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Uso de la terapia biológica en indicaciones no “aprobadas” Claudio Galarza Maldonado MD PhD UNERA Cuenca, Ecuador
Insidious Consequences of“evidence-based medicine” based only on randomized clinical trials  Implicit goal to rely on data from randomized clinical trials as the primary source for all clinical knowledge Rheumatologists are frequent authors of manuscripts and presenters of lectures concerning clinical trials which they did not design or analyze, but rarely present data from their own clinical care.  Virtual abandonment by most clinicians of careful observation of their own clinical experience.   Theodore Pincus, M.D.
Acute exsudative inflammatory reaction I n f l a m a c i o n Celsus: The four cardinal symptoms of inflammation
endocrine response para- or autocrine response Cellular communication is mediated through cytokines receptor C signal C C
C Cytokines can activate their target cells differently target cell production of mediators C proliferation / cell division C differentiation / maturation C migration Z C (mediators: chemokines)
Cytokines can activate their target cells differently target cell but most often cytokines exert  an anti-apoptic action C apoptosis C Z
The correct response of the target cell to cytokines  is crucial magnitude  of respone too strong too long  normal response  too short too weak duration of response signal  new signal  C excessive      production         of            mediators C C C C C C C C C C C C C C C target cell mediator-independent activation (mutations) inefficient shut-down of the signal cascade too many receptors  possible disease development overshooting response of the target cell
Evolution of Biotechnology Monoclonalantibodiesproduced Recombinanthuman insulin approved DNA double helix structure revealed Biologicals approved for clinical use DNAcloned Polymerase chain reactions Genetic codeelucidated First therapeutic MAb approved  (muromonab) Human genome mapped First human protein synthesized (growth hormone) 2000+ 1953 1961-1965 1973 1975 1977 1982 1986 1983 (1962)–MedicineWatson, Crick,Wilkins (1968)–MedicineHolley, Khorana,Nirenberg (1980)–ChemistryBerg, Gilbert,Sanger (1984)–MedicineJerne, Köhler,Milstein (1993)–ChemistryMullis Nobel Prizes (Year Awarded) Historical Events in Biotechnology. Available at: www.biotechinstitute.org/what_is/timeline.html. Accessed August 10, 2007. All Nobel Laureates. Available at: www./nobelprize.org. Accessed August 10, 2007
INFLIXIMAB RITUXIMAB ETANERCEPT ADALIMUMAB
TNF Plays a Central Role in I.M.I.D.s Crohn’s Disease Rheumatoid Arthritis Ankylosing  Spondylitis Psoriasis TNF Uveitis Psoriatic Arthritis
I.M.I.D.s: Cytokines and Disease Phenotype
Asthma Allergy CD3 Neutrophil IL-13 IL-5 IL-4 IgE TNFa IL-8 TH2 Mast/Basophil B TH1 Eosinophil Macrophage CD3 APC RA         		Type I DM UC Crohn’s		MS Psoriasis	COPD       Uveitis Sarcoidosis Osteoarthritis Graft Rejection TP CD3 Neutrophil TREG Ig TC TNFa CD3 MCP-1 IL-18 IL-1 Monocyte IL-6 IL-23 IL-21 B IL-12 Neutrophil Pathogenic T Cell Development Imbalance  Local Tissue Inflammation  Tissue damage Fibrosis Sensitization  I.M.I.D.s: Patogenesis.
Agentes anti-TNFα Infliximab  Adalimumab Etanercept  Murine (mouse) Fab  TNF binding region Extracellular domain of  Human p75 TNF receptor Human Fab  TNF binding region Human Fc region Human Fc region  Human Fc region  Mikuls TR, et al. Curr Rheumatol Rep. 2003,5:270.
INFLIXIMAB LUPUS SINDROME ANTIFOSFOLIPIDICO VASCULITIS
Autoimmun REV2011 May 18.  Therapeutic blockade of TNF in patients with SLE-Promising or crazy? Aringer M, Smolen JS
Neumonitis lupica aguda
Terapia de inducciòn a cortoplazo Infliximab en LUPUS
RITUXIMAB EN DOSIS MENORES A LAS APROBADAS EN ARTRITIS REUMATOIDE. EN LUPUS, DOSIS DE 500X2.
Alcanzar la remisión y si esto no es posible, lograr la mínima actividad de la enfermedad. Evitar la perdida de la capacidad funcional Controlar la inflamación Evitar la progresión radiológica Mejorar la calidad de vida
RolPotencial de lasCélula B en la Immunopatogénesis de la AR Secreción de citokinaspro-inflamatorias Presentaciónde Antigeno ActivaciónCel. T Producción deAuto-anticuerpos y superpetuación SeñalIntracelular Cell B Cell B Cell B Dendritic cell CellPlasmática cell T  IL-6 IL-10 TNF- RF TNF- RF RF Macrofago RF RF Fija complemento IL-1 IL-10 TNF- Daño inflamatorio IL-6 Sinoviainflamada Pérdida de cartilago Edwards 1999, Gause 2001, Zhang 1986, Takemura 2001, Dörner 2003, Shaw 2003
Some Pragmatic Limitations of Randomized Controlled Clinical Trials in Chronic DiseasesJ ClinEpidemiol  41:1037,1988; Arthritis Rheum  48:313, 2003  Statistically significant results not necessarily clinically important, and vice versa Tuulikki Sokka, Theodore Pincus
HIPOTESIS Inducción de remisión en pacientes con LES, bajo el tratamiento de Rituximab en dosis 500x2.
ENSAYO PILOTO CON DOS PAUTAS TERAPEUTICAS Все пациенты получали унифицированную терапию БПВП:  Глюкокортикостероиды + Микофенолата мофетил + Гидроксихлорохин
RTX 1000X2 VS RTX 500 X 2 RTX1000 RTX500
NO MAME GALLO !!!
Mario  Cardiel MD MSc Jefe de la Unidad de Investigación “Dr. Mario Alvizouri Muñoz” del Hospital General “Dr. Miguel Silva” de la Secretaría de Salud del Estado de Michoacán  Julio Molineros, Ph.D. Associate Research Scientist Arthritis & Clinical Immunology Research ProgramOklahoma Medical Research Foundation
ETANERCEPT SINDROME ANTIFOSFOLIPIDICO OBSTETRICO GOTA
SÍNDROME ANTIFOSFOLIPÍDICO Y EMBARAZO Pérdidas fetales Prematuridad Retraso del crecimiento intrauterino Pre-eclampsia
Desprendimiento laminar placentario14-08-08 Hematoma retrocorial de 22 x 6 mm agudo
28-08-2008 Hematoma retrocorial con disminución de tamaño a 17 mm.
17-10-2008 Reabsorción de hematoma, con placenta de características normales.
11 02 2009Embarazo de 36 semanas de gestación promedio, crecimiento normal.  
D.A. Clark / Journal of Reproductive Immunology 85 (2010) 15–24
ADALIMUMAB EN ARTRITIS TEMPRANA 40 MG AL MES
Do Conventional Methods Give Us What We Need?  X-ray at month 9 -Gd +Gd -Gd +Gd STIR Baseline -Gd +Gd -Gd +Gd STIR 9 months later Østergaard, et al. Ann Rheum Dis 2005; 64: 1503-1506
Joint Erosions Occur Early in RA MTP Hand  All ,[object Object]
Erosions can be detected by MRI within 4 months of RA onset
Rate of progression is significantly (p<0.05) more rapid in the first year than in the second and third yearsMaximum joints affected %  Year Fuchs, et al. J Rheumatol 1989;16:585–591 McQueen, et al. Ann Rheum Dis 1998;57:350–356 van der Heijde, et al. J Rheumatol 1995;22:1792–1796
TIGHT CONTROL
Toda verdad pasa por tres fases:- Primera,  es ridiculizada.- Segunda, es combatida violentamente. - Tercera, es aceptada como evidente por sí misma Arthur Schopenhauer
Educacionen ARTRITIS PREMIO ILAR 2011 www.educ-ar.com/
REAL Red Excelencia Artritis Latinoamerica

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Posibles indicaciones y estrategias para el manejo "off label" de los biologicos

  • 1. Uso de la terapia biológica en indicaciones no “aprobadas” Claudio Galarza Maldonado MD PhD UNERA Cuenca, Ecuador
  • 2. Insidious Consequences of“evidence-based medicine” based only on randomized clinical trials Implicit goal to rely on data from randomized clinical trials as the primary source for all clinical knowledge Rheumatologists are frequent authors of manuscripts and presenters of lectures concerning clinical trials which they did not design or analyze, but rarely present data from their own clinical care. Virtual abandonment by most clinicians of careful observation of their own clinical experience. Theodore Pincus, M.D.
  • 3. Acute exsudative inflammatory reaction I n f l a m a c i o n Celsus: The four cardinal symptoms of inflammation
  • 4.
  • 5. endocrine response para- or autocrine response Cellular communication is mediated through cytokines receptor C signal C C
  • 6. C Cytokines can activate their target cells differently target cell production of mediators C proliferation / cell division C differentiation / maturation C migration Z C (mediators: chemokines)
  • 7. Cytokines can activate their target cells differently target cell but most often cytokines exert an anti-apoptic action C apoptosis C Z
  • 8. The correct response of the target cell to cytokines is crucial magnitude of respone too strong too long normal response too short too weak duration of response signal new signal C excessive production of mediators C C C C C C C C C C C C C C C target cell mediator-independent activation (mutations) inefficient shut-down of the signal cascade too many receptors  possible disease development overshooting response of the target cell
  • 9. Evolution of Biotechnology Monoclonalantibodiesproduced Recombinanthuman insulin approved DNA double helix structure revealed Biologicals approved for clinical use DNAcloned Polymerase chain reactions Genetic codeelucidated First therapeutic MAb approved (muromonab) Human genome mapped First human protein synthesized (growth hormone) 2000+ 1953 1961-1965 1973 1975 1977 1982 1986 1983 (1962)–MedicineWatson, Crick,Wilkins (1968)–MedicineHolley, Khorana,Nirenberg (1980)–ChemistryBerg, Gilbert,Sanger (1984)–MedicineJerne, Köhler,Milstein (1993)–ChemistryMullis Nobel Prizes (Year Awarded) Historical Events in Biotechnology. Available at: www.biotechinstitute.org/what_is/timeline.html. Accessed August 10, 2007. All Nobel Laureates. Available at: www./nobelprize.org. Accessed August 10, 2007
  • 11. TNF Plays a Central Role in I.M.I.D.s Crohn’s Disease Rheumatoid Arthritis Ankylosing Spondylitis Psoriasis TNF Uveitis Psoriatic Arthritis
  • 12. I.M.I.D.s: Cytokines and Disease Phenotype
  • 13. Asthma Allergy CD3 Neutrophil IL-13 IL-5 IL-4 IgE TNFa IL-8 TH2 Mast/Basophil B TH1 Eosinophil Macrophage CD3 APC RA Type I DM UC Crohn’s MS Psoriasis COPD Uveitis Sarcoidosis Osteoarthritis Graft Rejection TP CD3 Neutrophil TREG Ig TC TNFa CD3 MCP-1 IL-18 IL-1 Monocyte IL-6 IL-23 IL-21 B IL-12 Neutrophil Pathogenic T Cell Development Imbalance Local Tissue Inflammation Tissue damage Fibrosis Sensitization I.M.I.D.s: Patogenesis.
  • 14. Agentes anti-TNFα Infliximab Adalimumab Etanercept Murine (mouse) Fab TNF binding region Extracellular domain of Human p75 TNF receptor Human Fab TNF binding region Human Fc region Human Fc region Human Fc region Mikuls TR, et al. Curr Rheumatol Rep. 2003,5:270.
  • 15. INFLIXIMAB LUPUS SINDROME ANTIFOSFOLIPIDICO VASCULITIS
  • 16. Autoimmun REV2011 May 18. Therapeutic blockade of TNF in patients with SLE-Promising or crazy? Aringer M, Smolen JS
  • 17.
  • 19.
  • 20.
  • 21.
  • 22.
  • 23. Terapia de inducciòn a cortoplazo Infliximab en LUPUS
  • 24. RITUXIMAB EN DOSIS MENORES A LAS APROBADAS EN ARTRITIS REUMATOIDE. EN LUPUS, DOSIS DE 500X2.
  • 25.
  • 26. Alcanzar la remisión y si esto no es posible, lograr la mínima actividad de la enfermedad. Evitar la perdida de la capacidad funcional Controlar la inflamación Evitar la progresión radiológica Mejorar la calidad de vida
  • 27. RolPotencial de lasCélula B en la Immunopatogénesis de la AR Secreción de citokinaspro-inflamatorias Presentaciónde Antigeno ActivaciónCel. T Producción deAuto-anticuerpos y superpetuación SeñalIntracelular Cell B Cell B Cell B Dendritic cell CellPlasmática cell T IL-6 IL-10 TNF- RF TNF- RF RF Macrofago RF RF Fija complemento IL-1 IL-10 TNF- Daño inflamatorio IL-6 Sinoviainflamada Pérdida de cartilago Edwards 1999, Gause 2001, Zhang 1986, Takemura 2001, Dörner 2003, Shaw 2003
  • 28.
  • 29.
  • 30. Some Pragmatic Limitations of Randomized Controlled Clinical Trials in Chronic DiseasesJ ClinEpidemiol 41:1037,1988; Arthritis Rheum 48:313, 2003 Statistically significant results not necessarily clinically important, and vice versa Tuulikki Sokka, Theodore Pincus
  • 31.
  • 32.
  • 33.
  • 34. HIPOTESIS Inducción de remisión en pacientes con LES, bajo el tratamiento de Rituximab en dosis 500x2.
  • 35. ENSAYO PILOTO CON DOS PAUTAS TERAPEUTICAS Все пациенты получали унифицированную терапию БПВП: Глюкокортикостероиды + Микофенолата мофетил + Гидроксихлорохин
  • 36. RTX 1000X2 VS RTX 500 X 2 RTX1000 RTX500
  • 37.
  • 38.
  • 40. Mario Cardiel MD MSc Jefe de la Unidad de Investigación “Dr. Mario Alvizouri Muñoz” del Hospital General “Dr. Miguel Silva” de la Secretaría de Salud del Estado de Michoacán Julio Molineros, Ph.D. Associate Research Scientist Arthritis & Clinical Immunology Research ProgramOklahoma Medical Research Foundation
  • 41.
  • 42.
  • 43.
  • 45. SÍNDROME ANTIFOSFOLIPÍDICO Y EMBARAZO Pérdidas fetales Prematuridad Retraso del crecimiento intrauterino Pre-eclampsia
  • 46.
  • 47.
  • 48. Desprendimiento laminar placentario14-08-08 Hematoma retrocorial de 22 x 6 mm agudo
  • 49. 28-08-2008 Hematoma retrocorial con disminución de tamaño a 17 mm.
  • 50. 17-10-2008 Reabsorción de hematoma, con placenta de características normales.
  • 51. 11 02 2009Embarazo de 36 semanas de gestación promedio, crecimiento normal.  
  • 52.
  • 53.
  • 54.
  • 55.
  • 56. D.A. Clark / Journal of Reproductive Immunology 85 (2010) 15–24
  • 57.
  • 58. ADALIMUMAB EN ARTRITIS TEMPRANA 40 MG AL MES
  • 59. Do Conventional Methods Give Us What We Need? X-ray at month 9 -Gd +Gd -Gd +Gd STIR Baseline -Gd +Gd -Gd +Gd STIR 9 months later Østergaard, et al. Ann Rheum Dis 2005; 64: 1503-1506
  • 60.
  • 61. Erosions can be detected by MRI within 4 months of RA onset
  • 62. Rate of progression is significantly (p<0.05) more rapid in the first year than in the second and third yearsMaximum joints affected % Year Fuchs, et al. J Rheumatol 1989;16:585–591 McQueen, et al. Ann Rheum Dis 1998;57:350–356 van der Heijde, et al. J Rheumatol 1995;22:1792–1796
  • 63.
  • 64.
  • 65.
  • 67. Toda verdad pasa por tres fases:- Primera, es ridiculizada.- Segunda, es combatida violentamente. - Tercera, es aceptada como evidente por sí misma Arthur Schopenhauer
  • 68.
  • 69. Educacionen ARTRITIS PREMIO ILAR 2011 www.educ-ar.com/
  • 70. REAL Red Excelencia Artritis Latinoamerica