FibroTest/FibroSURE (ARCHIVED)

Policy ID: L-223-001

Section: Laboratory

Effective Date: July 01, 2018

Revised Date: May 14, 2018

Revision Effective Date: January 01, 2020

Last Reviewed: May 20, 2021

Applies To: Commercial and Medicaid Expansion

This policy has been archived effective January 1, 2020. Click the archive tab above for more information.

Policy ID: L-223-001

Section: Laboratory

Effective Date: July 01, 2018

Revised Date: May 14, 2018

Revision Effective Date: January 01, 2020

Last Reviewed: May 20, 2021

Archived Date: January 01, 2020

Applies To: Commercial Only

BCBSND contracts with eviCore for its Laboratory Management Program. eviCore is an independent company providing specific medical policy and precertification services to BCBSND. Effective January 1, 2020, Lab Management (molecular and genomic testing) is delegated to eviCore.

Description

FibroTest (licensed in the United States as FibroSURE) is a serum biomarker test. It was developed to be an alternative to liver biopsy in the assessment of liver fibrosis for individuals with chronic viral hepatitis B or C, alcoholic liver disease, and metabolic steatohepatitis (for those who are overweight, have diabetes, or hyperlipidemia).

This policy is designed to address medical guidelines that are appropriate for the majority of individuals with a particular disease, illness, or condition. Each person's unique clinical circumstances may warrant individual consideration, based on review of applicable medical records.

Criteria

Coverage is subject to the specific terms of the member's benefit plan.

The FibroSure test to assess liver fibrosis is considered experimental/investigational, and therefore, non-covered because the safety and/or effectiveness of this service cannot be established by the available published peer-reviewed literature.

Experimental/Investigational (E/I) molecular and genomic (MolGen) tests refer to assays involving chromosomes, DNA, RNA, or gene products that have insufficient data to determine the net health impact, which typically means there is insufficient data to support that a test accurately assesses the outcome of interest (analytical and clinical validity), significantly improves health outcomes (clinical utility), and/or performs better than an existing standard of care medical management option. Such tests are also not generally accepted as standard of care in the evaluation or management of a particular condition.
In the case of MolGen testing, FDA clearance is not a reliable standard given the number of laboratory developed tests that currently fall outside of FDA oversight and FDA clearance often does not assess clinical utility.

Procedure Codes

81599

Professional Statements and Societal Positions

No specific evidence-based U.S. testing guidelines were identified.
World Health Organization (2016): The recommendations in the WHO document entitled Guidelines for the Screening, Care and Treatment of Persons with Chronic Hepatitis C Infection differ slightly than the recommendations in the 2015 document on HBV. The 2015 document lists FibroSURE as a possibility in settings where resources are not an issue, whereas the 2016 document does not make that same recommendation:
- Assessing degree of liver fibrosis and cirrhosis: in resource-limited settings, it is suggested that the aminotransferase/platelet ratio index (APRI) or FIB-4 tests be used for the assessment of hepatic fibrosis rather than other noninvasive tests that require more resources such as elastography or FibroTest. (Conditional recommendation, low quality of evidence)
World Health Organization (2015): In the WHO guidelines for chronic hepatitis B treatment, FibroSURE is listed as a possible non-invasive assessment tool for staging liver disease:
- Aspartate aminotransferase (AST)-to-platelet ratio index (APRI) is recommended as the preferred non-invasive test (NIT) to assess for the presence of cirrhosis (APRI score >2 in adults) in resource limited settings. Transient elastography (e.g., FibroScan) or FibroTest may be the preferred NITs in settings where they are available and cost is not a major constraint. (Conditional recommendation, low quality of evidence)
European Association for the Study of the Liver (EASL) (2015): In the guidelines entitled Non-invasive test for evaluation of liver disease severity and prognosis, EASL discusses the pros and cons of serum biomarkers of liver disease. The document states that further validation is warranted.
World Gastroenterology Organization (2014): In recommendations on Esophageal varices, the WGO states that the predictive accuracy is still unsatisfactory for noninvasive markers such as FibroSURE.
British HIV Association (2013): The Writing Group suggests hepatic transient elastography (TE) (FibroScan or Acoustic Radiation Force Impulse [ARFI]) as the non-invasive investigation of choice (2B) but if unavailable, or when reliable TE readings are not obtained, a blood panel test (aspartate transaminase to platelet ratio index [APRI], FIB-4, enhanced liver fibrosis [ELF], Fibrometer, Forns Index, FibroTest) as an alternative (2C).
Several systematic reviews evaluating evidence of FibroSURE have pooled results of multiple studies; one review found AUROCs in the range of 0.75 to 0.84 for fibrosis; from 0.81-0.92 for cirrhosis in individuals with HCV; 0.72-0.90 for detecting fibrosis; and from 0.75-0.92 for detecting cirrhosis in individuals with HBV. Another systematic review reported an HSROC of 0.84 for fibrosis, and 0.87 for cirrhosis in individuals with HBV. A pooled meta-analysis estimated a sensitivity of 71.2% and a specificity of 81.4% in individuals with HBV. In individuals with ALD, the sensitivity for detecting fibrosis was 85% and specificity was 66%; for detecting cirrhosis, sensitivity rose to 91% and specificity to 87%. Different analysis methods resulted in different AUROCs for diagnosing NAFLD; a weighting method produced an AUROC of 0.85, while a random effects model yielded an AUROC of 0.72. Despite many different types of studies and analysis methods, the diagnostic accuracy of FibroSURE seems generally seems to fall within a consistent, albeit moderate range. FibroSURE also generally seems to perform better in diagnosing cirrhosis than fibrosis.
FibroSURE is intended as an alternative to liver biopsy, currently considered the gold standard for staging liver fibrosis and cirrhosis. As a blood-based test, FibroSURE is an appealing alternative to the invasive nature of a biopsy. However, the evidence as a whole is insufficient and does not yet fully support using FibroSURE as a stand-alone test. Furthermore, several guideline organizations have published evidence-based recommendations regarding the treatment of liver disease and do not definitively recommend FibroSURE as a first-line choice; instead, they recommend the test as an alternative after other preferred tests, or in settings where resources are not constrained.

Diagnosis Codes

Not Applicable

Professional Statements and Societal Positions Guidelines

Not Applicable

ND Committee Review

Internal Medical Policy Committee 5-20-21 ND will archive their policy since the 1 code in the policy is in ND010; meaning all those codes are eviCore codes.

Links

Not Applicable

Disclaimer

Current medical policy is to be used in determining a Member's contract benefits on the date that services are rendered. Contract language, including definitions and specific inclusions/exclusions, as well as state and federal law, must be considered in determining eligibility for coverage. Members must consult their applicable benefit plans or contact a Member Services representative for specific coverage information. Likewise, medical policy, which addresses the issue(s) in any specific case, should be considered before utilizing medical opinion in adjudication. Medical technology is constantly evolving, and the Company reserves the right to review and update medical policy periodically.

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FibroTest/FibroSURE (ARCHIVED)

This policy has been archived effective January 1, 2020. Click the archive tab above for more information.

Description

Criteria

Procedure Codes

Professional Statements and Societal Positions

Diagnosis Codes

Professional Statements and Societal Positions Guidelines

ND Committee Review

Links

Disclaimer