New Data Presented at CHEST 2023 Demonstrate the Clinical Utility of Veracyte’s Envisia Genomic Classifier for Patients with Interstitial Lung Disease

Two studies highlight the value of adding Envisia results to standard-of-care procedures for identifying patients at increased risk of progressive disease


Veracyte, Inc. (Nasdaq: VCYT) today announced that new data presented at the American College of Chest Physicians (CHEST) Annual Meeting 2023 demonstrate the clinical utility of the company’s Envisia Genomic Classifier, which is used by physicians to improve diagnostic and prognostic confidence of interstitial lung diseases. The studies also underscore the challenge of identifying usual interstitial pneumonia (UIP) in patients being evaluated for ILD.

Interstitial lung disease is a broad group of disorders that lead to fibrosis, or scarring, of the lungs. People with ILD may find it difficult to breathe, and their condition often worsens over time. Among patients who have ILD, it is essential to identify those with UIP, which is a hallmark of idiopathic pulmonary fibrosis and is also associated with ILDs that are more likely to progress over time. Knowing that UIP is present may help a physician make more-informed treatment recommendations for their patients with ILD. However, UIP can be difficult to diagnose because it is challenging to detect using the standard approach of high-resolution computerized tomography (HRCT) and pathology-based diagnoses from a procedure such as cryobiopsy.

The studies presented at the CHEST Annual Meeting show that adding the Envisia Genomic Classifier to the diagnostic process can improve the ability to detect UIP.

In an independent study, researchers at UCLA Health evaluated electronic medical records for 83 patients to determine whether adding the Envisia Genomic Classifier to transbronchial lung cryobiopsy (TBLC) testing altered the diagnostic yield for UIP. Using just TBLC, a clear diagnosis could be made for only 46% of patients. That rate was even lower for patients with indeterminate HRCT results (23%). Adding results from the Envisia Genomic Classifier improved the diagnostic yield in both cases. Overall, combining the cryobiopsy procedure with the genomic classifier allowed for a diagnosis in 61% of cases. For patients with indeterminate HRCT results, adding the Envisia Genomic Classifier more than doubled the UIP diagnostic yield to 49%.

“We found that incorporating Envisia testing significantly increased the diagnostic yield of cryobiopsy for ILD in our overall cohort, as well as in the patients with indeterminate results on high-resolution CT,” said Augustine Chung, M.D., pulmonary director of the Connective Tissue Disease-Interstitial Lung Disease Clinic at UCLA Health and an author of the study. “A higher diagnostic yield could help physicians recommend the most appropriate treatment for their patients with ILD.”

The second study focused on the potentially subjective nature of results found on HRCT that was performed on patients with suspected ILD. Two expert thoracic radiologists independently reviewed and interpreted tomography scans for 74 cases of ILD, using the criteria recommended by current guidelines to look for the presence of UIP. Their conclusions were then compared to better understand variability between readers. The analysis showed that results were concordant in just 61% of cases, indicating that CT results may be less reliable than expected when used without a complementary test such as the Envisia Genomic Classifier. The lack of agreement was especially pronounced among cases that did not meet criteria for “typical” UIP, with concordance on “Probable UIP” seen in only 50% of cases and concordance on “Indeterminate for UIP” seen in 0% of cases.

“Collectively, these studies underscore the clinical value of the Envisia Genomic Classifier test for helping physicians determine whether UIP is present in patients with ILD,” said Bill Bulman, M.D., Veracyte’s medical director for Pulmonology. “They also support the clinical utility of using the Envisia test as a complement to current diagnostic procedures to improve ILD diagnostic and prognostic confidence.”