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ATTR (transthyretin amyloid) Amyloidosis Prior Authorization with Quantity Limit Program Summary

Policy Number: PH-91107

This program applies to Commercial, Blue Partner, GenPlus, NetResults A series, SourceRx and Health Insurance Marketplace.

POLICY REVIEW CYCLE                                                                                                                                                                           

Effective Date

Date of Origin 

4/1/2024

7/1/2019

FDA APPROVED INDICATIONS AND DOSAGE

Agent(s)

FDA Indication(s)

Notes

Ref#

Tegsedi®

(inotersen)

Subcutaneous injection

Treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis in adults

1

Vyndamax®

(tafamidis)

Capsule

Treatment of the cardiomyopathy of wild type or hereditary transthyretin-mediated amyloidosis (ATTR-CM) in adults to reduce cardiovascular mortality and cardiovascular-related hospitalization

2

Vyndaqel®

(tafamidis meglumine)

Capsule

Treatment of the cardiomyopathy of wild type or hereditary transthyretin-mediated amyloidosis (ATTR-CM) in adults to reduce cardiovascular mortality and cardiovascular-related hospitalization

2

WAINUA™

(eplontersen)

Subcutaneous injection

Treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis in adults

9

See package insert for FDA prescribing information:  https://dailymed.nlm.nih.gov/dailymed/index.cfm

CLINICAL RATIONALE

Amyloidosis

Amyloidosis is a protein disorder in which proteins misfold, then bind together to form amyloid fibrils which deposit into organs.(3) Transthyretin (TTR) is a protein primarily synthesized in the liver and carries thyroxine and retinol-binding protein. Dissociation of TTR followed by aggregation and misfolding of the TTR protein causes formation of insoluble amyloid fibrils. These fibrils deposit systemically, causing multisystem disease with rapidly progressing polyneuropathy and other systemic manifestations, particularly cardiomyopathy.(4,5) There are two types of ATTR (transthyretin amyloid) amyloidosis: hereditary ATTR (hATTR or ATTRm) and wild-type ATTR (ATTRwt). Hereditary ATTR results from an inherited mutation in the DNA that encodes for an unstable TTR protein, making TTR more likely to form amyloid fibrils. Wild-type ATTR is a result of aging and sex; as one gets older, normal TTR protein becomes unstable, misfolding and forming amyloid fibrils.(3)

Neuropathy

A range of sensory and motor impairments are reported by patients with hATTR amyloidosis with polyneuropathy. The most common of these include neuropathic pain, altered sensation (i.e., decreased pain sensation), numbness, and tingling, along with muscle weakness and impaired balance which lead to difficulty walking. The pathologic process typically involves small-fiber damage early in the disease course, often with subsequent damage to peripheral motor and sensory nerves that results in sensorimotor polyneuropathy. Autonomic impairment is also frequently observed, and includes nausea and vomiting, changes in gastrointestinal motility, orthostatic hypotension, bladder dysfunction, and erectile dysfunction. Historically, measuring the disease has utilized the Familial Amyloidotic Polyneuropathy (FAP) staging system and/or the polyneuropathy disability (PND) scoring system. However, these scales provide only a generic indicator of overall disease status and are not sensitive to track disease progression in the short-term period. Recently developed and used in hATTR amyloidosis studies is the modified Neuropathy Impairment Score +7 (NIS+7). This system is highly standardized, quantitative, and referenced assessments to quantify decreased muscle weakness, muscle stretch reflexes, sensory loss, and autonomic impairment. NIS+7 is more sensitive to disease progression over shorter time periods and better at capturing the different features of polyneuropathy. This scale has been further modified (mNIS+7 Alnylam and mNIS+7 Ionis) to afford more sensitive detection of disease progression.(5,7)

Diagnosis of hATTR neuropathy can be challenging without positive family history as clinical presentation may mimic various peripheral neuropathies. In patients with peripheral neuropathy of otherwise undetermined etiology, early search for associated clinical features, especially cardiac involvement can help reveal amyloidosis. Diagnosis can be confirmed by demonstration of amyloid in a biopsy sample and/or detection of any amyloidogic mutation by TTR genetic testing.(7)

Cardiomyopathy

Cardiomyopathy is a manifestation of ATTR amyloidosis in which transthyretin protein misfolds to form fibrils that deposit in the myocardium, leading to cardiomyopathy and symptoms of heart failure. Transthyretin amyloid cardiomyopathy (ATTR-CM) is a late-onset disease; symptoms are predominately manifested in male patients 60 years of age or older. The condition can be inherited as an autosomal dominant trait caused by pathogenic mutations in the transthyretin gene TTR (ATTRm) or by the deposition of wild-type transthyretin protein (ATTRwt). There are more than 120 pathogenic mutations in TTR that result in a variable phenotypic presentation. The prevalence of ATTRwt is uncertain, some studies have reported a prevalence of 13% among patients with heart failure with a preserved ejection fraction, 16% among patients undergoing transcatheter aortic-valve replacement for severe aortic stenosis, and 5% among patients with presumed hypertrophic cardiomyopathy. Treatments have previously been limited to supportive care.  Median survival in untreated patients is reported to be 2.5 years after diagnosis for ATTRm caused by the TTR Val122Ile mutation and 3.6 years for ATTRwt.(6) Patients with ATTR-CM often show common signs and symptoms of heart failure, such as dyspnea, orthopnea, paroxysmal nocturnal dyspnea, edema, fatigue, exercise intolerance, dizziness/syncope, palpitations, electrical conduction abnormalities, and arrhythmias. Therefore, ATTR-CM is sometimes mistakenly diagnosed as hypertrophic cardiomyopathy or as generic, undifferentiated heart failure with preserved ejection fraction rather than as amyloidosis.(6,8)

Patients with suspected ATTR-CM should include testing for monoclonal protein followed by scintigraphy or biopsy. Nuclear imaging can also be performed for additive information. In some cases, endomyocardial biopsy is necessary for a definitive diagnosis but if no monoclonal protein is detected and a diagnosis of light chain amyloidosis (AL) has been ruled out, scintigraphy alone can definitively diagnose ATTR-CM. If ATTR-CM is identified, TTR genotyping should be performed.(8)

Efficacy

Inotersen is an antisense oligonucleotide (ASO) that causes degradation of mutant and wild-type transthyretin (TTR) mRNA through binding to the TTR mRNA, which results in a reduction of serum TTR protein and TTR protein deposits in tissues. The efficacy of Tegsedi was demonstrated in the NEURO-TTR trial, a randomized, double-blind, placebo-controlled, multicenter clinical trial in adult patients with polyneuropathy cause by hATTR amyloidsis (Study 1; NCT 01737398) Patients were randomized  in a 2:1 ratio to receive either Tegsedi (113 patients) or placebo (60 patients), as a subcutaneous injection once per week for 65 weeks. Seventy seven percent of Tegsedi-treated patients and 87% of patients on placebo completed 66 weeks. Patients were FAP stage 1 or 2 (ambulatory or ambulatory with assistance, respectively) and had no prior liver transplant or anticipated liver transplant within 1 year of screening. Primary endpoints were the change in the mNIS+7 score and the change in the Norfolk QoL-DN score. At 66 weeks, both primary efficacy assessments favored inotersen. The least squares mean change from baseline was -19.7 points (95% CI, -26.4 to -13.0; p<0.001) for the mNIS+7 and -11.7 points (95% CI, -18.3 to -5.1; P<0.001) for the Norfolk QoL-DN score.(1)

Tafamidis is a selective stabilizer of TTR. Tafamidis binds to TTR at the thyroxine binding sites, stabilizing the tetramer and slowing dissociation into monomers, the rate-limiting step in the amyloidogenic process. Efficacy was demonstrated in a multicenter, international, randomized, double-blind, placebo-controlled study in 441 patients with wild type or hereditary ATTR-cardiomyopathy (ATTR-CM), with no prior liver or heart transplantation. Patients were randomized in a 1:2:2 ratio to receive Vyndaqel 20 mg (88 patients), Vyndaqel 80 mg (176 patients), or placebo (177 patients) once daily for 30 months, in addition to standard of care (e.g., diuretics). Treatment assignment was stratified by the presence or absence of a variant TTR genotype as well as baseline disease severity (NYHA Class). The primary analysis points were all-cause mortality and frequency of cardiovascular-related hospitalizations. The analysis demonstrated a significant reduction in all-cause mortality and frequency of cardiovascular-related hospitalizations in the pooled Vyndaqel group.(2)

Eplontersen is a transthyretin-directed ASO that causes degradation of mutant and wild-type TTR mRNA through binding to the TTR mRNA, which results in a reduction of serum TTR protein and TTR protein deposits in tissues. The efficacy of WAINUA was demonstrated in a randomized, open-label, multicenter trial and adult patients with polyneuropathy caused by hATTR amyloidosis (Study 1; NCT04136184). Patients were randomized in a 6:1 ration to receive subcutaneous injections of either 45mg of WAINUA once every 4 weeks (144 patients), or 284mg of inotersen once weekly (24 patients), respectively. Efficacy assessments were based on a comparison of the WAINUA arm of Study 1 with an external placebo group (60 patients) from another study (NCT01737398) of a comparable population of adult patients with the same indication. Endpoint was change from baseline to week 35 in the mNIS+7 composite score and change from baseline to week 35 in the QoL-DN total score. Treatment with WAINUA resulted in statistically significant improvements in the mNIS+7 and Norfolk QoL-DH total scores compared to placebo control (p<0.001) at week 35. The least squares mean change from baseline was -9.0 points (95% CI, -13.5 to -4.5; p<0.001) for the mNIS+7 and -11.8 points (95% CI, -16.5 to -6.8; P<0.001) for the Norfolk QoL-DN score.(9)

Safety

Tegsedi has a the following boxed warnings:(1)

  • Thrombocytopenia: Tegsedi causes reductions in platelet count that may result in sudden and unpredictable thrombocytopenia, which can be life-threatening. Tegsedi is contraindicated in patients with a platelet count below 100 x 10^9/L. Prior to starting Tegsedi, obtain a platelet count. During treatment, monitor platelet counts weekly if values are 75 x 10^9/L or greater, and more frequently if values are less than 75 x10^9/L.
  • Glomerulonephritis: Tegsedi can cause glomerulonephritis that may require immunosuppressive treatment and may result in dialysis-dependent renal failure. Tegsedi should generally not be initiated in patients with urinary protein to creatinine ratio (UPCR) of 1000 mg/g or higher. Prior to starting Tegsedi, measure serum creatinine, estimated glomerular filtration rate (eGFR), UPCR, and perform a urinalysis. During treatment, monitor serum creatinine, eGFR urinalysis, and UPCR every two weeks. Tegsedi should not be given to patients who develop a UPCR of 1000 mg/g or higher, or eGFR below 45 mL/minute/1.73 m^2, pending further evaluation of the cause. If a dose is held, once eGFR increases to greater than or equal to 45 mL/minute/1.73 m^2, UPCR decreases to below 1000 mg/g, or the underlying cause of the decline in renal function is corrected, weekly dosing may be reinitiated. In patients with UPCR of 2000 mg/g or higher, perform further evaluation for acute glomerulonephritis, as clinically indicated. If acute glomerulonephritis is confirmed, Tegsedi should be permanently discontinued. 
  • Tegsedi REMS Program: Because of the risks of serious bleeding caused by severe thrombocytopenia and because of glomerulonephritis, both of which require frequent monitoring, Tegsedi is available only through a restricted distribution program under a Risk Evaluation and Mitigation Strategy (REMS).

Tegsedi has the following contraindications:(1)

  • Platelet count below 100 x10^9/L
  • History of acute glomerulonephritis caused by inotersen
  • History of a hypersensitivity reaction to inotersen

Vyndaqel and Vyndamax have no FDA labeled contraindications for use.(2)

WAINUA has no FDA labeled contraindications for use.(9)

REFERENCES                                                                                                                                                                            

Number

Reference

1

Tegsedi prescribing Information. Akcea Pharmaceuticals, Inc. June 2022.

2

Vyndaqel and Vyndamax prescribing information. Pfizer Inc. April 2023.

3

Cleveland Clinic. Amyloidosis: ATTR. https://my.clevelandclinic.org/health/diseases/17855-amyloidosis-attr

4

Kapoor M, Rossor AM, Laura M, et al. Clinical Presentation, Diagnosis and Treatment of TTR Amyloidosis. Journal of Neuromuscular Diseases. 6 (2019) 189-199. https://content.iospress.com/download/journal-of-neuromuscular-diseases/jnd180371?id=journal-of-neuromuscular-diseases%2Fjnd180371

5

Dyck PJ, Gonzalez-Duarte A, Obici L, et al. Development of Measures of Polyneuropathy Impairment in hATTR Amyloidosis: From NIS to mNIS+7. Journal of the Neurological Sciences. Volume 405, 15 October 2019. https://www.sciencedirect.com/science/article/pii/S0022510X19303569 

6

Maurer MS, Schwartz JH, Gundapeneni B, et al. Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy. N Engl J Med 2018; 379:1007-16. https://www.nejm.org/doi/full/10.1056/NEJMoa1805689

7

Luigetti M, Romano A, Di Paolantonio A, Bisogni G, Sabatelli M. Diagnosis and Treatment of Hereditary Transthyretin Amyloidosis (hATTR) Polyneuropathy: Current Perspectives on Improving Patient Care. Ther Clin Risk Manag. 2020;16:109-123. doi:10.2147/TCRM.S219979.

8

Maurer MS, Bokhari S, Damy T, et al. Expert Consensus Recommendations for the Suspicion and Diagnosis of Transthyretin Cardiac Amyloidosis. Circ Heart Fail. 2019;12(9):e006075. doi:10.1161/CIRCHEARTFAILURE.119.006075.

9

WAINUA prescribing information. AstraZeneca Pharmaceuticals LP. December 2023. 

POLICY AGENT SUMMARY PRIOR AUTHORIZATION

Target Brand Agent(s)

Target Generic Agent(s)

Strength

Targeted MSC

Available MSC

Final Age Limit

Preferred Status

Wainua

eplontersen sodium subcutaneous soln auto-inj

45 MG/0.8ML

M ; N ; O ; Y

N

Tegsedi

inotersen sod subcutaneous pref syr

284 MG/1.5ML

M ; N ; O ; Y

N

Vyndamax

tafamidis cap

61 MG

M ; N ; O ; Y

N

Vyndaqel

tafamidis meglumine (cardiac) cap

20 MG

M ; N ; O ; Y

N

POLICY AGENT SUMMARY QUANTITY LIMIT

Target Brand Agent Name(s)

Target Generic Agent Name(s)

Strength

QL Amount

Dose Form

Day Supply

Duration

Addtl QL Info

Allowed Exceptions

Targeted NDCs When Exclusions Exist

Tegsedi

Inotersen Sod Subcutaneous Pref Syr 284 MG/1.5ML (Base Eq)

284 MG/1.5ML

4

Syringes

28

DAYS

Vyndamax

Tafamidis Cap 61 MG

61 MG

30

Capsules

30

DAYS

Vyndaqel

Tafamidis Meglumine (Cardiac) Cap 20 MG

20 MG

120

Capsules

30

DAYS

Wainua

eplontersen sodium subcutaneous soln auto-inj

45 MG/0.8ML

1

Pen

30

DAYS

CLIENT SUMMARY – PRIOR AUTHORIZATION

Target Brand Agent Name(s)

Target Generic Agent Name(s)

Strength

Client Formulary

Tegsedi

inotersen sod subcutaneous pref syr

284 MG/1.5ML

Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx

Vyndamax

tafamidis cap

61 MG

Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx

Vyndaqel

tafamidis meglumine (cardiac) cap

20 MG

Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx

Wainua

eplontersen sodium subcutaneous soln auto-inj

45 MG/0.8ML

Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx

CLIENT SUMMARY – QUANTITY LIMITS

Target Brand Agent Name(s)

Target Generic Agent Name(s)

Strength

Client Formulary

Tegsedi

Inotersen Sod Subcutaneous Pref Syr 284 MG/1.5ML (Base Eq)

284 MG/1.5ML

Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx

Vyndamax

Tafamidis Cap 61 MG

61 MG

Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx

Vyndaqel

Tafamidis Meglumine (Cardiac) Cap 20 MG

20 MG

Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx

Wainua

eplontersen sodium subcutaneous soln auto-inj

45 MG/0.8ML

Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx

PRIOR AUTHORIZATION CLINICAL CRITERIA FOR APPROVAL

Module

Clinical Criteria for Approval

Initial Evaluation

Target Agent(s) will be approved when ALL of the following are met:

  1. The patient has ONE of the following:
    1. ALL of the following:
      1. A diagnosis of polyneuropathy of hereditary transthyretin-mediated amyloidosis confirmed by testing (e.g., genetic testing, biopsy) AND
      2. The requested agent is FDA approved for use in polyneuropathy of hereditary transthyretin-mediated amyloidosis AND
      3. The patient has clinical manifestations of polyneuropathy (e.g., neuropathic pain, altered sensation, numbness, tingling, impaired balance, motor disability) OR
    2. ALL of the following:
      1. A diagnosis of cardiomyopathy of wild type or hereditary transthyretin-mediated amyloidosis confirmed by testing [e.g., stannous pyrophosphate (PYP) scanning, monoclonal antibody studies, biopsy, scintigraphy, genetic testing (TTR genotyping)] AND
      2. The requested agent is FDA approved for use in cardiomyopathy of wild type or hereditary transthyretin-mediated amyloidosis AND
      3. The patient has clinical manifestations of cardiomyopathy (e.g., dyspnea, fatigue, orthostatic hypotension, syncope, peripheral edema) OR
    3. The patient has another FDA approved indication for the requested agent and route of administration AND
  2. If the patient has an FDA approved indication, then ONE of the following:
    1. The patient’s age is within FDA labeling for the requested indication for the requested agent OR
    2. The prescriber has provided information in support of using the requested agent for the patient’s age for the requested indication AND
  3. The patient has NOT received a liver transplant AND
  4. The prescriber is a specialist in the area of the patient’s diagnosis (e.g., cardiologist, geneticist, neurologist) or the prescriber has consulted with a specialist in the area of the patient’s diagnosis AND
  5. The patient will NOT be using the requested agent in combination with another agent targeted in this program, Onpattro (patisiran), OR Amvuttra (vutrisiran) for the requested indication AND
  6. The patient does NOT have any FDA labeled contraindications to the requested agent 

Length of Approval: 12 months

NOTE: If Quantity Limit applies, please refer to Quantity Limit Criteria.

 

Renewal Evaluation

Target Agent(s) will be approved when ALL of the following are met:

  1. The patient has been previously approved for the requested agent through the plan’s Prior Authorization process AND
  2. The patient has had clinical benefit with the requested agent AND
  3. The prescriber is a specialist in the area of the patient’s diagnosis (e.g., cardiologist, geneticist, neurologist) or the prescriber has consulted with a specialist in the area of the patient’s diagnosis AND
  4. The patient has NOT received a liver transplant AND
  5. The patient will NOT be using the requested agent in combination with another agent targeted in this program, Onpattro (patisiran), OR Amvuttra (vutrisiran) for the requested indication AND
  6. The patient does NOT have any FDA labeled contraindications to the requested agent

Length of Approval: 12 months

NOTE: If Quantity Limit applies, please refer to Quantity Limit Criteria.

QUANTITY LIMIT CLINICAL CRITERIA FOR APPROVAL

Module

Clinical Criteria for Approval

QL with PA

Quantity Limit for the Target Agent(s) will be approved when ONE of the following is met:

  1. The requested quantity (dose) does NOT exceed the program quantity limit OR
  2. ALL of the following:
    1. The requested quantity (dose) exceeds the program quantity limit AND
    2. The requested quantity (dose) does NOT exceed the maximum FDA labeled dose for the requested indication AND
    3. The requested quantity (dose) cannot be achieved with a lower quantity of a higher strength that does NOT exceed the program quantity limit

Length of Approval: 12 months

This pharmacy policy is not an authorization, certification, explanation of benefits or a contract. Eligibility and benefits are determined on a case-by-case basis according to the terms of the member’s plan in effect as of the date services are rendered. All pharmacy policies are based on (i) information in FDA approved package inserts (and black box warning, alerts, or other information disseminated by the FDA as applicable); (ii) research of current medical and pharmacy literature; and/or (iii) review of common medical practices in the treatment and diagnosis of disease as of the date hereof. Physicians and other providers are solely responsible for all aspects of medical care and treatment, including the type, quality, and levels of care and treatment.

The purpose of Blue Cross and Blue Shield of Alabama’s pharmacy policies are to provide a guide to coverage. Pharmacy policies are not intended to dictate to physicians how to practice medicine. Physicians should exercise their medical judgment in providing the care they feel is most appropriate for their patients.

Neither this policy, nor the successful adjudication of a pharmacy claim, is guarantee of payment.

 

 

 

ALBP _  Commercial _ PS _ ATTR_Amyloidosis_PAQL _ProgSum_ 04-01-2024