Specialty Pharmacy Clinical Policy Bulletins Aetna Non-Medicare Prescription Drug Plan
Subject: infliximab-Remicade and Biosimilars 2182-A SGM P2022a
Drug
REMICADE(infliximab)
AVSOLA(infliximab-axxq)
INFLECTRA(infliximab-dyyb)
RENFLEXIS(infliximab-abda)
infliximab
Policy:
I. INDICATIONS
The indications below including FDA-approved indications and compendial uses are considered a covered benefit provided that all the approval criteria are met and the member has no exclusions to the prescribed therapy.
A. FDA-Approved Indications 1. Adult patients with moderately to severely active Crohn’s disease (CD) and fistulizing CD who have had an inadequate response to conventional therapy 2. Pediatric patients 6 years of age and older with moderately to severely active Crohn’s disease who have had an inadequate response to conventional therapy 3. Moderately to severely active ulcerative colitis (UC) in patients 6 years of age or older who have had an inadequate response to conventional therapy 4. Adult patients with moderately to severely active rheumatoid arthritis (RA), in combination with methotrexate 5. Adult patients with active ankylosing spondylitis (AS) 6. Adult patients with active psoriatic arthritis (PsA) 7. Adult patients with chronic severe plaque psoriasis (PsO) who are candidates for systemic therapy and when other systemic therapies are medically less appropriate
All other indications are considered experimental/investigational and not medically necessary.
II. DOCUMENTATION
Submission of the following information is necessary to initiate the prior authorization review:
A. Crohn’s disease (CD) and ulcerative colitis (UC) Continuation requests: Chart notes or medical record documentation supporting positive clinical response to therapy or remission.
B. Rheumatoid arthritis (RA) 1. For initial requests: i. Chart notes, medical record documentation, or claims history supporting previous medications tried (if applicable), including response to therapy. If therapy is not advisable, documentation of clinical reason to avoid therapy. ii. Laboratory results, chart notes, or medical record documentation of biomarker testing (i.e., rheumatoid factor [RF], anti-cyclic citrullinated peptide [anti- CCP], and C-reactive protein [CRP] and/or erythrocyte sedimentation rate [ESR]) (if applicable). 2. For continuation requests: Chart notes or medical record documentation supporting positive clinical response.
C. Ankylosing spondylitis (AS), non-radiographic axial spondyloarthritis (nr-axSpA), psoriatic arthritis (PsA), reactive arthritis, hidradenitis suppurativa, and uveitis 1. Initial requests: Chart notes, medical record documentation, or claims history supporting previous medications tried (if applicable), including response to therapy. If therapy is not advisable, documentation of clinical reason to avoid therapy. 2. Continuation requests: Chart notes or medical record documentation supporting positive clinical response.
D. Plaque psoriasis (PsO) 1. Initial requests: i. Chart notes or medical record documentation of affected area(s) and body surface area (BSA) affected (if applicable). ii. Chart notes, medical record documentation, or claims history supporting previous medications tried (if applicable), including response to therapy. If therapy is not advisable, documentation of clinical reason to avoid therapy. 2. Continuation requests: Chart notes or medical record documentation of decreased body surface area (BSA) affected and/or improvement in signs and symptoms.
E. Behcet’s disease (initial requests only) Chart notes, medical record documentation, or claims history supporting previous medications tried, including response to therapy (if applicable).
F. Pyoderma gangrenosum, sarcoidosis, Takayasu’s arteritis, immune checkpoint inhibitor toxicity, and acute graft versus host disease (initial requests only) Chart notes, medical record documentation, or claims history supporting previous medications tried (if applicable), including response to therapy. If therapy is not advisable, documentation of clinical reason to avoid therapy.
III. PRESCRIBER SPECIALTIES
This medication must be prescribed by or in consultation with one of the following: A. Crohn’s disease and ulcerative colitis: gastroenterologist B. Rheumatoid arthritis, ankylosing spondylitis, non- radiographic axial spondyloarthritis, Behcet’s disease, Takayasu’s arteritis, and reactive arthritis: rheumatologist C. Psoriatic arthritis and hidradenitis suppurativa:60 rheumatologist or dermatologist D. Plaque psoriasis and pyoderma gangrenosum: dermatologist E. Sarcoidosis: dermatologist or pulmonologist F. Uveitis: ophthalmologist or rheumatologist G. Immune checkpoint inhibitor toxicity and acute graft versus host disease: oncologist or hematologist
IV. CRITERIA FOR INITIAL APPROVAL
A. Crohn’s disease (CD) Authorization of 12 months may be granted for members 6 years of age or older for treatment of moderately to severely active CD.
B. Ulcerative colitis (UC) Authorization of 12 months may be granted for members 6 years of age or older for treatment of moderately to severely active UC.
C. Rheumatoid arthritis (RA) 1. Authorization of 12 months may be granted for adult members who have previously received a biologic or targeted synthetic drug (e.g., Rinvoq, Xeljanz) indicated for moderately to severely active rheumatoid arthritis. The requested medication must be prescribed in combination with methotrexate or leflunomide unless the member has a clinical reason not to use methotrexate or leflunomide (see Appendix).
2. Authorization of 12 months may be granted for adult members for treatment of moderately to severely active RA when all of the following criteria are met: i. Member meets either of the following criteria: a. Member has been tested for either of the following biomarkers and the test was positive: 1. Rheumatoid factor (RF) 2. Anti-cyclic citrullinated peptide (anti-CCP) b. Member has been tested for ALL of the following biomarkers: 1. RF 2. Anti-CCP 3. C-reactive protein (CRP) and/or erythrocyte sedimentation rate (ESR) ii. Member is prescribed the requested medication in combination with methotrexate or leflunomide, or has a clinical reason not to use methotrexate or leflunomide (see Appendix). iii. Member meets either of the following criteria: a. Member has experienced an inadequate response to at least a 3-month trial of methotrexate despite adequate dosing (i.e., titrated to at least 15 mg/week). b. Member has an intolerance or contraindication to methotrexate (see Appendix).
D. Ankylosing spondylitis (AS) and non-radiographicaxial spondyloarthritis (nr-axSpA) 1. Authorization of 12 months may be granted for adult members who have previously received a biologic or targeted synthetic drug (e.g., Rinvoq, Xeljanz) indicated for active ankylosing spondylitis or active non- radiographic axial spondyloarthritis.
2. Authorization of 12 months may be granted for adult members for treatment of active ankylosing spondylitis or active non-radiographic axial spondyloarthritis when either of the following criteria is met: i. Member has experienced an inadequate response to at least two non-steroidal anti-inflammatory drugs (NSAIDs). ii. Member has an intolerance or contraindication to two or more NSAIDs.
E. Psoriatic arthritis (PsA) 1. Authorization of 12 months may be granted for adult members who have previously received a biologic or targeted synthetic drug (e.g., Rinvoq, Otezla) indicated for active psoriatic arthritis.
2. Authorization of 12 months may be granted for adult members for treatment of active psoriatic arthritis when either of the following criteria is met: i. Member has mild to moderate disease and meets one of the following criteria: a. Member has had an inadequate response to methotrexate, leflunomide, or another conventional synthetic drug (e.g., sulfasalazine) administered at an adequate dose and duration. b. Member has an intolerance or contraindication to methotrexate or leflunomide (see Appendix), or another conventional synthetic drug (e.g., sulfasalazine). c. Member has enthesitis or predominantly axial disease. ii. Member has severe disease.
F. Plaque psoriasis (PsO) 1. Authorization of 12 months may be granted for adult members who have previously received a biologic or targeted synthetic drug (e.g., Sotyktu, Otezla) indicated for treatment of moderate to severe plaque psoriasis.
2. Authorization of 12 months may be granted for adult members for treatment of moderate to severe plaque psoriasis when any of the following criteria is met: i. Crucial body areas (e.g., hands, feet, face, neck, scalp, genitals/groin, intertriginous areas) are affected. ii. At least 10% of body surface area (BSA) is affected. iii. At least 3% of body surface area (BSA) is affected and the member meets either of the following criteria: a. Member has had an inadequate response or intolerance to either phototherapy (e.g., UVB, PUVA) or pharmacologic treatment with methotrexate, cyclosporine, or acitretin. b. Member has a clinical reason to avoid pharmacologic treatment with methotrexate, cyclosporine, and acitretin (see Appendix).
G. Behcet’s disease 1. Authorization of 12 months may be granted for members who have previously received Otezla or a biologic indicated for the treatment of Behcet’s disease.
2. Authorization of 12 months may be granted for the treatment of Behcet’s disease when the member has had an inadequate response to at least one non-biologic medication for Behcet’s disease (e.g., apremilast, colchicine, systemic glucocorticoids, azathioprine).
H. Hidradenitis suppurativa 1. Authorization of 12 months may be granted for members who have previously received a biologic indicated for treatment of severe, refractory hidradenitis suppurativa.
2. Authorization of 12 months may be granted for treatment of severe, refractory hidradenitis suppurativa when either of the following is met: i. Member has experienced an inadequate response to an oral antibiotic for at least 90 days. ii. Member has an intolerance or contraindication to oral antibiotics.
I. Pyoderma gangrenosum 1. Authorization of 12 months may be granted for members who have previously received a biologic indicated for treatment of pyoderma gangrenosum.
2. Authorization of 12 months may be granted for treatment of pyoderma gangrenosum when either of the following is met: i. Member has experienced an inadequate response to corticosteroids or immunosuppressive therapy (e.g., cyclosporine or mycophenolate mofetil). ii. Member has an intolerance or contraindication to corticosteroids and immunosuppressive therapy (e.g., cyclosporine, mycophenolate mofetil).
J. Sarcoidosis Authorization of 12 months may be granted for treatment of sarcoidosis in members when either of the following criteria is met: 1. Member has experienced an inadequate response to corticosteroids or immunosuppressive therapy. 2. Member has an intolerance or contraindication to corticosteroids and immunosuppressive therapy.
K. Takayasu’s arteritis Authorization of 12 months may be granted for treatment of refractory Takayasu’s arteritis when either of the following criteria is met: 1. Member has experienced an inadequate response to corticosteroids or immunosuppressive therapy (e.g., methotrexate, azathioprine, or mycophenolate mofetil). 2. Member has an intolerance or contraindication to corticosteroids and immunosuppressive therapy (e.g., methotrexate, azathioprine, or mycophenolate mofetil).
L. Uveitis 1. Authorization of 12 months may be granted for members who have previous received a biologic indicated for uveitis.
2. Authorization of 12 months may be granted for treatment of uveitis when either of the following criteria is met: i. Member has experienced an inadequate response to corticosteroids or immunosuppressive therapy (e.g., methotrexate, azathioprine, or mycophenolate mofetil). ii. Member has an intolerance or contraindication to corticosteroids and immunosuppressive therapy (e.g., methotrexate, azathioprine, or mycophenolate mofetil).
M. Reactive arthritis 1. Authorization of 12 months may be granted for members who have previously received a biologic indicated for reactive arthritis.
2. Authorization of 12 months may be granted for treatment of reactive arthritis when either of the following criteria is met: i. Member has experienced an inadequate response to at least a 3-month trial of one of the following despite adequate dosing or maximally tolerated dose: a. Sulfasalazine (i.e., titrated to 1000 mg twice daily) b. Methotrexate (i.e., titrated to at least 15 mg/week) ii. Member has an intolerance or contraindication to methotrexate (see Appendix) and sulfasalazine (e.g., porphyria, intestinal or urinary obstruction). N. Immune checkpoint inhibitor toxicity 1. Authorization of 6 months may be granted for treatment of immune checkpoint inhibitor toxicity when either of the following criteria is met: i. Member has experienced an inadequate response, intolerance, or contraindication to corticosteroids. ii. Member has moderate or severe diarrhea or colitis.
2. Authorization of 12 months may be granted for treatment of immune checkpoint inhibitor toxicity when the member has severe inflammatory arthritis and has experienced an inadequate response, intolerance, or contraindication to corticosteroids.
O. Acute graft versus host disease Authorization of 12 months may be granted for treatment of acute graft versus host disease when either of the following criteria is met: 1. Member has experienced an inadequate response to systemic corticosteroids. 2. Member has an intolerance or contraindication to corticosteroids.
V. CONTINUATION OF THERAPY
A. Crohn’s disease (CD) 1. Authorization of 12 months may be granted for all members 6 years of age or older (including new members) who are using the requested medication for moderately to severely active Crohn’s disease and who achieve or maintain remission.
2. Authorization of 12 months may be granted for all members 6 years of age or older (including new members) who are using the requested medication for moderately to severely active Crohn’s disease and who achieve or maintain a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms of the condition when there is improvement in any of the following from baseline: i. Abdominal pain or tenderness ii. Diarrhea iii. Body weight iv. Abdominal mass v. Hematocrit vi. Appearance of the mucosa on endoscopy, computed tomography enterography (CTE), magnetic resonance enterography (MRE), or intestinal ultrasound vii. Improvement on a disease activity scoring tool (e.g., Crohn’s Disease Activity Index [CDAI] score)
B. Ulcerative colitis (UC) 1. Authorization of 12 months may be granted for all members 6 years of age or older (including new members) who are using the requested medication for moderately to severely active ulcerative colitis and who achieve or maintain remission.
2. Authorization of 12 months may be granted for all members 6 years of age or older (including new members) who are using the requested medication for moderately to severely active ulcerative colitis and who achieve or maintain a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms of the condition when there is improvement in any of the following from baseline: i. Stool frequency ii. Rectal bleeding iii. Urgency of defecation iv. C-reactive protein (CRP) v. Fecal calprotectin (FC) vi. Appearance of the mucosa on endoscopy, computed tomography enterography (CTE), magnetic resonance enterography (MRE), or intestinal ultrasound vii. Improvement on a disease activity scoring tool (e.g., Ulcerative Colitis Endoscopic Index of Severity [UCEIS], Mayo score)
C. Rheumatoid arthritis (RA) Authorization of 12 months may be granted for all adult members (including new members) who are using the requested medication for moderately to severely active rheumatoid arthritis and who achieve or maintain a positive clinical response as evidenced by disease activity improvement of at least 20% from baseline in tender joint count, swollen joint count, pain, or disability.
D. Ankylosing spondylitis (AS) and non-radiographicaxial spondyloarthritis (nr-axSpA) Authorization of 12 months may be granted for all adult members (including new members) who are using the requested medication for active ankylosing spondylitis or active non-radiographic axial spondyloarthritis and who achieve or maintain a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms of the condition when there is improvement in any of the following from baseline: 1. Functional status 2. Total spinal pain 3. Inflammation (e.g., morning stiffness)
E. Psoriatic arthritis (PsA) Authorization of 12 months may be granted for all adult members (including new members) who are using the requested medication for psoriatic arthritis and who achieve or maintain a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms of the condition when there is improvement in any of the following from baseline: 1. Number of swollen joints 2. Number of tender joints 3. Dactylitis 4. Enthesitis 5. Axial disease 6. Skin and/or nail involvement
F. Plaque psoriasis (PsO) Authorization of 12 months may be granted for all adult members (including new members) who are using the requested medication for moderate to severe plaque psoriasis and who achieve or maintain a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms of the condition when either of the following is met: 1. Reduction in body surface area (BSA) affected from baseline 2. Improvement in signs and symptoms from baseline (e.g., itching, redness, flaking, scaling, burning, cracking, pain)
G. Hidradenitis suppurativa Authorization of 12 months may be granted for all members (including new members) who are using the requested medication for severe, refractory hidradenitis suppurativa and who achieve or maintain a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms of the condition when any of the following is met: 1. Reduction in abscess and inflammatory nodule count from baseline 2. Reduced formation of new sinus tracts and scarring 3. Decrease in frequency of inflammatory lesions from baseline 4. Reduction in pain from baseline 5. Reduction in suppuration from baseline 6. Improvement in frequency of relapses from baseline 7. Improvement in quality of life from baseline 8. Improvement on a disease severity assessment tool from baseline
H. Uveitis Authorization of 12 months may be granted for all members (including new members) who are using the requested medication for uveitis and who achieve or maintain a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms of the condition when the patient meets any of the following: 1. Reduced frequency of recurrence compared to baseline 2. Zero anterior chamber inflammation or reduction in anterior chamber inflammation compared to baseline 3. Decreased reliance on topical corticosteroids
I. Reactive arthritis Authorization of 12 months may be granted for all members (including new members) who are using the requested medication for reactive arthritis and who achieve or maintain a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms of the condition (e.g., tender joint count, swollen joint count, pain).
J. Immune checkpoint inhibitor toxicity and acute graft versus host disease All members (including new members) requesting authorization for continuation of therapy must meet all initial authorization criteria.
K. All other indications Authorization of 12 months may be granted for all members (including new members) who are using the requested medication for an indication outlined in Section IV and who achieve or maintain a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms of the condition.
VI. OTHER
For all indications: Member has had a documented negative tuberculosis (TB) test (which can include a tuberculosis skin test [PPD], an interferon-release assay [IGRA], or a chest x-ray)* within 6 months of initiating therapy for persons who are naïve to biologic drugs or targeted synthetic drugs associated with an increased risk of TB.
* If the screening testing for TB is positive, there must be further testing to confirm there is no active disease. Do not administer the requested medication to members with active TB infection. If there is latent disease, TB treatment must be started before initiation of the requested medication.
For all indications: Member cannot use the requested medication concomitantly with any other biologic drug or targeted synthetic drug.
VII. DOSAGE AND ADMINISTRATION
Approvals may be subject to dosing limits in accordance with FDA-approved labeling, accepted compendia, and/or evidence- based practice guidelines.
VIII. APPENDIX
Examples of Clinical Reasons to Avoid Pharmacologic Treatment with Methotrexate, Cyclosporine, Acitretin, or Leflunomide 1. Clinical diagnosis of alcohol use disorder, alcoholic liver disease, or other chronic liver disease 2. Drug interaction 3. Risk of treatment-related toxicity 4. Pregnancy or currently planning pregnancy 5. Breastfeeding 6. Significant comorbidity prohibits use of systemic agents (e.g., liver or kidney disease, blood dyscrasias, uncontrolled hypertension) 7. Hypersensitivity 8. History of intolerance or adverse event
Place of Service:
Outpatient
The above policy is based on the following references:
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Smolen JS, Aletaha D. Assessment of rheumatoid arthritis activity in clinical trials and clinical practice. In: UpToDate, Post TW (Ed), UpToDate, Waltham, MA. Available with subscription. URL: www.uptodate.com. Accessed March 19, 2021.
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Azulfidine [package insert]. New York, NY: Pfizer; August 2021.
Copyright Aetna Inc. All rights reserved. Pharmacy Clinical Policy Bulletins are developed by Aetna to assist in administering plan benefits and constitute neither offers of coverage nor medical advice. This Clinical Policy Bulletin contains only a partial, general description of plan or program benefits and does not constitute a contract. Aetna does not provide health care services and, therefore, cannot guarantee any results or outcomes. Participating providers are independent contractors in private practice and are neither employees nor agents of Aetna or its affiliates. Treating providers are solely responsible for medical advice and treatment of members. This Clinical Policy Bulletin may be updated and therefore is subject to change.
