dosages at any time (p=0.601 at 12 months, p=0.149 at 24 months and p=0.311 at 36 months). The reduction in total WOMAC score and pain subscore was numerically greater with treatment than placebo at every visit, with a significant between-group difference for pain subscore at 36 months (p=0.029 for 2 g/day). The treatment-placebo difference in radiological and radioclinical progressors was significant in both treatment groups at every visit (figure 3).
Strontium ranelate was well tolerated (table 3).19 The rate of venous thromboembolic events was <1% in all groups, and there were no cases of drug reaction with eosinophilia and systemic symptoms. There were no relevant differences in clinical or laboratory parameters, with the possible exception of creatine phosphokinase, which increased from baseline with treatment (11.7±85.6 and 20.7±104.4 IU/l with 1 and 2 g/day, respectively), but not placebo (−0.4±68.1 IU/l); eight patients (three, one and four patients in the 1 g/day, 2 g/day, and placebo groups, respectively) had values greater than five times the upper limit of normal.
Our results demonstrate that strontium ranelate has structure-modifying activity in patients with knee osteoarthritis, with significantly smaller degradations in JSW over the study (p<0.001 for 1 g/day and p=0.018 for 2 g/day vs placebo). There were fewer patients with radiographical and radioclinical progression of osteoarthritis in the treatment groups. Additionally to this structural effect, symptomatic improvement was observed, with a significant impact on WOMAC total score and pain subscore (p=0.045 and p=0.028, respectively), and a trend towards improvement in global knee pain (p=0.065) at 2 g/day, but not 1 g/day. The safety profile of strontium ranelate was satisfactory, in line with knowledge of this agent.20 ,21 There was a slight mean increase in creatine phosphokinase in the treated groups as previously described for strontium ranelate.20 Pooled analysis in osteoporotic patients treated with strontium ranelate showed that increases were mainly mild, transient and reversible22; they were not associated with any clinical muscular symptoms.
These results come from a single study with a large sample size. The robustness of our observation of a structure-modifying effect for strontium ranelate is demonstrated by a range of sensitivity analyses and the rigorous methodology used for radiography acquisition and reading.10 In this context, the trial was carried out in accordance with current European and US regulatory guidelines,23 ,24 in terms of design and efficacy evaluation.
Osteoarthritis is not a uniform disease entity, and different phenotypes clearly exist, driven by variable changes in bone, cartilage and synovium; the links between these phenotypes are unclear.1 Strontium ranelate may exert structure-modifying effects through influences on chondrocyte and bone cell function. Evidence to support an action on cartilage via chondrocytes includes: the treatment-placebo difference in urinary CTX-II in our study, which suggests lower cartilage metabolism and possibly reduced osteophyte formation; a report that strontium ranelate stimulates cartilage matrix formation in vitro,5 implying restoration of the balance between chondrocyte formation and resorption; a direct effect of strontium ranelate on proteoglycan synthesis5; and an indirect effect on insulin growth factor-1 (IGF-1).6 ,25
Strontium ranelate is known to influence bone; however, it is unclear whether its effect on cartilage is direct or secondary to an effect on subchondral bone. Defective subchondral bone metabolism in osteoarthritis could modify chondrocytes in cartilage via local factors released during subchondral bone remodelling.26 Strontium ranelate may decrease in vitro subchondral bone resorption via the osteoprotegerin/RANK ligand pathway in subchondral osteoblasts and by downregulating metalloproteases 2 and 9.4 Similar findings have been reported for strontium ranelate in osteoporotic bone.27 ,28 These effects on subchondral bone may directly alter the progression of osteoarthritis, or modify cartilage response to mechanical loading.
We observed differential effects of the two doses of strontium ranelate: structure appeared to be modified at both 1 and 2 g/day, while symptoms required 2 g/day for significant amelioration. This supports published evidence for different aetiological pathways in structural and symptomatic osteoarthritis.29 Osteoarthritic pain may have several causes (synovitis, osteophytes and bone marrow oedema), which are all related to inflammation or bone, rather than cartilage, which is considered to be aneural. We could hypothesise that both dosages affect the aetiological pathways leading to structure modification, but only 2 g/day has an additional effect on pain, possibly through its action on bone though further clinical and preclinical studies are required to explore this in more depth. In line with this, strontium ranelate has strong dose-dependent effects on bone mineral density in osteoporosis with a clinical effect at 2 g/day.30 Further evidence to support heterogeneity between structure and symptoms is the inconsistency noted between radiological grade and knee pain or function.31 ,32 Alternative interpretations include floor and ceiling effects in pain outcome measures; and the fluctuating symptomatic natural history of osteoarthritis.33 These results raise the interesting question of whether structure modification and pain relief can both be gained by a single drug or whether a combination of drugs would be necessary in osteoarthritis.
Strontium ranelate 2 g/day would therefore be the most appropriate dosage for clinical practice since it was associated with a 27% reduction in radiological JSN (a surrogate of cartilage loss) versus placebo. This translates into nearly a year of average radiological osteoarthritis progression saved over 3 years. Moreover, our results imply that 14 patients (95% CI 9 to 57) would need to be treated with 2 g/day strontium ranelate over the study duration to prevent one case of radiological progression ≥0.5 mm, a threshold known to predict osteoarthritis-related surgery.34 Moreover, the modification of structure observed in patients with knee osteoarthritis with strontium ranelate in our study is clinically relevant, since it is accompanied by a beneficial effect on symptoms.
There are several limitations to our study. One is the difficulty of evaluating the magnitude of pain changes due to both a relatively high placebo response, which is common to all other osteoarthritis trials,35 and the difficult interpretation of changes evaluated as means as opposed to individual improvements. The dropout rate (14% annualised; mostly for non-medical reasons (consent withdrawal)) could be regarded as a limitation; however, the annualised rate is similar to those reported for other osteoarthritis trials (11% to 16%).17 ,33 ,36–40 Aside from a possible role of the disease itself, the rate of withdrawals may be affected by study duration and the number of assessments in a relatively young population. This was anticipated in the sample size calculations, and sensitivity analyses demonstrated minimal impact of missing data. Moreover, the baseline characteristics of dropouts were similar to those of the ITT population and completers, implying that premature withdrawal did not lead to the selection of a particular subpopulation. Another limitation is the possibility of different phenotypes in osteoarthritis,1 suggesting that strontium ranelate might be more effective in certain subgroups of osteoarthritis patients, for example, those with dominant subchondral bone changes. Finally, like all studies of this type, potential causes of radiographical JSN other than cartilage thinning, such as meniscal extrusion, cannot be excluded.
In conclusion, treatment with strontium ranelate 1 and 2 g/day was associated with a significant effect on structure in patients with knee osteoarthritis. Additionally to this structure-modifying activity, there was a beneficial effect on symptoms at 2 g/day.
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Files in this Data Supplement:
Contributors All authors participated in the design of the study, the interpretation of the data, and the writing of the article. The statistical analysis was done by the sponsor and the main analysis was independently confirmed by the Department of Public Health Epidemiology and Health Economics, University of Liege, Belgium. All authors have read and approved the final version. Study committees, coordinators and investigators are listed in an online appendix.
Funding Servier, France.
Competing interests JYR, JB, NB, WB, RC, XC, CC, HG, FN, EN, PNS, TDS and CC have received fees, research grants, or both from Servier. JYR has also received consulting fees, paid advisory boards, lecture fees, and/or grant support from Novartis, Negma, Lilly, Wyeth, Amgen, GlaxoSmithKline, Roche, Merckle, Nycomed, NPS, Theramex, UCB, Merck Sharp and Dohme, Rottapharm, IBSA, Genevrier, Teijin, Teva, Ebewee Pharma, Zodiac, Analis, Novo-Nordisk and Bristol Myers Squibb. NB is the registered copyright and trademark holder of the WOMAC Index, and the trademark and registered copyright holder of the AUSCAN index. HG has also received consulting fees or honoraria from Amgen, Novartis, Lilly, Roche, GSK, BMS, Pfizer and Merck. TDS has received fees for consulting or advisory boards from Ono Pharma, Expanscience, MSD and Amgen. CC has received consulting fees and paid advisory boards for Alliance for Better Bone Health, Glaxo Smith Kline, Roche, Merck Sharp and Dohme, Lilly, Amgen, Wyeth, Novartis and Nycomed.
Ethics approval Ethics committees or institutional review boards of every site.
Provenance and peer review Not commissioned; externally peer reviewed.
Open Access This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/