Specialty Pharmacy Clinical Policy Bulletins Aetna Non-Medicare Prescription Drug Plan
Subject: SCIG 2043-A SGM P2023a
Drug
Subcutaneous Immune Globulin (SCIG)
Hizentra®, HyQvia®, Cutaquig®, Cuvitru™ and Xembify®
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. Cutaquig (Immune Globulin Subcutaneous [Human] - hipp, 16.5% Solution) Cutaquig is indicated as replacement therapy for primary humoral immunodeficiency (PI) in adults and pediatric patients 2 years of age and older. 2. Cuvitru (Immune Globulin Subcutaneous [Human], 20% Solution) Cuvitru is indicated as replacement therapy for primary humoral immunodeficiency in adult and pediatric patients two years of age and older. 3. Hizentra (Immune Globulin Subcutaneous [Human], 20% Liquid) a. Hizentra is indicated as replacement therapy for primary humoral immunodeficiency in adults and pediatric patients 2 years of age and older. b. Hizentra is indicated for the treatment of adult patients with chronic inflammatory demyelinating polyneuropathy (CIDP) as maintenance therapy to prevent relapse of neuromuscular disability and impairment. Limitations of Use: Hizentra maintenance therapy in CIDP has been systematically studied for 6 months and for a further 12 months in a follow-up study. Maintenance therapy beyond these periods should be individualized based upon the patient’s response and need for continued therapy. 4. HyQvia (Immune Globulin Infusion 10% [Human] with Recombinant Human Hyaluronidase) a. HyQvia is indicated for the treatment of primary immunodeficiency in adults and pediatric patients two years of age and older. b. HyQvia is indicated for the treatment of chronic inflammatory demyelinating polyneuropathy (CIDP) as maintenance therapy to prevent relapse of neuromuscular disability and impairment in adults. 5. Xembify (Immune Globulin Subcutaneous [Human} – klhw, 20% Solution) Xembify is indicated for treatment of primary humoral immunodeficiency (PI) in patients 2 years of age and older.
B. Compendial Uses 1. Idiopathic thrombocytopenic purpura (ITP) 2. Multifocal motor neuropathy 3. Kawasaki syndrome 4. B-cell chronic lymphocytic leukemia (CLL) 5. Prophylaxis of bacterial infections in pediatric human immunodeficiency virus (HIV) infection 6. Bone marrow transplant (BMT)/hematopoietic stem cell transplant (HSCT) 7. Dermatomyositis 8. Polymyositis 9. Myasthenia gravis 10. Guillain-Barré syndrome 11. Lambert-Eaton myasthenic syndrome 12. Fetal/neonatal alloimmune thrombocytopenia 13. Parvovirus B19-induced pure red cell aplasia 14. Stiff-person syndrome 15. Management of immune checkpoint inhibitor-related toxicities 16. Acquired red cell aplasia 17. Acute disseminated encephalomyelitis 18. Autoimmune mucocutaneous blistering diseases 19. Autoimmune hemolytic anemia 20. Autoimmune neutropenia 21. Birdshot retinochoroidopathy 22. BK virus associated nephropathy 23. Churg-Strauss Syndrome 24. Enteroviral meningoencephalitis 25. Hematophagocytic lymphohistiocytosis (HLH) or macrophage activation syndrome (MAS) 26. Hemolytic disease of newborn 27. HIV-associated thrombocytopenia 28. Hyperimmunoblobulinemia E Syndrome 29. Hypogammaglobulinemia from chimeric antigen receptor T (CAR-T) therapy 30. Multiple myeloma 31. Neonatal hemochromatosis, prophylaxis 32. Opsoclonus-myoclonus 33. Paraneoplastic opsonus-myoclonus ataxia associated with neuroblastoma 34. Post-transfusion purpura 35. Rasmussen encephalitis 36. Renal transplantation from a live donor with ABO incompatibility or positive cross match 37. Secondary immunosuppression associated with major surgery, hematological malignancy, major burns, and collagen-vascular diseases 38. Solid organ transplantation, for allosensitized members 39. Toxic epidermal necrolysis and Stevens-Johnson syndrome 40. Toxic shock syndrome 41. Systemic lupus erythematosus (SLE) 42. Toxic necrotizing fasciitis due to group A streptococcus 43. Measles (Rubeola) prophylaxis 44. Tetanus treatment and prophylaxis 45. Varicella prophylaxis
All other indications are considered experimental/investigational and not medically necessary.
II. DOCUMENTATION The following information is necessary to initiate the prior authorization review: A. Primary immunodeficiency 1. Diagnostic test results a. Copy of laboratory report with serum immunoglobulin levels: IgG, IgA, IgM, and IgG subclasses b. Vaccine response to pneumococcal polysaccharide vaccine (post-vaccination Streptococcus pneumoniae antibody titers) c. Pertinent genetic or molecular testing in members with a known genetic disorder d. Copy of laboratory report with lymphocyte subset enumeration by flow cytometry 2. IgG trough level for those continuing with IG therapy B. Myasthenia gravis 1. Clinical records describing standard treatments tried and failed C. Secondary hypogammaglobulinemia (CLL, HIV, BMT/HSCT recipient) 1. Copy of laboratory report with pre-treatment serum IgG level D. Chronic inflammatory demyelinating polyneuropathy (CIDP) and multifocal motor neuropathy (MMN) 1. Pre-treatment electrodiagnostic studies (electromyography [EMG] or nerve conduction studies [NCS]) E. Dermatomyositis and polymyositis 1. Clinical records describing standard treatments tried and failed F. Lambert-Eaton Myasthenic Syndrome (LEMS) 1. Neurophysiology studies (e.g., electromyography) 2. A positive anti- P/Q type voltage-gated calcium channel antibody test G. Idiopathic thrombocytopenic purpura 1. Laboratory report with pre-treatment/current platelet count 2. Chronic/persistent ITP: copy of medical records supporting trial and failure with corticosteroid or anti-D therapy (unless contraindicated) H. Parvovirus B19-indicated Pure Red Cell Aplasia (PRCA) 1. Copy of test result confirming presence of parvovirus B19 I. Stiff-person syndrome 1. Anti-glutamic acid decarboxylase (GAD) antibody testing results 2. Clinical records describing standard treatments tried and failed J. Toxic shock syndrome or toxic necrotizing fasciitis due to group A streptococcus 1. Documented presence of fasciitis (toxic necrotizing fasciitis due to group A streptococcus only) 2. Microbiological data (culture or Gram stain)
III. CRITERIA FOR INITIAL APPROVAL
A. Primary Immunodeficiency Initial authorization of 6 months may be granted for members with any of the following diagnoses: 1. Severe combined immunodeficiency (SCID) or congenital agammaglobulinemia (e.g., X-linked or autosomal recessive agammaglobulinemia) a. Diagnosis confirmed by genetic or molecular testing, or b. Pretreatment IgG level < 200 mg/dL, or c. Absence or very low number of T cells (CD3 T cells < 300/microliter) or the presence of maternal T cells in the circulation (SCID only)
2. Wiskott-Aldrich syndrome, DiGeorge syndrome, or ataxia-telangiectasia (or other non-SCID combined immunodeficiency) a. Diagnosis confirmed by genetic or molecular testing (if applicable), and b. History of recurrent bacterial infections (e.g., pneumonia, otitis media, sinusitis, sepsis, gastrointestinal), and c. Impaired antibody response to pneumococcal polysaccharide vaccine (see Appendix A)
3. Common variable immunodeficiency (CVID) a. Age 2 years or older, and b. Other causes of immune deficiency have been excluded (e.g., drug induced, genetic disorders, infectious diseases such as HIV, malignancy), and c. Pretreatment IgG level < 500 mg/dL or ≥ 2 SD below the mean for age, and d. History of recurrent bacterial infections, and e. Impaired antibody response to pneumococcal polysaccharide vaccine (see Appendix A)
4. Hypogammaglobulinemia (unspecified), IgG subclass deficiency, selective IgA deficiency, selective IgM deficiency, or specific antibody deficiency a. History of recurrent bacterial infections, and b. Impaired antibody response to pneumococcal polysaccharide vaccine (see Appendix A), and c. Any of the following pre-treatment laboratory findings: i. Hypogammaglobulinemia: IgG < 500 mg/dL or ≥ 2 SD below the mean for age ii. Selective IgA deficiency: IgA level < 7 mg/dL with normal IgG and IgM levels iii. Selective IgM deficiency: IgM level < 30 mg/dL with normal IgG and IgA levels iv. IgG subclass deficiency: IgG1, IgG2, or IgG3 ≥ 2 SD below mean for age assessed on at least 2 occasions; normal IgG (total) and IgM levels, normal/low IgA levels v. Specific antibody deficiency: normal IgG, IgA and IgM levels
5. Other predominant antibody deficiency disorders must meet a., b., and c.i. in section 4. above.
6. Other combined immunodeficiency must meet criteria in section 2. above.
Re-authorization of 12 months may be granted when the following criteria are met: 1. A reduction in the frequency of bacterial infections has been demonstrated since initiation of IG therapy, AND 2. IgG trough levels are monitored at least yearly and maintained at or above the lower range of normal for age (when applicable for indication), OR 3. The prescriber will re-evaluate the dose of IG and consider a dose adjustment (when appropriate).
B. Myasthenia Gravis 1. Authorization of 1 month may be granted to members who are prescribed IG for worsening weakness, acute exacerbation, or in preparation for surgery. a. Worsening weakness includes an increase in any of the following symptoms: diplopia, ptosis, blurred vision, difficulty speaking (dysarthria), difficulty swallowing (dysphagia), difficulty chewing, impaired respiratory status, fatigue, and limb weakness. Acute exacerbations include more severe swallowing difficulties and/or respiratory failure b. Pre-operative management (e.g., prior to thymectomy) 2. Authorization of 6 months may be granted to members with refractory myasthenia gravis who have tried and failed 2 or more of standard therapies (e.g., corticosteroids, azathioprine, cyclosporine, mycophenolate mofetil, rituximab).
C. Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) 1. Initial authorization of 3 months may be granted when the following criteria are met: a. Disease course is progressive or relapsing/remitting for 2 months or longer b. Moderate to severe functional disability c. The diagnosis was confirmed by electrodiagnostic studies 2. Re-authorization of 6 months may be granted when the following criteria are met: a. Significant improvement in disability and maintenance of improvement since initiation of IG therapy b. IG is being used at the lowest effective dose and frequency
D. Dermatomyositis or Polymyositis 1. Initial authorization of 3 months may be granted when the following criteria are met: a. Member has at least 4 of the following: i. Proximal muscle weakness (upper or lower extremity and trunk) ii. Elevated serum creatine kinase (CK) or aldolase level iii. Muscle pain on grasping or spontaneous pain iv. Myogenic changes on EMG (short-duration, polyphasic motor unit potentials with spontaneous fibrillation potentials) v. Positive for anti-synthetase antibodies (e.g., anti-Jo-1, also called histadyl tRNA synthetase) vi. Non-destructive arthritis or arthralgias vii. Systemic inflammatory signs (fever: more than 37°C at axilla, elevated serum CRP level or accelerated ESR of more than 20 mm/h by the Westergren method) viii. Pathological findings compatible with inflammatory myositis (inflammatory infiltration of skeletal evidence of active regeneration may be seen), and b. Standard first-line treatments (corticosteroids) and second-line treatments (immunosuppressants) have been tried but were unsuccessful or not tolerated, or c. Member is unable to receive standard first-line and second-line therapy because of a contraindication or other clinical reason. 2. Re-authorization of 6 months may be granted when the following criterion is met: a. Significant improvement in disability and maintenance of improvement since initiation of IG therapy
E. Idiopathic Thrombocytopenic Purpura ITP/(Immune Thrombocytopenia) 1. Newly diagnosed ITP (diagnosed within the past 3 months) or initial therapy: authorization of 1 month may be granted when the following criteria are met a. Children (< 18 years of age) i. Significant bleeding symptoms (mucosal bleeding or other moderate/severe bleeding) or ii. High risk for bleeding* (see Appendix B), or iii. Rapid increase in platelets is required* (e.g., surgery or procedure) b. Adults (≥ 18 years of age) i. Platelet count < 30,000/mcL, or ii. Platelet count < 50,000/mcL and significant bleeding symptoms, high risk for bleeding or rapid increase in platelets is required*, and iii. Corticosteroid therapy is contraindicated and IG will be used alone or IG will be used in combination with corticosteroid therapy 2. Chronic/persistent ITP (≥ 3 months from diagnosis) or ITP unresponsive to first-line therapy: authorization of 6 months may be granted when the following criteria are met: a. Platelet count < 30,000/mcL, or b. Platelet count < 50,000/mcL and significant bleeding symptoms, high risk for bleeding* or rapid increase in platelets is required*, and c. Relapse after previous response to IG or inadequate response/intolerance/contraindication to corticosteroid or anti-D therapy 3. Adults with refractory ITP after splenectomy: authorization of 6 months may be granted when either of the following criteria is met: a. Platelet count < 30,000/mcL, or b. Significant bleeding symptoms 4. ITP in pregnant women: authorization through delivery may be granted to pregnant women with ITP.
* The member’s risk factor(s) for bleeding (see Appendix B) or reason requiring a rapid increase in platelets must be provided.
F. B-cell Chronic Lymphocytic Leukemia (CLL) 1. Initial authorization of 6 months may be granted when all of the following criteria are met: a. IG is prescribed for prophylaxis of bacterial infections. b. Member has a history of recurrent sinopulmonary infections requiring intravenous antibiotics or hospitalization. c. Member has a pretreatment serum IgG level <500 mg/dL. 2. Re-authorization of 6 months may be granted when a reduction in the frequency of bacterial infections has been demonstrated since initiation of IG therapy.
G. Prophylaxis of Bacterial Infections in HIV-Infected Pediatric Patients 1. Initial authorization of 6 months may be granted to pediatric members with HIV infection when any of the following criteria are met: a. IG is prescribed for primary prophylaxis of bacterial infections and pretreatment serum IgG < 400 mg/dL, or b. IG is prescribed for secondary prophylaxis of bacterial infections for members with a history of recurrent bacterial infections (> 2 serious bacterial infections in a 1-year period), or c. Member has failed to form antibodies to common antigens, such as measles, pneumococcal, and/or Haemophilus influenzae type b vaccine, or d. Member lives in an area where measles is highly prevalent and who have not developed an antibody response after two doses of measles, mumps, and rubella virus vaccine live, or e. Member has been exposed to measles and request is for a single dose, or f. Member has chronic bronchiectasis that is suboptimally responsive to antimicrobial and pulmonary therapy
2. Re-authorization of 6 months may be granted when a reduction in the frequency of bacterial infections has been demonstrated since initiation of IG therapy.
H. Bone marrow transplant/hemopoietic stem cell transplant (BMT/HSCT) 1. Initial authorization of 6 months may be granted to members who are BMT/HSCT recipients when the following criteria are met: a. Therapy will be used to prevent the risk of acute graft-versus-host disease, associated interstitial pneumonia (infectious or idiopathic), septicemia, and other infections (e.g., cytomegalovirus infections [CMV], recurrent bacterial infection) b. Either of the following: i. IG is requested within the first 100 days post- transplant. ii. Member has a pretreatment serum IgG < 400 mg/dL. 2. Re-authorization of 6 months may be granted when a reduction in the frequency of bacterial infections has been demonstrated since initiation of IG therapy.
I. Multifocal Motor Neuropathy (MMN) 1. Initial authorization of 3 months may be granted when the following criteria are met: a. Member experienced progressive, multifocal, asymmetrical weakness without objective sensory loss in 2 or more nerves for at least 1 month b. The diagnosis was confirmed by electrodiagnostic studies 2. Re-authorization of 6 months may be granted when significant improvement in disability and maintenance of improvement have occurred since initiation of IG therapy
J. Guillain-Barre Syndrome (GBS) Authorization of 1 month total may be granted for GBS when the following criteria are met: 1. Member has severe disease with significant weakness (e.g., inability to stand or walk without aid, respiratory weakness) 2. Onset of neurologic symptoms occurred less than 4 weeks from the anticipated start of therapy
K. Lambert-Eaton Myasthenic Syndrome (LEMS) 1. Initial authorization of 6 months may be granted for LEMS when the following criteria are met: a. Diagnosis has been confirmed by either of the following: i. Neurophysiology studies (e.g., electromyography) ii. A positive anti- P/Q type voltage-gated calcium channel antibody test b. Anticholinesterases (e.g., pyridostigmine) and amifampridine (e.g., 3,4-diaminopyridine phosphate, Firdapse) have been tried but were unsuccessful or not tolerated c. Weakness is severe or there is difficulty with venous access for plasmapheresis 2. Re-authorization of 6 months may be granted when member is responding to therapy (i.e., there is stability or improvement in symptoms relative to the natural course of LEMS).
L. Kawasaki Syndrome Authorization of 1 month may be granted for pediatric members with Kawasaki syndrome.
M. Fetal/Neonatal Alloimmune Thrombocytopenia (F/NAIT) Authorization of 6 months may be granted for treatment of F/NAIT.
N. Parvovirus B19-induced Pure Red Cell Aplasia (PRCA) Authorization of 6 months may be granted for severe, refractory anemia associated with bone marrow suppression, with parvovirus B19 viremia.
O. Stiff-person Syndrome Authorization of 6 months may be granted for stiff-person syndrome when the following criteria are met: 1. Diagnosis has been confirmed by anti-glutamic acid decarboxylase (GAD) antibody testing 2. Member had an inadequate response to first-line treatment (benzodiazepines and/or baclofen)
P. Management of immune checkpoint inhibitor-related toxicities Authorization of 1 month may be granted for management of immune checkpoint-inhibitor toxicities when all of the following criteria are met: 1. Member has experienced a moderate or severe adverse event to a PD-1 or PD-L1 inhibitor (e.g., pembrolizumab, nivolumab, atezolizumab, avelumab, durvalumab) 2. The offending medication has been held or discontinued 3. Member experienced one or more of the following nervous system adverse events: myocarditis, bullous dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, pneumonitis, myasthenia gravis, peripheral neuropathy, encephalitis, transverse myelitis, severe inflammatory arthritis, Guillain-Barre syndrome, or steroid-refractory myalgias or myositis
Q. Acquired Red Cell Aplasia Authorization of 6 months may be granted for acquired red cell aplasia.
R. Acute Disseminated Encephalomyelitis Authorization of 1 month may be granted for acute disseminated encephalomyelitis in members who have had an insufficient response or a contraindication to intravenous corticosteroid treatment.
S. Autoimmune Mucocutaneous Blistering Disease Authorization of 6 months may be granted for autoimmune mucocutaneous blistering disease (includes pemphigus vulgaris, pemphigus foliaceus, bullous pemphigoid, mucous membrane pemphigoid, and epidermolysis bullosa aquisita) when the following criteria are met: 1. Diagnosis has been proven by biopsy and confirmed by pathology report, and 2. Condition is rapidly progressing, extensive or debilitating, and 3. Member has failed or experienced significant complications (e.g., diabetes, steroid-induced osteoporosis) from standard treatment (corticosteroids, immunosuppressive agents).
T. Autoimmune Hemolytic Anemia Authorization of 6 months may be granted for warm-type autoimmune hemolytic anemia in members who do not respond or have a contraindication to corticosteroids or splenectomy.
U. Autoimmune Neutropenia Authorization of 6 months may be granted for autoimmune neutropenia where treatment with G-CSF (granulocyte colony stimulating factor) is not appropriate.
V. Birdshot Retinochoroidopathy Authorization of 6 months may be granted for birdshot (vitiliginous) retinochoroidopathy that is not responsive to immunosuppressives (e.g., corticosteroids, cyclosporine).
W. BK Virus Associated Nephropathy Authorization of 6 months may be granted for BK virus associated nephropathy.
X. Churg-Strauss Syndrome Authorization of 6 months may be granted for severe, active Churg-Strauss syndrome as adjunctive therapy for members who have experienced failure, intolerance, or are contraindicated to other interventions.
Y. Enteroviral Meningoencephalitis Authorization of 6 months may be granted for severe cases of enteroviral meningoencephalitis.
Z. Hematophagocytic Lymphohistiocytosis (HLH) or Macrophage Activation Syndrome (MAS) Authorization of 6 months may be granted for treatment of hypogammaglobulinemia in HLH or MAS when total IgG is less than 400 mg/dL or two standard deviations below the mean for age.
AA. Hemolytic Disease of Newborn Authorization of 6 months may be granted for isoimmune hemolytic disease in neonates. BB. HIV-associated Thrombocytopenia Authorization of 6 months may be granted for HIV- associated thrombocytopenia when the following criteria are met: 1. Pediatric members with IgG < 400 mg/dL and has one of the following: a. 2 or more bacterial infections in a 1-year period despite antibiotic chemoprophylaxis with TMP-SMZ or another active agent, or b. Received 2 doses or measles vaccine and lives in a region with a high prevalence or measles, or c. HIV-associated thrombocytopenia despite anti- retroviral therapy, or d. Chronic bronchiectasis that is suboptimally responsive to antimicrobial and pulmonary therapy, or e. T4 cell count ≥ 200/mm3 2. Adult members with significant bleeding, platelet count < 20,000/mcL, and failure of RhIG in Rh-positive patients
CC. Hyperimmunoglobulinemia E Syndrome Authorization of 6 months may be granted to treat severe eczema in hyperimmunoglobulinemia E syndrome.
DD. Hypogammaglobulinemia from CAR-T therapy Authorization of 6 months may be granted for members with IgG < 400 mg/dL receiving treatment with CAR-T therapy (including but not limited to idecabtagene vicleucel [Abecma], tisagenlecleucel [Kymriah], or axicabtagene ciloleucel [Yescarta]).
EE. Multiple Myeloma Authorization of 6 months may be granted for multiple myeloma in members who have recurrent, serious infections despite the use of prophylactic antibiotics.
FF. Neonatal Hemochromatosis Authorization of 6 months may be granted for prophylaxis in members who are pregnant with a history of pregnancy ending in documented neonatal hemochromatosis.
GG. Opsoclonus-myoclonus Authorization of 6 months may be granted for treatment of either of the following: 1. Paraneoplastic opsoclonus-myoclonus-ataxia associated with neuroblastoma 2. Refractory opsoclonus-myoclonus, as last-resort treatment
HH. Post-transfusion Purpura Authorization of 1 month may be granted for post- transfusion purpura.
II. Rasmussen Encephalitis Authorization of 6 months may be granted for Rasmussen encephalitis in members whose symptoms do not improve with anti-epileptic drugs and corticosteroids.
JJ. Renal Transplantation Authorization of 6 months may be granted for a member undergoing renal transplantation from a live donor with ABO incompatibility or positive cross match.
KK. Secondary Immunosuppression Associated with Major Surgery, Hematological Malignancy, Major Burns, and Collagen-Vascular Diseases Authorization of 6 months may be granted to prevent or modify recurrent bacterial or viral infections in members with secondary immunosuppression (IgG < 400 mg/dL) associated with major surgery, hematological malignancy, extensive burns, or collagen-vascular disease.
LL. Solid Organ Transplantation Authorization of 6 months may be granted for solid organ transplantation for allosensitized members.
MM. Toxic Epidermal Necrolysis and Stevens-Johnson Syndrome Authorization of 1 month may be granted for severe cases of toxic epidermal necrolysis or Stevens-Johnson syndrome.
NN. Toxic Shock Syndrome Authorization of 1 month may be granted for staphylococcal or streptococcal toxic shock syndrome when the infection is refractory to several hours of aggressive therapy, an undrainable focus is present, or the member has persistent oliguria with pulmonary edema.
OO. Systemic Lupus Erythematosus Authorization of 6 months may be granted for severe, active SLE in members who have experienced inadequate response, intolerance or have a contraindication to first and second line therapies (e.g., hydroxychloroquine, glucocorticoids, anifrolumab, rituximab).
PP. Measles (Rubeola) prophylaxis Authorization of 1 month may be granted for postexposure prophylaxis to prevent or modify symptoms of measles (rubeola) in susceptible members exposed to the disease less than 6 days previously.
QQ. Tetanus treatment and prophylaxis Authorization of 1 month may be granted for treatment or postexposure prophylaxis of tetanus as an alternative when tetanus immune globulin (TIG) is unavailable.
RR. Varicella prophylaxis Authorization of 1 month may be granted for postexposure prophylaxis of varicella in susceptible individuals when varicella-zoster immune globulin (VZIG) is unavailable.
SS. Toxic Necrotizing Fasciitis Due To Group A Streptococcus Authorization of 1 month may be granted for members with fasciitis due to invasive streptococcal infection.
IV. CONTINUATION OF THERAPY
Authorization may be granted for continuation of therapy when either the following criteria is met: A. For conditions with reauthorization criteria listed under section III: Members who are currently receiving IG therapy must meet the applicable reauthorization criteria for the member’s condition. B. For all other conditions, all members (including new members) must meet initial authorization criteria.
V. APPENDICES
Appendix A: Impaired Antibody Response to Pneumococcal Polysaccharide Vaccine • Age 2 years and older: impaired antibody response demonstrated to vaccination with a pneumococcal polysaccharide vaccine • Not established for children less than 2 years of age • Excludes the therapy initiated in the hospital setting
Appendix B: Examples of Risk Factors for Bleeding (not all inclusive) • Undergoing a medical or dental procedure where blood loss is anticipated • Comorbidity (e.g., peptic ulcer disease, hypertension) • Mandated anticoagulation therapy • Profession or lifestyle predisposes patient to trauma (e.g., construction worker, fireman, professional athlete)
Place of Service:
Outpatient
The above policy is based on the following references:
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Cuvitru [package insert]. Lexington, MA: Baxalta US Inc.; March 2023.
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HyQvia [package insert]. Lexington, MA: Baxalta US Inc.; January 2024.
Xembify [package insert]. Research Triangle Park, NC: Grifols Therapeutics LLC; August 2020.
Asceniv [package insert]. Boca Raton, FL: ADMA Biologics; April 2019.
Bivigam [package insert]. Boca Raton, FL: ADMA Biologics; December 2020.
Flebogamma 10% DIF [package insert]. Los Angeles, CA: Grifols Biologicals, Inc.; September 2019.
Flebogamma 5% DIF [package insert]. Los Angeles, CA: Grifols Biologicals, Inc.; September 2019.
Gammagard Liquid [package insert]. Westlake Village, CA: Baxalta US Inc.; March 2023.
Gammagard S/D [package insert]. Lexington, MA: Baxalta US Inc.; March 2023.
Gammagard S/D IgA less than 1 mcg/mL [package insert]. Westlake Village, CA: Baxalta US Inc.; September 2016.
Gammaked [package insert]. Research Triangle Park, NC: Grifols Therapeutics LLC; January 2020.
Gammaplex 5% [package insert]. Hertfordshire, United Kingdom: Bio Products Laboratory; November 2021.
Gammaplex 10% [package insert]. Hertfordshire, United Kingdom: Bio Products Laboratory; November 2021.
Gamunex-C [package insert]. Research Triangle Park, NC: Grifols Therapeutics Inc.; January 2020.
Octagam 10% [package insert]. Hoboken, NJ: Octapharma USA, Inc.; April 2022.
Octagam 5% [package insert]. Hoboken, NJ: Octapharma USA, Inc.; April 2022.
Panzyga [package insert]. Hoboken, NJ: Octapharma USA.; February 2021.
Privigen [package insert]. Kankakee, IL: CSL Behring LLC; March 2022.
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Van den Bergh PY, Hadden RD, van Doorn PA, et al. European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society - second revision. Eur J Neurol. 2021;28(11):3556-3583.
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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.
