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Recent advances in rheumatoid arthritis
DR. Satyabrata sahoo
DM Resident Clinical Pharmacology
Department of Clinical & Experimental Pharmacology
School of Tropical Medicine, Kolkata
10/29/2021 1
Content
• Introduction
• Pathophysiology
• Clinical feaures
• Lab findings
• Complications
• Quality of life
• Recent advances in management
• Clinical trials
• summary
10/29/2021 2
Introduction
• Rheumatoid arthritis (RA): a chronic autoimmune inflammatory disorder of
unknown etiology that occurs in approximately 1% of the population (Albani and
Carson 1997).
• Common autoimmune disease associated with progressive disability, systemic
complications, early death and socioeconomic costs.
• More prevalent among women than men
• Develops in the fourth and fifth decades of life(Kavanaugh and Lipsky 1996).
• Symptoms are pain, stiffness, and swelling of the joints resulting in impaired
physical function.
• Often accompanied by constitutional symptoms such as fever and malaise (Grassi
et al. 1998).
• Synovial inflammation
10/29/2021 3
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Clinical features
• Joint pain
• Swelling
• Fever
• Fatigue
• Morning stiffness
• Deformity etc.
10/29/2021 8
Lab findings
• CRP ,ESR
• Anti CCP antibody- most specific
• Anti MCV antibody-most sensitive
• MRI- synovitis, joint effusion, bone marrow edema
• Ultrasound-synovitis, erosion
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Management
• Non pharmacological:
 Physiotherapy
 Occupational therapy
 Hand exercise programmes
 Podiatry
 Psychological interventions
 Diet and complementary therapies
 surgery
• Pharmacological therapy:
 NSAIDs, cDMARDs, steroids, biologicals, biosimilars
• New therapies in research: gene therapy, nanotherapy, stem cell
therapy etc
10/29/2021 15
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• Background: To evaluate the effect of Filgotinib vs placebo on the
signs and symptoms of RA in a treatment refractory population
• Method: Randomised placebo controlled multinational phase 3 trial
• Intervention: Filgotinib 200mg(n=148), Filgotinib 100mg(n=153)or
placebo(n=148)
• Result: Among 448 patients 360 women [80.4%]; mean [SD] DAS28-
CRP score, 5.9 [0.96]; 105 [23.4%] with3 prior bDMARDs), 381(85%)
completed the study.
• At week 12, more patients receiving filgotinib, 200mg (66.0%) or
100mg (57.5%), achieved ACR20 response (placebo, 31.1%)P < .001
• Conclusion: significantly greater proportion of clinical response by
Filgotinib
10/29/2021 22
Background: Methotrexate+adalimumab is more effective than ADA monotherapy.
Assessment of toxicity of different doses of Methotrexate and treatment efficacy of
ADA+MTX in two trials
Method: Data originated from Concerto, efficacy assessed by ACR50
Result: In CONCERTO, ACR50 rates increased over time,ranging from 54% to 68% at
week 26, while AE rates remained steady, ranging from 2.4% to 17.8% at week 26
• In MUSICA, ACR50 rates increased over time, and were 32.3% and 37.5% at week
24, while MTX related AE rates remained steady and were 6.5% at week24
Conclusion: In patients with RA initiating ADA+MTX combination, treatment
efficacy was achieved and increased throughout both trials, while rates of MTX
related AEs remained steady.
10/29/2021 23
Summary
• The recent developments in the management strategies for
rheumatoid arthritis have made significant contribution to reducing
the disease progression and improving outcomes of the patients.
• Identifying the candidates early in 'window of opportunity" and
aggressive target oriented approach can prove to be a boon to the
patients in long run.
• The addition of biologic agents to the armamentarium of available
disease modifying agents early in course of the disease can result in
satisfying functional recovery and even remission in patients of RA.
• With judicious use of medications and careful monitoring quality of
life of patients with RA can be surely improved.
10/29/2021 24
References
1.Goodman & Gilman’s the pharmacological basis of therapeutics 13th edition
2. J MGIMS, September 2012, Vol 17, No (ii), 6 – 127 M Joshi
3. J R Coll Physicians Edinb 2005; 35:239–245
© 2005 RCPE
4. www.tcd.ie/tsmj
5. www.co-rheumatology.com
6. Burmester GR, et al. RMD Open 2017;3:e000465. doi:10.1136/rmdopen-
2017-000465
7. NICE guideline
8. N Engl J Med 2011;365:2205-19.Copyright © 2011 Massachusetts Medical
Society.
9. P.A. Borea (ed.), A 291 3 Adenosine Receptors from Cell Biology to
Pharmacology and Therapeutics, DOI 10.1007/978-90-481-3144-0_15.
10/29/2021 25
THANK YOU
10/29/2021 26

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Recent advances in rheumatoid arthritis

  • 1. Recent advances in rheumatoid arthritis DR. Satyabrata sahoo DM Resident Clinical Pharmacology Department of Clinical & Experimental Pharmacology School of Tropical Medicine, Kolkata 10/29/2021 1
  • 2. Content • Introduction • Pathophysiology • Clinical feaures • Lab findings • Complications • Quality of life • Recent advances in management • Clinical trials • summary 10/29/2021 2
  • 3. Introduction • Rheumatoid arthritis (RA): a chronic autoimmune inflammatory disorder of unknown etiology that occurs in approximately 1% of the population (Albani and Carson 1997). • Common autoimmune disease associated with progressive disability, systemic complications, early death and socioeconomic costs. • More prevalent among women than men • Develops in the fourth and fifth decades of life(Kavanaugh and Lipsky 1996). • Symptoms are pain, stiffness, and swelling of the joints resulting in impaired physical function. • Often accompanied by constitutional symptoms such as fever and malaise (Grassi et al. 1998). • Synovial inflammation 10/29/2021 3
  • 8. Clinical features • Joint pain • Swelling • Fever • Fatigue • Morning stiffness • Deformity etc. 10/29/2021 8
  • 9. Lab findings • CRP ,ESR • Anti CCP antibody- most specific • Anti MCV antibody-most sensitive • MRI- synovitis, joint effusion, bone marrow edema • Ultrasound-synovitis, erosion 10/29/2021 9
  • 15. Management • Non pharmacological:  Physiotherapy  Occupational therapy  Hand exercise programmes  Podiatry  Psychological interventions  Diet and complementary therapies  surgery • Pharmacological therapy:  NSAIDs, cDMARDs, steroids, biologicals, biosimilars • New therapies in research: gene therapy, nanotherapy, stem cell therapy etc 10/29/2021 15
  • 22. • Background: To evaluate the effect of Filgotinib vs placebo on the signs and symptoms of RA in a treatment refractory population • Method: Randomised placebo controlled multinational phase 3 trial • Intervention: Filgotinib 200mg(n=148), Filgotinib 100mg(n=153)or placebo(n=148) • Result: Among 448 patients 360 women [80.4%]; mean [SD] DAS28- CRP score, 5.9 [0.96]; 105 [23.4%] with3 prior bDMARDs), 381(85%) completed the study. • At week 12, more patients receiving filgotinib, 200mg (66.0%) or 100mg (57.5%), achieved ACR20 response (placebo, 31.1%)P < .001 • Conclusion: significantly greater proportion of clinical response by Filgotinib 10/29/2021 22
  • 23. Background: Methotrexate+adalimumab is more effective than ADA monotherapy. Assessment of toxicity of different doses of Methotrexate and treatment efficacy of ADA+MTX in two trials Method: Data originated from Concerto, efficacy assessed by ACR50 Result: In CONCERTO, ACR50 rates increased over time,ranging from 54% to 68% at week 26, while AE rates remained steady, ranging from 2.4% to 17.8% at week 26 • In MUSICA, ACR50 rates increased over time, and were 32.3% and 37.5% at week 24, while MTX related AE rates remained steady and were 6.5% at week24 Conclusion: In patients with RA initiating ADA+MTX combination, treatment efficacy was achieved and increased throughout both trials, while rates of MTX related AEs remained steady. 10/29/2021 23
  • 24. Summary • The recent developments in the management strategies for rheumatoid arthritis have made significant contribution to reducing the disease progression and improving outcomes of the patients. • Identifying the candidates early in 'window of opportunity" and aggressive target oriented approach can prove to be a boon to the patients in long run. • The addition of biologic agents to the armamentarium of available disease modifying agents early in course of the disease can result in satisfying functional recovery and even remission in patients of RA. • With judicious use of medications and careful monitoring quality of life of patients with RA can be surely improved. 10/29/2021 24
  • 25. References 1.Goodman & Gilman’s the pharmacological basis of therapeutics 13th edition 2. J MGIMS, September 2012, Vol 17, No (ii), 6 – 127 M Joshi 3. J R Coll Physicians Edinb 2005; 35:239–245 © 2005 RCPE 4. www.tcd.ie/tsmj 5. www.co-rheumatology.com 6. Burmester GR, et al. RMD Open 2017;3:e000465. doi:10.1136/rmdopen- 2017-000465 7. NICE guideline 8. N Engl J Med 2011;365:2205-19.Copyright © 2011 Massachusetts Medical Society. 9. P.A. Borea (ed.), A 291 3 Adenosine Receptors from Cell Biology to Pharmacology and Therapeutics, DOI 10.1007/978-90-481-3144-0_15. 10/29/2021 25