Ulcerative Colitis Therapy. Faculty Disclosure. Acknowledgements 28/11/2013. Amy Morse November 30/13

Similar documents
Efficacy and Safety of Treatment for Pediatric IBD

Indications for use of Infliximab

Efficacy and Safety of Treatment for Pediatric IBD

Medical Therapy for Pediatric IBD: Efficacy and Safety

Biologic Therapy for Inflammatory. Is Top-Down Too Top-Heavy? S. Devi Rampertab, MD, FACG, AGAF Associate Professor of Medicine University of Florida

Treatment Options. Suresh Pola, MD Kaiser San Diego

Ali Keshavarzian MD Rush University Medical Center

Doncaster & Bassetlaw Medicines Formulary

IBD Understanding Your Medications. Thomas V. Aguirre, MD Santa Barbara GI Consultants

Practical Risk Management Tools for Patients with IBD. Garth Swanson MD Rush University Medical Center

Moderately to severely active ulcerative colitis

To help protect your privacy, PowerPoint prevented this external picture from being automatically downloaded. To download and display this picture,

Slide 1 Medications in inflammatory bowel disease a primer for health care providers. Slide 2. Slide 3 Theory of pathogenesis. IBD - epidemiology

CCFA. Crohns Disease vs UC: What is the best treatment for me? November

IBD Module 2: Medication and Patient Management. Kami Roake, PharmD Rheumatology & Gastroenterology Pharmacist University of Utah Hospitals & Clinics

An Update on the Biologic Treatment for Patients with Inflammatory Bowel Disease. David A. Schwartz, MD

Of Treatment For Inflammatory Bowel Diseases

Treatment Goals. Current Therapeutic Pyramids Crohn s Disease Ulcerative Colitis 11/14/10

1. Background: Infliximab is administered parenterally; therefore, it is not covered under retail pharmacy benefits.

Pharmacotherapy of Inflammatory Bowel Disorder

Update on Biologics in Ulcerative Colitis. Scott Plevy, MD University of North Carolina Chapel Hill, NC

Dr. Elmer Schabel, MD. Bundesinstitut für Arzneimittel und Medizinprodukte, Bonn, Germany (No conflicts of interest)

New treatment options in UC. Rob Bryant IBD Consultant Royal Adelaide Hospital

COPYRIGHT. Inflammatory Bowel Disease What Every Clinician Needs to Know. Adam S. Cheifetz, MD. Director, Center for Inflammatory Bowel Disease

Anne Griffiths MD, FRCPC. SickKids Hospital, University of Toronto. Buenos Aires, August 16, 2014

September 12, 2015 Millie D. Long MD, MPH, FACG

Pharmacotherapy of Inflammatory Bowel Disorder

Treatment of Inflammatory Bowel Disease. Michael Weiss MD, FACG

Definitions. Clinical remission: Resolution of symptoms (stool frequency 3/day, no bleeding and no urgency)

Positioning Biologics in Ulcerative Colitis

The legally binding text is the original French version TRANSPARENCY COMMITTEE OPINION. 3 October 2012

How do I choose amongst medicines for inflammatory bowel disease. Maria T. Abreu, MD

Therapy for Inflammatory Bowel Disease

Anti tumor necrosis factor (TNF) agents have

IBD Updates. Themes in IBD IBD management journey. New tools for therapeutic monitoring. First-line treatment in IBD

Positioning New Therapies

Outline. Biologic Drugs in Inflammatory Bowel Disease Dr. Jason Etzel MD The Vancouver Clinic. Biologic Drugs. Biologic Drugs. Biologic Drugs Anti-TNF

National Institute for Health and Care Excellence

Medical therapies and IBD

Understanding Your Benefits and Risks

Emerging g therapies for IBD: A practical approach to positioning. Sequential Therapies for IBD

Pediatric Inflammatory Bowel Diseases

My Child Has Inflammatory Bowel Disease : Why? What now? What s next?

PEDIATRIC INFLAMMATORY BOWEL DISEASE

The following slides are provided as presented by the author during the live educa7onal ac7vity and are intended for reference purposes only.

Title: Author: Journal:

IBD Medical Treatments 2018

Crohn s Disease. Resident Lecture 1/17/19

Improving outcome of Inflammatory Bowel Disease in children

Top 10 Things you need to know about IBD. Suresh Pola, MD Kaiser San Diego

How to Optimize Induction and Maintenance Responses: Definitions and Dosing Advances in Inflammatory Bowel Disease December 6, 2009

Crohn's Disease. The What, When, and Why of Treatment

Drugs and Applicable Coding: J-code: Enbrel-J1438; Humira-J0135; Remicade-J1745; Inflectra-Q5102; Cimzia-J0718; Simponi-J1602 Renflexis - pending

Best Practices in the Diagnosis and Treatment of Inflammatory Bowel Disease

Pharmacotherapy of Inflammatory Bowel Disorder

Treating Crohn s and Colitis in the ASC

Best Practices in the Diagnosis and Treatment of Inflammatory Bowel Disease

Position of Biologics in IBD Circa 2006: Top Down vs. Step Up Therapy

ULCERATIVE COLITIS. Sean Lynch, MD and Richard Bloomfeld, MD Wake Forest University School of Medicine Winston-Salem, NC

TRANSPARENCY COMMITTEE

IBD in teenagers Biological and Transition

Azathioprine for Induction and Maintenance of Remission in Crohn s Disease

Inflammatory Bowel Disease

Disclosures. What Do I Do When Anti-TNF Therapy Is Not Working Anymore? Fadi Hamid, M.D. Saint Luke s GI Specialists

P a g e 1. Inflammatory Bowel Disease Guidelines

Medical Management of Inflammatory Bowel Disease

Mucosal Healing in Crohn s Disease. Geert D Haens MD, PhD University Hospital Gasthuisberg University of Leuven Leuven, Belgium

Chronic Granulomatous Disease Managing GI Issues

10/23/2014. Program Goals

Effective Health Care Program

Regulatory Status FDA-approved indications: Entyvio is an α4β7integrin receptor antagonist indicated for: (1)

Primary & Secondary Care Inflammatory Bowel Disease Pathway February 2018

Addressing Risks and Benefits In IBD

I B D. etter than this. isease UNDERSTANDING INFLAMMATORY BOWEL DISEASES

Inflammatory bowel disease (IBD) Overview of the Paediatric investigation plans. Presented by: Richard Veselý. An agency of the European Union

INFLIXIMAB Remicade (infliximab), Inflectra (infliximab-dyyb), Ixifi* (infliximabqbtx), Renflexis (infliximab-abda)

Biologics in IBD. Brian P. Bosworth, MD, NYSGEF Associate Professor of Medicine Weill Cornell Medical College

Understanding Inflammatory Bowel Diseases (IBD):

Regional vs. Systemic Therapy. Corticosteroids. Regional vs. Systemic Therapy for Uveitis. Considerations

The legally binding text is the original French version TRANSPARENCY COMMITTEE OPINION. 20 October 2010

Crohn's disease CAUSES COURSE OF CROHN'S DISEASE TREATMENT. Sulfasalazine

2nd Nottingham IBD Masterclass, 2017

NEW CONCEPTS IN CROHN S DISEASE GLENDON BURRESS, MD PEDIATRIC GASTROENTEROLOGY ROCKFORD, IL

Selection and use of the non-anti- TNF biological therapies: Who? When? How?

ENTYVIO (VEDOLIZUMAB)

Achieving Success in Ulcerative Colitis: the Role of Infliximab

This program is supported by an educational grant from Janssen Biotech Inc., Shire, Inc., and a sponsorship from Takeda

Synopsis (C0168T37 ACT 1)

INFLAMMATORY BOWEL DISEASE. Brittany Palasik, PharmD, BCPS University of North Texas System College of Pharmacy

Managing. Inflammatory Bowel Disease. Slide 1. Slide 2. Slide 3. Disclosures. Vijay Yajnik, MD., PhD 01/25/14. None relevant to this talk

Beyond Anti TNFs: positioning of other biologics for Crohn s disease. Christina Ha, MD Cedars Sinai Inflammatory Bowel Disease Center

Biologic Therapy for Ulcerative Colitis in 2015

Regulatory Status FDA- approved indication: Simponi and Simponi ARIA are tumor necrosis factor (TNF) blockers indicated for the treatment of: (2-3)

Carefirst.+.V Family of health care plans

Biologics in Ulcerative Colitis. Chris Probert

The clinical trial information provided in this public disclosure synopsis is supplied for informational purposes only.

Pharmacy Prior Authorization

Are Biologicals Safe Enough?

Optimizing the effectiveness of anti-tnf therapy in paediatric IBD

CADTH CANADIAN DRUG EXPERT COMMITTEE FINAL RECOMMENDATION

Transcription:

Ulcerative Colitis Therapy Amy Morse November 30/13 GI for GP s Jasper AB Faculty Disclosure Faculty: Amy Morse Relationships with commercial interests: Grants/Research Support: Therapeutic Fellowship funded by Olympus, Pentax and CIHR Speakers Bureau/Honoraria: Takeda Consulting Fees: Advisory Board, Shire Other: None Acknowledgements Karen Kroeker has kindly let me sample from her slide bank for this presentation 1

Objectives Goals of therapy in UC Review common therapies Review side effects Review biologic therapy What options When its used Contraindications Chronic inflammatory bowel disease only affects the colon (starts bum up ) proctitis, proctosigmoiditis, L sided, pancolitis Ulcerative Colitis Severity: mild, moderate, severe fulminant 2

Etiology Schematic Diagram What are the goals of therapy? 1. Induce and maintain remission Steroid free remission 2. Prevent complications 3. Improve QOL 4. Avoid surgery 5.? Mucosal healing 3

Treatment of IBD TWO PHASES: INDUCTION of Remission 5 ASA Corticosteroids MTX Anti TNF Surgery MAINTENANCE of Remission 5 ASA Imuran/6 MP, MTX Anti TNF IBD Treatment Pyramid Surgery Biologic Therapy AZA/6 MP MTX Prednisone Budesonide 5 ASA Antibiotics Aminosalicylates (5 ASA) TWO TYPES: Sulfasalazine: sulfapyridine + mesalamine Mesalamine: mesalamine + mesalamine Pentasa, Asacol, Salofalk, MMX Different release characteristics 4

Side Effects 5 ASA Sulfasalazine Anorexia N/V Neutropenia, agranulocytosis Hemolysis Macrocytosis (folate deficiency) Reversible male infertility Plus mesalamine SE Mesalamine Headache Drug fever, rash Paradoxical exacerbation of diarrhea Pancreatitis Hepatitis Pericarditis Nephritis Generally well tolerated 5 ASA in Ulcerative Colitis IBD Treatment Pyramid Mainstay of treatment in mild moderate UC Effective for induction & maintenance No need more more than daily or BID therapy Combination oral & rectal therapy improves remission rates Glucocorticoids for Ulcerative Colitis VERY EFFECTIVE FOR INDUCTION OF REMISSION: Prednisone 40 60mg/day plus taper Effective for inducing remission Budesonide Not effective FOR IN PATIENTS: Solumedrol (methylprednisone) 20 30mg IV BID 5

Side Effects Prednisone Sleep & mood disturbance Acne, alopecia Striae, central obesity Hirsutism Adrenal suppression Proximal myopathy Glucose intolerence Hypertension Weight gain Glaucoma Cataracts Infection Pseudotumor cerebri Edema Impaired wound healing Growth retardation Osteopenia/osteoporosis Avascular necrosis Immunosuppressives Azathioprine 2.5 mg/kg/d 6 mercaptopurine 1.5 mg/kg/d (Methotrexate 15 25mg/week (PO/SC)) AZA/6 MP Crohn s Disease & UC Azathioprine 2.5mg/kg/d 6 mercaptopurine 1.5mg/kg/d Not effective in inducing remission 70% effective in maintaining remission Need to follow bloodwork (CBC, liver enzymes for side effects) 6

Side Effects AZA/6 MP Nausea Drug fever Rash Arthralgias Leukopenia Thrombocytopenia Bone marrow suppression Pancreatitis Hepatitis Infection Lymphoma Anti TNF: Biologic Therapy Anti TNF α Infliximab (Remicade ) Adalimumab (Humira ) Certolizumab Golimumab(Simponi ) (New) Why anti TNF? Pts with UC have high levels of TNF in the colon mucosa, produced by lamina propria mononuclear cells TNF key player in the inflammatory cascade Shut it off and decrease inflammation 7

Anti TNFα (available in Canada) Infliximab (intravenous) Chimeric monoclonal antibody to soluble and membranebound TNFα Adalimumab (subcutaneous) Human monoclonal antibody to soluble TNFα but not to lymphotoxin Golimumab (subcutaneous) IgG1 monoclonal antibody against TNF Subcutaneous administration (also tested IV data not published) AKA: CNTO 148 Binds membrane bound and soluble TNF Who we use it on? Outpatients failing other therapies Fulminant/severe not responding to steroids Oxford rule Oxford Rule In patient Severe/Fulminant Colitis Day 3 8 BM/day or 3 8 BM/day and CRP > 45 85% chance of colectomy Day 7 > 3 BM/day or visible blood 60% chance of continuing Sx and 40% of requiring colectomy 8

Evidence for Infliximab in Steroid Refractory UC (Jarnerot) % Colectomy 100% 90% 80% 70% 60% 50% 40% 30% 20% 10% 0% p=0.017 p=0.012 3 Months 3 Years None of the pts in endoscopic remission at 3months had a colectomy; versus 50% who were not in remission (p=0.02) Infliximab Placebo Infliximab Ulcerative Colitis Outpatients ACT I&II (NEJM 2005; 353:2462) Outpatient trial 2 DR, RCT of 364 pts with mod severe UC (Mayo 6 12; with endo score 2+) randomized to placebo, 5, 10 mg/kg at 0, 2, 6 & q8wk DEFINITIONS: Response: decrease Mayo 3 (at least 50%) with bleeding decreasing by 1+ (absolute score 0 1) Remission: Mayo 2, endo score 0 1 Mucosal healing: Absolute score 0 1 ACT I&II Clinical Response 8 wks 69% better with infliximab vs placebo 37% (steroid+/ aza) 9

ACT I&II Remission 8 weeks 38% REMISSION with infliximab vs placebo 15% (steroid+/ aza) ACT I&II Mucosal Healing 8 wks ACT I&II Sustained Remission 10

Side Effects Anti TNF Infusion reactions (fever, headache, nausea, flushing, dyspnea, anaphylaxis) Serum sickness (myalgia, arthralgia, facial edema, urticaria) Infection URTI, UTI, abscess Re activation of TB CNS optic neuritis, MS Malignancy lymphoma, hepatosplenic T cell lymphoma CHF contraindicated in heart failure Why we test for TB prior to starting anti TNF Macrophages activated by TB need TNF which is needed to form granuloma and trap the TB bug and contain the infection Anti TNF Summary Anti TNF therapy are useful for induction and maintenance of remission in both Crohn s Disease and UC No stopping rules Often used in combination therapy 11

Surgery in Ulcerative Colitis Cure for UC Indications: 1. Refractory to medical therapy 2. Toxic megacolon/fulminant colitis 3. Malignancy or dysplasia 4. Patient preference Goals of therapy 1. Induce and maintain remission Steroid free remission 2. Prevent complications 3. Improve QOL 4. Avoid surgery 5.? Mucosal healing Questions????? 12

What is Golimumab? IgG1 monoclonal antibody against TNF Subcutaneous administration (also tested IV data not published) AKA: CNTO 148 Binds membrane bound and soluble TNF Golimumab for UC INDUCTION (PURSUIT SC) Combined with Phase 2 dose finding study 1064 pts 4 dosing groups: 100/50, 200/100, 400/200, placebo P: 774 pts with mod severe UC (Mayo 6 12, endo 2+) TNF naïve I: 200/100, 400/200 at wks 0, 2 C: placebo O: Wk 6 clinical response 2ndary: clinical remission, mucosal healing, IBDQ Golimumab Induction 60% 50% 40% 30% 20% 10% 0% CLINICAL RESPONSE P<0.0001 Placebo 200/100 mg 400/200 mg 13

Golimumab Induction 2ndary Outcomes Placebo N=256 200/100 N=257 Clinical Remission 6.3% 18.7% P<0.0001 Mucosal Healing 28.5% 43.2% P=0.0005 Change in IBDQ 14.6 27.4 P<0.0001 400/200 N=258 17.8% P<0.0001 45.3% P<0.0001 27.0 P<0.0001 Golimumab for UC MAINTENANCE P: 464 pts who responded to Induction Golimumab I: 50 or 100mg q4wks C: placebo O: Wk 54 clinical response 2ndary: clinical remission, mucosal healing at wk 30 & 54 Golimumab for UC MAINTENANCE P: 464 pts who responded to Induction Golimumab I: 50 or 100mg q4wks C: placebo O: Wk 54 clinical response 2ndary: clinical remission, mucosal healing at wk 30 & 54 14

Golimumab Maintenance 60% 50% 40% 30% 20% 10% 0% CLINICAL RESPONSE AT WK 54 P=0.01 P<0.001 Placebo 50mg 100mg Golimumab Maintenance 35% 30% 25% 20% 15% 10% 5% 0% CLINICAL RESPONSE AT BOTH WK 30 & 54 P=0.003 P=0.091 Placebo 50mg 100mg Golimumab Maintenance 50% 40% MUCOSAL HEALING AT WK 30 & 54 P=0.011 P=0.001 30% 20% 10% 0% Placebo 50mg 100mg 15

Golimumab Maintenance 2ndary Outcomes Clinical Remission at Wk 30 Clinical Remission at Wk 54 Steroid Use at Baseline Placebo N=156 200/100 N=153 22.4% 35.9% P=0.009 22.4% 33.3% P=0.071 400/200 N=154 40.9% P<0.001 34.4% P=0.01 87 79 83 Steroid free at Wk 54 20.7% 38.0% P=0.031 31.3% P=0.112 Golimumab Maintenance Adverse Reactions SAE: 7.7%, 8.4%, 14.3% (P, 50, 100) Serious infections: 1.9%, 3.2%, 3.2% 4 pts developed active TB 3 deaths: sepsis, TB, cardiac failure (all in 100mg group) Golimumab Dosing Ulcerative colitis: U.S. labeling: SubQ: Induction: 200 mg at week 0, then 100 mg at week 2, followed by maintenance therapy of 100 mg every 4 weeks Canadian labeling: SubQ: Induction: 200 mg at week 0, then 100 mg at week 2, followed by maintenance therapy of 50 mg every 4 weeks (maintenance dose may be increased to 100 mg every 4 weeks if needed) Uptodate.com 16