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UnitedHealthcare® West Medical Management Guideline Genetic Testing for Neuromuscular Disorders Guideline Number: MMG165.C Effective Date: May 1, 2021 Instructions for Use Table of Contents Page Related Medical Management Guidelines Coverage Rationale ....................................................................... 1 • Chromosome Microarray Testing (Non-Oncology Documentation Requirements ...................................................... 2 Conditions) Definitions ...................................................................................... 3 • Genetic Testing for Cardiac Disease Applicable Codes .......................................................................... 3 • Whole Exome and Whole Genome Sequencing Description of Services ................................................................. 4 Clinical Evidence ........................................................................... 4 Related Benefit Interpretation Policy U.S. Food and Drug Administration ........................................... 22 • Genetic Testing References ................................................................................... 22 Guideline History/Revision Information ..................................... 26 Instructions for Use ..................................................................... 26 Coverage Rationale Multi-gene panel testing for the diagnosis of Neuromuscular Disorders is proven and medically necessary for the following: Suspected dystroglycanopathy (e.g., Walker Warburg syndrome, muscle-eye-brain disease, Fukuyama congenital muscular dystrophy, congenital muscular dystrophy 1C and 1D) in members with: o Age of onset of symptoms at 2 years old or less; or o Hypotonia, low muscle tone; or o Gross developmental delay; and o Evidence of muscle weakness; and o Elevated serum creatine kinase (CK) levels; and o One or more of the following: . Structural eye abnormalities . Intellectual disabilities . Epilepsy . Brain malformation Suspected congenital muscular dystrophy or myopathy in members with: o Age of onset of symptoms 2 years old or less; or o Hypotonia, low muscle tone; or o Gross developmental delay; and o Evidence of muscle weakness; and o Additional clinical testing such as muscle biopsy or electromyelogram (EMG) is not available or is equivocal and does not aid in the differential diagnosis; and o There is a high likelihood that the condition is inherited; and o Targeted single gene genetic testing is negative; or o The phenotype could be explained by more than one gene found in the requested multi-gene panel Suspected Limb Girdle Muscular Dystrophy (LGMD) in members with: o Muscle weakness or wasting of the shoulders, upper arms, pelvic area, and thighs; and o One or more of the following: Genetic Testing for Neuromuscular Disorders Page 1 of 26 UnitedHealthcare West Medical Management Guideline Effective 05/01/2021 Proprietary Information of UnitedHealthcare. Copyright 2021 United HealthCare Services, Inc. Muscle biopsy is not available or not informative for a specific LGMD sub-type . Initial targeted genetic testing is not informative Suspected glycogen storage disease in members with: o Adolescent or adult with exercise intolerance, muscle weakness, and muscle cramps; and o Normal or equivocal CK results; and o One of the following conditions is met: Exercise testing is unavailable or uninformative; or Muscle biopsy is unavailable or uninformative; or Targeted genetic testing was negative; or o Infant or child with unexplained liver disease, or muscle weakness, or heart dysfunction; and o One of the following conditions is met: o Muscle biopsy is unavailable or uninformative; or o Enzyme testing was unavailable or uninformative; or o Targeted genetic testing was negative Suspected mitochondrial disease in members with: o Progressive external ophthalmoplegia; or o Proximal weakness; or o Muscle cramping, fatigue, or exercise intolerance; and o One of the following conditions is met: o Muscle biopsy or other clinical testing was uninformative; or o Persistently unexplained elevated lactic acid; or o Targeted genetic testing was negative Suspected hereditary peripheral neuropathy in members with: o A high degree of suspicion of having a hereditary neuropathy based on medical history, family history, and other clinical tests; or o Electrodiagnostic testing is not possible, or results are equivocal; or o Targeted genetic testing was negative Suspected hereditary spastic paraplegia (HSP) or ataxia in members with: o Peripheral neuropathy; or o Ataxia; and o One of the following condition is met: . A family history suggestive of a HSP or ataxia where a diagnosis has not been determined; or . Other clinical testing such as routine lab tests, imaging, muscle biopsy, or nerve conduction tests are inconclusive; or . Targeted genetic testing was negative Suspected distal myopathy or myofibrillar in members with: o Muscle weakness or wasting of the distal muscles i.e. hands, feet; and o One or more of the following: . Clinical features do not suggest a specific distal myopathy or myofibrillar sub-type . Muscle biopsy is not informative for a specific distal myopathy or myofibrillar sub-type . Initial targeted genetic testing is not informative . Cardiomyopathy Multi-gene neuromuscular disease panels are unproven and not medically necessary for all other indications due to insufficient evidence of efficacy. Documentation Requirements Benefit coverage for health services is determined by the member specific benefit plan document and applicable laws that may require coverage for a specific service. The documentation requirements outlined below are used to assess whether the member meets the clinical criteria for coverage but do not guarantee coverage of the service requested. Genetic Testing for Neuromuscular Disorders Page 2 of 26 UnitedHealthcare West Medical Management Guideline Effective 05/01/2021 Proprietary Information of UnitedHealthcare. Copyright 2021 United HealthCare Services, Inc. Required Clinical Information Genetic Testing for Neuromuscular Disorders Medical notes documenting all of the following: Personal history of the condition, if applicable, including age at diagnosis Complete family history (usually three-generation pedigree) relevant to condition being tested Genetic testing results of family member, if applicable, and reason for testing Ethnicity/ancestry (e.g., Ashkenazi Jewish), if reason for testing Any prior genetic testing results How clinical management will be impacted based on results of genetic testing Genetic counseling (if available) Definitions Comparative Genomic Hybridization (CGH): CGH is a technology that can be used for the detection of genomic copy number variations (CNVs). Tests can use a variety of probes or single nucleotide polymorphisms (SNPS) to provide copy number and gene differentiating information. All platforms share in common that tumor (patient) and reference DNA are labelled with dyes or fluorescing probes and hybridized on the array, and a scanner measures differences in intensity between the probes, and the data is expressed as having greater or less intensity than the reference DNA (Piluso et al. 2011). Neuromuscular Disorders (NMD): Are group of inherited diseases that represent a number of conditions that result from impairment of nerves that control the muscles, or direct impairment of the muscles (Piluso et al. 2011). Next Generation Sequencing (NGS): High-throughput DNA sequencing of large numbers of genes in a single reaction (Efthymiou et al. 2016) Variant of Unknown Significance (VUS): A variation in a genetic sequence that has an unknown association with disease. It may also be called an unclassified variant (Efthymiou et al. 2016) Whole Exome Sequencing (WES): About 1% of a person’s DNA makes protein. These protein making sections are called exons. All the exons together are called the exome. WES is a DNA analysis technique that looks at all of the exons in a person, or a tissue type such as a tumor, at one time, rather than gene by gene (U.S. National Library of Medicine, 2020a). Whole Genome Sequencing (WGS): WGS determines the sequence of the entire DNA in a person, or a tissue type, such as a tumor, which includes the protein making (coding) as well as non-coding DNA elements (U.S. National Library of Medicine, 2020b). Applicable Codes The following list(s) of procedure and/or diagnosis codes is provided for reference purposes only and may not be all inclusive. Listing of a code in this guideline does not imply that the service described by the code is a covered or non-covered health service. Benefit coverage for health services is determined by the member specific benefit plan document and applicable laws that may require coverage for a specific service. The inclusion of a code does not imply any right to reimbursement or guarantee claim payment. Other Policies and Guidelines may apply. CPT Code Description 0216U Neurology (inherited ataxias), genomic DNA sequence analysis of 12 common genes including small sequence changes, deletions, duplications, short tandem repeat gene expansions, and variants in non- uniquely mappable regions, blood or saliva, identification and categorization of genetic variants 0217U Neurology (inherited ataxias), genomic DNA sequence analysis of 51 genes