There have been a couple
of publications on sarilumab at the ACR 2015 Annual Meeting in San Francisco. I
guess that the proliferation of studies hints at Sanofi thinks to bring
sarilumab to the market. I think, it’s still too soon to apply for FDA approval.
But let’s look at some of the studies; I’ll quote all studies under references
with a link to the ACR Meeting Abstracts.
Vibeke Strand and
colleagues presented: “Impact of Sarilumab on Fatigue, Pain, Morning Stiffness,
Productivity, and Health Related Quality of Life (HRQoL) in Patients with
Active Rheumatoid Arthritis Who Were Inadequate Responders or Intolerant of
Anti-TNF-α Therapy: Results from a Phase 3 Study (RCT)” This Phase 3 RCT [randomized
controlled trial] showed statistically significant and clinically meaningful
changes from baseline in fatigue, morning stiffness, pain, productivity and
participation, rheumatoid arthritis impact scores and health related quality of
life at Week 24.
There were several studies
that looked at different dosages and combinations like the one presented by Roy
Fleischmann et al. (Abstract No. 970 / Sarilumab in combination with CsDMARDs
in patients with active RA and inadequate responders or intolerant of Anti–TNF-alpha
Therapy), Arthur Kavanaugh et al. ( ABSTRACT No. 2760 / Efficacy and safety of
sarilumab plus MTX in patients with RA), Mark C. Genovese et al. (ABSTRACT No.
2770 / Efficacy of sarilumab plus methotrexate in achieving clinical Remission
in patients with active, moderate-to-severe RA), Maxime Dougados et al. (ABSTRACT
No. 2761 / IL-6R blockade with sarilumab plus methotrexate results in changes
in clinical and laboratory parameters associated with chronic inflammation), or
another evalution by Vibeke Strand et al. (ABSTRACT No. 2313 / Responder rates
and numbers needed to treat).
Paul Emery and colleagues
presented: “Safety and Tolerability of Subcutaneous Sarilumab Compared to
Intravenous Tocilizumab in Patients with RA”. Conclusion: “Overall, there was
no clinically meaningful difference between the treatment groups with regards
to clinical adverse events. Laboratory changes noted in the sarilumab groups
were within the same range as those noted in the tocilizumab groups. […]”.
Gerd Burmester and colleagues
looked at: “Sarilumab Dose Reduction to Manage Laboratory Abnormalities in an
Open-Label Extension Study in RA Patients”. Conclusions: “In this study,
reducing the dose from 200 mg q2w to 150 mg q2w to manage laboratory
abnormalities allowed the majority of patients to continue in the study for a
mean duration of >1.5 years. For patients continuing in the study, these
laboratory abnormalities improved during the 6 months following dose reduction,
and efficacy was maintained.” Two points: 1. necessity to reduce dose at all
makes me uneasy, 2. if efficacy is maintained, why use a higher dosage at all?
There might be at least a subgroup of patients, in whom a lower dosage could be
possible.
Now, we come to Anita Boyapati and colleagues, who presented: “Evaluation
of Bone and Joint Proteins for Prognostic Association with Radiographic
Progression and Disease Activity in Methotrexate Inadequate Responder
Rheumatoid Arthritis Patients in a Sarilumab Phase 3 Study”. Methods: “Serum markers
[RANKL, MMP-3 and MMP-cleaved fragments of collagen types 1 and 3 (C1M and C3M)]
were measured at baseline and posttreatment in patients receiving Pbo +MTX
(n=128) or subcutaneous SAR 200 mg q2w + MTX (n=131).” Conclusion: “Analysis of
markers […] showed correlation in MOBILITY patients. These data suggest that
multivariate analysis of markers may be necessary to identify increased risk of
joint destruction and elevated disease activity in patients with established RA.”
And it shows, what isn’ seen – the necessity of results on radiographic
progression. But it isn’t a shortcoming of this study.
I’m following the development around sarilumab for a couple of years
now. I still hope that the drug comes to the market. But … do we need
sarilumab? What could sarilumab give us, which we can’t get from tocilizumab? Will
I split up my IL-6 inhibitor patients in two groups? Right now I can’t answer
these questions. And still we need data on radiographic progression.
References:
Strand V, Kosinski M, Graham N, Chen CI, Joseph GJ, Bauer D, Lin Y,
Pacheco-Tena C, Fleischmann R. Impact of Sarilumab on Fatigue, Pain, Morning
Stiffness, Productivity, and Health Related Quality of Life (HRQoL) in Patients
with Active Rheumatoid Arthritis Who Were Inadequate Responders or Intolerant of
Anti-TNF-α Therapy: Results from a Phase 3 Study (RCT) [abstract]. Arthritis Rheumatol. 2015; 67 (suppl
10). http://acrabstracts.org/abstract/impact-of-sarilumab-on-fatigue-pain-morning-stiffness-productivity-and-health-related-quality-of-life-hrqol-in-patients-with-active-rheumatoid-arthritis-who-were-inadequate-responders-or-intoler/.
Accessed November 17, 2015.
Fleischmann R,
Castelar-Pinheiro G, Brzezicki J, Hrycaj P, Lin Y, van Adelsberg J, Graham N,
van Hoogstraten H, Bauer D, Burmester G. Efficacy and Safety of Sarilumab in
Combination with Csdmards in Patients with Active Rheumatoid Arthritis Who Were
Inadequate Responders or Intolerant of Anti–TNF-α Therapy: Results from a
Phase 3 Study [abstract]. Arthritis
Rheumatol. 2015; 67 (suppl 10). http://acrabstracts.org/abstract/efficacy-and-safety-of-sarilumab-in-combination-with-csdmards-in-patients-with-active-rheumatoid-arthritis-who-were-inadequate-responders-or-intolerant-of-antiaetnf-i%c2%b1-therapy-results-f/.
Accessed November 17, 2015.
Kavanaugh A, Kivitz AJ,
Miranda P, Fiore S, Fay J, Fan C, van Adelsberg J, Huizinga TWJ. Efficacy and
Safety of Sarilumab Plus MTX in Subgroups of Patients with Rheumatoid Arthritis
in a Phase 3 Study [abstract]. Arthritis
Rheumatol. 2015; 67 (suppl 10). http://acrabstracts.org/abstract/efficacy-and-safety-of-sarilumab-plus-mtx-in-subgroups-of-patients-with-rheumatoid-arthritis-in-a-phase-3-study/.
Accessed November 17, 2015.
Genovese MC, Stanislav M, van Hoogstraten H, Martincova R, Fan C, van
Adelsberg J. Efficacy of Sarilumab Plus Methotrexate in Achieving Clinical
Remission, Using 4 Different Definitions, in Patients with Active,
Moderate-to-Severe Rheumatoid Arthritis in a Phase 3 Study [abstract]. Arthritis Rheumatol. 2015; 67 (suppl
10). http://acrabstracts.org/abstract/efficacy-of-sarilumab-plus-methotrexate-in-achieving-clinical-remission-using-4-different-definitions-in-patients-with-active-moderate-to-severe-rheumatoid-arthritis-in-a-phase-3-study/.
Accessed November 17, 2015.
Dougados M, Choy EH, Kameda H, van Adelsberg J, Fay J, Fiore S, Fan C,
Schett G. IL-6R Blockade with Sarilumab Plus Methotrexate Results in Changes in
Clinical and Laboratory Parameters Associated with Chronic Inflammation in
Patients with Moderate-to-Severe RA in a Phase 3 Study [abstract]. Arthritis Rheumatol. 2015; 67 (suppl
10). http://acrabstracts.org/abstract/il-6r-blockade-with-sarilumab-plus-methotrexate-results-in-changes-in-clinical-and-laboratory-parameters-associated-with-chronic-inflammation-in-patients-with-moderate-to-severe-ra-in-a-phase-3-study/.
Accessed November 17, 2015.
Strand V, Rendas-Baum R, Joseph GJ, Chen CI, van Hoogstraten H, Huizinga
TWJ, Genovese MC. Responder Rates and Numbers Needed to Treat Based on
Clinically Meaningful Improvements in Patient Reported Outcomes (PROs)
Including Health-Related Quality of Life (HRQoL) after Sarilumab Treatment
during a Phase III Randomized Controlled Trial (RCT) [abstract]. Arthritis Rheumatol. 2015; 67 (suppl
10). http://acrabstracts.org/abstract/responder-rates-and-numbers-needed-to-treat-based-on-clinically-meaningful-improvements-in-patient-reported-outcomes-pros-including-health-related-quality-of-life-hrqol-after-sarilumab-treatment-d/.
Accessed November 17, 2015.
Emery P, Rondon J, Garg A,
van Hoogstraten H, Graham N, Liu M, Parrino J, Spindler AJ, Liu N. Safety and
Tolerability of Subcutaneous Sarilumab Compared to Intravenous Tocilizumab in
Patients with RA [abstract]. Arthritis Rheumatol. 2015; 67
(suppl 10). http://acrabstracts.org/abstract/safety-and-tolerability-of-subcutaneous-sarilumab-compared-to-intravenous-tocilizumab-in-patients-with-ra/.
Accessed November 17, 2015.
Burmester G, Garg A, van
Hoogstraten H, Graham N, Boddy A, Parrino J, Genovese MC. Sarilumab Dose
Reduction to Manage Laboratory Abnormalities in an Open-Label Extension Study
in RA Patients [abstract]. Arthritis
Rheumatol. 2015; 67 (suppl 10). http://acrabstracts.org/abstract/sarilumab-dose-reduction-to-manage-laboratory-abnormalities-in-an-open-label-extension-study-in-ra-patients/.
Accessed November 17, 2015.
Boyapati A, Msihid J, Hamilton JD, Gabay C, Graham N, Fiore S.
Evaluation of Bone and Joint Proteins for Prognostic Association with
Radiographic Progression and Disease Activity in Methotrexate Inadequate Responder
Rheumatoid Arthritis Patients in a Sarilumab Phase 3 Study [abstract]. Arthritis Rheumatol. 2015; 67 (suppl
10). http://acrabstracts.org/abstract/evaluation-of-bone-and-joint-proteins-for-prognostic-association-with-radiographic-progression-and-disease-activity-in-methotrexate-inadequate-responder-rheumatoid-arthritis-patients-in-a-sarilumab-ph/.
Accessed November 17, 2015.
Sarilumab at the EULAR 2014 Meeting in Paris http://rheumatologe.blogspot.de/2014/06/sarilumab-at-eular-2014-meeting-in-paris.html
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