Inflammatory Bowel Disease (IBD)

CCFA Northern California Chapter Oakland Patient & Family Education Symposium November 7, 2015 is due to an An Update in Inappropriate Inflammatory Response to Inflammatory Bowel Disease Medications Intestinal Microbes in a Genetically Susceptible Host Ronald Hsu MD FACG, FASGE, AGAF, FACP Medical Director, Sutter Roseville Endoscopy Center Clinical Professor of Medicine, University of California, School of Medicine

Abraham et al: NEJM 2009

Medications in IBD Targets and Effects

Corticosteroids 5-ASA • Target at stopping inflammation • Different formulations • • Budesonide • Aminosalicylates (5-ASA) and/or are effective in Mild to Moderate Disease and Acute Flares • Biologics and combination with immunomodulators Immune modulators Biologics are more efficacious in Moderate and Severe Disease • Thiopurines IBD • Anti-TNF for • Methotrexate • Anti-Integrin – achieving mucosal healing – decreasing disease complications Antibiotics Others – needing surgery • Probiotics • Cipro • Fecal Microbiota • Metronidazole Transplantation (FMT) • Worms UC CD Crohn’s Disease and Ulcerative Colitis are part of a 1950’s sulfasalazine spectrum of Inflammatory Bowel Disease steroids New FDA Approved Medications 1997 Asacol (mesalamine) 1998 Remicade (inflixmab) *adult 2000 Colazal (basalazide) 2001 Entocort (budesonide) 2006 Remicade (inflixmab) *peds Crohn’s Ulcerative 2007 Liada (mesalamine) Humira (adalimumab) Disease CD/UC Colitis 2008 Apriso (mesalamine) Tysabri (natalizumab) Cimzia (certolizumab pegol) 10% 2011 Remicade (inflixmab) *adult 2012 Humira (adalimumab) 2013 Uceris (budesonide) Delzicol (mesalamine) Incidence: CD =7 in 100,000 ; UC = 10-15 in 100,000 Simponi (golimumab)

2014 Entyvio (vedolizumab) Entyvio (vedolizumab)

IBD Medications (Route of Delivery) Aminosalicylate (5-ASA) Formulations

1 Aminosalicylate (5-ASA) Oral Sulfasalazine (AZULFADINE) Drug linked to sulfapyridine - delayed released tablet Enema Suppository Basalazide (COLAZAL) Drug linked to inert molecule - capsule 2 / Oral Osalazine (DIPENTUM) Drug linked to drug (mesalamine-mesalamine) capsule Immunosuppressive Rectal Mesalamine (PENTASA) Time released (ethylcellulose-coated microgranule) Intravenous capsule 3 Immunomodulator Oral Mesalamine (LIADA) MMX drug released at pH ≥7 (gastro resistant polymer Injection film-coated) tablet 4 Biologic Injection Mesalamine ( ASACOL HD) Delayed release tablet Infusion 5 Antibiotic Oral Mesalamine (APRISO) Extended release capsule Intravenous Mesalamine (DELZICOL) Delayed release capsule 6 Probiotic Oral Mesalamine enema (ROWASA) Topical directly in the left distal colon Rectal 7 Fecal Microbiota Transplant Oral Mesalamine suppository (CANASA) Topical mesalamine directly in rectum (investigational) Rectal

8 Worm (small studies) Oral Side Effects of 5-ASA Corticosteroid Preparations sulfasalazine headache, nausea, loss of appetite, rash, fever, low prednisone oral WBC count, pancreatitis budesonide oral (EC, MMX), rectal foams mesalamine abdominal pain, cramps, diarrhea, gas, nausea, hair methyl-prednisone intravenous, enemas loss, headache, dizziness, decrease kidney function hydrocortisone intravenous, enemas, rectal foams olsalazine diarrhea most common enemas balsalazide headache, abdominal pain

MMX technology vs Enteric Coated Delivery System Side Effects of Corticosteroid

• high blood pressure • rounding of the face • high blood sugar levels "moon face” • increased risk of infection • acne • cataracts • increased facial hair • osteoporosis (weakened • stretch marks bones) • weight gain • osteonecrosis (avascular • mood swings necrosis) • psychosis and other psychiatric symptoms • insomnia (difficulty sleeping) in IBD Corticosteroid usage - Caveats (Moderate to Severe Disease)

UC (n=63) CD (n=74) • Steroids cannot be stopped abruptly after prolonged use. Dose adjustments must be gradual reductions to zero over Remission No Remission Steroid No several weeks dependent change dependent change • Half of patients treated with steroids become steroid 1-month 54% (34) 16% (19) 58% (43) 16% (10) dependent or steroid resistant responses* • 30% acute IBD may not respond to steroids 12- months 49% (31) 22% (14) 29% (18) 32% (24) 28% (21) 38% (28) responses Surgery Surgery

*30 days after initiating corticosteroid therapy >50% will fail steroids in 1 year

Faubion W et al. Gastroenterology 2001;121:225

Off Label Prescription Immunomodulators

• Immunomodulators Purines oral – Azathioprine (Imuran) is approved for rheumatoid arthritis and to prevent organ • Azathioprine (IMURAN) rejection after a transplant • 6-mercaptopurine (PURANTOL) – Methotrexate is approved to treat cancer and severe cases of and rheumatoid arthritis • Immunosuppressives – Cyclosporine: approved for organ transplant; iv cyclosporine is effective in Methotrexate (ABITREXATE, FOLEX, MEXATE) oral (not effective), injection (sq fulminant UC not CD – Tacrolimus (FK506): approved for organ transplant; effective in refractory UC & or im 25mg/week for Crohn’s) • Antibiotics – metronidazole (Flagyl) and ciprofloxacin (Cipro) in treating Crohn’s disease absence of infection Uses of Immunomodulators Immunomodulators- Caveats

• not responsive to 5-ASA or corticosteroids Purines MTX • steroid-dependent disease • Need to monitor for liver • Monitor of liver toxicity and • experienced side effects with corticosteroid treatment toxicity and bone marrow bone marrow suppression • perineal disease that does not respond to antibiotics suppression and kidney • Use folate supplement • fistulas (abnormal channels between two loops of damage intestine, or between the intestine and another • Check for TPMT level structure—such as the ) • Monitor 6-TG level • to maintain remission • Use folate supplement • Combine with biologics for moderate to severe disease for both UC, CD

Rate of Non-Hodgkin Lymphoma associated with Immunomodulator and anti-tumor Necrosis Factor treatment Imuran (azathioprine) Tablets and Injection

Serious Infections (February 2014) Progressive Multifocal Leukoencephalopathy. ….Cases of JC virus- associated infection resulting in progressive multifocal leukoencephalopathy (PML), sometimes fatal, have been reported in patients treated with immunosuppressants, including Imuran.

Malignancy (May 2011) Lymphoma and Hepatosplenic T-cell lymphoma (HSTCL) ….Reports of malignancy include post-transplant lymphoma and hepatosplenic T-cell lymphoma (HSTCL) in patients with inflammatory bowel disease. INCIDENCE is RARE About 1 in 8 (12%) women in the US will develop invasive cancer during their lifetime. discuss with your doctor; overall, thiopurines are safe to use Biologic Biologic Medications for IBD

• genetically engineered medications made from living organisms • target at specific molecular players in the inflammatory process such as cytokines— specialized proteins that play a role in increasing or decreasing inflammation • targets include tumor necrosis factor (TNF)-alpha, interleukins, adhesion molecules, colony-stimulating factors, and others

Administration of Biologics Caveats of using Biologics

Intravenous Infusions Subcutaneous Injections • TB skin testing prior to treatment • Vaccination (inactivated influenza, tetanus, HPV, meningococcus, HAV, Infliximab, Vedolizumab Adalimumab HBV); Live, attenuated influenza (intranasal vaccine) – Schedule – Schedule: q2weeks • Contraindicated live vaccines: – Dose: 4,2,1 (40mg @) – Varicella zoster vaccine • Induction: 0,2,6 weeks Certolizumab – Herpes zoster (live zoster vaccine) • Maintenance: q 8 weeks – Yellow fever vaccine – Schedule: – Measles-mumps-rubella vaccine – Dose • Induction: 0,2,4 weeks – Typhoid live oral vaccine • – Smallpox vaccine • IFX (5mg/Kg) Maintenance q 4 weeks – Dose: 1 – Tuberculosis Bacillus Calmette-Guérin vaccine • Vedo (300mg @) – Polio live oral vaccine Golimumab – Anthrax vaccine – Schedule: • Skin examination surveillance for skin cancer • Induction q2 weeks 1st 2 shots • Trough drug level after loading dose prior to maintenance therapy • Maintenance q 4 weeks • Antibody testing if decreasing response – Dose: 2,1(100mg @) • Monitor for risk for infection Adverse Effects of Anti-TNF Therapy Adverse Effects of Anti-integrin Therapy

• Infusion-related reactions • Adverse effects of immunosuppression but less • Infection and malignancy frequent than anti-TNF – Serous infection • Progressive Multifocal Leukoencephalopathy (PML) a – Lymphoma and HSTCL (adalimumab, infliximab) JC Virus infection in the brain was reported in • Reactivation of HBV, TB natalizumab (anti-α4β1 integrin) not vedolizumab (anti-α4β7 integrin) use • Skin cancer • Psoriasis • Autoimmunity (lupus-like syndrome) • Immunogenecity – antibodies to anti-TNF • Demyelinating disorder, CHF, liver toxicity

Other Therapies in IBD Crohn’s Disease Ulcerative Colitis

Bacteriotherapy Worm (Trichuris Suis Ovum) Therapy • Probiotics – effective in • CD trial (N=36): no response pouchitis • UC trial (n=54) 12 weeks: • FMT – – positive response; – mixed results in UC ; – êUCDAI ≥ 4: – TSO:placebo = 43%:16.7% (p=0.04) – Larger studies are ongoing

Features of CD: Features of UC: Penetrating Inflammatory Stricturing Inflammatory Severity of UC Sequential Therapies for IBD

FULMINANT SEVERITY • >10 stools/day MODERATE • >6 bloody • Continuous stools/day MILD • ≥4 stools/day bleeding • Fever • Toxicity +/- blood • Tachycardia • <4 stools/day • • Abdominal Minimal signs of • é ESR +/- blood toxicity tenderness/ • Normal ESR distension • No signs of • Transfusion toxicity requirment • Colonic dilation on X-ray Hanauer

Mild to Moderate UC Role of Biologics Rx in Moderate to Severe UC

Biologic

Hanauer Hanauer Clinical Remission Rates in CD Patients Early initiation of Biologic Rx to with Conventional Therapies Prevent Progression of CD

• Aminosalicylates – Mild-Moderate Disease ~45-55%

• Antibiotics – Few controlled trials – Mild-Moderate Disease ~50%

• Budesonide – Mild-Moderate Disease ~65-75%

• Corticosteroids – Moderate to Severe Disease~70-80%

Risk Factors for Progression of CD Reasons for Medications Failure

• Age of onset <40 • Smoking • Non-adherence • Elevated CRP • Severe endoscopic • Inadequate dose • Initial requirement of • Antibodies formation to biologics steroids • Stricturing, penetrating • Other causes e.g. coexisting infection • Perianal fistulizing behaviour disease • Terminal ileum locaion • Misdiagnosis • Genetic markers • Serological markers • Allergic/sensitive/intolerance to drug – NOD2/IBD5 – ASCA/ANCA

Vargas et al Gastro DDW 2013 Abs 557 Danese S Aliment Pharmacol Ther 2011;33;857 Beaugerie L et al Gastroenterology 2006;130:650-6 Goals of Medical Treatment Take Home Message (I)

1950’S • Medications don’t work if you don’t take them. • Symptoms control 1980 • Maintenance therapy is needed in the majority of 1990 • Improve quality of life patients. 2000 • Mucosal healing • Improvement of symptoms may not reflect mucosal healing. • Decrease hospitalization • Cohn's Disease can run a more complicated course • Avoid surgery than ulcerative colitis. It can progress to fibrostenotic 2015 or fistulizing disease. Biologic therapies can decrease SUSTAINED DISEASE CONTROL progression when use in the early phase of the disease in high risk patients. Hsu

Take Home Message (II) Take Home Message (III)

• 5-ASAs are effective in mild to moderate disease. • Biologics are very effective in stopping inflammation. • Corticosteroids and immunosuppressive drugs can Special measures and monitoring are necessary to control flares but should not be used for long term avoid infection and enhance drug responsiveness. maintenance. • More biologics are being developed. Update the • Immunomodulators are used in maintenance therapy advances in IBD treatments from reliable resources. for moderate to severe disease. They are also used in • Work with your doctor to achieve our common Goals combination with biologics to decrease of Medical Treatment. immunogenicity and potentiate effectiveness.

Hsu Hsu