Last Review Date: 10/01/2020

Date of Origin: 01/01/2012

Dates Reviewed: 06/2012, 02/2013, 04/2014, 09/2014, 07/2015, 07/2016, 09/2016, 12/2016, 03/2017, 06/2017, 09/2017, 12/2017, 03/2018, 06/2018, 10/2018, 10/2019, 10/2020

1. Length of Authorization

Coverage will be provided for six months and may be renewed; Management of Immune Checkpoint Inhibitor-Related Toxicity may NOT be renewed.

2. Dosing Limits

A.  Quantity Limit (max daily dose) [Pharmacy Benefit]:

• Xolair 75 mg single-dose prefilled syringe: 1 syringe every 14 days
• Xolair 150 mg single-dose prefilled syringe: 2 syringes every 14 days
• Xolair 150mg powder for injection: 3 vials every 14 days

B.  Max Units (per dose and over time) [Medical Benefit]:

     Allergic Asthma

• 90 billable units every 14 days

  All other indications

• 60 billable units every 28 days

3. Initial Approval Criteria

Coverage is provided in the following conditions:

• Patient is at least 18 years of age (unless otherwise specified); AND

Universal Criteria ¹

• Must not be used in combination with another monoclonal antibody (e.g., benralizumab mepolizumab, reslizumab, etc.); AND

Moderate-to-severe persistent allergic asthma † ^1,2,3,20

• Patient is at least 6 years of age; AND
• Will not be used for treatment of acute bronchospasm, status asthmaticus, or allergic conditions (other than indicated); AND
• Patient has a positive skin test or in vitro reactivity to a perennial aero-allergen; AND
• Patient must weigh between 20 kg (44 lbs.) and 150 kg (330 lbs.); AND
• Patient has a serum total IgE level, measured before the start of treatment, of either:
  • ≥ 30 IU/mL and ≤ 700 IU/mL in patients age ≥ 12 years; OR
  • ≥ 30 IU/mL and ≤ 1300 IU/mL in patients age 6 to <12 years; AND
• Patient has documented ongoing symptoms of moderate-to-severe asthma* with a minimum (3) month trial on previous combination therapy including medium- or high-dose inhaled corticosteroids PLUS another controller medication (e.g., long-acting beta-2 agonist, leukotriene receptor antagonist, theophylline, etc.)

Chronic idiopathic urticaria (CIU) † ^1,4,5,6,8

• Patient is at least 12 years of age; AND
• The underlying cause of the patient’s condition is NOT considered to be any other allergic condition(s) or other form(s) of urticaria; AND
• Patient is avoiding triggers (e.g., NSAIDs, etc.); AND
• Documented baseline score from an objective clinical evaluation tool, such as: urticaria activity score (UAS7), angioedema activity score (AAS), Dermatology Life Quality Index (DLQI), Angioedema Quality of Life (AE-QoL), or Chronic Urticaria Quality of Life Questionnaire (CU-Q₂oL); AND
• Patient had an inadequate response to a one or more month trial on previous therapy with scheduled dosing of a second-generation H1-antihistamine product**; AND
• Patient had an inadequate response to a one or more month trial on previous therapy with scheduled dosing of at least one of the following:
  • Up-dosing/dose advancement (up to 4-fold) of a second generation H1-antihistamine**
  • Add-on therapy with a leukotriene antagonist (e.g., montelukast, zafirlukast, etc.)
  • Add-on therapy with another H1-antihistamine**
  • Add-on therapy with a H2-antagonist (e.g. ranitidine, etc.)
  • Add-on therapy with cyclosporine

Note: renewal will require submission of a current (within 30 days) score from an objective clinical evaluation tool (i.e., UAS7, AAS, DLQI, AE-QoL or CU-Q₂oL).

Management of Immune Checkpoint Inhibitor-Related Toxicity ‡ ^9,10

• Patient has been receiving therapy with an immune checkpoint inhibitor (e.g. nivolumab, pembrolizumab, atezolizumab, avelumab, durvalumab, cemiplimab, ipilimumab, etc.); AND
• Patient has refractory and severe (i.e., grade 3: intense or widespread, constant, limiting self-care activities of daily living or sleep) pruritis; AND
• Patient has an increased serum IgE level above the upper limit of normal of the laboratory reference value

Systemic Mastocytosis ‡ ^7,9,11

• Used for the prevention of one of the following:
  • Chronic mast cell mediator-related cardiovascular (e.g., pre-syncope, tachycardia, etc.) or pulmonary (e.g., wheezing, throat-swelling, etc.) symptoms insufficiently controlled by conventional therapy (e.g., H1 or H2 blockers or corticosteroids); OR
  • Unprovoked anaphylaxis; OR
  • Hymenoptera or food-induced anaphylaxis in patients with a negative test for specific IgE antibodies or a negative skin test; OR
• Used to improve tolerance while on immunotherapy (i.e., venom immunotherapy [VIT])

† FDA-approved indication(s); ‡ Compendia recommended indication(s)

4. Renewal Criteria ¹

• Patient continues to meet the universal and other indication-specific relevant criteria identified in section III; AND
• Absence of unacceptable toxicity from the drug. Examples of unacceptable toxicity include the following: symptoms of anaphylaxis (bronchospasm, hypotension, syncope, urticaria, and/or angioedema), malignancy, symptoms similar to serum sickness (fever, arthralgia, and rash), parasitic (helminth) infection, eosinophilic conditions (e.g. vasculitic rash, worsening pulmonary symptoms, cardiac complications, and/or neuropathy, especially upon reduction of oral corticosteroids), etc.; AND

Moderate-to-severe persistent allergic asthma

• Patient must weigh between 20 kg (44 lbs.) and 150 kg (330 lbs.); AND
• Treatment has resulted in clinical improvement as documented by one or more of the following:

• Decreased utilization of rescue medications; OR
• Decreased frequency of exacerbations (defined as worsening of asthma that requires increase in inhaled corticosteroid dose or treatment with systemic corticosteroids); OR
• Improvement in lung function (increase in percent predicted FEV₁ or PEF) from pre-treatment baseline; OR
• Reduction in reported symptoms (e.g., decrease in asthma symptom score), as evidenced by decreases in frequency or magnitude of one or more of the following symptoms:

• Asthma attacks
• Chest tightness or heaviness
• Coughing or clearing throat
• Difficulty taking deep breath or difficulty breathing out
• Shortness of breath
• Sleep disturbance, night wakening, or symptoms upon awakening
• Tiredness
• Wheezing/heavy breathing/fighting for air; AND
  • •  
• Patient is periodically checked to reassess the need for continued therapy based upon the patient’s disease severity and level of asthma control

Chronic idiopathic urticaria (CIU)

• Treatment with Xolair (omalizumab) has resulted in clinical improvement as documented by improvement from baseline using objective clinical evaluation tools such as the urticaria activity score (UAS7), angioedema activity score (AAS), Dermatology Life Quality Index (DLQI), Angioedema Quality of Life (AE-QoL), or Chronic Urticaria Quality of Life Questionnaire(CU-Q₂oL); AND
• Submitted current UAS7, AAS, DLQI, AE-QoL, or Cu-Q₂oL was recorded within the past 30 days.

Management of Immune Checkpoint Inhibitor-Related Toxicity

• May not be renewed

Systemic Mastocytosis

• Disease response as indicated by improvement in signs and symptoms compared to baseline or a decreased frequency of exacerbations

5. Dosage/Administration

6. Billing Code/Availability Information

HCPCS Code:

• • •  
• J2357 – Injection, omalizumab, 5 mg; 1 billable unit = 5 mg

NDC:

• Xolair 75 mg single-dose prefilled syringe: 50242-0214-xx
• Xolair 150 mg single-dose prefilled syringe: 50242-0215-xx
• Xolair 150 mg single-use vial powder for injection: 50242-0040-xx

   VII.  References

1. Xolair [package insert]. South San Francisco, CA; Genentech, Inc.; May 2019. Accessed September 2020.
2. National Asthma Education and Prevention Program (NAEPP). Guidelines for the diagnosis and management of asthma. Expert Panel Report 3. Bethesda, MD: National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI); August 2007.
3. Global Initiative for Asthma (GINA).Global Strategy for Asthma Management and Prevention. 2018 Update.  Available from: http://www.ginasthma.org. Accessed April 2018.
4. Baiardini I, Braido F, Bindslev-Jensen C, et al.  Recommendations for assessing patient-reported outcomes and health-related quality of life in patients with urticaria: a GA (2) LEN taskforce position paper. Allergy. 2011 Jul;66(7):840-4. doi: 10.1111/j.1398-9995.2011.02580.x. Epub 2011 Mar 9.
5. Zuberbier T, Aberer W, Asero R, et al.  EAACI/GA (2) LEN/EDF/WAO guideline for the Definition, Classification, Diagnosis and Management of Urticaria. The 2017 Revision and Update. Allergy. 2018 Jan 15. doi: 10.1111/all.13397.
6. Maurer M, Rosén K, Hsieh HJ, et al.  Omalizumab for the treatment of chronic idiopathic or spontaneous urticaria.  N Engl J Med. 2013 Mar 7;368(10):924-35. doi: 10.1056/NEJMoa1215372. Epub 2013 Feb 24.
7. Siles RI, Hsieh FH. Allergy blood testing: A practical guide for clinicians. Cleve Clin J Med. 2011 Sep;78(9):585-92. doi: 10.3949/ccjm.78a.11023.
8. Bernstein JA, Lang DM, Khan DA, et al. The diagnosis and management of acute and chronic urticaria: 2014 update. J Allergy Clin Immunol. 2014 May;133(5):1270-7.
9. Referenced with permission from the NCCN Drugs and Biologics Compendium (NCCN Compendium^®) Omalizumab. National Comprehensive Cancer Network, 2020. The NCCN Compendium^® is a derivative work of the NCCN Guidelines^®. NATIONAL COMPREHENSIVE CANCER NETWORK^®, NCCN^®, and NCCN GUIDELINES^® are trademarks owned by the National Comprehensive Cancer Network, Inc. To view the most recent and complete version of the Compendium, go online to NCCN.org. Accessed September 2020.
10. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines^®) for Management of Immunotherapy-Related Toxicities 1.2020. National Comprehensive Cancer Network, 2019. NATIONAL COMPREHENSIVE CANCER NETWORK^®, NCCN^®, and NCCN GUIDELINES^® are trademarks owned by the National Comprehensive Cancer Network, Inc. To view the most recent and complete version of the Guidelines, go online to NCCN.org. Accessed September 2020.
11. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines^®) for Systemic Mastocytosis Version 1.2020. National Comprehensive Cancer Network, 2020. NATIONAL COMPREHENSIVE CANCER NETWORK^®, NCCN^®, and NCCN GUIDELINES^® are trademarks owned by the National Comprehensive Cancer Network, Inc. To view the most recent and complete version of the Guidelines, go online to NCCN.org. Accessed September 2020.
12. Carter MC, Robyn JA, Bressler PB, Walker JC, Shapiro GG, Metcalfe DD. Omalizumab for the treatment of unprovoked anaphylaxis in patients with systemic mastocytosis. J Allergy Clin Immunol. 2007;119(6):1550-1551.
13. Slapnicar C, Trinkaus M, Hicks L, Vadas P. Efficacy of Omalizumab in Indolent Systemic Mastocytosis. Case Rep Hematol. 2019;2019:3787586. Published 2019 Sep 16.
14. Jendoubi, F, Gaudenzio, N, Gallini, A, et al. Omalizumab in the treatment of adult patients with mastocytosis: A systematic review. Clin Exp Allergy. 2020; 50: 654– 661.
15. Busse W, Corren J, Lanier BQ, et al. Omalizumab, anti-IgE recombinant humanized monoclonal antibody, for the treatment of severe allergic asthma. J Allergy Clin Immunol. 2001;108(2):184-190.
16. Solèr M, Matz J, Townley R, et al. The anti-IgE antibody omalizumab reduces exacerbations and steroid requirement in allergic asthmatics. Eur Respir J. 2001;18(2):254-261.
17. Lanier B, Bridges T, Kulus M, et al. Omalizumab for the treatment of exacerbations in children with inadequately controlled allergic (IgE-mediated) asthma. J Allergy Clin Immunol. 2009;124(6):1210-1216.
18. Milgrom H, Berger W, Nayak A, et al. Treatment of childhood asthma with anti-immunoglobulin E antibody (omalizumab). Pediatrics. 2001;108(2):E36.
19. Saini SS, Bindslev-Jensen C, Maurer M, et al. Efficacy and safety of omalizumab in patients with chronic idiopathic/spontaneous urticaria who remain symptomatic on H1 antihistamines: a randomized, placebo-controlled study. J Invest Dermatol. 2015;135(1):67-75.
20. Holguin F, Cardet JC, Chung KF, et al. Management of severe asthma: a European

Respiratory Society/American Thoracic Society guideline. Eur Respir J 2020; 55: 1900588 [https://doi.org/10.1183/13993003.00588-2019].

21. First Coast Service Options, Inc. Local Coverage Article: Billing and Coding: Omalizumab (A57658). Centers for Medicare & Medicare Services. Updated on 11/22/2019 with effective dates 10/03/2018. Accessed September 2020.
22. National Government Services, Inc. Local Coverage Article: Billing and Coding: Omalizumab (A52448). Centers for Medicare & Medicare Services. Updated on 11/01/2019 with effective dates 11/07/2019. Accessed September 2020.

Appendix 1 – Covered Diagnosis Codes

Appendix 2 – Centers for Medicare and Medicaid Services (CMS)

Medicare coverage for outpatient (Part B) drugs is outlined in the Medicare Benefit Policy Manual (Pub. 100-2), Chapter 15, §50 Drugs and Biologicals. In addition, National Coverage Determination (NCD), Local Coverage Determinations (LCDs), and Local Coverage Articles (LCAs) may exist and compliance with these policies is required where applicable. They can be found at: http://www.cms.gov/medicare-coverage-database/search/advanced-search.aspx. Additional indications may be covered at the discretion of the health plan.

Medicare Part B Covered Diagnosis Codes (applicable to existing NCD/LCD/LCA):